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

6 structures for P18146

Entry ID Method Resolution Chain Position Source
4R2A X-ray 159 A A 335-423 PDB
4R2C X-ray 189 A A 335-423 PDB
4R2D X-ray 209 A A 335-423 PDB
4X9J X-ray 141 A A 335-423 PDB
5N14 NMR - A 395-408 PDB
AF-P18146-F1 Predicted AlphaFoldDB

447 variants for P18146

Variant ID(s) Position Change Description Diseaes Association Provenance
CA361096271
rs1257729605
2 A>T No ClinGen
gnomAD
TCGA novel 2 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs768284319
CA3429954
6 A>G No ClinGen
ExAC
gnomAD
CA3429956
rs202023911
8 M>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs773869377
CA3429955
8 M>T No ClinGen
ExAC
TOPMed
gnomAD
CA361096414
rs1255059386
8 M>V No ClinGen
gnomAD
rs766886557
CA3429957
9 Q>* No ClinGen
ExAC
gnomAD
rs199695186
CA361096460
9 Q>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
NCI-TCGA
gnomAD
rs990682316
CA128180013
9 Q>L No ClinGen
Ensembl
CA3429958
rs754190894
10 L>M No ClinGen
ExAC
gnomAD
rs759886974
CA3429959
13 P>L No ClinGen
ExAC
gnomAD
CA361096571
rs759886974
13 P>R No ClinGen
ExAC
gnomAD
rs765498015
CA3429960
14 L>V No ClinGen
ExAC
gnomAD
CA3429962
rs550077220
15 Q>E No ClinGen
1000Genomes
ExAC
TOPMed
rs550077220
CA361096611
15 Q>K No ClinGen
1000Genomes
ExAC
TOPMed
rs371476752
CA3429963
15 Q>L No ClinGen
ESP
ExAC
rs76865845
CA128180036
17 S>P No ClinGen
Ensembl
CA3429965
rs751640347
19 P>R No ClinGen
ExAC
gnomAD
CA361096712
rs1278496666
19 P>S No ClinGen
gnomAD
rs532091505
CA3429967
20 F>C No ClinGen
1000Genomes
ExAC
gnomAD
CA3429966
rs532091505
20 F>S No ClinGen
1000Genomes
ExAC
gnomAD
CA361096811
COSM1235205
rs1302695548
21 G>E Variant assessed as Somatic; impact. haematopoietic_and_lymphoid_tissue [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
rs374447937
CA3429968
24 P>A No ClinGen
ESP
ExAC
gnomAD
rs547507736
CA361096906
24 P>H No ClinGen
1000Genomes
ExAC
gnomAD
CA3429969
rs547507736
24 P>L Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
gnomAD
TCGA novel 25 H>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs149170181
CA3429970
26 S>P No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs547794631
CA361096998
28 T>A No ClinGen
1000Genomes
ExAC
gnomAD
CA128180061
VAR_052712
rs13181973
28 T>I No ClinGen
UniProt
Ensembl
dbSNP
rs547794631
CA3429971
28 T>P No ClinGen
1000Genomes
ExAC
gnomAD
CA128180079
rs1048942238
29 M>I No ClinGen
TOPMed
rs768374163
CA3429972
29 M>L No ClinGen
ExAC
TOPMed
gnomAD
CA3429974
rs142306373
29 M>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs142306373
CA128180077
29 M>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs768374163
CA3429973
29 M>V Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA361097127
rs1262523327
31 N>K No ClinGen
TOPMed
rs1427288402
CA361097149
32 Y>C No ClinGen
gnomAD
rs199793033
CA3429975
32 Y>D No ClinGen
1000Genomes
ExAC
gnomAD
rs1393783755
CA361097192
33 P>R Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs1173635872
CA361097174
33 P>S No ClinGen
gnomAD
TCGA novel 34 K>E Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3429978
rs368477832
34 K>N Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ESP
NCI-TCGA
TOPMed
gnomAD
CA361097204
rs1421945241
34 K>Q No ClinGen
gnomAD
CA361097221
rs1299144028
34 K>T No ClinGen
gnomAD
rs558452520
CA3429981
35 L>V Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
rs764350788
CA3429985
36 E>A No ClinGen
ExAC
gnomAD
COSM1317146
CA128180119
rs895031869
37 E>K haematopoietic_and_lymphoid_tissue [Cosmic] No ClinGen
cosmic curated
TOPMed
gnomAD
TCGA novel 39 M>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA361097333
rs1561813673
39 M>L No ClinGen
Ensembl
rs577004119
CA3429986
39 M>T No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA3429987
rs538748263
40 L>M Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
gnomAD
rs538748263
CA128180139
40 L>V No ClinGen
1000Genomes
ExAC
gnomAD
rs1283240843
CA361097348
41 L>Q No ClinGen
gnomAD
CA361097345
rs1240644594
41 L>V No ClinGen
gnomAD
TCGA novel 41 L>missing Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 42 S>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3429988
rs767439005
42 S>N No ClinGen
ExAC
gnomAD
CA3429990
rs147932034
43 N>S No ClinGen
ESP
ExAC
rs1561813700
CA361097364
44 G>R No ClinGen
Ensembl
CA361097386
rs1488875491
45 A>V No ClinGen
TOPMed
gnomAD
CA128180153
rs749068859
47 Q>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
CA3429993
rs141704626
48 F>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 49 L>F Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3429995
rs747666166
50 G>D No ClinGen
ExAC
gnomAD
rs778619028
CA3429994
50 G>S No ClinGen
ExAC
gnomAD
CA128180169
rs902327219
52 A>G No ClinGen
TOPMed
rs371909472
CA3429998
52 A>T No ClinGen
ESP
ExAC
gnomAD
CA361097515
rs902327219
52 A>V No ClinGen
TOPMed
rs1350089260
CA361097532
53 G>E No ClinGen
gnomAD
rs202143124
CA128180173
54 A>T No ClinGen
Ensembl
CA361097550
rs1323268510
54 A>V No ClinGen
TOPMed
gnomAD
CA3430001
rs763303660
55 P>A No ClinGen
ExAC
TOPMed
gnomAD
rs763303660
CA361097559
55 P>S No ClinGen
ExAC
TOPMed
gnomAD
CA3430002
rs377338719
56 E>G No ClinGen
ESP
ExAC
gnomAD
CA361097594
rs774647977
57 G>C No ClinGen
ExAC
CA3430003
rs774647977
57 G>S No ClinGen
ExAC
CA128180198
rs933295010
58 S>T No ClinGen
TOPMed
gnomAD
rs1032087174 59 G>missing Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs761876801
CA3430005
59 G>S No ClinGen
ExAC
gnomAD
rs201549947
CA3430006
59 G>V No ClinGen
1000Genomes
ExAC
gnomAD
TCGA novel 60 S>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA361097649
rs750479341
60 S>N No ClinGen
ExAC
CA3430007
rs750479341
60 S>T No ClinGen
ExAC
rs957730983
CA128180211
61 N>S No ClinGen
TOPMed
TCGA novel 61 N>Y Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3430013
rs753748601
63 S>N No ClinGen
ExAC
gnomAD
CA361097719
rs1232793156
63 S>R No ClinGen
gnomAD
CA3430015
rs544126669
64 S>G No ClinGen
1000Genomes
ExAC
gnomAD
CA128180214
rs200514514
64 S>N Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
NCI-TCGA
gnomAD
TCGA novel 64 S>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1401759112
CA361097764
65 S>G No ClinGen
gnomAD
rs1465687054
CA361097775
65 S>N No ClinGen
gnomAD
rs747838420
CA3430016
66 S>N No ClinGen
ExAC
gnomAD
rs1449990055
CA361097799
66 S>R No ClinGen
gnomAD
rs747838420
CA361097791
66 S>T No ClinGen
ExAC
gnomAD
rs541266469
CA361097811
67 S>T No ClinGen
1000Genomes
TOPMed
rs140268489
RCV000961140
67 S>missing No ClinVar
dbSNP
rs199973871
CA3430017
67 S>G No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs541266469
CA128180220
67 S>N No ClinGen
1000Genomes
TOPMed
rs199973871
CA3430018
67 S>R No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA128180222
CA128180224
rs200940543
68 G>R No ClinGen
TOPMed
gnomAD
rs770357422
CA3430020
69 G>D No ClinGen
ExAC
gnomAD
CA361097838
rs1320164238
69 G>S No ClinGen
gnomAD
CA361097854
rs1272976358
70 G>D No ClinGen
gnomAD
CA361097851
rs1580990888
70 G>S No ClinGen
Ensembl
CA3430021
rs775964046
71 G>R No ClinGen
ExAC
gnomAD
CA361097870
rs1297360019
73 G>D No ClinGen
TOPMed
rs749738681
CA3430022
73 G>S No ClinGen
ExAC
gnomAD
rs1017146935
CA128180230
74 G>E No ClinGen
Ensembl
rs769071689
CA3430023
74 G>R No ClinGen
ExAC
gnomAD
rs774542019
CA3430024
75 G>D No ClinGen
ExAC
TOPMed
gnomAD
CA361097878
rs1382558474
75 G>S No ClinGen
gnomAD
CA361097885
rs1580990912
76 G>D No ClinGen
Ensembl
TCGA novel 77 S>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA361097894
rs1394276325
77 S>R No ClinGen
gnomAD
CA3430025
rs558985780
77 S>T No ClinGen
1000Genomes
ExAC
gnomAD
CA361097899
rs1561813866
78 N>S No ClinGen
Ensembl
CA3430029
rs772158966
79 S>N No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 80 S>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA361097917
rs1374692082
80 S>R No ClinGen
gnomAD
rs773461593
CA3430030
82 S>C No ClinGen
ExAC
gnomAD
rs773461593
CA361097927
82 S>G No ClinGen
ExAC
gnomAD
TCGA novel 82 S>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs898320714
CA361097928
82 S>N Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA128180254
rs898320714
82 S>T Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs1342573008
CA361097937
83 S>N No ClinGen
gnomAD
TCGA novel 84 S>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1580990956
CA361097943
84 S>N No ClinGen
Ensembl
CA361097953
rs1338036973
85 T>I No ClinGen
gnomAD
TCGA novel 86 F>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA361097966
rs1221374503
87 N>S No ClinGen
gnomAD
TCGA novel 87 N>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1281661940
CA361097975
88 P>L No ClinGen
TOPMed
gnomAD
rs760828546
CA361097993
90 A>E No ClinGen
ExAC
TOPMed
gnomAD
rs760828546
CA361097995
90 A>G No ClinGen
ExAC
TOPMed
gnomAD
CA128180260
rs1022820772
90 A>T No ClinGen
Ensembl
rs760828546
CA3430031
90 A>V No ClinGen
ExAC
TOPMed
gnomAD
rs766482111
CA3430032
91 D>N No ClinGen
ExAC
TOPMed
gnomAD
CA3430034
rs753839059
92 T>A No ClinGen
ExAC
rs200340767
CA3430037
94 E>K No ClinGen
ExAC
TOPMed
gnomAD
CA3430038
rs529757041
95 Q>E No ClinGen
1000Genomes
ExAC
gnomAD
CA361098084
rs529757041
95 Q>K No ClinGen
1000Genomes
ExAC
gnomAD
rs201259281
CA361098108
96 P>A No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
TCGA novel 96 P>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3430039
rs201259281
96 P>S Variant assessed as Somatic; 5.524e-05 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1394377857
CA361098133
97 Y>C No ClinGen
TOPMed
gnomAD
CA3430040
rs777399498
97 Y>N No ClinGen
ExAC
gnomAD
CA361098130
rs1394377857
97 Y>S No ClinGen
TOPMed
gnomAD
rs1299769797
CA361098168
99 H>D No ClinGen
TOPMed
gnomAD
rs140129794
CA3430041
100 L>P No ClinGen
ESP
ExAC
CA128180274
rs879195239
101 T>S No ClinGen
Ensembl
CA361098224
rs1317735632
102 A>S No ClinGen
TOPMed
gnomAD
TCGA novel 102 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3430042
rs756776870
102 A>V No ClinGen
ExAC
gnomAD
rs200402937
CA128180674
103 E>G No ClinGen
TOPMed
gnomAD
rs1458032586
CA361100801
105 F>L No ClinGen
gnomAD
rs779279352
CA3430063
112 N>H No ClinGen
ExAC
gnomAD
CA128180680
rs150291660
113 E>K No ClinGen
ESP
TOPMed
rs772577529
CA3430065
121 Y>S No ClinGen
ExAC
gnomAD
CA128180699
rs200134168
122 P>S No ClinGen
Ensembl
CA361101346
rs1341880364
123 S>R No ClinGen
TOPMed
CA361101439
rs1292289866
128 L>V No ClinGen
gnomAD
rs1332106692
CA361101456
129 P>A No ClinGen
gnomAD
CA3430068
rs199627951
129 P>L No ClinGen
ExAC
gnomAD
CA361101470
rs199627951
129 P>R No ClinGen
ExAC
gnomAD
rs1332106692
CA361101461
129 P>S No ClinGen
gnomAD
rs1332106692
CA361101455
129 P>T No ClinGen
gnomAD
CA3430070
rs745933125
131 I>N No ClinGen
ExAC
gnomAD
CA3430071
rs769829111
133 Y>C No ClinGen
ExAC
TOPMed
gnomAD
CA361101630
rs1257926984
136 R>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs1359191813
CA361101636
136 R>L Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
rs797019589
CA128180717
138 S>* No ClinGen
Ensembl
CA361101696
rs1322007068
138 S>F No ClinGen
TOPMed
CA361101722
rs1394454708
140 E>K No ClinGen
TOPMed
CA128180725
rs28365166
VAR_029330
144 N>K No ClinGen
UniProt
TOPMed
dbSNP
CA361101811
rs1188987693
144 N>Y No ClinGen
gnomAD
CA128180735
rs28365164
VAR_029331
145 S>R No ClinGen
UniProt
Ensembl
dbSNP
rs762815487
CA3430073
146 G>D No ClinGen
ExAC
gnomAD
CA361101882
rs1474289680
147 N>I No ClinGen
gnomAD
rs1580991567
CA361101890
148 T>P No ClinGen
Ensembl
CA361101934
rs1580991589
150 W>C No ClinGen
Ensembl
rs137878468
CA361101938
151 P>A No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA3430075
rs137878468
151 P>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA3430077
rs767122422
152 E>K Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs1415768432
CA361102053
156 S>T No ClinGen
TOPMed
gnomAD
CA3430080
rs765856772
163 S>C No ClinGen
ExAC
gnomAD
rs767618259
CA128180748
163 S>R No ClinGen
Ensembl
rs753147814
CA3430081
163 S>T No ClinGen
ExAC
gnomAD
rs758932198
CA3430082
164 M>I No ClinGen
ExAC
TOPMed
gnomAD
CA361102243
rs1382203641
164 M>T No ClinGen
gnomAD
rs778302593
CA3430083
165 T>N No ClinGen
ExAC
gnomAD
rs1580991627
CA361102285
166 N>K No ClinGen
Ensembl
CA3430084
rs747347984
167 P>S No ClinGen
ExAC
gnomAD
rs1209850719
CA361102320
168 P>L No ClinGen
TOPMed
gnomAD
rs1209850719
CA361102315
168 P>Q No ClinGen
TOPMed
gnomAD
CA361102318
rs1209850719
168 P>R No ClinGen
TOPMed
gnomAD
rs1211585763
CA361102328
169 A>P No ClinGen
TOPMed
rs1211585763
CA361102332
169 A>T No ClinGen
TOPMed
CA128180753
rs200714449
169 A>V No ClinGen
Ensembl
rs973407190
CA128180757
170 S>A No ClinGen
Ensembl
rs149488084
CA128180760
170 S>C No ClinGen
ESP
TOPMed
gnomAD
rs199700793
CA361102370
171 S>* No ClinGen
TOPMed
gnomAD
CA3430086
rs781257455
171 S>A No ClinGen
ExAC
gnomAD
rs199700793
CA128180766
171 S>L No ClinGen
TOPMed
gnomAD
CA3430090
rs201570244
172 S>A No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA361102382
rs774169562
172 S>C No ClinGen
ExAC
gnomAD
CA3430089
rs201570244
172 S>P No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA3430091
rs201570244
172 S>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs774169562
CA3430092
172 S>Y No ClinGen
ExAC
gnomAD
CA361102402
rs1173363390
174 A>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
TCGA novel 175 P>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs201215035
CA128180789
177 P>S No ClinGen
TOPMed
rs202015917
CA128180793
178 A>G No ClinGen
TOPMed
gnomAD
rs202015917
CA128180796
178 A>V No ClinGen
TOPMed
gnomAD
CA361102456
rs1289081010
179 A>V No ClinGen
gnomAD
CA3430095
rs767254414
183 S>A No ClinGen
ExAC
TOPMed
gnomAD
CA361102477
rs1305588383
183 S>F Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA361102480
rs1389045967
COSM1567499
184 A>T large_intestine Variant assessed as Somatic; impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
NCI-TCGA
TOPMed
CA3430099
rs753338388
186 Q>* No ClinGen
ExAC
gnomAD
TCGA novel 186 Q>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1242903292
CA361102554
189 P>L No ClinGen
gnomAD
rs1242903292
CA361102551
189 P>R No ClinGen
gnomAD
CA128180817
rs200284757
191 S>I No ClinGen
Ensembl
rs1255480636
CA361102609
193 A>E No ClinGen
TOPMed
gnomAD
rs759021865
CA3430100
193 A>S No ClinGen
ExAC
gnomAD
TCGA novel 193 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1255480636
CA361102612
193 A>V No ClinGen
TOPMed
gnomAD
TCGA novel 194 V>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3430101
rs764695759
195 P>Q No ClinGen
ExAC
gnomAD
rs774242130
CA128180823
196 S>C No ClinGen
TOPMed
rs757711179
CA3430103
197 N>K No ClinGen
ExAC
gnomAD
CA3430104
rs781553250
198 D>H No ClinGen
ExAC
gnomAD
CA361102696
rs1453932337
199 S>N No ClinGen
TOPMed
TCGA novel 205 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3430107
rs780048789
208 T>P No ClinGen
ExAC
gnomAD
TCGA novel 210 P>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs768644189
CA3430109
210 P>S No ClinGen
ExAC
gnomAD
rs201793207
CA3430110
211 T>P No ClinGen
ExAC
gnomAD
CA3430111
rs748017067
212 P>L No ClinGen
ExAC
TOPMed
gnomAD
CA361102901
rs1224108899
212 P>S No ClinGen
TOPMed
gnomAD
CA128180854
rs947294211
214 T>S No ClinGen
TOPMed
gnomAD
rs201717898
CA128180858
215 D>E No ClinGen
Ensembl
rs201581445
CA3430113
216 I>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 218 P>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1276413762
CA361103062
218 P>L No ClinGen
TOPMed
CA128180876
rs28365165
VAR_029332
219 E>D No ClinGen
UniProt
Ensembl
dbSNP
CA3430115
rs770593593
222 S>N No ClinGen
ExAC
gnomAD
rs1210402337
CA361103201
223 Q>R No ClinGen
gnomAD
rs200345348
CA3430116
225 F>L No ClinGen
ExAC
TOPMed
gnomAD
CA128180890
rs995882489
226 P>L No ClinGen
gnomAD
rs1032115273
CA128180886
226 P>S No ClinGen
TOPMed
CA128180894
rs957347240
227 G>A No ClinGen
TOPMed
gnomAD
rs957347240
CA361103292
227 G>V Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
CA3430119
rs201406048
229 A>S No ClinGen
1000Genomes
ESP
ExAC
gnomAD
CA3430118
rs201406048
229 A>T No ClinGen
1000Genomes
ESP
ExAC
gnomAD
rs762346051
CA3430120
229 A>V No ClinGen
ExAC
gnomAD
rs1356175294
CA361103413
232 A>V No ClinGen
gnomAD
rs1580991917
CA361103450
235 Y>S No ClinGen
Ensembl
CA361103463
rs767798551
236 P>L No ClinGen
ExAC
gnomAD
rs767798551
CA3430121
236 P>R No ClinGen
ExAC
gnomAD
rs1372641336
CA361103480
237 P>L No ClinGen
TOPMed
CA361103501
rs1372891950
239 A>T No ClinGen
gnomAD
CA361103533
rs1226733615
240 Y>S No ClinGen
gnomAD
rs780315115
CA3430124
243 A>T No ClinGen
ExAC
gnomAD
CA361103675
rs1288382551
245 G>S No ClinGen
gnomAD
rs755060107
CA3430126
246 G>S No ClinGen
ExAC
gnomAD
CA361103802
rs1412243365
249 V>F No ClinGen
gnomAD
CA3430127
rs778893817
249 V>G No ClinGen
ExAC
gnomAD
CA361103842
rs1482275326
251 M>V No ClinGen
gnomAD
rs777476660
CA3430130
255 Y>H No ClinGen
ExAC
gnomAD
rs200832114
CA128180952
258 P>L No ClinGen
TOPMed
gnomAD
CA3430132
rs770548315
258 P>S No ClinGen
ExAC
gnomAD
rs1174428885
CA361104077
259 Q>H No ClinGen
TOPMed
CA128180956
rs200009922
260 Q>H No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA3430134
rs759198636
263 D>N No ClinGen
ExAC
TOPMed
gnomAD
rs759198636
CA361104193
263 D>Y No ClinGen
ExAC
TOPMed
gnomAD
rs1580992009
CA361104227
265 G>S No ClinGen
Ensembl
CA361104262
rs1416365751
267 G>D No ClinGen
gnomAD
rs775094635
CA3430136
268 T>I No ClinGen
ExAC
gnomAD
CA128180981
rs199646874
269 P>Q No ClinGen
Ensembl
CA128180984
rs199646874
269 P>R No ClinGen
Ensembl
rs865781599
CA128180989
270 D>G No ClinGen
Ensembl
CA3430138
rs762279773
270 D>N No ClinGen
ExAC
TOPMed
gnomAD
rs1485160735
CA361104334
271 Q>L No ClinGen
TOPMed
rs1215737762
CA361104365
273 P>T No ClinGen
gnomAD
CA128180998
rs974073836
275 Q>* No ClinGen
TOPMed
CA128181002
rs866895287
276 G>C No ClinGen
Ensembl
TCGA novel 276 G>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3430141
rs568294551
279 S>N No ClinGen
1000Genomes
ExAC
gnomAD
rs200710842
CA3430143
279 S>R No ClinGen
ExAC
gnomAD
rs1485114313
CA361104501
280 R>C No ClinGen
gnomAD
CA361104513
rs1580992102
281 T>P No ClinGen
Ensembl
CA3430144
rs755152311
281 T>S No ClinGen
ExAC
gnomAD
CA128181026
rs868815253
283 Q>P No ClinGen
Ensembl
rs200056344
CA128181030
284 P>A No ClinGen
gnomAD
rs1167309548
CA361104611
285 S>L No ClinGen
gnomAD
rs969339195
CA128181043
291 T>I No ClinGen
Ensembl
CA128181050
rs201032646
296 A>V No ClinGen
gnomAD
CA128181061
rs201493880
297 T>S No ClinGen
Ensembl
rs1580992177
CA361104888
302 Q>R No ClinGen
Ensembl
CA3430148
rs777755202
303 D>V No ClinGen
ExAC
TOPMed
gnomAD
CA128181069
rs371702129
304 L>P No ClinGen
ESP
TOPMed
rs201017327
CA3430149
306 A>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs757080248
CA3430150
306 A>V No ClinGen
ExAC
gnomAD
CA361105099
rs1431546100
307 L>I No ClinGen
TOPMed
gnomAD
CA3430151
rs781094908
308 N>K No ClinGen
ExAC
gnomAD
rs1236988714
CA361105199
309 T>I No ClinGen
TOPMed
gnomAD
CA361105197
rs1236988714
309 T>S No ClinGen
TOPMed
gnomAD
rs201637316
CA3430152
310 S>G No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA128181084
rs1046797670
310 S>N No ClinGen
TOPMed
rs769551859
CA3430153
312 Q>R No ClinGen
ExAC
gnomAD
CA3430154
rs146282587
313 S>F No ClinGen
ESP
ExAC
TOPMed
CA128181105
rs201831925
314 Q>H No ClinGen
Ensembl
TCGA novel 315 L>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1385084693
CA361105395
316 I>V No ClinGen
gnomAD
rs1285902502
CA361105455
317 K>N No ClinGen
gnomAD
rs1235440886
CA361105480
318 P>S No ClinGen
TOPMed
TCGA novel 320 R>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA361105526
rs1191792029
320 R>L No ClinGen
gnomAD
rs772509529
CA3430156
322 R>H No ClinGen
ExAC
gnomAD
CA3430157
rs773779462
323 K>E No ClinGen
ExAC
gnomAD
rs1442427059
CA361105662
323 K>R No ClinGen
TOPMed
CA361105805
rs1464342926
326 N>K No ClinGen
TOPMed
gnomAD
rs988622254
CA128181133
327 R>W No ClinGen
Ensembl
TCGA novel 330 K>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs555144693
CA3430158
330 K>R No ClinGen
1000Genomes
ExAC
gnomAD
CA361105990
rs1387378079
331 T>A No ClinGen
gnomAD
rs1230522969
COSM1433393
CA361105998
331 T>M large_intestine Variant assessed as Somatic; impact. central_nervous_system [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
rs1580992292
CA361106012
332 P>S No ClinGen
Ensembl
CA3430162
rs776931076
333 P>H No ClinGen
ExAC
TOPMed
gnomAD
rs776931076
CA128181145
333 P>L No ClinGen
ExAC
TOPMed
gnomAD
CA3430161
rs776931076
333 P>R No ClinGen
ExAC
TOPMed
gnomAD
rs201213506
CA3430164
334 H>D No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA3430163
rs201213506
334 H>N No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs746692720 334 H>P Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No NCI-TCGA
rs1304806674
CA361106107
334 H>Q No ClinGen
gnomAD
rs746692720 334 H>T Variant assessed as Somatic; 4.65e-05 impact. [NCI-TCGA] No NCI-TCGA
CA3430165
rs201213506
334 H>Y No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs764015540
CA3430166
338 Y>F No ClinGen
ExAC
TOPMed
gnomAD
CA361106257
rs202118818
339 A>G No ClinGen
TOPMed
gnomAD
rs202118818
CA128181161
339 A>V No ClinGen
TOPMed
gnomAD
rs745631772
CA3430171
344 S>A No ClinGen
ExAC
gnomAD
CA361106448
rs1431269827
346 D>N No ClinGen
TOPMed
gnomAD
CA361106483
rs1183670804
347 R>H No ClinGen
gnomAD
rs201517117
CA128181194
348 R>C No ClinGen
ExAC
gnomAD
rs201517117
CA3430173
348 R>G No ClinGen
ExAC
gnomAD
CA3430174
rs748831364
348 R>H No ClinGen
ExAC
TOPMed
CA128181201
rs577439715
350 S>P No ClinGen
1000Genomes
CA361106551
rs1158530364
351 R>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
TCGA novel 351 R>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1411364349
CA361106577
352 S>C No ClinGen
TOPMed
rs773690840
CA3430176
356 T>P No ClinGen
ExAC
gnomAD
rs931624345
CA128181214
359 I>T No ClinGen
gnomAD
CA361106794
rs1286054246
362 H>Y No ClinGen
gnomAD
TCGA novel 364 G>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
COSM1186840
CA3430182
rs775787059
371 R>H lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
CA361107242
rs1487438114
379 R>C No ClinGen
gnomAD
TCGA novel 385 T>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3430185
rs751573105
390 H>D No ClinGen
ExAC
gnomAD
rs1437446571
CA361107838
401 C>Y No ClinGen
TOPMed
CA361108079
rs1561814597
411 R>H No ClinGen
Ensembl
rs1440102254
CA361108124
413 R>K No ClinGen
TOPMed
CA361108165
rs1561814606
414 H>L No ClinGen
Ensembl
CA361108158
rs1397728528
414 H>Y No ClinGen
gnomAD
rs535038686
CA361108307
419 L>M No ClinGen
1000Genomes
ExAC
gnomAD
CA361108362
rs1166693992
420 R>P No ClinGen
TOPMed
TCGA novel 420 R>W Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3430189
rs755983566
423 D>N No ClinGen
ExAC
TOPMed
gnomAD
rs779644730
CA3430190
424 K>R No ClinGen
ExAC
gnomAD
CA361108583
rs1229612199
426 A>T No ClinGen
gnomAD
CA361108651
rs1166167763
428 K>E No ClinGen
TOPMed
CA3430193
rs373411522
431 V>A No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA361108822
rs1390264560
434 S>P No ClinGen
TOPMed
TCGA novel 435 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA361108873
rs1580992480
436 T>P No ClinGen
Ensembl
rs201394271
CA3430197
437 S>P No ClinGen
ExAC
TOPMed
gnomAD
rs534778183
CA128181276
441 S>C No ClinGen
Ensembl
CA3430200
rs746308508
442 Y>S No ClinGen
ExAC
gnomAD
CA361109072
rs1422118092
443 P>R No ClinGen
gnomAD
CA361109116
rs1173220892
445 P>L No ClinGen
gnomAD
rs201552434
CA128181289
447 A>T No ClinGen
TOPMed
CA361109241
rs1167047514
449 S>C No ClinGen
gnomAD
CA361109291
rs1376911505
451 P>L No ClinGen
gnomAD
rs1376911505
CA361109289
451 P>Q No ClinGen
gnomAD
rs1365462911
CA361109319
453 P>S No ClinGen
TOPMed
CA128181302
rs865951226
454 V>A No ClinGen
gnomAD
CA3430205
rs763286707
454 V>L No ClinGen
ExAC
gnomAD
rs149798677
CA128181304
455 T>A No ClinGen
1000Genomes
ESP
TOPMed
gnomAD
rs768733193
CA3430207
456 T>I No ClinGen
ExAC
gnomAD
CA361109411
rs1364304172
457 S>F No ClinGen
gnomAD
rs1282108476
CA361109483
459 P>L No ClinGen
gnomAD
CA3430210
rs774561952
459 P>S No ClinGen
ExAC
gnomAD
rs1348315466
CA361109542
461 P>L No ClinGen
TOPMed
gnomAD
rs1370589212
CA361109554
462 A>T No ClinGen
TOPMed
CA3430212
rs767650411
463 T>A No ClinGen
ExAC
gnomAD
rs200048883
CA128181327
464 T>S No ClinGen
Ensembl
CA3430214
rs760644725
465 S>L No ClinGen
ExAC
gnomAD
CA3430215
rs370248873
469 P>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1192140857
CA361109783
471 P>H No ClinGen
TOPMed
rs753553653
CA3430216
472 T>A No ClinGen
ExAC
TOPMed
gnomAD
rs1435715856
CA361109852
474 F>L No ClinGen
gnomAD
CA3430219
rs202226814
477 P>A No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1387817209
COSM735540
CA361109984
480 S>L lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
rs922456828
CA128181347
481 T>I No ClinGen
TOPMed
CA361110014
rs1580992644
482 Y>S No ClinGen
Ensembl
CA128181350
rs955227243
485 P>R No ClinGen
TOPMed
CA361110107
rs1580992653
487 H>P No ClinGen
Ensembl
TCGA novel 489 G>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1286256447
CA361110185
490 F>C No ClinGen
TOPMed
CA3430227
rs768984243
492 S>F No ClinGen
ExAC
gnomAD
rs199867643
CA3430226
492 S>P No ClinGen
ExAC
gnomAD
CA361110248
COSM1061394
rs1296620472
493 P>L Variant assessed as Somatic; impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
CA361110278
rs1561814777
495 V>A No ClinGen
Ensembl
CA3430228
rs774453334
496 A>P No ClinGen
ExAC
gnomAD
CA3430229
rs140128606
497 T>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA361110332
rs1207458162
498 T>M No ClinGen
gnomAD
rs1372874718
CA361110355
499 Y>* No ClinGen
TOPMed
gnomAD
rs1396385681
CA361110379
501 S>P No ClinGen
gnomAD
CA3430231
rs773373715
503 P>S No ClinGen
ExAC
gnomAD
rs766194467
CA361110452
505 A>S No ClinGen
ExAC
gnomAD
CA3430233
rs766194467
505 A>T No ClinGen
ExAC
gnomAD
CA128181378
rs200268457
507 P>L No ClinGen
TOPMed
gnomAD
CA128181375
rs376532290
507 P>S No ClinGen
ESP
TOPMed
rs915368252
CA128181407
510 V>A No ClinGen
Ensembl
TCGA novel 512 S>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs145540497
CA3430236
512 S>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1327890220
CA361110624
513 F>L No ClinGen
gnomAD
rs757997080
CA3430238
517 A>T No ClinGen
ExAC
gnomAD
rs751040100
CA3430240
519 T>S No ClinGen
ExAC
gnomAD
rs758418994
CA128181424
522 F>I No ClinGen
gnomAD
rs1319830395
CA361110750
523 S>G No ClinGen
TOPMed
gnomAD
CA361110749
rs1319830395
523 S>R No ClinGen
TOPMed
gnomAD
rs1226620293
CA361110781
524 A>D No ClinGen
gnomAD
rs147752848
CA361110773
524 A>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs147752848
CA3430242
524 A>T No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA3430243
rs749750277
526 T>S No ClinGen
ExAC
TOPMed
gnomAD
rs371059427
CA3430244
529 S>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA128181436
rs748400232
530 D>G No ClinGen
ExAC
TOPMed
gnomAD
CA3430246
rs748400232
530 D>V No ClinGen
ExAC
TOPMed
gnomAD
CA3430247
rs772398081
531 M>T No ClinGen
ExAC
gnomAD
rs773465307
CA3430248
532 T>A No ClinGen
ExAC
gnomAD
rs202136756
CA128181442
534 T>N No ClinGen
TOPMed
rs1166405541
CA361111048
536 S>P No ClinGen
gnomAD
rs1404629415
CA361111153
540 I>T No ClinGen
gnomAD
rs776445332
CA3430251
540 I>V No ClinGen
ExAC
gnomAD
rs759479225
CA3430252
542 I>V No ClinGen
ExAC
TOPMed
gnomAD
CA3430253
rs764964083
543 C>Y No ClinGen
ExAC
TOPMed
gnomAD

No associated diseases with P18146

5 regional properties for P18146

Type Name Position InterPro Accession
domain Protein kinase domain 12 - 264 IPR000719
domain NAF domain 294 - 351 IPR004041
active_site Serine/threonine-protein kinase, active site 130 - 142 IPR008271
binding_site Protein kinase, ATP binding site 18 - 41 IPR017441
domain NAF/FISL domain 291 - 315 IPR018451

Functions

Description
EC Number
Subcellular Localization
  • Nucleus
  • Cytoplasm
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

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.
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.

14 GO annotations of molecular function

Name Definition
DNA binding Any molecular function by which a gene product interacts selectively and non-covalently with DNA (deoxyribonucleic acid).
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 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 activity, RNA polymerase II-specific A DNA-binding transcription factor activity that modulates the transcription of specific gene sets transcribed by RNA polymerase II.
double-stranded methylated DNA binding Binding to double-stranded methylated DNA. Methylation of cytosine or adenine in DNA is an important mechanism for establishing stable heritable epigenetic marks.
hemi-methylated DNA-binding Binding to double-stranded hemi-methylated DNA at replication foci (one strand methylated, while the other strand is unmethylated). Methylation of cytosine or adenine in DNA is an important mechanism for establishing stable heritable epigenetic marks.
histone acetyltransferase binding Binding to an histone acetyltransferase.
promoter-specific chromatin binding Binding to a section of chromatin that is associated with gene promoter sequences of DNA.
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.
RNA polymerase II transcription regulatory region sequence-specific DNA binding Binding to a specific sequence of DNA that is part of a regulatory region that controls the transcription of a gene or cistron 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 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.
zinc ion binding Binding to a zinc ion (Zn).

35 GO annotations of biological process

Name Definition
BMP signaling pathway The series of molecular signals initiated by the binding of a member of the BMP (bone morphogenetic protein) family to a receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.
cellular response to gamma radiation 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 gamma radiation stimulus. Gamma radiation is a form of electromagnetic radiation (EMR) or light emission of a specific frequency produced from sub-atomic particle interaction, such as electron-positron annihilation and radioactive decay. Gamma rays are generally characterized as EMR having the highest frequency and energy, and also the shortest wavelength, within the electromagnetic radiation spectrum.
cellular response to heparin 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 heparin stimulus.
cellular response to interleukin-8 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 an interleukin-8 stimulus.
cellular response to mycophenolic acid 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 mycophenolic acid stimulus.
circadian regulation of gene expression Any process that modulates the frequency, rate or extent of gene expression such that an expression pattern recurs with a regularity of approximately 24 hours.
circadian temperature homeostasis Any homeostatic process in which an organism modulates its internal body temperature at different values with a regularity of approximately 24 hours.
estrous cycle A type of ovulation cycle, which occurs in most mammalian therian females, where the endometrium is resorbed if pregnancy does not occur.
glomerular mesangial cell proliferation The multiplication or reproduction of glomerular mesangial cells, resulting in the expansion of the population.
interleukin-1-mediated signaling pathway The series of molecular signals initiated by interleukin-1 binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.
locomotor rhythm The rhythm of the locomotor activity of an organism during its 24 hour activity cycle.
negative regulation of canonical Wnt signaling pathway Any process that decreases 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.
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.
positive regulation of chemokine production Any process that activates or increases the frequency, rate, or extent of chemokine production.
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 gene expression Any process that increases the frequency, rate or extent of gene expression. Gene expression is the process in which a gene's coding sequence is converted into a mature gene product (protein or RNA).
positive regulation of glomerular metanephric mesangial cell proliferation Any process that increases the frequency, rate or extent of metanephric glomerular mesangial cell proliferation.
positive regulation of hormone biosynthetic process Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of hormones.
positive regulation of interleukin-1 beta production Any process that activates or increases the frequency, rate, or extent of interleukin-1 beta production.
positive regulation of miRNA transcription Any process that activates or increases the frequency, rate or extent of microRNA (miRNA) gene transcription.
positive regulation of neuron death Any process that activates or increases the frequency, rate or extent of neuron death.
positive regulation of post-translational protein modification Any process that activates or increases the frequency, rate or extent of post-translational protein modification.
positive regulation of tau-protein kinase activity Any process that activates or increases the frequency, rate or extent of tau-protein kinase activity.
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.
regulation of apoptotic process Any process that modulates the occurrence or rate of cell death by apoptotic process.
regulation of progesterone biosynthetic process Any process that modulates the frequency, rate or extent of progesterone biosynthetic process.
regulation of protein sumoylation Any process that modulates the frequency, rate or extent of the addition of SUMO groups to a protein.
regulation of transcription by RNA polymerase II Any process that modulates the frequency, rate or extent of transcription mediated by RNA polymerase II.
regulation of transcription from RNA polymerase II promoter in response to hypoxia Any process that modulates the frequency, rate or extent of transcription from an RNA polymerase II promoter as a result of a hypoxia stimulus.
response to glucose Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a glucose stimulus.
response to hypoxia Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus indicating lowered oxygen tension. Hypoxia, defined as a decline in O2 levels below normoxic levels of 20.8 - 20.95%, results in metabolic adaptation at both the cellular and organismal level.
response to insulin Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an insulin stimulus. Insulin is a polypeptide hormone produced by the islets of Langerhans of the pancreas in mammals, and by the homologous organs of other organisms.
response to ischemia Any process that results in a change in state or activity of an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a inadequate blood supply.
skeletal muscle cell differentiation The process in which a relatively unspecialized cell acquires specialized features of a skeletal muscle cell, a somatic cell located in skeletal muscle.
T cell differentiation The process in which a precursor cell type acquires characteristics of a more mature T-cell. A T cell is a type of lymphocyte whose definin characteristic is the expression of a T cell receptor complex.

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
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
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
Q9HBE1 PATZ1 POZ-, AT hook-, and zinc finger-containing protein 1 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
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
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
Q8N680 ZBTB2 Zinc finger and BTB domain-containing protein 2 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
Q5TC79 ZBTB37 Zinc finger and BTB domain-containing protein 37 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
Q9Y330 ZBTB12 Zinc finger and BTB domain-containing protein 12 Homo sapiens (Human) PR
Q13105 ZBTB17 Zinc finger and BTB domain-containing protein 17 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
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
P41182 BCL6 B-cell lymphoma 6 protein 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
Q8TD17 ZNF398 Zinc finger protein 398 Homo sapiens (Human) PR
P52739 ZNF131 Zinc finger protein 131 Homo sapiens (Human) PR
A6NGD5 ZSCAN5C Zinc finger and SCAN domain-containing protein 5C Homo sapiens (Human) PR
Q7Z398 ZNF550 Zinc finger protein 550 Homo sapiens (Human) PR
Q9Y2K1 ZBTB1 Zinc finger and BTB domain-containing protein 1 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
P24278 ZBTB25 Zinc finger and BTB domain-containing protein 25 Homo sapiens (Human) PR
Q96N38 ZNF714 Zinc finger protein 714 Homo sapiens (Human) PR
Q86YH2 ZNF280B Zinc finger protein 280B Homo sapiens (Human) PR
Q05215 EGR4 Early growth response protein 4 Homo sapiens (Human) PR
Q9Y5W3 KLF2 Krueppel-like factor 2 Homo sapiens (Human) PR
Q06889 EGR3 Early growth response protein 3 Homo sapiens (Human) PR
Q9Y4X4 KLF12 Krueppel-like factor 12 Homo sapiens (Human) PR
Q99612 KLF6 Krueppel-like factor 6 Homo sapiens (Human) PR
O75840 KLF7 Krueppel-like factor 7 Homo sapiens (Human) PR
P57682 KLF3 Krueppel-like factor 3 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
P41183 Bcl6 B-cell lymphoma 6 protein homolog 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
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
P08046 Egr1 Early growth response protein 1 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
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
P43301 Egr3 Early growth response protein 3 Rattus norvegicus (Rat) PR
P08154 Egr1 Early growth response protein 1 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
Q6P882 zbtb8a.2 Zinc finger and BTB domain-containing protein 8A.2 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
A4II20 egr1 Early growth response protein 1 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
MAAAKAEMQL MSPLQISDPF GSFPHSPTMD NYPKLEEMML LSNGAPQFLG AAGAPEGSGS
70 80 90 100 110 120
NSSSSSSGGG GGGGGGSNSS SSSSTFNPQA DTGEQPYEHL TAESFPDISL NNEKVLVETS
130 140 150 160 170 180
YPSQTTRLPP ITYTGRFSLE PAPNSGNTLW PEPLFSLVSG LVSMTNPPAS SSSAPSPAAS
190 200 210 220 230 240
SASASQSPPL SCAVPSNDSS PIYSAAPTFP TPNTDIFPEP QSQAFPGSAG TALQYPPPAY
250 260 270 280 290 300
PAAKGGFQVP MIPDYLFPQQ QGDLGLGTPD QKPFQGLESR TQQPSLTPLS TIKAFATQSG
310 320 330 340 350 360
SQDLKALNTS YQSQLIKPSR MRKYPNRPSK TPPHERPYAC PVESCDRRFS RSDELTRHIR
370 380 390 400 410 420
IHTGQKPFQC RICMRNFSRS DHLTTHIRTH TGEKPFACDI CGRKFARSDE RKRHTKIHLR
430 440 450 460 470 480
QKDKKADKSV VASSATSSLS SYPSPVATSY PSPVTTSYPS PATTSYPSPV PTSFSSPGSS
490 500 510 520 530 540
TYPSPVHSGF PSPSVATTYS SVPPAFPAQV SSFPSSAVTN SFSASTGLSD MTATFSPRTI
EIC