Q03014
Gene name |
HHEX (HEX, PRH, PRHX) |
Protein name |
Hematopoietically-expressed homeobox protein HHEX |
Names |
Homeobox protein HEX, Homeobox protein PRH |
Species |
Homo sapiens (Human) |
KEGG Pathway |
hsa:3087 |
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

2 structures for Q03014
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
2E1O | NMR | - | A | 138-194 | PDB |
AF-Q03014-F1 | Predicted | AlphaFoldDB |
219 variants for Q03014
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
CA212069963 rs890175536 |
2 | Q>R | No |
ClinGen TOPMed |
|
rs1564728388 CA377810847 |
4 | P>L | No |
ClinGen Ensembl |
|
CA377810842 rs1455869041 |
4 | P>S | No |
ClinGen gnomAD |
|
CA377810851 rs1589621587 |
5 | H>P | No |
ClinGen Ensembl |
|
CA212069965 rs1014685241 |
6 | P>R | No |
ClinGen TOPMed |
|
CA377810863 rs1190097525 |
7 | G>R | No |
ClinGen TOPMed |
|
CA212069967 rs546230628 |
8 | P>L | No |
ClinGen 1000Genomes gnomAD |
|
rs546230628 CA377810870 |
8 | P>Q | No |
ClinGen 1000Genomes gnomAD |
|
rs1231813088 CA377810883 |
10 | A>V | No |
ClinGen gnomAD |
|
rs1183185221 CA377810889 |
11 | G>A | No |
ClinGen gnomAD |
|
rs1423720818 CA377810890 |
12 | A>T | No |
ClinGen gnomAD |
|
CA377810898 rs1355791757 |
13 | V>L | No |
ClinGen gnomAD |
|
CA377810896 rs1355791757 |
13 | V>M | No |
ClinGen gnomAD |
|
CA377810904 rs1168959334 CA377810903 |
14 | G>R | No |
ClinGen gnomAD |
|
TCGA novel rs748494650 CA5604578 |
15 | V>G | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen ExAC gnomAD NCI-TCGA |
CA212069968 rs973237946 |
15 | V>L | No |
ClinGen TOPMed |
|
CA377810915 rs1335185921 |
16 | P>L | No |
ClinGen gnomAD |
|
rs1335185921 CA377810917 |
16 | P>Q | No |
ClinGen gnomAD |
|
CA212069970 rs867687942 |
19 | A>E | No |
ClinGen Ensembl |
|
rs867687942 CA377810935 |
19 | A>G | No |
ClinGen Ensembl |
|
rs1218689152 CA377810932 |
19 | A>P | No |
ClinGen TOPMed |
|
rs1218689152 CA377810931 |
19 | A>T | No |
ClinGen TOPMed |
|
rs1245578903 CA377810941 |
20 | P>L | No |
ClinGen gnomAD |
|
rs1194519827 CA377810948 |
22 | P>T | No |
ClinGen gnomAD |
|
CA377810967 rs1470860448 |
25 | Q>P | No |
ClinGen TOPMed |
|
rs749396288 CA5604581 |
26 | P>A | No |
ClinGen ExAC gnomAD |
|
rs917914135 CA212069973 |
26 | P>R | No |
ClinGen TOPMed gnomAD |
|
CA377810978 rs1240771743 |
27 | A>T | No |
ClinGen gnomAD |
|
CA377810995 rs1188874146 |
29 | P>L | No |
ClinGen TOPMed gnomAD |
|
CA377810994 rs1188874146 |
29 | P>R | No |
ClinGen TOPMed gnomAD |
|
CA377810999 rs1295181822 |
30 | T>K | No |
ClinGen TOPMed gnomAD |
|
CA377811001 rs1295181822 |
30 | T>M | No |
ClinGen TOPMed gnomAD |
|
CA377811002 rs1391782171 |
31 | P>T | No |
ClinGen gnomAD |
|
rs949426439 CA212069974 |
33 | Y>C | No |
ClinGen TOPMed |
|
CA377811017 rs1474310402 |
33 | Y>H | No |
ClinGen gnomAD |
|
TCGA novel | 33 | Y>T | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA5604582 rs770977782 |
34 | I>M | No |
ClinGen ExAC gnomAD |
|
rs1156313218 CA377811036 |
35 | E>D | No |
ClinGen TOPMed |
|
CA212069975 rs943618846 |
36 | D>N | No |
ClinGen gnomAD |
|
rs1184570903 CA377811071 |
41 | G>E | No |
ClinGen TOPMed |
|
CA377811078 rs1338751519 |
42 | P>L | No |
ClinGen TOPMed gnomAD |
|
CA5604586 rs771793065 |
44 | A>V | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1298618123 CA377811096 |
45 | P>L | No |
ClinGen gnomAD |
|
CA5604587 rs775302104 |
48 | A>T | No |
ClinGen ExAC TOPMed gnomAD |
|
CA377811111 rs1253856328 |
48 | A>V | No |
ClinGen gnomAD |
|
CA5604588 rs760441003 |
50 | T>K | No |
ClinGen ExAC TOPMed gnomAD |
|
TCGA novel | 50 | T>R | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs1208900235 CA377811134 |
52 | P>L | No |
ClinGen TOPMed gnomAD |
|
rs1208900235 CA377811133 |
52 | P>Q | No |
ClinGen TOPMed gnomAD |
|
rs776542212 CA5604590 |
53 | S>F | No |
ClinGen ExAC gnomAD |
|
rs932231605 CA212069978 |
54 | P>L | No |
ClinGen TOPMed gnomAD |
|
CA377811150 rs1170180635 |
55 | N>S | No |
ClinGen TOPMed gnomAD |
|
rs1418617550 CA377811165 |
57 | S>F | No |
ClinGen TOPMed |
|
rs764744029 CA5604592 |
59 | T>I | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1427205880 CA377811182 |
60 | S>N | No |
ClinGen gnomAD |
|
rs750063118 CA377811194 CA5604593 |
62 | V>L | No |
ClinGen ExAC TOPMed gnomAD |
|
CA377811203 rs1321412297 |
63 | S>F | No |
ClinGen gnomAD |
|
CA5604596 rs142036619 |
64 | P>H | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA5604597 rs142036619 |
64 | P>L | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA5604598 rs142036619 |
64 | P>R | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
rs766112006 CA5604595 |
64 | P>S | No |
ClinGen ExAC gnomAD |
|
CA377811211 rs1244380185 |
65 | Y>F | No |
ClinGen TOPMed |
|
CA377811207 rs1332097827 |
65 | Y>H | No |
ClinGen gnomAD |
|
CA377811214 rs1225884461 |
66 | R>G | No |
ClinGen gnomAD |
|
CA212069982 rs868255183 |
66 | R>Q | No |
ClinGen gnomAD |
|
rs754315134 CA212069983 |
67 | T>A | No |
ClinGen ExAC TOPMed gnomAD |
|
rs757308946 CA5604600 |
67 | T>I | No |
ClinGen ExAC TOPMed gnomAD |
|
CA5604599 rs754315134 |
67 | T>S | No |
ClinGen ExAC TOPMed gnomAD |
|
rs757308946 CA377811220 |
67 | T>S | No |
ClinGen ExAC TOPMed gnomAD |
|
CA5604603 rs745904454 |
68 | P>L | No |
ClinGen ExAC gnomAD |
|
CA5604602 rs745904454 |
68 | P>R | No |
ClinGen ExAC gnomAD |
|
CA377811233 rs1204238532 |
70 | Y>D | No |
ClinGen gnomAD |
|
rs780241760 CA5604604 |
71 | E>G | No |
ClinGen ExAC gnomAD |
|
rs746868626 CA5604605 |
72 | P>H | No |
ClinGen ExAC gnomAD |
|
rs1442714190 CA377811256 |
73 | T>M | No |
ClinGen gnomAD |
|
TCGA novel | 75 | I>M | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs1589621770 CA377811275 |
76 | H>P | No |
ClinGen Ensembl |
|
rs1248379400 CA377811289 |
78 | A>V | No |
ClinGen TOPMed |
|
TCGA novel | 79 | F>L | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA377811303 rs1320151050 |
80 | S>L | No |
ClinGen TOPMed |
|
rs1480129873 CA377811309 |
81 | H>P | No |
ClinGen gnomAD |
|
CA377811311 rs1589621781 |
81 | H>Q | No |
ClinGen Ensembl |
|
CA377811317 rs1159967487 |
82 | H>R | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed gnomAD |
CA377811325 rs1365657343 |
83 | S>F | No |
ClinGen gnomAD |
|
rs1451879808 CA377811326 |
84 | A>T | No |
ClinGen gnomAD |
|
rs1391826173 CA377811334 |
85 | A>T | No |
ClinGen gnomAD |
|
TCGA novel | 86 | A>V | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs769590079 CA377811350 |
88 | A>S | No |
ClinGen ExAC gnomAD |
|
CA5604609 rs769590079 |
88 | A>T | No |
ClinGen ExAC gnomAD |
|
CA377811357 rs1345400029 |
89 | A>V | No |
ClinGen gnomAD |
|
CA377811364 rs1418387 |
90 | A>G | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs1418387 CA5604610 |
90 | A>V | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA377811369 rs1308497933 |
91 | Y>C | No |
ClinGen gnomAD |
|
CA212069989 rs867605493 COSM1741957 |
92 | G>R | Variant assessed as Somatic; 0.0 impact. urinary_tract [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated NCI-TCGA gnomAD |
rs751190903 CA5604613 |
93 | P>S | No |
ClinGen ExAC TOPMed gnomAD |
|
rs867066260 CA212069990 |
94 | G>S | No |
ClinGen Ensembl |
|
rs1290819766 CA377811390 |
95 | G>C | No |
ClinGen gnomAD |
|
CA377811391 rs1483331825 |
95 | G>D | No |
ClinGen gnomAD |
|
CA377811403 rs1348962571 |
97 | G>R | No |
ClinGen TOPMed |
|
rs370000570 CA212069991 |
99 | P>L | No |
ClinGen ESP TOPMed gnomAD |
|
rs754334398 CA5604616 |
99 | P>T | No |
ClinGen ExAC gnomAD |
|
CA377811419 rs1386125639 |
100 | L>V | No |
ClinGen gnomAD |
|
CA377811428 rs1422263508 |
101 | Y>S | No |
ClinGen TOPMed |
|
rs1426832512 CA377811436 |
102 | P>L | No |
ClinGen TOPMed gnomAD |
|
rs1192192366 CA377811433 |
102 | P>S | No |
ClinGen TOPMed |
|
CA377811450 rs1365407216 |
104 | P>Q | No |
ClinGen gnomAD |
|
CA377811447 rs1162031192 |
104 | P>S | No |
ClinGen TOPMed gnomAD |
|
CA377811461 rs1430945151 |
106 | T>M | No |
ClinGen gnomAD |
|
rs779264732 CA5604618 |
107 | V>M | No |
ClinGen ExAC gnomAD |
|
CA212069992 rs994627049 |
109 | D>N | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed |
CA212069993 rs1026326163 |
113 | A>S | No |
ClinGen gnomAD |
|
CA5604620 rs540724252 |
113 | A>V | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
CA5604622 rs747172564 |
115 | L>F | No |
ClinGen ExAC TOPMed gnomAD |
|
CA212069994 rs993173166 |
116 | R>C | No |
ClinGen TOPMed gnomAD |
|
rs1206459587 CA377811521 |
116 | R>P | No |
ClinGen TOPMed gnomAD |
|
rs1024947210 CA377811527 |
117 | H>L | No |
ClinGen TOPMed gnomAD |
|
CA212069995 rs1024947210 |
117 | H>P | No |
ClinGen TOPMed gnomAD |
|
CA377811536 rs987560198 CA212069996 |
118 | D>E | No |
ClinGen TOPMed gnomAD |
|
CA377811542 rs1243872043 |
119 | P>L | No |
ClinGen gnomAD |
|
CA377811546 rs1298456522 |
120 | L>P | No |
ClinGen TOPMed |
|
rs1384927212 CA377811548 |
121 | G>S | No |
ClinGen gnomAD |
|
CA5604633 rs777102021 |
123 | P>S | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA gnomAD |
rs762070983 CA5604634 |
124 | L>P | No |
ClinGen ExAC gnomAD |
|
CA5604635 rs765838543 |
128 | P>L | No |
ClinGen ExAC gnomAD |
|
rs1413060810 CA377811609 |
128 | P>S | No |
ClinGen TOPMed |
|
CA5604636 rs750824236 |
129 | F>L | No |
ClinGen ExAC gnomAD |
|
rs1325695460 CA377811627 |
131 | Q>E | No |
ClinGen gnomAD |
|
rs538680375 CA5604637 |
132 | R>K | No |
ClinGen 1000Genomes ExAC gnomAD |
|
CA5604638 rs150804177 |
133 | P>S | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA377811652 rs1564729118 |
135 | H>Y | No |
ClinGen Ensembl |
|
rs1240715324 CA377811668 |
137 | R>K | No |
ClinGen TOPMed gnomAD |
|
rs1200714119 CA377811714 |
144 | F>I | No |
ClinGen gnomAD |
|
CA377811727 rs1271715312 |
145 | S>C | No |
ClinGen gnomAD |
|
CA377811735 rs1293929865 |
146 | N>K | No |
ClinGen gnomAD |
|
rs781261088 CA5604642 |
147 | D>E | No |
ClinGen ExAC TOPMed gnomAD |
|
rs867064568 CA212070245 |
147 | D>N | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen Ensembl NCI-TCGA |
rs571252950 CA5604643 |
148 | Q>* | No |
ClinGen 1000Genomes ExAC gnomAD |
|
rs777779960 CA5604645 |
150 | I>V | No |
ClinGen ExAC gnomAD |
|
rs751797640 CA5604648 |
151 | E>D | No |
ClinGen ExAC TOPMed gnomAD |
|
CA5604647 rs770598208 |
151 | E>Q | No |
ClinGen ExAC gnomAD |
|
rs745348021 TCGA novel CA5604649 |
154 | K>N | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen ExAC gnomAD NCI-TCGA |
rs1458326195 CA377811786 |
154 | K>T | No |
ClinGen TOPMed |
|
CA377811791 rs1343529616 |
155 | K>E | No |
ClinGen gnomAD |
|
rs1274323168 CA377811809 |
157 | E>G | No |
ClinGen gnomAD |
|
rs771813965 CA5604650 |
157 | E>K | No |
ClinGen ExAC gnomAD |
|
rs765458169 CA5604653 |
159 | Q>R | No |
ClinGen ExAC TOPMed gnomAD |
|
CA377811838 rs1162165582 |
161 | Y>C | No |
ClinGen TOPMed |
|
CA377811851 rs1223732746 |
163 | S>Y | No |
ClinGen gnomAD |
|
rs755049912 CA5604658 |
165 | P>L | No |
ClinGen ExAC gnomAD |
|
rs751698879 CA5604657 |
165 | P>S | No |
ClinGen ExAC gnomAD |
|
TCGA novel | 168 | K>M | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
CA5604660 rs752804342 |
168 | K>R | No |
ClinGen ExAC gnomAD |
|
CA212070246 rs17851141 |
171 | A>T | No |
ClinGen Ensembl |
|
CA5604661 rs755960214 |
173 | M>R | No |
ClinGen ExAC gnomAD |
|
CA5604662 rs777393392 |
175 | Q>H | No |
ClinGen ExAC gnomAD |
|
CA377811936 rs1292554684 |
177 | S>R | No |
ClinGen Ensembl |
|
rs753656580 CA5604663 |
178 | E>G | No |
ClinGen ExAC gnomAD |
|
CA212070247 rs979370507 |
178 | E>Q | No |
ClinGen Ensembl |
|
TCGA novel | 188 | R>* | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
TCGA novel | 193 | R>K | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
TCGA novel | 197 | Q>* | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs749658938 CA5604691 |
197 | Q>H | No |
ClinGen ExAC gnomAD |
|
CA377812110 rs1589623553 |
198 | E>K | No |
ClinGen Ensembl |
|
rs1465729223 CA377812124 |
199 | N>K | No |
ClinGen TOPMed gnomAD |
|
CA377812127 rs780836792 |
200 | P>S | No |
ClinGen ExAC TOPMed gnomAD |
|
CA5604707 rs780836792 |
200 | P>T | No |
ClinGen ExAC TOPMed gnomAD |
|
rs139182180 CA5604708 |
202 | S>N | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA5604709 rs757653686 |
203 | N>S | No |
ClinGen ExAC gnomAD |
|
rs757653686 CA5604710 |
203 | N>T | No |
ClinGen ExAC gnomAD |
|
TCGA novel | 206 | E>K | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs770553856 | 207 | E>missing | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No | NCI-TCGA |
rs1300666221 CA377812178 |
207 | E>Q | No |
ClinGen TOPMed |
|
rs1224472544 CA377812181 |
207 | E>V | No |
ClinGen TOPMed |
|
rs746224197 CA5604712 |
208 | L>Q | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1280797145 CA377812188 |
209 | E>* | No |
ClinGen TOPMed gnomAD |
|
rs1330004120 CA377812192 |
209 | E>G | No |
ClinGen gnomAD |
|
rs1280797145 CA377812189 |
209 | E>Q | No |
ClinGen TOPMed gnomAD |
|
rs1348222290 CA377812207 |
211 | L>S | No |
ClinGen gnomAD |
|
rs1375795368 CA377812223 |
213 | S>I | No |
ClinGen TOPMed |
|
rs1375795368 CA377812221 |
213 | S>N | No |
ClinGen TOPMed |
|
rs747061001 CA5604716 |
213 | S>R | No |
ClinGen ExAC gnomAD |
|
CA5604717 rs149951495 |
214 | S>Y | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs777011688 CA5604718 |
215 | C>S | No |
ClinGen ExAC gnomAD |
|
rs1301655370 CA377812240 |
216 | D>Y | No |
ClinGen gnomAD |
|
rs1347616290 CA377812271 |
220 | D>Y | No |
ClinGen gnomAD |
|
rs1159187572 CA377812283 |
221 | L>F | No |
ClinGen TOPMed |
|
CA5604719 rs762086181 |
223 | S>G | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1365794476 CA377812318 |
225 | Q>H | No |
ClinGen gnomAD |
|
rs1468837966 CA377812363 |
228 | G>D | No |
ClinGen TOPMed gnomAD |
|
rs909818705 CA212070418 |
228 | G>S | No |
ClinGen Ensembl |
|
rs939992398 CA212070419 |
229 | A>T | No |
ClinGen Ensembl |
|
rs775389812 CA212070420 |
230 | S>A | No |
ClinGen Ensembl |
|
rs1366647435 CA377812403 |
231 | L>S | No |
ClinGen gnomAD |
|
rs772927960 CA5604721 |
232 | D>N | No |
ClinGen ExAC TOPMed gnomAD |
|
rs772927960 CA377812415 |
232 | D>Y | No |
ClinGen ExAC TOPMed gnomAD |
|
rs762793686 CA5604722 |
233 | S>I | No |
ClinGen ExAC gnomAD |
|
CA5604725 RCV000950750 rs184882393 |
234 | S>C | No |
ClinGen ClinVar 1000Genomes ExAC TOPMed dbSNP gnomAD |
|
rs751457715 CA5604724 |
234 | S>P | No |
ClinGen ExAC gnomAD |
|
rs755816063 CA5604728 |
236 | C>Y | No |
ClinGen ExAC TOPMed gnomAD |
|
CA5604729 rs777471219 |
237 | S>L | No |
ClinGen ExAC TOPMed gnomAD |
|
CA212070421 rs201876873 |
238 | P>L | No |
ClinGen Ensembl |
|
CA377812535 rs1264817116 |
240 | P>S | No |
ClinGen gnomAD |
|
CA377812552 rs1488175634 |
241 | A>V | No |
ClinGen gnomAD |
|
rs758719291 CA5604731 |
243 | Q>* | No |
ClinGen ExAC gnomAD |
|
rs1252818021 CA377812578 |
243 | Q>L | No |
ClinGen gnomAD |
|
rs1217153454 CA377812595 |
244 | E>G | No |
ClinGen TOPMed |
|
rs780435092 CA5604732 |
246 | L>I | No |
ClinGen ExAC gnomAD |
|
rs200052261 COSM921488 CA5604733 |
249 | E>D | Variant assessed as Somatic; 0.0 impact. liver endometrium [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ExAC NCI-TCGA TOPMed gnomAD |
rs1386188015 CA377812670 |
250 | I>M | No |
ClinGen gnomAD |
|
rs1286564454 CA377812711 |
256 | Q>R | No |
ClinGen TOPMed |
|
TCGA novel | 259 | D>N | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs1227981903 CA377812741 |
260 | I>T | No |
ClinGen TOPMed |
|
CA377812763 rs1368365223 |
263 | D>G | No |
ClinGen gnomAD |
|
CA5604736 rs374722314 |
264 | K>E | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
TCGA novel | 264 | K>N | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
rs368062383 CA212070422 |
265 | S>R | No |
ClinGen ESP |
|
rs1394138052 COSM3978903 CA377812800 |
268 | N>S | lung [Cosmic] | No |
ClinGen cosmic curated TOPMed |
rs773419319 CA5604738 |
271 | G>L | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1445495335 CA377812817 |
271 | G>R | No |
ClinGen gnomAD |
No associated diseases with Q03014
4 regional properties for Q03014
Type | Name | Position | InterPro Accession |
---|---|---|---|
domain | Homeobox domain | 135 - 199 | IPR001356 |
conserved_site | Homeobox, conserved site | 170 - 193 | IPR017970 |
domain | Homeobox domain, metazoa | 159 - 170 | IPR020479-1 |
domain | Homeobox domain, metazoa | 174 - 193 | IPR020479-2 |
4 GO annotations of cellular component
Name | Definition |
---|---|
chromatin | The ordered and organized complex of DNA, protein, and sometimes RNA, that forms the chromosome. |
cytoplasm | The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures. |
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. |
protein-DNA complex | A macromolecular complex containing both protein and DNA molecules. |
11 GO annotations of molecular function
Name | Definition |
---|---|
DNA binding, bending | The activity of binding selectively and non-covalently to and distorting the original structure of DNA, typically a straight helix, into a bend, or increasing the bend if the original structure was intrinsically bent due to its sequence. |
DNA-binding transcription activator activity, RNA polymerase II-specific | A DNA-binding transcription factor activity that activates or increases transcription of specific gene sets transcribed by RNA polymerase II. |
DNA-binding transcription factor activity, RNA polymerase II-specific | A DNA-binding transcription factor activity that modulates the transcription of specific gene sets transcribed by RNA polymerase II. |
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. |
eukaryotic initiation factor 4E binding | Binding to eukaryotic initiation factor 4E, a polypeptide factor involved in the initiation of ribosome-mediated translation. |
protein homodimerization activity | Binding to an identical protein to form a homodimer. |
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. |
TBP-class protein binding | Binding to a member of the class of TATA-binding proteins (TBP), including any of the TBP-related factors (TRFs). |
transcription cis-regulatory region binding | Binding to a specific sequence of DNA that is part of a regulatory region that controls transcription of that section of the DNA. The transcribed region might be described as a gene, cistron, or operon. |
21 GO annotations of biological process
Name | Definition |
---|---|
anterior/posterior pattern specification | The regionalization process in which specific areas of cell differentiation are determined along the anterior-posterior axis. The anterior-posterior axis is defined by a line that runs from the head or mouth of an organism to the tail or opposite end of the organism. |
B cell differentiation | The process in which a precursor cell type acquires the specialized features of a B cell. A B cell is a lymphocyte of B lineage with the phenotype CD19-positive and capable of B cell mediated immunity. |
cell differentiation | The process in which relatively unspecialized cells, e.g. embryonic or regenerative cells, acquire specialized structural and/or functional features that characterize the cells, tissues, or organs of the mature organism or some other relatively stable phase of the organism's life history. Differentiation includes the processes involved in commitment of a cell to a specific fate and its subsequent development to the mature state. |
DNA conformation change | A cellular process that results in a change in the spatial configuration of a DNA molecule. A conformation change can bend DNA, or alter the, twist, writhe, or linking number of a DNA molecule. |
mRNA export from nucleus | The directed movement of mRNA from the nucleus to the cytoplasm. |
negative regulation of angiogenesis | Any process that stops, prevents, or reduces the frequency, rate or extent of angiogenesis. |
negative regulation of cyclin-dependent protein serine/threonine kinase activity | Any process that stops, prevents, or reduces the frequency, rate or extent of cyclin-dependent protein serine/threonine kinase activity. |
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 transcription by competitive promoter binding | Any process that stops, prevents, or reduces the frequency, rate or extent of DNA-dependent transcription using a mechanism that involves direct competition for interaction with a promoter binding site. |
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. |
negative regulation of transcription by transcription factor localization | Any process that stops, prevents, or reduces the frequency, rate or extent of DNA-dependent transcription using a mechanism that involves the localization of a transcription factor. |
negative regulation of vascular endothelial growth factor receptor signaling pathway | Any process that stops, prevents, or reduces the frequency, rate or extent of vascular endothelial growth factor receptor signaling pathway activity. |
poly(A)+ mRNA export from nucleus | The directed movement of poly(A)+ mRNA out of the nucleus into the cytoplasm. |
positive regulation of canonical Wnt signaling pathway | Any process that increases the rate, frequency, or extent of the Wnt signaling pathway through beta-catenin, the series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell, followed by propagation of the signal via beta-catenin, and ending with a change in transcription of target genes. |
positive regulation of DNA-templated transcription | Any process that activates or increases the frequency, rate or extent of cellular DNA-templated transcription. |
positive regulation of transcription by RNA polymerase II | Any process that activates or increases the frequency, rate or extent of transcription from an RNA polymerase II promoter. |
positive regulation of Wnt signaling pathway | Any process that activates or increases the frequency, rate or extent of Wnt signal transduction. |
protein localization to nucleus | A process in which a protein transports or maintains the localization of another protein to the nucleus. |
regulation of leukocyte proliferation | Any process that modulates the frequency, rate or extent of leukocyte proliferation. |
regulation of transcription by RNA polymerase II | Any process that modulates the frequency, rate or extent of transcription mediated by RNA polymerase II. |
Wnt signaling pathway | The series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell and ending with a change in cell state. |
8 homologous proteins in AiPD
UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
---|---|---|---|---|
Q6H6S3 | HOX24 | Homeobox-leucine zipper protein HOX24 | Oryza sativa subsp japonica (Rice) | PR |
Q7XUJ5 | HOX22 | Homeobox-leucine zipper protein HOX22 | Oryza sativa subsp japonica (Rice) | PR |
Q5VPE5 | HOX28 | Homeobox-leucine zipper protein HOX28 | Oryza sativa subsp japonica (Rice) | PR |
A3BYC1 | HOX25 | Homeobox-leucine zipper protein HOX25 | Oryza sativa subsp japonica (Rice) | PR |
P46603 | HAT9 | Homeobox-leucine zipper protein HAT9 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9FN29 | ATHB-52 | Homeobox-leucine zipper protein ATHB-52 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9M276 | ATHB-12 | Homeobox-leucine zipper protein ATHB-12 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9IAV3 | hhex | Hematopoietically-expressed homeobox protein hhex | Danio rerio (Zebrafish) (Brachydanio rerio) | PR |
10 | 20 | 30 | 40 | 50 | 60 |
MQYPHPGPAA | GAVGVPLYAP | TPLLQPAHPT | PFYIEDILGR | GPAAPTPAPT | LPSPNSSFTS |
70 | 80 | 90 | 100 | 110 | 120 |
LVSPYRTPVY | EPTPIHPAFS | HHSAAALAAA | YGPGGFGGPL | YPFPRTVNDY | THALLRHDPL |
130 | 140 | 150 | 160 | 170 | 180 |
GKPLLWSPFL | QRPLHKRKGG | QVRFSNDQTI | ELEKKFETQK | YLSPPERKRL | AKMLQLSERQ |
190 | 200 | 210 | 220 | 230 | 240 |
VKTWFQNRRA | KWRRLKQENP | QSNKKEELES | LDSSCDQRQD | LPSEQNKGAS | LDSSQCSPSP |
250 | 260 | ||||
ASQEDLESEI | SEDSDQEVDI | EGDKSYFNAG |