P41182
Gene name |
BCL6 (BCL5, LAZ3, ZBTB27, ZNF51) |
Protein name |
B-cell lymphoma 6 protein |
Names |
BCL-6, B-cell lymphoma 5 protein, BCL-5, Protein LAZ-3, Zinc finger and BTB domain-containing protein 27, Zinc finger protein 51 |
Species |
Homo sapiens (Human) |
KEGG Pathway |
hsa:604 |
EC number |
|
Protein Class |
|

Descriptions
The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.
Autoinhibitory domains (AIDs)
Target domain |
|
Relief mechanism |
|
Assay |
cis-regPred |
Accessory elements
No accessory elements
Autoinhibited structure

Activated structure

109 structures for P41182
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
1R28 | X-ray | 220 A | A/B | 5-129 | PDB |
1R29 | X-ray | 130 A | A | 5-129 | PDB |
1R2B | X-ray | 220 A | A/B | 5-129 | PDB |
2EN2 | NMR | - | A | 598-626 | PDB |
2EOS | NMR | - | A | 626-654 | PDB |
2LCE | NMR | - | A | 540-602 | PDB |
2YRM | NMR | - | A | 515-544 | PDB |
3BIM | X-ray | 260 A | A/B/C/D/E/F/G/H | 5-129 | PDB |
3E4U | X-ray | 210 A | A/B/C/D/E/F | 5-129 | PDB |
3LBZ | X-ray | 230 A | A/B | 5-129 | PDB |
4CP3 | X-ray | 230 A | A/B | 9-128 | PDB |
4U2M | X-ray | 223 A | A/B/C/D | 5-129 | PDB |
5H7G | X-ray | 185 A | A/B | 5-129 | PDB |
5H7H | X-ray | 195 A | A | 5-129 | PDB |
5MW2 | X-ray | 235 A | A | 5-129 | PDB |
5MW6 | X-ray | 165 A | A/B | 5-129 | PDB |
5MWD | X-ray | 185 A | A | 5-129 | PDB |
5N1X | X-ray | 172 A | PDB | ||
5N1Z | X-ray | 181 A | A | 6-128 | PDB |
5N20 | X-ray | 138 A | A | 6-128 | PDB |
5N21 | X-ray | 158 A | A/B | 7-128 | PDB |
5X4M | X-ray | 165 A | A | 5-129 | PDB |
5X4N | X-ray | 194 A | A | 5-129 | PDB |
5X4O | X-ray | 205 A | A | 5-129 | PDB |
5X4P | X-ray | 206 A | A | 5-129 | PDB |
5X4Q | X-ray | 200 A | A | 5-129 | PDB |
5X9O | X-ray | 158 A | A | 5-129 | PDB |
5X9P | X-ray | 186 A | A | 5-129 | PDB |
6C3L | X-ray | 146 A | A/B | 5-129 | PDB |
6C3N | X-ray | 253 A | A/B | 1-129 | PDB |
6CQ1 | X-ray | 170 A | A/B | 1-129 | PDB |
6EW6 | X-ray | 139 A | A | 6-128 | PDB |
6EW7 | X-ray | 160 A | A/B | 7-128 | PDB |
6EW8 | X-ray | 184 A | A | 6-129 | PDB |
6TBT | X-ray | 163 A | A/B | 6-129 | PDB |
6TCJ | X-ray | 213 A | A/B | 6-129 | PDB |
6TOF | X-ray | 167 A | A | 5-129 | PDB |
6TOG | X-ray | 169 A | A | 5-129 | PDB |
6TOH | X-ray | 158 A | A | 5-129 | PDB |
6TOI | X-ray | 158 A | A | 5-129 | PDB |
6TOJ | X-ray | 185 A | A | 5-129 | PDB |
6TOK | X-ray | 143 A | A | 5-129 | PDB |
6TOL | X-ray | 164 A | A | 5-129 | PDB |
6TOM | X-ray | 190 A | A | 5-129 | PDB |
6TON | X-ray | 236 A | A | 5-129 | PDB |
6TOO | X-ray | 153 A | A | 5-129 | PDB |
6XMX | EM | 370 A | A/B/C/D/E/F/G/H | 5-360 | PDB |
6XWF | X-ray | 160 A | A | 6-129 | PDB |
6XXS | X-ray | 325 A | A/B/E/F | 6-129 | PDB |
6XYX | X-ray | 144 A | A/B | 6-129 | PDB |
6XZZ | X-ray | 139 A | A | 6-129 | PDB |
6Y17 | X-ray | 156 A | A/B | 6-129 | PDB |
6ZBU | X-ray | 246 A | A/B/E/F/I/J | 6-129 | PDB |
7BDE | X-ray | 204 A | A | 5-129 | PDB |
7LWE | X-ray | 117 A | A | 1-129 | PDB |
7LWF | X-ray | 122 A | A | 5-129 | PDB |
7LWG | X-ray | 130 A | A/B | 5-129 | PDB |
7LZQ | X-ray | 171 A | A | 1-129 | PDB |
7LZR | X-ray | 134 A | A/B/C/D | 5-129 | PDB |
7LZS | X-ray | 149 A | A | 5-129 | PDB |
7OKD | X-ray | 194 A | A | 5-129 | PDB |
7OKE | X-ray | 148 A | A | 5-129 | PDB |
7OKF | X-ray | 160 A | A | 5-129 | PDB |
7OKG | X-ray | 132 A | A | 5-129 | PDB |
7OKH | X-ray | 152 A | A | 5-129 | PDB |
7OKI | X-ray | 161 A | A | 5-129 | PDB |
7OKJ | X-ray | 143 A | A | 5-129 | PDB |
7OKK | X-ray | 205 A | A | 5-129 | PDB |
7OKL | X-ray | 120 A | A | 5-129 | PDB |
7OKM | X-ray | 148 A | A | 5-129 | PDB |
7Q7R | X-ray | 170 A | A | 5-129 | PDB |
7Q7S | X-ray | 144 A | A | 5-129 | PDB |
7Q7T | X-ray | 146 A | A | 5-129 | PDB |
7Q7U | X-ray | 178 A | A | 5-129 | PDB |
7Q7V | X-ray | 181 A | A | 5-129 | PDB |
7QK0 | X-ray | 196 A | A | 5-129 | PDB |
7RUW | X-ray | 130 A | A | 5-129 | PDB |
7RUX | X-ray | 130 A | A | 5-129 | PDB |
7RUY | X-ray | 127 A | A | 5-129 | PDB |
7RUZ | X-ray | 162 A | A | 5-129 | PDB |
7RV0 | X-ray | 145 A | A | 5-129 | PDB |
7RV1 | X-ray | 117 A | A | 5-129 | PDB |
7RV2 | X-ray | 129 A | A | 5-129 | PDB |
7RV3 | X-ray | 135 A | A | 5-129 | PDB |
7RV4 | X-ray | 125 A | A | 5-129 | PDB |
7RV5 | X-ray | 221 A | A | 5-129 | PDB |
7RV6 | X-ray | 168 A | A | 5-129 | PDB |
7RV7 | X-ray | 163 A | A | 5-129 | PDB |
7RV8 | X-ray | 125 A | A | 5-129 | PDB |
7RV9 | X-ray | 150 A | A | 5-129 | PDB |
7T0S | X-ray | 186 A | A/B/C | 5-129 | PDB |
7T0T | X-ray | 200 A | A/B/C/D/E/F | 5-129 | PDB |
7T0U | X-ray | 149 A | A/B/C/D | 5-129 | PDB |
7ZWN | X-ray | 205 A | A | 5-129 | PDB |
7ZWO | X-ray | 139 A | A | 5-129 | PDB |
7ZWP | X-ray | 185 A | A | 5-129 | PDB |
7ZWQ | X-ray | 165 A | A | 5-129 | PDB |
7ZWR | X-ray | 147 A | A | 5-129 | PDB |
7ZWS | X-ray | 153 A | A | 5-129 | PDB |
7ZWT | X-ray | 194 A | A | 5-129 | PDB |
7ZWU | X-ray | 156 A | A | 5-129 | PDB |
7ZWV | X-ray | 152 A | A | 5-129 | PDB |
7ZWW | X-ray | 167 A | A | 5-129 | PDB |
7ZWX | X-ray | 138 A | A | 5-129 | PDB |
7ZWY | X-ray | 165 A | A | 5-129 | PDB |
7ZWZ | X-ray | 140 A | A | 5-129 | PDB |
8AS9 | X-ray | 340 A | A/B | 6-129 | PDB |
8C78 | X-ray | 180 A | A | 5-129 | PDB |
AF-P41182-F1 | Predicted | AlphaFoldDB |
502 variants for P41182
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
rs1455072478 CA355750181 |
2 | A>G | No |
ClinGen gnomAD |
|
rs200997613 CA89694417 |
2 | A>T | No |
ClinGen 1000Genomes ESP TOPMed gnomAD |
|
TCGA novel | 3 | S>A | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA2750941 rs145456310 |
3 | S>L | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs768405263 CA2750939 |
4 | P>L | No |
ClinGen ExAC TOPMed gnomAD |
|
CA2750937 rs776004818 |
9 | I>L | No |
ClinGen ExAC |
|
CA355750130 rs1403542460 |
10 | Q>* | No |
ClinGen gnomAD |
|
rs1204164230 CA355750121 |
11 | F>S | No |
ClinGen gnomAD |
|
rs772289458 CA2750936 |
12 | T>P | No |
ClinGen ExAC gnomAD |
|
TCGA novel | 14 | H>L | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs746411980 CA2750935 |
24 | R>C | No |
ClinGen ExAC gnomAD |
|
rs752260228 CA89694403 |
24 | R>H | No |
ClinGen Ensembl |
|
rs779268890 CA2750934 |
26 | R>W | No |
ClinGen ExAC TOPMed gnomAD |
|
CA2750933 rs11545363 |
28 | R>* | No |
ClinGen ExAC gnomAD |
|
TCGA novel | 29 | D>G | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
TCGA novel | 35 | V>A | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
TCGA novel | 35 | V>F | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs778027285 CA2750931 |
39 | S>N | No |
ClinGen ExAC gnomAD |
|
rs147478441 CA2750930 |
40 | R>C | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs147478441 CA355749935 |
40 | R>G | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA2750928 rs573866973 |
40 | R>H | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
CA2750929 rs573866973 |
40 | R>L | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
CA355749918 rs1413816021 |
42 | Q>H | No |
ClinGen TOPMed |
|
CA157267 rs200263685 RCV000120197 |
48 | T>M | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ClinVar ESP ExAC NCI-TCGA TOPMed dbSNP gnomAD |
rs1415288002 CA355749801 |
57 | F>L | No |
ClinGen gnomAD |
|
CA2750903 rs752436963 |
59 | S>G | No |
ClinGen ExAC gnomAD |
|
CA355749790 rs1474668374 |
59 | S>N | No |
ClinGen gnomAD |
|
rs955595035 CA89693979 |
60 | I>T | No |
ClinGen Ensembl |
|
CA355749784 rs1260913176 |
60 | I>V | No |
ClinGen gnomAD |
|
rs1327801709 CA355749772 |
61 | F>L | No |
ClinGen TOPMed |
|
rs767073067 CA2750902 |
68 | N>K | No |
ClinGen ExAC gnomAD |
|
rs911170380 COSM1617302 CA89693973 |
68 | N>S | liver [Cosmic] | No |
ClinGen cosmic curated TOPMed gnomAD |
CA355749693 rs1202329522 |
73 | N>D | No |
ClinGen TOPMed gnomAD |
|
rs760006045 CA2750901 COSM730010 |
73 | N>S | lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] | No |
ClinGen cosmic curated ExAC NCI-TCGA TOPMed gnomAD |
CA355749679 rs1579816551 |
75 | D>Y | No |
ClinGen Ensembl |
|
CA355749660 rs1275125976 |
77 | E>D | No |
ClinGen gnomAD |
|
CA2750900 rs774593110 |
78 | I>M | No |
ClinGen ExAC gnomAD |
|
rs771261860 CA2750899 |
79 | N>S | No |
ClinGen ExAC |
|
rs763472780 CA2750898 |
80 | P>S | No |
ClinGen ExAC gnomAD |
|
CA355749615 rs1225779160 |
84 | C>S | No |
ClinGen TOPMed gnomAD |
|
CA2750896 rs769899811 |
85 | I>V | No |
ClinGen ExAC gnomAD |
|
rs148348997 CA89693962 |
89 | F>L | No |
ClinGen ESP TOPMed |
|
rs768771889 CA2750893 |
94 | R>Q | Variant assessed as Somatic; 9.239e-05 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
rs781532443 CA2750894 |
94 | R>W | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
rs1391779185 CA355749524 |
98 | R>P | No |
ClinGen gnomAD |
|
rs1391779185 CA355749525 |
98 | R>Q | No |
ClinGen gnomAD |
|
rs867240773 CA89693940 |
98 | R>W | No |
ClinGen gnomAD |
|
CA2750889 rs377166099 |
100 | G>D | No |
ClinGen ESP ExAC gnomAD |
|
rs757071785 CA2750890 |
100 | G>S | No |
ClinGen ExAC TOPMed gnomAD |
|
rs777825559 CA2750888 |
103 | M>I | No |
ClinGen ExAC TOPMed gnomAD |
|
CA89693930 rs200844445 |
105 | V>G | No |
ClinGen Ensembl |
|
CA89693923 rs201271781 |
106 | M>V | No |
ClinGen Ensembl |
|
rs752135848 CA2750886 |
107 | A>T | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1026114025 CA89693919 |
108 | T>A | No |
ClinGen TOPMed |
|
CA2750884 rs754593601 |
113 | Q>K | No |
ClinGen ExAC gnomAD |
|
rs1218169171 CA355749402 |
116 | H>R | No |
ClinGen gnomAD |
|
rs866452181 CA89693913 |
117 | V>F | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen Ensembl NCI-TCGA |
CA2750883 rs751185760 |
119 | D>N | No |
ClinGen ExAC gnomAD |
|
CA2750881 COSM1042459 rs372779365 |
122 | R>Q | Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated 1000Genomes ESP ExAC NCI-TCGA TOPMed gnomAD |
rs551620719 CA2750882 |
122 | R>W | No |
ClinGen 1000Genomes ExAC gnomAD |
|
CA355749362 rs1579816227 |
123 | K>E | No |
ClinGen Ensembl |
|
CA2750880 rs773775457 |
123 | K>R | No |
ClinGen ExAC gnomAD |
|
rs1579816201 CA355749356 |
124 | F>V | No |
ClinGen Ensembl |
|
CA2750879 rs765718723 |
126 | K>R | No |
ClinGen ExAC |
|
rs1368125173 CA355749333 |
127 | A>P | No |
ClinGen gnomAD |
|
CA355749309 rs1309836914 |
128 | S>R | No |
ClinGen TOPMed |
|
rs1261239948 CA355749306 |
129 | E>* | No |
ClinGen gnomAD |
|
CA2750851 rs748058804 |
130 | A>T | No |
ClinGen ExAC gnomAD |
|
CA2750849 rs376615026 |
131 | E>D | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
rs1258651142 CA355749279 |
133 | V>I | No |
ClinGen gnomAD |
|
CA89693241 rs922510534 |
134 | S>F | No |
ClinGen Ensembl |
|
rs1210690719 CA355749271 |
134 | S>P | No |
ClinGen gnomAD |
|
rs1236418654 CA355749266 |
135 | A>S | No |
ClinGen Ensembl |
|
CA355749260 rs1484945872 |
136 | I>V | No |
ClinGen gnomAD |
|
CA2750848 rs746514494 |
138 | P>A | No |
ClinGen ExAC gnomAD |
|
rs555800838 CA2750847 |
138 | P>L | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
rs555800838 CA89693238 |
138 | P>R | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
rs746514494 CA355749224 |
138 | P>S | No |
ClinGen ExAC gnomAD |
|
rs750032802 CA2750845 |
139 | P>L | No |
ClinGen ExAC gnomAD |
|
rs758046316 CA2750846 |
139 | P>S | No |
ClinGen ExAC TOPMed gnomAD |
|
CA2750844 rs779270221 |
140 | R>C | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA gnomAD |
rs536118071 COSM1421602 CA89693225 |
140 | R>H | Variant assessed as Somatic; 0.0 impact. large_intestine central_nervous_system [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated 1000Genomes ExAC NCI-TCGA TOPMed gnomAD |
rs536118071 CA2750843 |
140 | R>L | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
CA89693216 rs777622359 |
142 | E>A | No |
ClinGen Ensembl |
|
rs1398495055 CA355749102 |
144 | L>F | No |
ClinGen gnomAD |
|
rs144416315 CA2750842 |
144 | L>H | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA89693209 rs944713285 |
145 | N>H | No |
ClinGen TOPMed gnomAD |
|
rs760727857 CA2750840 |
147 | R>Q | No |
ClinGen ExAC TOPMed gnomAD |
|
CA89693206 rs754091486 |
147 | R>W | No |
ClinGen TOPMed gnomAD |
|
CA2750839 rs201608619 |
148 | M>T | No |
ClinGen 1000Genomes ExAC gnomAD |
|
CA355748983 rs1279740465 |
150 | M>T | No |
ClinGen TOPMed gnomAD |
|
CA355748992 rs1187601998 |
150 | M>V | No |
ClinGen gnomAD |
|
rs1253230088 CA355748962 |
151 | P>R | No |
ClinGen TOPMed gnomAD |
|
CA2750838 rs766610723 |
151 | P>S | No |
ClinGen ExAC TOPMed gnomAD |
|
rs373679379 CA2750837 |
152 | Q>R | No |
ClinGen ESP ExAC gnomAD |
|
CA355748910 rs1249095205 |
154 | I>V | No |
ClinGen gnomAD |
|
TCGA novel | 155 | M>I | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs774667475 CA2750836 |
156 | A>V | No |
ClinGen ExAC gnomAD |
|
CA2750833 rs776489192 |
157 | Y>C | No |
ClinGen ExAC gnomAD |
|
CA355748820 rs372638471 |
158 | R>L | No |
ClinGen ExAC TOPMed gnomAD |
|
CA2750829 rs372638471 |
158 | R>P | No |
ClinGen ExAC TOPMed gnomAD |
|
CA2750830 rs372638471 |
158 | R>Q | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
CA2750831 rs746850741 |
158 | R>W | No |
ClinGen ExAC gnomAD |
|
rs745566677 CA2750828 |
159 | G>V | No |
ClinGen ExAC gnomAD |
|
CA2750827 rs778509539 |
160 | R>C | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
CA2750826 rs138532510 |
160 | R>H | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA355748718 rs1579813358 |
162 | V>G | No |
ClinGen Ensembl |
|
rs1463088347 CA355748735 |
162 | V>L | No |
ClinGen gnomAD |
|
CA89693168 rs61752081 CA157275 RCV000120201 |
164 | E>D | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD ClinVar dbSNP |
|
CA355748627 rs1365905276 |
165 | N>K | No |
ClinGen gnomAD |
|
rs756650083 CA2750824 |
165 | N>S | No |
ClinGen ExAC gnomAD |
|
rs753216447 CA2750823 |
166 | N>T | No |
ClinGen ExAC gnomAD |
|
rs1418942018 CA355748589 |
167 | L>P | No |
ClinGen TOPMed gnomAD |
|
CA2750822 rs767730014 |
168 | P>S | No |
ClinGen ExAC TOPMed gnomAD |
|
rs767730014 CA355748583 |
168 | P>T | No |
ClinGen ExAC TOPMed gnomAD |
|
CA355748515 rs1316769730 |
171 | S>N | No |
ClinGen TOPMed |
|
CA355748507 rs751896144 |
171 | S>R | No |
ClinGen ExAC TOPMed gnomAD |
|
CA2750818 rs568417048 |
172 | A>T | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
CA2750817 rs370494696 |
174 | G>R | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA89693147 rs77274617 |
175 | C>S | No |
ClinGen ExAC gnomAD |
|
CA2750816 rs77274617 |
175 | C>Y | No |
ClinGen ExAC gnomAD |
|
CA2750815 rs768291789 |
177 | S>R | No |
ClinGen ExAC gnomAD |
|
rs368005490 CA2750814 |
179 | A>T | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs1473954844 CA355748329 |
181 | A>S | No |
ClinGen TOPMed |
|
rs1473954844 CA355748326 |
181 | A>T | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed |
rs1419000487 CA355748292 |
183 | S>G | No |
ClinGen TOPMed |
|
rs960367912 COSM1131519 CA89693143 |
183 | S>N | Variant assessed as Somatic; 0.0 impact. prostate [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated NCI-TCGA TOPMed gnomAD |
rs771608305 CA2750812 |
183 | S>R | No |
ClinGen ExAC gnomAD |
|
TCGA novel | 184 | L>H | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA2750810 rs773937915 |
186 | S>G | No |
ClinGen ExAC gnomAD |
|
TCGA novel | 188 | L>P | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs1579813093 CA355748176 |
189 | S>P | No |
ClinGen Ensembl |
|
rs374814697 CA2750808 |
190 | T>A | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs374814697 CA355748159 |
190 | T>P | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs778230721 CA2750807 |
191 | P>L | No |
ClinGen ExAC TOPMed gnomAD |
|
rs150319050 CA2750804 |
192 | P>S | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
TCGA novel | 195 | Y>* | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA355748105 rs1282265946 |
197 | M>I | No |
ClinGen gnomAD |
|
rs758674166 CA2750800 |
197 | M>K | No |
ClinGen ExAC gnomAD |
|
CA2750801 rs766302625 |
197 | M>V | No |
ClinGen ExAC gnomAD |
|
rs1347130242 CA355748096 |
198 | Y>* | No |
ClinGen gnomAD |
|
CA355748101 rs1234897185 |
198 | Y>H | No |
ClinGen gnomAD |
|
CA355748088 rs1449890100 |
199 | S>R | No |
ClinGen TOPMed |
|
rs1579812945 CA355748083 |
200 | H>P | No |
ClinGen Ensembl |
|
rs1286763475 CA355748074 |
201 | L>F | No |
ClinGen TOPMed |
|
rs1022534258 CA89693107 |
204 | S>N | No |
ClinGen TOPMed |
|
CA2750798 rs151194132 |
210 | D>H | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA2750797 rs151194132 |
210 | D>N | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA355747875 rs1579812861 |
211 | E>K | No |
ClinGen Ensembl |
|
CA89693104 rs767911394 |
212 | E>K | No |
ClinGen ExAC TOPMed gnomAD |
|
rs767911394 CA2750796 |
212 | E>Q | No |
ClinGen ExAC TOPMed gnomAD |
|
CA89693092 rs911074942 |
214 | R>Q | No |
ClinGen TOPMed gnomAD |
|
CA2750795 rs189037992 |
214 | R>W | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
COSM1131520 CA2750792 rs142220629 |
217 | R>Q | Variant assessed as Somatic; 4.635e-05 impact. prostate [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ESP ExAC NCI-TCGA TOPMed gnomAD |
rs376246678 CA2750793 |
217 | R>W | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA355747731 rs1266907236 |
218 | M>T | No |
ClinGen TOPMed |
|
CA355747649 rs1480124716 |
223 | P>T | No |
ClinGen TOPMed |
|
CA355747592 rs1259353913 |
225 | P>L | No |
ClinGen gnomAD |
|
rs772718103 CA2750790 |
225 | P>S | No |
ClinGen ExAC gnomAD |
|
CA2750786 rs755544927 |
228 | R>Q | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
CA2750787 rs371023739 |
228 | R>W | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA355747515 rs1341531795 |
230 | L>R | No |
ClinGen gnomAD |
|
rs1270887193 CA355747509 |
231 | P>S | No |
ClinGen gnomAD |
|
rs1343118986 CA355747397 |
234 | S>N | No |
ClinGen TOPMed |
|
CA2750781 rs765371056 |
235 | A>T | No |
ClinGen ExAC gnomAD |
|
CA355747346 rs1375333353 |
236 | R>K | No |
ClinGen gnomAD |
|
rs372568524 CA2750779 |
237 | P>Q | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA355747250 rs1166884305 |
238 | V>D | No |
ClinGen gnomAD |
|
CA2750778 rs767237085 |
238 | V>L | No |
ClinGen ExAC TOPMed gnomAD |
|
CA2750777 rs759501076 |
239 | P>L | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
CA355747207 rs759501076 |
239 | P>R | No |
ClinGen ExAC TOPMed gnomAD |
|
CA2750776 rs147671000 |
240 | G>R | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs1560150982 CA355747148 |
241 | E>A | No |
ClinGen Ensembl |
|
CA2750773 rs772973428 |
244 | R>Q | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
rs529677174 CA2750774 |
244 | R>W | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
COSM1042456 rs560916500 CA2750772 |
245 | P>L | endometrium [Cosmic] | No |
ClinGen cosmic curated 1000Genomes ExAC gnomAD |
rs1198106559 CA355746938 |
247 | L>M | No |
ClinGen gnomAD |
|
CA355746806 rs1579812469 |
249 | V>G | No |
ClinGen Ensembl |
|
CA355746823 rs369204237 |
249 | V>L | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA2750769 rs369204237 |
249 | V>M | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA2750768 rs747597566 |
252 | N>D | No |
ClinGen ExAC TOPMed gnomAD |
|
CA2750767 VAR_052709 rs34463990 |
252 | N>S | No |
ClinGen UniProt ESP ExAC TOPMed dbSNP gnomAD |
|
rs886560305 CA89693024 |
253 | V>M | No |
ClinGen Ensembl |
|
CA355746612 rs1355692033 |
255 | H>R | No |
ClinGen gnomAD |
|
CA355746587 rs1379487528 |
256 | S>N | No |
ClinGen TOPMed |
|
rs868239399 CA89693022 |
257 | N>D | No |
ClinGen Ensembl |
|
CA355746496 rs1463632569 |
258 | I>T | No |
ClinGen gnomAD |
|
rs772259307 CA355746471 |
259 | Y>C | No |
ClinGen ExAC gnomAD |
|
rs772259307 CA2750766 |
259 | Y>S | No |
ClinGen ExAC gnomAD |
|
rs1405489754 CA355746440 |
261 | P>A | No |
ClinGen TOPMed gnomAD |
|
rs745925127 CA2750765 |
262 | K>T | No |
ClinGen ExAC gnomAD |
|
CA355746388 rs1460631604 |
263 | E>K | No |
ClinGen gnomAD |
|
rs1411351491 CA355746367 |
263 | E>V | No |
ClinGen gnomAD |
|
CA89693012 rs1048274829 |
265 | I>V | No |
ClinGen TOPMed |
|
CA2750762 rs754024282 |
266 | P>T | No |
ClinGen ExAC TOPMed gnomAD |
|
CA355746287 rs1323707063 |
268 | E>G | No |
ClinGen TOPMed |
|
rs1276130642 CA355746275 COSM399947 |
269 | A>S | lung [Cosmic] | No |
ClinGen cosmic curated Ensembl |
CA2750761 rs780987785 |
270 | R>Q | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
rs1456520855 CA355746251 |
271 | S>N | No |
ClinGen gnomAD |
|
rs139857005 CA355746219 |
273 | M>L | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs960338136 CA89692996 |
273 | M>T | No |
ClinGen TOPMed |
|
COSM1131521 CA2750760 rs139857005 |
273 | M>V | prostate [Cosmic] | No |
ClinGen cosmic curated ESP ExAC TOPMed gnomAD |
TCGA novel | 274 | H>L | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs1214523775 CA355746193 |
274 | H>P | No |
ClinGen gnomAD |
|
CA355746181 rs1242688298 |
275 | Y>H | No |
ClinGen TOPMed |
|
CA2750758 rs766224934 |
276 | S>N | No |
ClinGen ExAC gnomAD |
|
CA2750757 rs762888381 |
278 | A>P | No |
ClinGen ExAC gnomAD |
|
CA2750756 rs201424809 |
278 | A>V | No |
ClinGen ExAC TOPMed gnomAD |
|
CA2750755 rs764799764 |
279 | E>Q | No |
ClinGen ExAC gnomAD |
|
rs1210638938 CA16040238 |
280 | G>S | No |
ClinGen TOPMed |
|
rs776396654 CA2750753 |
284 | A>V | No |
ClinGen ExAC gnomAD |
|
CA2750752 rs760940345 |
286 | P>L | No |
ClinGen ExAC gnomAD |
|
CA2750751 rs760940345 |
286 | P>R | No |
ClinGen ExAC gnomAD |
|
rs1457084745 CA355746033 |
288 | A>V | No |
ClinGen gnomAD |
|
rs776120197 CA2750750 |
289 | R>Q | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA gnomAD |
CA2750749 rs772472637 |
291 | A>T | No |
ClinGen ExAC gnomAD |
|
CA2750748 rs746322343 |
291 | A>V | No |
ClinGen ExAC gnomAD |
|
CA355746014 rs1292171577 |
292 | P>S | No |
ClinGen TOPMed |
|
TCGA novel | 293 | Y>T | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs1156748714 CA355745996 |
294 | F>L | No |
ClinGen gnomAD |
|
rs1455565982 CA355745993 |
295 | P>A | No |
ClinGen gnomAD |
|
CA2750747 rs774632128 |
296 | C>G | No |
ClinGen ExAC TOPMed gnomAD |
|
rs774632128 CA89692975 |
296 | C>R | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1194417942 CA355745976 |
297 | D>E | No |
ClinGen gnomAD |
|
CA355745981 rs1220888989 |
297 | D>H | No |
ClinGen gnomAD |
|
TCGA novel | 301 | K>I | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA157271 rs587778091 RCV000120199 |
302 | E>G | No |
ClinGen ClinVar ExAC TOPMed dbSNP gnomAD |
|
CA2750745 rs777942698 |
303 | E>K | No |
ClinGen ExAC gnomAD |
|
CA355745933 rs1322466271 |
303 | E>V | No |
ClinGen gnomAD |
|
rs200317307 CA89692958 |
304 | E>D | No |
ClinGen 1000Genomes |
|
rs1472287277 CA355745930 |
304 | E>K | No |
ClinGen TOPMed |
|
rs1303425150 CA355745921 |
305 | R>K | No |
ClinGen gnomAD |
|
rs751323271 CA2750743 |
306 | P>S | No |
ClinGen ExAC gnomAD |
|
CA355745915 rs751323271 |
306 | P>T | No |
ClinGen ExAC gnomAD |
|
rs779829722 CA2750742 |
307 | S>C | No |
ClinGen ExAC TOPMed gnomAD |
|
rs779829722 CA355745907 |
307 | S>F | No |
ClinGen ExAC TOPMed gnomAD |
|
rs369445234 CA2750741 |
308 | S>L | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA355745879 rs1359631290 |
311 | E>K | No |
ClinGen gnomAD |
|
TCGA novel | 313 | A>T | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs988570451 CA89692949 |
315 | H>R | No |
ClinGen Ensembl |
|
CA2750738 rs542190544 |
317 | E>K | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
rs763822826 CA2750736 |
318 | P>L | No |
ClinGen ExAC TOPMed gnomAD |
|
rs753608577 CA355745724 |
318 | P>S | No |
ClinGen ExAC TOPMed gnomAD |
|
rs753608577 CA2750737 |
318 | P>T | No |
ClinGen ExAC TOPMed gnomAD |
|
CA355745701 rs775725915 |
319 | P>H | No |
ClinGen ExAC TOPMed gnomAD |
|
rs775725915 CA2750734 |
319 | P>L | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1262902643 CA355745706 |
319 | P>S | No |
ClinGen TOPMed gnomAD |
|
rs1262902643 CA355745710 |
319 | P>T | No |
ClinGen TOPMed gnomAD |
|
CA355745687 rs1411489406 |
320 | N>D | No |
ClinGen TOPMed gnomAD |
|
TCGA novel | 320 | N>M | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs759988632 CA2750732 |
320 | N>S | No |
ClinGen ExAC TOPMed gnomAD |
|
COSM1471537 rs1231829175 CA355745669 |
321 | A>T | Variant assessed as Somatic; 0.0 impact. prostate [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated NCI-TCGA TOPMed gnomAD |
rs377059215 CA157273 RCV000120200 |
321 | A>V | No |
ClinGen ClinVar ESP ExAC TOPMed dbSNP gnomAD |
|
rs771040247 CA2750731 |
322 | P>A | No |
ClinGen ExAC gnomAD |
|
CA2750729 rs147914986 |
325 | R>Q | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
rs749366850 CA2750730 |
325 | R>W | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1016920638 CA89692891 |
327 | G>C | No |
ClinGen TOPMed gnomAD |
|
CA355745551 rs1464515353 |
327 | G>V | No |
ClinGen gnomAD |
|
CA2750728 rs769911330 |
328 | L>P | No |
ClinGen ExAC gnomAD |
|
rs149798354 CA2750727 |
329 | V>I | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
TCGA novel | 335 | Q>H | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA355745408 rs1423186282 |
335 | Q>L | No |
ClinGen gnomAD |
|
CA2750726 rs779735759 |
336 | K>T | No |
ClinGen ExAC gnomAD |
|
CA2750723 rs778985564 |
351 | K>M | No |
ClinGen ExAC |
|
CA355745021 rs1467680757 |
352 | N>H | No |
ClinGen TOPMed |
|
TCGA novel | 352 | N>T | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA355744960 COSM1184596 rs1258718328 |
354 | C>Y | large_intestine [Cosmic] | No |
ClinGen cosmic curated gnomAD |
CA355744942 rs756882169 |
355 | I>L | No |
ClinGen ExAC gnomAD |
|
rs756882169 CA2750722 |
355 | I>V | No |
ClinGen ExAC gnomAD |
|
rs1252542876 CA355744797 |
361 | S>P | No |
ClinGen gnomAD |
|
CA2750720 rs763596354 |
362 | P>L | No |
ClinGen ExAC gnomAD |
|
CA2750719 rs755757577 |
363 | P>A | No |
ClinGen ExAC TOPMed gnomAD |
|
CA89692854 rs1008921188 |
364 | A>V | No |
ClinGen TOPMed |
|
TCGA novel | 365 | K>N | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs767821014 CA355744602 |
368 | T>I | No |
ClinGen ExAC gnomAD |
|
rs767821014 CA2750717 |
368 | T>S | No |
ClinGen ExAC gnomAD |
|
CA355744557 rs1394202381 |
370 | P>H | No |
ClinGen gnomAD |
|
rs759914346 CA2750716 |
372 | A>S | No |
ClinGen ExAC |
|
CA355744287 rs1336404127 |
380 | F>L | No |
ClinGen TOPMed |
|
rs1375458531 CA355744284 |
381 | I>V | No |
ClinGen gnomAD |
|
rs1218233420 CA355744268 |
382 | V>M | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed |
CA2750714 rs766860585 |
385 | S>N | No |
ClinGen ExAC gnomAD |
|
rs1579811386 CA355744196 |
385 | S>R | No |
ClinGen Ensembl |
|
CA355744147 rs1056932 |
387 | N>K | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA355744122 rs1168767265 |
389 | N>D | No |
ClinGen gnomAD |
|
RCV000120198 rs150656653 CA157269 |
389 | N>S | No |
ClinGen ClinVar 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
rs769861975 CA2750712 |
391 | K>R | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA gnomAD |
rs748367275 CA2750711 |
392 | P>L | No |
ClinGen ExAC gnomAD |
|
CA2750710 rs1056933 |
393 | E>G | No |
ClinGen ExAC gnomAD |
|
rs1178677766 CA355743956 |
395 | P>H | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA gnomAD |
CA2750707 rs142017472 |
397 | Q>H | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs34145295 CA89692817 |
398 | A>D | No |
ClinGen Ensembl |
|
rs1344041493 CA355743886 |
398 | A>T | No |
ClinGen TOPMed |
|
CA2750706 rs757267633 |
399 | E>D | No |
ClinGen ExAC gnomAD |
|
rs36011786 CA89692813 |
400 | L>M | No |
ClinGen ExAC TOPMed gnomAD |
|
rs777170865 CA2750704 |
401 | G>C | No |
ClinGen ExAC gnomAD |
|
CA2750703 rs769386051 |
402 | R>C | No |
ClinGen ExAC |
|
RCV000903689 CA2750702 rs139744042 |
402 | R>H | No |
ClinGen ClinVar 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
CA355743787 rs139744042 |
402 | R>L | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
rs780897268 CA2750701 |
403 | L>I | No |
ClinGen ExAC TOPMed gnomAD |
|
rs780897268 CA355743781 |
403 | L>V | No |
ClinGen ExAC TOPMed gnomAD |
|
CA355743744 rs1391743154 |
405 | P>A | No |
ClinGen TOPMed gnomAD |
|
rs1391743154 CA355743740 |
405 | P>S | No |
ClinGen TOPMed gnomAD |
|
CA2750698 rs369842677 |
406 | R>P | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs369842677 CA2750699 |
406 | R>Q | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ESP ExAC NCI-TCGA TOPMed gnomAD |
CA89692785 rs891639094 |
407 | A>D | No |
ClinGen TOPMed gnomAD |
|
CA355743686 rs1235812657 |
408 | Y>C | No |
ClinGen gnomAD |
|
rs1439689589 CA355743695 |
408 | Y>H | No |
ClinGen gnomAD |
|
rs763470720 CA2750697 |
409 | T>M | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1266269631 CA355743650 |
410 | A>P | No |
ClinGen gnomAD |
|
CA2750695 rs765268974 |
410 | A>V | No |
ClinGen ExAC TOPMed gnomAD |
|
CA2750694 rs146386826 |
411 | P>L | No |
ClinGen ESP ExAC gnomAD |
|
CA2750691 rs760912020 |
412 | P>L | No |
ClinGen ExAC TOPMed gnomAD |
|
CA355743607 rs1239334107 |
412 | P>S | No |
ClinGen gnomAD |
|
rs1307107486 CA355743554 |
414 | C>Y | No |
ClinGen gnomAD |
|
CA2750690 rs774320115 |
415 | Q>R | No |
ClinGen ExAC gnomAD |
|
rs376807699 CA2750688 |
417 | P>A | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA2750687 rs142387697 CA2750686 |
418 | M>L | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
TCGA novel | 419 | E>D | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs747683215 CA2750685 |
419 | E>V | No |
ClinGen ExAC TOPMed gnomAD |
|
CA355743426 rs1299252015 |
420 | P>S | No |
ClinGen TOPMed gnomAD |
|
rs780512791 CA2750684 |
421 | E>D | No |
ClinGen ExAC gnomAD |
|
CA355743406 rs1219665569 |
421 | E>Q | No |
ClinGen gnomAD |
|
CA355743365 CA355743366 rs1369675066 |
422 | N>K | No |
ClinGen TOPMed gnomAD |
|
rs754654517 CA2750683 |
423 | L>F | No |
ClinGen ExAC TOPMed gnomAD |
|
rs754654517 CA355743361 |
423 | L>I | No |
ClinGen ExAC TOPMed gnomAD |
|
rs780442173 CA355743261 |
426 | Q>P | No |
ClinGen ExAC gnomAD |
|
rs780442173 CA2750681 |
426 | Q>R | No |
ClinGen ExAC gnomAD |
|
CA89692740 rs939068114 |
428 | P>L | No |
ClinGen TOPMed |
|
CA2750680 rs758728015 |
429 | T>A | No |
ClinGen ExAC TOPMed gnomAD |
|
TCGA novel | 429 | T>I | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs753955082 CA2750676 |
435 | G>R | No |
ClinGen ExAC TOPMed gnomAD |
|
rs753955082 CA2750677 |
435 | G>W | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1579810846 CA355742868 |
438 | S>F | No |
ClinGen Ensembl |
|
CA355742851 rs1215648106 |
439 | T>I | No |
ClinGen gnomAD |
|
CA355742865 rs1579810828 |
439 | T>P | No |
ClinGen Ensembl |
|
CA355742816 rs1487231523 |
441 | P>S | No |
ClinGen gnomAD |
|
rs1282428338 CA355742770 |
443 | A>T | No |
ClinGen gnomAD |
|
rs761002552 CA2750674 |
445 | R>Q | No |
ClinGen ExAC TOPMed gnomAD |
|
CA89692722 rs967749286 |
445 | R>W | No |
ClinGen TOPMed gnomAD |
|
CA2750673 COSM479834 rs775834769 |
449 | I>V | kidney Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] | No |
ClinGen cosmic curated ExAC NCI-TCGA TOPMed gnomAD |
rs201771435 CA2750670 |
450 | V>I | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
rs201771435 CA2750671 |
450 | V>L | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA355742390 rs1235687781 |
454 | M>I | No |
ClinGen gnomAD |
|
rs764890174 CA2750650 |
454 | M>T | No |
ClinGen ExAC gnomAD |
|
rs775772146 CA2750651 |
454 | M>V | No |
ClinGen ExAC TOPMed gnomAD |
|
TCGA novel | 455 | T>A | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
RCV000120202 rs541016998 CA157277 |
455 | T>M | No |
ClinGen ClinVar 1000Genomes ExAC TOPMed dbSNP gnomAD |
|
rs1238920334 CA355742355 |
457 | S>P | No |
ClinGen gnomAD |
|
rs1044213121 CA89692486 |
458 | P>L | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen Ensembl NCI-TCGA |
CA157279 rs137878288 RCV000120203 |
459 | R>C | No |
ClinGen ClinVar 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
COSM1042450 rs143522266 CA2750649 |
459 | R>H | endometrium [Cosmic] | No |
ClinGen cosmic curated 1000Genomes ESP ExAC TOPMed gnomAD |
CA355742334 rs137878288 |
459 | R>S | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA355742273 rs368187258 |
462 | S>R | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA2750646 rs374228382 |
463 | E>K | No |
ClinGen ESP ExAC |
|
CA2750643 rs779359717 |
464 | S>I | No |
ClinGen ExAC gnomAD |
|
rs1401083474 CA355742173 |
469 | Y>H | No |
ClinGen gnomAD |
|
CA2750641 rs749842417 |
470 | M>V | No |
ClinGen ExAC gnomAD |
|
CA355742134 rs1245034066 |
471 | H>P | No |
ClinGen TOPMed |
|
rs1043642277 CA355742128 |
471 | H>Q | No |
ClinGen TOPMed gnomAD |
|
CA355742132 rs1245034066 |
471 | H>R | No |
ClinGen TOPMed |
|
rs1196017842 CA355742135 |
471 | H>Y | No |
ClinGen TOPMed |
|
CA355742114 rs1466913399 |
472 | P>L | No |
ClinGen gnomAD |
|
CA355742124 rs1444039618 |
472 | P>T | No |
ClinGen gnomAD |
|
CA2750638 rs752840713 |
473 | P>A | No |
ClinGen ExAC TOPMed gnomAD |
|
rs767642014 CA2750637 COSM174704 |
473 | P>L | Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ExAC NCI-TCGA TOPMed gnomAD |
rs752840713 CA355742107 |
473 | P>T | No |
ClinGen ExAC TOPMed gnomAD |
|
rs770320988 | 474 | K>E | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No | NCI-TCGA |
CA2750633 rs765118132 |
474 | K>R | No |
ClinGen ExAC gnomAD |
|
rs761505079 CA2750632 |
475 | C>F | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1160203866 CA355742055 |
475 | C>R | No |
ClinGen gnomAD |
|
CA355742046 rs761505079 |
475 | C>Y | No |
ClinGen ExAC TOPMed gnomAD |
|
rs535108808 COSM3846988 CA2750630 |
476 | T>M | Variant assessed as Somatic; 0.0 impact. breast [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ExAC NCI-TCGA gnomAD |
CA355742016 rs1319771401 |
477 | S>P | No |
ClinGen TOPMed |
|
CA2750628 rs775011229 |
478 | C>S | No |
ClinGen ExAC gnomAD |
|
rs138591566 CA2750627 |
478 | C>W | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA355741990 rs775011229 |
478 | C>Y | No |
ClinGen ExAC gnomAD |
|
CA2750625 rs376883234 |
479 | G>S | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs987361306 CA89692385 |
480 | S>P | No |
ClinGen TOPMed |
|
CA355741915 rs1242950510 |
482 | S>F | No |
ClinGen gnomAD |
|
TCGA novel | 484 | Q>* | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs749657541 CA2750623 |
485 | H>Q | No |
ClinGen ExAC gnomAD |
|
TCGA novel | 487 | E>D | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs778229277 CA2750622 |
487 | E>V | No |
ClinGen ExAC gnomAD |
|
CA2750621 rs770432763 |
488 | M>T | No |
ClinGen ExAC TOPMed gnomAD |
|
CA355741709 rs1422232189 |
489 | C>W | No |
ClinGen gnomAD |
|
CA2750620 rs748627517 |
491 | H>P | No |
ClinGen ExAC TOPMed gnomAD |
|
CA355741686 rs1347889080 |
491 | H>Q | No |
ClinGen gnomAD |
|
rs748627517 CA355741688 |
491 | H>R | No |
ClinGen ExAC TOPMed gnomAD |
|
CA355741666 rs2229362 |
493 | A>S | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
RCV000120204 VAR_019970 CA157281 rs2229362 |
493 | A>T | No |
ClinGen ClinVar UniProt 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
rs915322376 CA89692351 |
496 | T>A | No |
ClinGen TOPMed gnomAD |
|
CA2750618 rs375595181 |
496 | T>M | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ESP ExAC NCI-TCGA TOPMed gnomAD |
rs915322376 CA89692353 |
496 | T>P | No |
ClinGen TOPMed gnomAD |
|
rs1245283417 CA355741493 |
500 | E>D | No |
ClinGen gnomAD |
|
CA89692338 rs983410189 |
501 | M>I | No |
ClinGen TOPMed |
|
rs763834345 CA2750614 |
501 | M>V | No |
ClinGen ExAC gnomAD |
|
CA355741448 rs1488877472 |
503 | E>K | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA gnomAD |
CA2750612 rs752610881 |
506 | S>T | No |
ClinGen ExAC TOPMed gnomAD |
|
CA355741350 rs1313419031 |
507 | E>G | No |
ClinGen gnomAD |
|
CA355741304 rs1365056172 |
509 | S>P | No |
ClinGen gnomAD |
|
CA355741287 rs1159893808 |
510 | D>N | No |
ClinGen TOPMed |
|
rs758964515 CA2750610 |
513 | C>Y | No |
ClinGen ExAC gnomAD |
|
rs770507201 CA2750608 |
514 | E>K | No |
ClinGen ExAC gnomAD |
|
rs373425354 CA2750589 |
516 | G>R | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
RCV000120196 CA157265 rs587778090 |
517 | A>I | No |
ClinGen ClinVar Ensembl dbSNP |
|
rs762251488 CA2750587 |
517 | A>T | No |
ClinGen ExAC gnomAD |
|
COSM1421598 CA2750586 rs776993725 |
517 | A>V | Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ExAC NCI-TCGA gnomAD |
CA355749205 rs1385653267 |
519 | F>L | No |
ClinGen TOPMed |
|
rs769047717 CA2750585 |
519 | F>S | No |
ClinGen ExAC TOPMed gnomAD |
|
rs560242782 CA89711259 |
521 | N>S | No |
ClinGen TOPMed |
|
rs199997559 CA355749171 CA2750583 |
522 | E>D | No |
ClinGen 1000Genomes ExAC gnomAD |
|
rs747509903 CA2750584 |
522 | E>G | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1316988931 CA355749157 |
524 | D>H | No |
ClinGen TOPMed gnomAD |
|
TCGA novel | 524 | D>N | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA2750582 rs772115541 |
526 | R>C | No |
ClinGen ExAC gnomAD |
|
rs1246753673 CA355749131 |
526 | R>H | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed gnomAD |
CA355749088 rs1322215309 |
530 | E>D | No |
ClinGen gnomAD |
|
CA355749090 rs1368110797 |
530 | E>G | No |
ClinGen gnomAD |
|
CA2750581 rs746130585 |
532 | S>A | No |
ClinGen ExAC gnomAD |
|
CA355749051 rs1333525198 |
534 | K>N | No |
ClinGen TOPMed gnomAD |
|
rs565046748 CA2750579 |
534 | K>T | No |
ClinGen 1000Genomes ExAC gnomAD |
|
CA2750578 rs747910667 |
535 | R>G | No |
ClinGen ExAC gnomAD |
|
rs780977325 CA2750577 |
535 | R>K | No |
ClinGen ExAC gnomAD |
|
TCGA novel | 535 | R>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs780977325 CA355749046 |
535 | R>T | No |
ClinGen ExAC gnomAD |
|
CA2750575 rs545063119 |
537 | T>M | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
rs530287353 CA89711239 |
539 | Q>H | No |
ClinGen Ensembl |
|
rs940637288 CA89711235 |
540 | T>N | No |
ClinGen gnomAD |
|
rs1443386916 CA355748982 |
542 | S>G | No |
ClinGen TOPMed gnomAD |
|
rs1381617645 CA355748976 |
542 | S>N | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA gnomAD |
CA2750573 rs377588896 |
543 | D>E | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs112650365 CA89711233 |
543 | D>G | No |
ClinGen Ensembl |
|
rs750156065 CA2750572 |
545 | P>H | No |
ClinGen ExAC gnomAD |
|
rs764991882 CA2750571 |
546 | Y>H | No |
ClinGen ExAC |
|
rs1488674146 CA355748894 |
550 | R>C | No |
ClinGen gnomAD |
|
COSM1042448 rs147650939 CA2750568 |
550 | R>H | Variant assessed as Somatic; 0.0 impact. large_intestine endometrium [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ESP ExAC NCI-TCGA TOPMed gnomAD |
CA2750567 rs761133130 |
551 | C>Y | No |
ClinGen ExAC |
|
rs1300364346 CA355748867 |
552 | Q>H | No |
ClinGen Ensembl |
|
TCGA novel | 554 | S>missing | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA355748831 rs1248764498 |
556 | R>C | No |
ClinGen TOPMed |
|
rs774357645 CA2750563 |
560 | N>H | No |
ClinGen ExAC gnomAD |
|
CA2750562 rs771146799 |
560 | N>T | No |
ClinGen ExAC gnomAD |
|
CA89711196 rs867768344 |
561 | L>I | No |
ClinGen Ensembl |
|
rs749489926 CA2750561 |
561 | L>P | No |
ClinGen ExAC gnomAD |
|
rs77733730 CA2750558 |
562 | A>P | No |
ClinGen ExAC gnomAD |
|
rs77733730 COSM1484950 CA2750559 |
562 | A>T | breast [Cosmic] | No |
ClinGen cosmic curated ExAC gnomAD |
CA2750557 rs780123797 |
566 | T>P | No |
ClinGen ExAC gnomAD |
|
CA355748676 rs1438511659 |
567 | V>I | No |
ClinGen gnomAD |
|
CA355748043 rs753499318 |
572 | K>N | No |
ClinGen ExAC gnomAD |
|
rs777469418 CA2750534 |
573 | P>A | No |
ClinGen ExAC gnomAD |
|
rs1458680123 CA355748026 |
574 | Y>C | No |
ClinGen TOPMed |
|
CA2750533 rs755666072 |
575 | R>C | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA gnomAD |
rs1262719853 CA355748017 |
575 | R>H | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed gnomAD |
TCGA novel | 577 | N>I | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA355747954 rs1386949361 |
581 | A>S | No |
ClinGen TOPMed |
|
rs1302792965 CA355747926 |
584 | N>H | No |
ClinGen TOPMed |
|
CA355747922 rs1579805151 |
584 | N>T | No |
ClinGen Ensembl |
|
CA2750529 rs752044631 |
594 | R>* | No |
ClinGen ExAC gnomAD |
|
TCGA novel | 603 | K>N | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA355747712 rs1466914215 |
605 | E>K | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA gnomAD |
CA2750527 rs763086743 |
606 | T>A | No |
ClinGen ExAC |
|
CA355747697 rs1272912974 |
606 | T>N | No |
ClinGen TOPMed |
|
CA2750526 rs773103820 |
607 | C>S | No |
ClinGen ExAC gnomAD |
|
CA89710809 rs1042221684 |
608 | G>R | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA gnomAD |
TCGA novel | 611 | F>L | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA2750524 rs370028442 |
612 | V>I | No |
ClinGen ESP ExAC gnomAD |
|
CA89710500 rs867576130 |
618 | R>C | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed |
CA2750477 rs766041104 COSM350824 |
618 | R>H | lung [Cosmic] | No |
ClinGen cosmic curated ExAC TOPMed gnomAD |
rs766041104 CA2750476 |
618 | R>L | No |
ClinGen ExAC TOPMed gnomAD |
|
CA355747215 rs1441588327 |
630 | Y>N | No |
ClinGen gnomAD |
|
TCGA novel | 635 | C>G | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs1176821201 CA355747044 |
638 | R>C | Variant assessed as Somatic; 9.239e-05 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed gnomAD |
rs1468858377 CA355747038 |
638 | R>H | No |
ClinGen gnomAD |
|
TCGA novel | 639 | F>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
TCGA novel | 641 | H>Q | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA355746798 rs1222785450 |
649 | L>P | No |
ClinGen gnomAD |
|
TCGA novel | 656 | K>* | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA355745842 rs1478407186 |
662 | K>N | No |
ClinGen gnomAD |
|
CA2750446 rs771597612 |
665 | L>V | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1426858162 CA355745782 |
668 | R>H | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed |
rs1202633041 CA355745726 |
674 | R>* | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA gnomAD |
VAR_014825 CA2750445 rs1056936 |
676 | H>Y | No |
ClinGen UniProt ExAC dbSNP gnomAD |
|
TCGA novel | 683 | A>D | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA355745640 rs1230004461 |
683 | A>S | No |
ClinGen gnomAD |
|
rs1230004461 COSM1042444 CA355745642 |
683 | A>T | Variant assessed as Somatic; 0.0 impact. skin endometrium [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated NCI-TCGA gnomAD |
rs558388208 CA2750441 |
684 | I>V | No |
ClinGen 1000Genomes ExAC gnomAD |
|
CA355745622 rs1579800375 |
685 | T>P | No |
ClinGen Ensembl |
|
rs1579800370 CA355745603 |
687 | T>P | No |
ClinGen Ensembl |
|
CA355745557 rs1579800349 |
691 | Y>S | No |
ClinGen Ensembl |
|
rs755174150 CA2750440 |
692 | R>C | No |
ClinGen ExAC gnomAD |
|
COSM3408501 CA2750439 rs750212558 |
692 | R>H | Variant assessed as Somatic; 0.0 impact. central_nervous_system [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ExAC NCI-TCGA gnomAD |
rs200887028 CA2750437 |
693 | V>M | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
rs753741309 CA2750436 |
694 | S>P | No |
ClinGen ExAC gnomAD |
|
rs1579800273 CA355745509 |
697 | D>A | No |
ClinGen Ensembl |
|
CA355745495 rs1363605252 |
699 | P>S | No |
ClinGen Ensembl |
|
CA2750434 rs760088914 |
700 | P>L | No |
ClinGen ExAC TOPMed gnomAD |
|
rs760088914 CA355745479 |
700 | P>R | No |
ClinGen ExAC TOPMed gnomAD |
|
CA355745481 rs1182456613 |
700 | P>S | No |
ClinGen gnomAD |
|
CA355745449 rs1224498201 |
703 | P>L | No |
ClinGen TOPMed |
|
rs771627344 CA2750432 |
705 | A>G | No |
ClinGen ExAC gnomAD |
|
CA355745406 rs771627344 |
705 | A>V | No |
ClinGen ExAC gnomAD |
3 associated diseases with P41182
Without disease ID
7 regional properties for P41182
Type | Name | Position | InterPro Accession |
---|---|---|---|
domain | BTB/POZ domain | 22 - 129 | IPR000210 |
domain | Zinc finger C2H2-type | 518 - 546 | IPR013087-1 |
domain | Zinc finger C2H2-type | 546 - 573 | IPR013087-2 |
domain | Zinc finger C2H2-type | 574 - 601 | IPR013087-3 |
domain | Zinc finger C2H2-type | 602 - 629 | IPR013087-4 |
domain | Zinc finger C2H2-type | 630 - 657 | IPR013087-5 |
domain | Zinc finger C2H2-type | 658 - 681 | IPR013087-6 |
5 GO annotations of cellular component
Name | Definition |
---|---|
Golgi apparatus | A membrane-bound cytoplasmic organelle of the endomembrane system that further processes the core oligosaccharides (e.g. N-glycans) added to proteins in the endoplasmic reticulum and packages them into membrane-bound vesicles. The Golgi apparatus operates at the intersection of the secretory, lysosomal, and endocytic pathways. |
nucleolus | A small, dense body one or more of which are present in the nucleus of eukaryotic cells. It is rich in RNA and protein, is not bounded by a limiting membrane, and is not seen during mitosis. Its prime function is the transcription of the nucleolar DNA into 45S ribosomal-precursor RNA, the processing of this RNA into 5.8S, 18S, and 28S components of ribosomal RNA, and the association of these components with 5S RNA and proteins synthesized outside the nucleolus. This association results in the formation of ribonucleoprotein precursors; these pass into the cytoplasm and mature into the 40S and 60S subunits of the ribosome. |
nucleoplasm | That part of the nuclear content other than the chromosomes or the nucleolus. |
nucleus | A membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. In most cells, the nucleus contains all of the cell's chromosomes except the organellar chromosomes, and is the site of RNA synthesis and processing. In some species, or in specialized cell types, RNA metabolism or DNA replication may be absent. |
paraspeckles | Discrete subnuclear bodies in the interchromatin nucleoplasmic space, often located adjacent to nuclear specks. 10-20 paraspeckles are typically found in human cell nuclei. |
12 GO annotations of molecular function
Name | Definition |
---|---|
chromatin binding | Binding to chromatin, the network of fibers of DNA, protein, and sometimes RNA, that make up the chromosomes of the eukaryotic nucleus during interphase. |
chromatin DNA binding | Binding to DNA that is assembled into chromatin. |
DNA-binding transcription factor activity | A transcription regulator activity that modulates transcription of gene sets via selective and non-covalent binding to a specific double-stranded genomic DNA sequence (sometimes referred to as a motif) within a cis-regulatory region. Regulatory regions include promoters (proximal and distal) and enhancers. Genes are transcriptional units, and include bacterial operons. |
DNA-binding transcription factor binding | Binding to a DNA-binding transcription factor, a protein that interacts with a specific DNA sequence (sometimes referred to as a motif) within the regulatory region of a gene to modulate transcription. |
DNA-binding transcription repressor activity, RNA polymerase II-specific | A DNA-binding transcription factor activity that represses or decreases the transcription of specific gene sets transcribed by RNA polymerase II. |
identical protein binding | Binding to an identical protein or proteins. |
intronic transcription regulatory region sequence-specific DNA binding | Binding to an intronic DNA sequence that regulates the transcription of the transcript it is contained within. |
metal ion binding | Binding to a metal ion. |
RNA polymerase II cis-regulatory region sequence-specific DNA binding | Binding to a specific upstream regulatory DNA sequence (transcription factor recognition sequence or binding site) located in cis relative to the transcription start site (i.e., on the same strand of DNA) of a gene transcribed by RNA polymerase II. |
sequence-specific DNA binding | Binding to DNA of a specific nucleotide composition, e.g. GC-rich DNA binding, or with a specific sequence motif or type of DNA e.g. promotor binding or rDNA binding. |
sequence-specific double-stranded DNA binding | Binding to double-stranded DNA of a specific nucleotide composition, e.g. GC-rich DNA binding, or with a specific sequence motif or type of DNA, e.g. promotor binding or rDNA binding. |
transcription corepressor binding | Binding to a transcription corepressor, a protein involved in negative regulation of transcription via protein-protein interactions with transcription factors and other proteins that negatively regulate transcription. Transcription corepressors do not bind DNA directly, but rather mediate protein-protein interactions between repressing transcription factors and the basal transcription machinery. |
48 GO annotations of biological process
Name | Definition |
---|---|
actin cytoskeleton organization | A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of cytoskeletal structures comprising actin filaments and their associated proteins. |
B cell proliferation | The expansion of a B cell population by cell division. Follows B cell activation. |
cell morphogenesis | The developmental process in which the size or shape of a cell is generated and organized. |
cell-matrix adhesion | The binding of a cell to the extracellular matrix via adhesion molecules. |
cellular response to DNA damage stimulus | Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus indicating damage to its DNA from environmental insults or errors during metabolism. |
erythrocyte development | The process whose specific outcome is the progression of an erythrocyte over time, from its formation to the mature structure. |
germinal center formation | The process in which germinal centers form. A germinal center is a specialized microenvironment formed when activated B cells enter lymphoid follicles. Germinal centers are the foci for B cell proliferation and somatic hypermutation. |
histone deacetylation | The modification of histones by removal of acetyl groups. |
inflammatory response | The immediate defensive reaction (by vertebrate tissue) to infection or injury caused by chemical or physical agents. The process is characterized by local vasodilation, extravasation of plasma into intercellular spaces and accumulation of white blood cells and macrophages. |
isotype switching to IgE isotypes | The switching of activated B cells from IgM biosynthesis to IgE biosynthesis, accomplished through a recombination process involving an intrachromosomal deletion between switch regions that reside 5' of the IgM and IgE constant region gene segments in the immunoglobulin heavy chain locus. |
negative regulation of B cell apoptotic process | Any process that stops, prevents, or reduces the frequency, rate, or extent of B cell apoptotic process. |
negative regulation of cell growth | Any process that stops, prevents, or reduces the frequency, rate, extent or direction of cell growth. |
negative regulation of cell-matrix adhesion | Any process that stops, prevents, or reduces the rate or extent of cell adhesion to the extracellular matrix. |
negative regulation of cellular senescence | Any process that stops, prevents or reduces the frequency, rate or extent of cellular senescence. |
negative regulation of DNA-templated transcription | Any process that stops, prevents, or reduces the frequency, rate or extent of cellular DNA-templated transcription. |
negative regulation of isotype switching to IgE isotypes | Any process that stops, prevents, or reduces the frequency, rate or extent of isotype switching to IgE isotypes. |
negative regulation of leukocyte proliferation | Any process that stops, prevents, or reduces the frequency, rate or extent of leukocyte proliferation. |
negative regulation of mast cell cytokine production | Any process that stops, prevents, or reduces the frequency, rate, or extent of mast cell cytokine production. |
negative regulation of mitotic cell cycle DNA replication | Any process that stops, prevents or reduces the frequency, rate or extent of mitotic cell cycle DNA replication. |
negative regulation of Notch signaling pathway | Any process that stops, prevents, or reduces the frequency, rate or extent of the Notch signaling pathway. |
negative regulation of plasma cell differentiation | Any process that stops, prevents or reduces the frequency, rate or extent of plasma cell differentiation. |
negative regulation of Rho protein signal transduction | Any process that stops, prevents, or reduces the frequency, rate or extent of Rho protein signal transduction. |
negative regulation of T-helper 2 cell differentiation | Any process that stops, prevents, or reduces the frequency, rate or extent of T-helper 2 cell differentiation. |
negative regulation of transcription by RNA polymerase II | Any process that stops, prevents, or reduces the frequency, rate or extent of transcription mediated by RNA polymerase II. |
plasma cell differentiation | The process in which a B cell acquires the specialized features of a plasma cell. A plasma cell is a lymphocyte which develops from a B cell and produces high amounts of antibody. |
positive regulation of apoptotic process | Any process that activates or increases the frequency, rate or extent of cell death by apoptotic process. |
positive regulation of B cell proliferation | Any process that activates or increases the rate or extent of B cell proliferation. |
positive regulation of histone deacetylation | Any process that activates or increases the frequency, rate or extent of the removal of acetyl groups from histones. |
positive regulation of neuron differentiation | Any process that activates or increases the frequency, rate or extent of neuron differentiation. |
positive regulation of regulatory T cell differentiation | Any process that activates or increases the frequency, rate or extent of differentiation of regulatory T cells. |
protein localization | Any process in which a protein is transported to, or maintained in, a specific location. |
pyramidal neuron differentiation | The process in which a neuroblast or one of its progeny commits to a pyramidal neuron fate, migrates from the ventricular zone to the appropriate layer in the cortex and develops into a mature neuron. |
regulation of cell differentiation | Any process that modulates the frequency, rate or extent of cell differentiation, the process in which relatively unspecialized cells acquire specialized structural and functional features. |
regulation of cell population proliferation | Any process that modulates the frequency, rate or extent of cell proliferation. |
regulation of cytokine production | Any process that modulates the frequency, rate, or extent of production of a cytokine. |
regulation of germinal center formation | Any process that modulates the frequency, rate, or extent of germinal center formation. |
regulation of GTPase activity | Any process that modulates the rate of GTP hydrolysis by a GTPase. |
regulation of immune response | Any process that modulates the frequency, rate or extent of the immune response, the immunological reaction of an organism to an immunogenic stimulus. |
regulation of immune system process | Any process that modulates the frequency, rate, or extent of an immune system process. |
regulation of inflammatory response | Any process that modulates the frequency, rate or extent of the inflammatory response, the immediate defensive reaction (by vertebrate tissue) to infection or injury caused by chemical or physical agents. |
regulation of memory T cell differentiation | Any process that modulates the frequency, rate, or extent of memory T cell differentiation. |
regulation of T cell proliferation | Any process that modulates the frequency, rate or extent of T cell proliferation. |
regulation of transcription by RNA polymerase II | Any process that modulates the frequency, rate or extent of transcription mediated by RNA polymerase II. |
Rho protein signal transduction | The series of molecular signals within the cell that are mediated by a member of the Rho family of proteins switching to a GTP-bound active state. |
spermatogenesis | The developmental process by which male germ line stem cells self renew or give rise to successive cell types resulting in the development of a spermatozoa. |
T-helper 2 cell differentiation | The process in which a relatively unspecialized T cell acquires specialized features of a T-helper 2 (Th2) cell. A Th2 cell is a CD4-positive, alpha-beta T cell that has the phenotype GATA-3-positive and produces interleukin-4. |
transcription by RNA polymerase II | The synthesis of RNA from a DNA template by RNA polymerase II (RNAP II), originating at an RNA polymerase II promoter. Includes transcription of messenger RNA (mRNA) and certain small nuclear RNAs (snRNAs). |
type 2 immune response | An immune response which is associated with resistance to extracellular organisms such as helminths and pathological conditions such as allergy, which is orchestrated by the production of particular cytokines, most notably IL-4, IL-5, IL-10, and IL-13, by any of a variety of cell types including T-helper 2 cells, eosinophils, basophils, mast cells, and nuocytes, resulting in enhanced production of certain antibody isotypes and other effects. |
177 homologous proteins in AiPD
UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
---|---|---|---|---|
Q08DS3 | OSR1 | Protein odd-skipped-related 1 | Bos taurus (Bovine) | PR |
Q2VWH6 | FEZF2 | Fez family zinc finger protein 2 | Bos taurus (Bovine) | PR |
A6QNZ0 | ZSCAN26 | Zinc finger and SCAN domain-containing protein 26 | Bos taurus (Bovine) | PR |
A7MBI1 | ZFP69 | Zinc finger protein 69 homolog | Bos taurus (Bovine) | PR |
Q08705 | CTCF | Transcriptional repressor CTCF | Gallus gallus (Chicken) | PR |
O42409 | GFI1B | Zinc finger protein Gfi-1b | Gallus gallus (Chicken) | PR |
A2T6W2 | ZNF449 | Zinc finger protein 449 | Pan troglodytes (Chimpanzee) | PR |
Q9U405 | grau | Transcription factor grauzone | Drosophila melanogaster (Fruit fly) | PR |
Q7K0S9 | sug | Zinc finger protein GLIS2 homolog | Drosophila melanogaster (Fruit fly) | PR |
P20385 | Cf2 | Chorion transcription factor Cf2 | Drosophila melanogaster (Fruit fly) | PR |
Q86P48 | ATbp | AT-rich binding protein | Drosophila melanogaster (Fruit fly) | PR |
P28698 | MZF1 | Myeloid zinc finger 1 | Homo sapiens (Human) | PR |
Q9NTW7 | ZFP64 | Zinc finger protein 64 | Homo sapiens (Human) | PR |
O14978 | ZNF263 | Zinc finger protein 263 | Homo sapiens (Human) | PR |
O60304 | ZNF500 | Zinc finger protein 500 | Homo sapiens (Human) | PR |
P08151 | GLI1 | Zinc finger protein GLI1 | Homo sapiens (Human) | PR |
Q9UFB7 | ZBTB47 | Zinc finger and BTB domain-containing protein 47 | Homo sapiens (Human) | PR |
P18146 | EGR1 | Early growth response protein 1 | Homo sapiens (Human) | PR |
Q9Y5W3 | KLF2 | Krueppel-like factor 2 | Homo sapiens (Human) | PR |
Q9UNY5 | ZNF232 | Zinc finger protein 232 | Homo sapiens (Human) | PR |
Q96SZ4 | ZSCAN10 | Zinc finger and SCAN domain-containing protein 10 | Homo sapiens (Human) | PR |
P17028 | ZNF24 | Zinc finger protein 24 | Homo sapiens (Human) | PR |
P57682 | KLF3 | Krueppel-like factor 3 | Homo sapiens (Human) | PR |
P25490 | YY1 | Transcriptional repressor protein YY1 | Homo sapiens (Human) | SS |
O43296 | ZNF264 | Zinc finger protein 264 | Homo sapiens (Human) | PR |
P49711 | CTCF | Transcriptional repressor CTCF | Homo sapiens (Human) | PR |
Q9NQX1 | PRDM5 | PR domain zinc finger protein 5 | Homo sapiens (Human) | PR |
Q8TAX0 | OSR1 | Protein odd-skipped-related 1 | Homo sapiens (Human) | PR |
Q9UL58 | ZNF215 | Zinc finger protein 215 | Homo sapiens (Human) | PR |
Q8TBJ5 | FEZF2 | Fez family zinc finger protein 2 | Homo sapiens (Human) | PR |
Q96SR6 | ZNF382 | Zinc finger protein 382 | Homo sapiens (Human) | PR |
Q96IT1 | ZNF496 | Zinc finger protein 496 | Homo sapiens (Human) | PR |
Q96N95 | ZNF396 | Zinc finger protein 396 | Homo sapiens (Human) | PR |
Q9ULJ3 | ZBTB21 | Zinc finger and BTB domain-containing protein 21 | Homo sapiens (Human) | PR |
O75840 | KLF7 | Krueppel-like factor 7 | Homo sapiens (Human) | PR |
Q9H9D4 | ZNF408 | Zinc finger protein 408 | Homo sapiens (Human) | PR |
Q13127 | REST | RE1-silencing transcription factor | Homo sapiens (Human) | PR |
Q8IZM8 | ZNF654 | Zinc finger protein 654 | Homo sapiens (Human) | PR |
Q14526 | HIC1 | Hypermethylated in cancer 1 protein | Homo sapiens (Human) | PR |
P17022 | ZNF18 | Zinc finger protein 18 | Homo sapiens (Human) | PR |
Q86XF7 | ZNF575 | Zinc finger protein 575 | Homo sapiens (Human) | PR |
Q06889 | EGR3 | Early growth response protein 3 | Homo sapiens (Human) | PR |
Q8NAM6 | ZSCAN4 | Zinc finger and SCAN domain-containing protein 4 | Homo sapiens (Human) | PR |
Q08ER8 | ZNF543 | Zinc finger protein 543 | Homo sapiens (Human) | PR |
P17029 | ZKSCAN1 | Zinc finger protein with KRAB and SCAN domains 1 | Homo sapiens (Human) | PR |
O95625 | ZBTB11 | Zinc finger and BTB domain-containing protein 11 | Homo sapiens (Human) | PR |
Q9NPC7 | MYNN | Myoneurin | Homo sapiens (Human) | PR |
Q96BV0 | ZNF775 | Zinc finger protein 775 | Homo sapiens (Human) | PR |
Q8NF99 | ZNF397 | Zinc finger protein 397 | Homo sapiens (Human) | PR |
Q63HK3 | ZKSCAN2 | Zinc finger protein with KRAB and SCAN domains 2 | Homo sapiens (Human) | PR |
Q5FWF6 | ZNF789 | Zinc finger protein 789 | Homo sapiens (Human) | PR |
Q15776 | ZKSCAN8 | Zinc finger protein with KRAB and SCAN domains 8 | Homo sapiens (Human) | PR |
Q53GI3 | ZNF394 | Zinc finger protein 394 | Homo sapiens (Human) | PR |
O95125 | ZNF202 | Zinc finger protein 202 | Homo sapiens (Human) | PR |
Q05516 | ZBTB16 | Zinc finger and BTB domain-containing protein 16 | Homo sapiens (Human) | PR |
Q9H116 | GZF1 | GDNF-inducible zinc finger protein 1 | Homo sapiens (Human) | PR |
Q8N0Y2 | ZNF444 | Zinc finger protein 444 | Homo sapiens (Human) | PR |
Q6P9G9 | ZNF449 | Zinc finger protein 449 | Homo sapiens (Human) | PR |
Q8IW36 | ZNF695 | Zinc finger protein 695 | Homo sapiens (Human) | PR |
Q5VTD9 | GFI1B | Zinc finger protein Gfi-1b | Homo sapiens (Human) | PR |
Q6PG37 | ZNF790 | Zinc finger protein 790 | Homo sapiens (Human) | PR |
Q9NQV6 | PRDM10 | PR domain zinc finger protein 10 | Homo sapiens (Human) | PR |
Q9Y2D9 | ZNF652 | Zinc finger protein 652 | Homo sapiens (Human) | PR |
Q9Y4E5 | ZNF451 | E3 SUMO-protein ligase ZNF451 | Homo sapiens (Human) | PR |
Q8ND82 | ZNF280C | Zinc finger protein 280C | Homo sapiens (Human) | PR |
Q49AA0 | ZFP69 | Zinc finger protein 69 homolog | Homo sapiens (Human) | PR |
O43298 | ZBTB43 | Zinc finger and BTB domain-containing protein 43 | Homo sapiens (Human) | PR |
P51508 | ZNF81 | Zinc finger protein 81 | Homo sapiens (Human) | PR |
Q5JNZ3 | ZNF311 | Zinc finger protein 311 | Homo sapiens (Human) | PR |
Q9BRR0 | ZKSCAN3 | Zinc finger protein with KRAB and SCAN domains 3 | Homo sapiens (Human) | PR |
Q969J2 | ZKSCAN4 | Zinc finger protein with KRAB and SCAN domains 4 | Homo sapiens (Human) | PR |
P49910 | ZNF165 | Zinc finger protein 165 | Homo sapiens (Human) | PR |
Q9Y4X4 | KLF12 | Krueppel-like factor 12 | Homo sapiens (Human) | PR |
P10074 | ZBTB48 | Telomere zinc finger-associated protein | Homo sapiens (Human) | PR |
P17010 | ZFX | Zinc finger X-chromosomal protein | Homo sapiens (Human) | PR |
Q9H5H4 | ZNF768 | Zinc finger protein 768 | Homo sapiens (Human) | PR |
Q6NSZ9 | ZSCAN25 | Zinc finger and SCAN domain-containing protein 25 | Homo sapiens (Human) | PR |
Q9Y2L8 | ZKSCAN5 | Zinc finger protein with KRAB and SCAN domains 5 | Homo sapiens (Human) | PR |
Q86UZ6 | ZBTB46 | Zinc finger and BTB domain-containing protein 46 | Homo sapiens (Human) | PR |
Q9NX65 | ZSCAN32 | Zinc finger and SCAN domain-containing protein 32 | Homo sapiens (Human) | PR |
O14771 | ZNF213 | Zinc finger protein 213 | Homo sapiens (Human) | PR |
Q8IWY8 | ZSCAN29 | Zinc finger and SCAN domain-containing protein 29 | Homo sapiens (Human) | PR |
Q8NCP5 | ZBTB44 | Zinc finger and BTB domain-containing protein 44 | Homo sapiens (Human) | PR |
Q9NQX0 | PRDM6 | Putative histone-lysine N-methyltransferase PRDM6 | Homo sapiens (Human) | PR |
Q9BU19 | ZNF692 | Zinc finger protein 692 | Homo sapiens (Human) | PR |
Q08AG5 | ZNF844 | Zinc finger protein 844 | Homo sapiens (Human) | PR |
Q6R2W3 | ZBED9 | SCAN domain-containing protein 3 | Homo sapiens (Human) | PR |
P98182 | ZNF200 | Zinc finger protein 200 | Homo sapiens (Human) | PR |
Q9UK11 | ZNF223 | Zinc finger protein 223 | Homo sapiens (Human) | PR |
O15156 | ZBTB7B | Zinc finger and BTB domain-containing protein 7B | Homo sapiens (Human) | PR |
Q6ZMS7 | ZNF783 | Zinc finger protein 783 | Homo sapiens (Human) | PR |
P59923 | ZNF445 | Zinc finger protein 445 | Homo sapiens (Human) | PR |
Q8N859 | ZNF713 | Zinc finger protein 713 | Homo sapiens (Human) | PR |
Q99612 | KLF6 | Krueppel-like factor 6 | Homo sapiens (Human) | PR |
Q8TD17 | ZNF398 | Zinc finger protein 398 | Homo sapiens (Human) | PR |
A6NGD5 | ZSCAN5C | Zinc finger and SCAN domain-containing protein 5C | Homo sapiens (Human) | PR |
Q05215 | EGR4 | Early growth response protein 4 | Homo sapiens (Human) | PR |
Q7Z398 | ZNF550 | Zinc finger protein 550 | Homo sapiens (Human) | PR |
Q96N20 | ZNF75A | Zinc finger protein 75A | Homo sapiens (Human) | PR |
A6NJL1 | ZSCAN5B | Zinc finger and SCAN domain-containing protein 5B | Homo sapiens (Human) | PR |
A1YPR0 | ZBTB7C | Zinc finger and BTB domain-containing protein 7C | Homo sapiens (Human) | PR |
Q9NWS9 | ZNF446 | Zinc finger protein 446 | Homo sapiens (Human) | PR |
Q96N38 | ZNF714 | Zinc finger protein 714 | Homo sapiens (Human) | PR |
Q86YH2 | ZNF280B | Zinc finger protein 280B | Homo sapiens (Human) | PR |
Q9Y2K1 | ZBTB1 | Zinc finger and BTB domain-containing protein 1 | Homo sapiens (Human) | PR |
P24278 | ZBTB25 | Zinc finger and BTB domain-containing protein 25 | Homo sapiens (Human) | PR |
Q8N680 | ZBTB2 | Zinc finger and BTB domain-containing protein 2 | Homo sapiens (Human) | PR |
Q9Y330 | ZBTB12 | Zinc finger and BTB domain-containing protein 12 | Homo sapiens (Human) | PR |
Q5TC79 | ZBTB37 | Zinc finger and BTB domain-containing protein 37 | Homo sapiens (Human) | PR |
Q9HBE1 | PATZ1 | POZ-, AT hook-, and zinc finger-containing protein 1 | Homo sapiens (Human) | PR |
P52739 | ZNF131 | Zinc finger protein 131 | Homo sapiens (Human) | PR |
Q13105 | ZBTB17 | Zinc finger and BTB domain-containing protein 17 | Homo sapiens (Human) | PR |
O08584 | Klf6 | Krueppel-like factor 6 | Mus musculus (Mouse) | PR |
Q61164 | Ctcf | Transcriptional repressor CTCF | Mus musculus (Mouse) | PR |
Q810A1 | Znf18 | Zinc finger protein 18 | Mus musculus (Mouse) | PR |
Q8BGS3 | Zkscan1 | Zinc finger protein with KRAB and SCAN domains 1 | Mus musculus (Mouse) | PR |
Q00899 | Yy1 | Transcriptional repressor protein YY1 | Mus musculus (Mouse) | PR |
Q9DAI4 | Zbtb43 | Zinc finger and BTB domain-containing protein 43 | Mus musculus (Mouse) | PR |
O70237 | Gfi1b | Zinc finger protein Gfi-1b | Mus musculus (Mouse) | PR |
Q99KZ6 | Znf639 | Zinc finger protein 639 | Mus musculus (Mouse) | PR |
Q9Z1D9 | Znf394 | Zinc finger protein 394 | Mus musculus (Mouse) | PR |
Q9CXE0 | Prdm5 | PR domain zinc finger protein 5 | Mus musculus (Mouse) | PR |
P43300 | Egr3 | Early growth response protein 3 | Mus musculus (Mouse) | PR |
Q9DAU9 | Znf654 | Zinc finger protein 654 | Mus musculus (Mouse) | PR |
Q9R1Y5 | Hic1 | Hypermethylated in cancer 1 protein | Mus musculus (Mouse) | PR |
Q8R0T2 | Znf768 | Zinc finger protein 768 | Mus musculus (Mouse) | PR |
Q9WVG7 | Osr1 | Protein odd-skipped-related 1 | Mus musculus (Mouse) | PR |
Q8BI73 | Znf775 | Zinc finger protein 775 | Mus musculus (Mouse) | PR |
Q8VCZ7 | Zbtb7c | Zinc finger and BTB domain-containing protein 7C | Mus musculus (Mouse) | PR |
Q91VN1 | Znf24 | Zinc finger protein 24 | Mus musculus (Mouse) | PR |
Q9DB38 | Znf580 | Zinc finger protein 580 | Mus musculus (Mouse) | PR |
A7KBS4 | Zscan4d | Zinc finger and SCAN domain containing protein 4D | Mus musculus (Mouse) | PR |
Q91VW9 | Zkscan3 | Zinc finger protein with KRAB and SCAN domains 3 | Mus musculus (Mouse) | PR |
P10925 | Zfy1 | Zinc finger Y-chromosomal protein 1 | Mus musculus (Mouse) | PR |
P08046 | Egr1 | Early growth response protein 1 | Mus musculus (Mouse) | PR |
Q3TTC2 | Yy2 | Transcription factor YY2 | Mus musculus (Mouse) | PR |
Q3UTQ7 | Prdm10 | PR domain zinc finger protein 10 | Mus musculus (Mouse) | PR |
Q6P3Y5 | Znf280c | Zinc finger protein 280C | Mus musculus (Mouse) | PR |
Q9ERU3 | Znf22 | Zinc finger protein 22 | Mus musculus (Mouse) | PR |
Q8VIG1 | Rest | RE1-silencing transcription factor | Mus musculus (Mouse) | PR |
Q9Z1D8 | Zkscan5 | Zinc finger protein with KRAB and SCAN domains 5 | Mus musculus (Mouse) | PR |
Q8BID6 | Zbtb46 | Zinc finger and BTB domain-containing protein 46 | Mus musculus (Mouse) | PR |
P17012 | Zfx | Zinc finger X-chromosomal protein | Mus musculus (Mouse) | PR |
Q9WUK6 | Zbtb18 | Zinc finger and BTB domain-containing protein 18 | Mus musculus (Mouse) | PR |
O35738 | Klf12 | Krueppel-like factor 12 | Mus musculus (Mouse) | PR |
B2RXC5 | Znf382 | Zinc finger protein 382 | Mus musculus (Mouse) | PR |
O08900 | Ikzf3 | Zinc finger protein Aiolos | Mus musculus (Mouse) | PR |
Q5DU09 | Znf652 | Zinc finger protein 652 | Mus musculus (Mouse) | PR |
Q5RJ54 | Zscan26 | Zinc finger and SCAN domain-containing protein 26 | Mus musculus (Mouse) | PR |
Q8BLM0 | Klf8 | Krueppel-like factor 8 | Mus musculus (Mouse) | PR |
Q99JB0 | Klf7 | Krueppel-like factor 7 | Mus musculus (Mouse) | PR |
Q8R0A2 | Zbtb44 | Zinc finger and BTB domain-containing protein 44 | Mus musculus (Mouse) | PR |
P20662 | Zfy2 | Zinc finger Y-chromosomal protein 2 | Mus musculus (Mouse) | PR |
Q80VJ6 | Zscan4c | Zinc finger and SCAN domain containing protein 4C | Mus musculus (Mouse) | PR |
Q3URS2 | Zscan4f | Zinc finger and SCAN domain containing protein 4F | Mus musculus (Mouse) | PR |
Q60980 | Klf3 | Krueppel-like factor 3 | Mus musculus (Mouse) | PR |
Q8K3J5 | Znf131 | Zinc finger protein 131 | Mus musculus (Mouse) | PR |
P41183 | Bcl6 | B-cell lymphoma 6 protein homolog | Mus musculus (Mouse) | PR |
Q9Z2K3 | Znf394 | Zinc finger protein 394 | Rattus norvegicus (Rat) | PR |
Q642B9 | Znf18 | Zinc finger protein 18 | Rattus norvegicus (Rat) | PR |
B0K011 | Osr1 | Protein odd-skipped-related 1 | Rattus norvegicus (Rat) | PR |
D3ZUU2 | Gzf1 | GDNF-inducible zinc finger protein 1 | Rattus norvegicus (Rat) | PR |
B1WBU4 | Zbtb8a | Zinc finger and BTB domain-containing protein 8A | Rattus norvegicus (Rat) | PR |
Q7TNK3 | Znf24 | Zinc finger protein 24 | Rattus norvegicus (Rat) | PR |
O35819 | Klf6 | Krueppel-like factor 6 | Rattus norvegicus (Rat) | PR |
Q9R1D1 | Ctcf | Transcriptional repressor CTCF | Rattus norvegicus (Rat) | PR |
P43301 | Egr3 | Early growth response protein 3 | Rattus norvegicus (Rat) | PR |
P08154 | Egr1 | Early growth response protein 1 | Rattus norvegicus (Rat) | PR |
A0JPL0 | Znf382 | Zinc finger protein 382 | Rattus norvegicus (Rat) | PR |
Q4KLI1 | Zkscan1 | Zinc finger protein with KRAB and SCAN domains 1 | Rattus norvegicus (Rat) | PR |
A1L1J6 | Znf652 | Zinc finger protein 652 | Rattus norvegicus (Rat) | PR |
Q9SHD0 | ZAT4 | Zinc finger protein ZAT4 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q0P4X6 | zbtb44 | Zinc finger and BTB domain-containing protein 44 | Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) | PR |
A4II20 | egr1 | Early growth response protein 1 | Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) | PR |
Q6P882 | zbtb8a.2 | Zinc finger and BTB domain-containing protein 8A.2 | Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) | PR |
Q567C6 | znf367 | Zinc finger protein 367 | Danio rerio (Zebrafish) (Brachydanio rerio) | PR |
A7Y7X5 | znf711 | Zinc finger protein 711 | Danio rerio (Zebrafish) (Brachydanio rerio) | PR |
10 | 20 | 30 | 40 | 50 | 60 |
MASPADSCIQ | FTRHASDVLL | NLNRLRSRDI | LTDVVIVVSR | EQFRAHKTVL | MACSGLFYSI |
70 | 80 | 90 | 100 | 110 | 120 |
FTDQLKCNLS | VINLDPEINP | EGFCILLDFM | YTSRLNLREG | NIMAVMATAM | YLQMEHVVDT |
130 | 140 | 150 | 160 | 170 | 180 |
CRKFIKASEA | EMVSAIKPPR | EEFLNSRMLM | PQDIMAYRGR | EVVENNLPLR | SAPGCESRAF |
190 | 200 | 210 | 220 | 230 | 240 |
APSLYSGLST | PPASYSMYSH | LPVSSLLFSD | EEFRDVRMPV | ANPFPKERAL | PCDSARPVPG |
250 | 260 | 270 | 280 | 290 | 300 |
EYSRPTLEVS | PNVCHSNIYS | PKETIPEEAR | SDMHYSVAEG | LKPAAPSARN | APYFPCDKAS |
310 | 320 | 330 | 340 | 350 | 360 |
KEEERPSSED | EIALHFEPPN | APLNRKGLVS | PQSPQKSDCQ | PNSPTESCSS | KNACILQASG |
370 | 380 | 390 | 400 | 410 | 420 |
SPPAKSPTDP | KACNWKKYKF | IVLNSLNQNA | KPEGPEQAEL | GRLSPRAYTA | PPACQPPMEP |
430 | 440 | 450 | 460 | 470 | 480 |
ENLDLQSPTK | LSASGEDSTI | PQASRLNNIV | NRSMTGSPRS | SSESHSPLYM | HPPKCTSCGS |
490 | 500 | 510 | 520 | 530 | 540 |
QSPQHAEMCL | HTAGPTFPEE | MGETQSEYSD | SSCENGAFFC | NECDCRFSEE | ASLKRHTLQT |
550 | 560 | 570 | 580 | 590 | 600 |
HSDKPYKCDR | CQASFRYKGN | LASHKTVHTG | EKPYRCNICG | AQFNRPANLK | THTRIHSGEK |
610 | 620 | 630 | 640 | 650 | 660 |
PYKCETCGAR | FVQVAHLRAH | VLIHTGEKPY | PCEICGTRFR | HLQTLKSHLR | IHTGEKPYHC |
670 | 680 | 690 | 700 | ||
EKCNLHFRHK | SQLRLHLRQK | HGAITNTKVQ | YRVSATDLPP | ELPKAC |