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

13 structures for P35414

Entry ID Method Resolution Chain Position Source
2LOT NMR - A 1-55 PDB
2LOU NMR - A 1-55 PDB
2LOV NMR - A 1-55 PDB
2LOW NMR - A 1-55 PDB
5VBL X-ray 260 A PDB
6KNM X-ray 320 A PDB
7SUS X-ray 270 A PDB
7W0L EM 357 A Q/R 2-330 PDB
7W0M EM 371 A R 2-330 PDB
7W0N EM 421 A Q/R 2-330 PDB
7W0O EM 378 A R 2-330 PDB
7W0P EM 316 A R 2-330 PDB
AF-P35414-F1 Predicted AlphaFoldDB

353 variants for P35414

Variant ID(s) Position Change Description Diseaes Association Provenance
rs897353100
CA222674832
4 G>R No ClinGen
TOPMed
CA6002958
rs760885266
9 N>H No ClinGen
ExAC
TOPMed
gnomAD
rs1036113404
CA222674798
9 N>I No ClinGen
TOPMed
TCGA novel 9 N>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA380544900
rs1372426063
11 Y>C No ClinGen
TOPMed
gnomAD
rs1461556030
CA380544906
11 Y>H No ClinGen
TOPMed
gnomAD
TCGA novel 13 A>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs184417795
CA222674757
14 D>E No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA6002955
rs749004527
15 N>S No ClinGen
ExAC
gnomAD
rs1192596408
CA380544822
17 S>T No ClinGen
TOPMed
rs747713707
CA6002952
18 E>D No ClinGen
ExAC
gnomAD
rs769341289
CA6002953
18 E>V No ClinGen
ExAC
rs1565021402
CA380544769
20 E>D No ClinGen
Ensembl
CA380544742
rs1480062263
22 T>I No ClinGen
gnomAD
rs1193505336
CA380544748
22 T>S No ClinGen
gnomAD
CA222674736
rs866747209
23 D>N No ClinGen
Ensembl
CA6002950
rs754947275
23 D>V No ClinGen
ExAC
gnomAD
CA380544711
rs1201123037
24 W>* No ClinGen
gnomAD
CA380544691
rs564912523
25 K>N No ClinGen
1000Genomes
TOPMed
rs780061917
CA6002948
27 S>L Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA380544649
rs1332991096
29 A>T No ClinGen
TOPMed
gnomAD
CA222674703
rs1050060678
30 L>F No ClinGen
TOPMed
rs1288585000
CA380544622
31 I>N No ClinGen
TOPMed
CA6002945
COSM1746338
rs765581418
33 A>T urinary_tract [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
rs765076382
CA222674685
36 M>I No ClinGen
Ensembl
rs757373811
CA6002944
36 M>L No ClinGen
ExAC
gnomAD
TCGA novel 36 M>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA222674684
rs192352340
38 V>I No ClinGen
1000Genomes
TOPMed
rs923143520
CA222674679
40 L>F No ClinGen
TOPMed
rs764453655
CA6002942
41 L>V No ClinGen
ExAC
TOPMed
gnomAD
CA6002939
rs767906014
44 T>M Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
TCGA novel 47 G>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1238295474
CA380544414
47 G>S No ClinGen
TOPMed
gnomAD
TCGA novel 48 L>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA380544395
rs1460332643
49 V>M No ClinGen
gnomAD
rs776263345
CA6002934
50 L>F No ClinGen
ExAC
gnomAD
CA6002933
rs768473688
51 W>R No ClinGen
ExAC
gnomAD
CA380544343
rs145108815
CA380544342
53 V>L No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs145108815
CA6002931
RCV000906400
53 V>M No ClinGen
ClinVar
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
rs745691280
CA222674591
55 R>P No ClinGen
ExAC
TOPMed
gnomAD
CA6002929
rs745691280
55 R>Q Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs200201854
CA6002930
55 R>W No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA6002928
rs779214361
56 S>G No ClinGen
ExAC
gnomAD
rs753846480
CA6002926
COSM3415989
58 R>Q Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
rs370702287
CA6002927
58 R>W No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA380544251
rs1156413531
60 K>R No ClinGen
TOPMed
gnomAD
CA380544242
rs1452552982
61 R>G No ClinGen
TOPMed
gnomAD
rs1380549490
CA380544239
61 R>K No ClinGen
gnomAD
CA6002925
rs142394789
62 R>C No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs756545642
CA6002924
64 A>G No ClinGen
ExAC
gnomAD
CA6002923
rs753248942
67 F>S No ClinGen
ExAC
gnomAD
CA6002921
rs376527330
72 A>E No ClinGen
ESP
ExAC
gnomAD
CA6002920
rs376527330
72 A>V No ClinGen
ESP
ExAC
gnomAD
CA380544081
rs1308815903
74 A>V No ClinGen
gnomAD
rs761594364
CA6002917
77 T>I No ClinGen
ExAC
gnomAD
rs138423122
CA380544027
78 F>L No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs144634263
CA6002914
79 V>M No ClinGen
ESP
ExAC
gnomAD
rs538356535
CA6002913
81 T>M Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
rs994466745
CA222674531
86 A>V No ClinGen
TOPMed
gnomAD
CA222674526
rs752803395
89 T>K No ClinGen
ExAC
TOPMed
gnomAD
CA6002905
rs752803395
89 T>M No ClinGen
ExAC
TOPMed
gnomAD
rs752803395
CA6002906
89 T>R No ClinGen
ExAC
TOPMed
gnomAD
CA6002902
rs751917695
90 Y>D No ClinGen
ExAC
gnomAD
CA222674520
rs751917695
90 Y>N No ClinGen
ExAC
gnomAD
CA6002900
rs374221224
91 R>Q Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA6002901
rs200935550
91 R>W No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
TCGA novel 92 D>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs763688175
CA6002898
93 Y>C No ClinGen
ExAC
gnomAD
rs753483177
CA6002899
93 Y>D No ClinGen
ExAC
gnomAD
rs760167700
CA6002897
94 D>A No ClinGen
ExAC
gnomAD
CA6002896
rs767552266
94 D>E No ClinGen
ExAC
TOPMed
gnomAD
CA380543802
rs763318766
96 P>A No ClinGen
Ensembl
CA380543800
rs763318766
96 P>S No ClinGen
Ensembl
rs374473031
CA6002894
99 T>N No ClinGen
ESP
ExAC
gnomAD
rs527725306
CA222674451
104 L>F No ClinGen
1000Genomes
rs749056077
CA6002891
105 S>N No ClinGen
ExAC
gnomAD
CA6002890
rs773442045
106 S>G No ClinGen
ExAC
gnomAD
CA380543650
rs1590545274
107 Y>S No ClinGen
Ensembl
CA380543629
rs1173064610
109 I>N No ClinGen
TOPMed
TCGA novel 111 V>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs748168275
CA6002888
111 V>I Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA380543564
rs1296542035
113 M>I No ClinGen
TOPMed
CA6002887
rs781306328
113 M>L No ClinGen
ExAC
gnomAD
CA380543571
rs1394966975
113 M>T No ClinGen
gnomAD
CA6002886
rs755448440
114 Y>D No ClinGen
ExAC
gnomAD
rs1197749607
CA380543541
115 A>D No ClinGen
gnomAD
CA6002884
rs780449482
115 A>T No ClinGen
ExAC
gnomAD
rs750760773
CA6002882
COSM1245187
117 V>I Variant assessed as Somatic; 0.0 impact. oesophagus [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
rs772810549
CA6002881
121 T>I No ClinGen
ExAC
gnomAD
rs752254107
CA6002879
122 G>S Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs753116544
CA6002878
123 L>F No ClinGen
ExAC
gnomAD
CA380543433
rs1590545209
124 S>R No ClinGen
Ensembl
TCGA novel 126 D>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs766255831
CA6002875
126 D>N Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
CA6002874
rs762740856
127 R>C No ClinGen
ExAC
TOPMed
gnomAD
COSM93871
CA6002873
rs772893901
127 R>H lung [Cosmic] No ClinGen
cosmic curated
ExAC
gnomAD
TCGA novel 130 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA380543325
rs1466560631
132 V>A No ClinGen
gnomAD
CA6002871
rs562689168
132 V>M No ClinGen
ExAC
TOPMed
gnomAD
rs776670797
CA380543317
133 R>K No ClinGen
ExAC
gnomAD
CA6002870
rs776670797
133 R>M No ClinGen
ExAC
gnomAD
CA380543291
rs1469614549
136 A>S No ClinGen
gnomAD
rs1193200316
CA380543272
138 A>V No ClinGen
gnomAD
rs780546020
CA6002867
139 R>Q No ClinGen
ExAC
gnomAD
CA6002868
rs770716889
139 R>W No ClinGen
ExAC
TOPMed
gnomAD
rs1458114226
CA380543265
140 L>P No ClinGen
gnomAD
CA380543263
rs1590545160
141 R>G No ClinGen
Ensembl
CA6002866
rs200833984
143 R>Q No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA380543250
rs1201535000
COSM1704007
143 R>W skin [Cosmic] No ClinGen
cosmic curated
gnomAD
CA380543242
rs1590545135
144 V>G No ClinGen
Ensembl
rs1424540556
CA380543230
146 G>E No ClinGen
TOPMed
CA6002863
rs755793037
146 G>R Variant assessed as Somatic; 4.813e-05 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs576092494
CA222674311
148 V>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs576092494
CA6002861
148 V>M No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
TCGA novel 149 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs751033294
CA6002859
150 T>M Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA6002857
rs373482292
151 A>E No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
TCGA novel 151 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA380543197
rs1590545094
152 V>G No ClinGen
Ensembl
CA380543195
rs747848269
153 L>F Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs747848269
CA222674297
153 L>I No ClinGen
gnomAD
CA380543177
rs1590545089
155 V>G No ClinGen
Ensembl
CA6002856
rs552008634
157 A>P No ClinGen
ExAC
gnomAD
TCGA novel 157 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs761618705
CA6002854
158 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA6002853
rs776795599
158 A>V No ClinGen
ExAC
gnomAD
CA6002851
rs760691556
159 L>F No ClinGen
ExAC
TOPMed
gnomAD
rs772632870
CA6002849
160 L>P No ClinGen
ExAC
gnomAD
CA380543156
rs1237794048
160 L>V No ClinGen
TOPMed
gnomAD
rs746406904
CA6002848
161 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
rs1280191295
CA380543141
162 M>I No ClinGen
TOPMed
CA222674235
rs771369044
163 P>A No ClinGen
ExAC
TOPMed
gnomAD
CA380543136
rs1219170438
163 P>L No ClinGen
TOPMed
CA6002846
rs771369044
163 P>T No ClinGen
ExAC
TOPMed
gnomAD
CA380543135
rs1410486842
164 V>I No ClinGen
Ensembl
CA6002845
rs749698318
165 M>V No ClinGen
ExAC
gnomAD
CA6002844
rs780922972
166 V>A No ClinGen
ExAC
gnomAD
CA380543117
rs780922972
166 V>G No ClinGen
ExAC
gnomAD
rs373170562
COSM1354728
CA6002843
168 R>C Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA6002842
rs746176980
168 R>H No ClinGen
ExAC
TOPMed
gnomAD
rs746176980
CA222674209
168 R>L No ClinGen
ExAC
TOPMed
gnomAD
CA6002841
rs746176980
168 R>P No ClinGen
ExAC
TOPMed
gnomAD
CA380543104
rs1297186852
169 T>N No ClinGen
gnomAD
CA222674202
rs867095656
170 T>I No ClinGen
Ensembl
CA380543095
rs761532425
171 G>A No ClinGen
ExAC
TOPMed
gnomAD
rs761532425
CA6002837
171 G>E No ClinGen
ExAC
TOPMed
gnomAD
rs369317042
CA222674190
CA6002838
171 G>R No ClinGen
ESP
ExAC
gnomAD
CA6002835
rs764290440
172 D>N No ClinGen
ExAC
gnomAD
rs771174826
CA222674167
173 L>V No ClinGen
Ensembl
CA380543066
rs760876917
175 N>K No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 175 N>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs775613142
CA6002833
177 T>I No ClinGen
ExAC
gnomAD
CA6002832
rs200422749
178 K>R No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA6002831
rs759679942
179 V>E No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 180 Q>E Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA6002830
rs147862659
180 Q>H No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA380543041
rs1367901533
180 Q>K No ClinGen
TOPMed
CA222674099
rs1005685932
180 Q>R No ClinGen
TOPMed
CA380543016
rs1219421947
183 M>T No ClinGen
TOPMed
rs778339271
CA6002827
183 M>V No ClinGen
ExAC
gnomAD
CA6002826
rs768419160
184 D>G No ClinGen
ExAC
TOPMed
gnomAD
rs746680863
CA6002825
186 S>P No ClinGen
ExAC
gnomAD
CA380542982
rs1288897691
188 V>M No ClinGen
gnomAD
rs1322779715
CA380542969
190 T>A No ClinGen
gnomAD
rs1366574383
CA380542966
190 T>S No ClinGen
gnomAD
CA380542927
rs1315517697
196 A>P No ClinGen
gnomAD
rs757807794
CA6002823
196 A>V No ClinGen
ExAC
gnomAD
rs201345085
CA6002822
197 W>* No ClinGen
1000Genomes
ExAC
gnomAD
rs61731623
CA380542907
198 E>D No ClinGen
ExAC
TOPMed
gnomAD
CA6002820
rs748878685
199 V>G No ClinGen
ExAC
TOPMed
gnomAD
rs1214148172
CA380542905
199 V>M No ClinGen
TOPMed
rs375325181
CA222673967
201 L>V No ClinGen
ESP
CA222673963
rs987592819
202 G>R No ClinGen
Ensembl
rs763920197
CA6002818
203 V>I No ClinGen
ExAC
gnomAD
rs202019294
CA6002816
204 S>L Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA6002817
rs202019294
204 S>W No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs759463806
CA6002814
205 S>Y No ClinGen
ExAC
TOPMed
gnomAD
CA380542871
rs1590544856
206 T>P No ClinGen
Ensembl
rs766977824
CA6002812
206 T>S No ClinGen
ExAC
gnomAD
CA6002809
rs376646370
208 V>L No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA6002810
COSM429269
rs376646370
208 V>M Variant assessed as Somatic; 0.0 impact. breast [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
1000Genomes
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1000614668
CA222673906
209 G>V No ClinGen
gnomAD
CA6002808
rs748576901
211 V>L No ClinGen
ExAC
gnomAD
rs532639542
COSM429268
CA222673897
215 T>I Variant assessed as Somatic; impact. breast [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
Ensembl
NCI-TCGA
rs1354695548
CA380542812
216 I>V No ClinGen
gnomAD
rs1565194332
CA380542790
219 T>S No ClinGen
Ensembl
CA6002805
rs771771159
220 C>Y No ClinGen
ExAC
TOPMed
gnomAD
rs1565194327
CA599792486
221 Y>* No ClinGen
Ensembl
rs538012075
CA6002804
222 F>C No ClinGen
1000Genomes
ExAC
gnomAD
CA6002803
rs778464649
223 F>L No ClinGen
ExAC
TOPMed
gnomAD
CA380542751
rs144399813
224 I>M No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs749277146
CA6002801
225 A>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA6002800
rs140463390
225 A>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA380542733
rs1280620140
227 T>I No ClinGen
TOPMed
rs755821341
CA6002799
228 I>V No ClinGen
ExAC
gnomAD
CA380542726
rs767575528
229 A>P No ClinGen
ExAC
TOPMed
gnomAD
CA6002797
rs767575528
229 A>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs755284432
CA6002796
230 G>C No ClinGen
ExAC
gnomAD
rs200672348
COSM192517
CA6002795
233 R>C large_intestine [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
TOPMed
gnomAD
rs147193169
CA6002794
233 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs147193169
COSM93870
CA222673824
233 R>L lung [Cosmic] No ClinGen
cosmic curated
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA222673819
rs771201022
235 E>D No ClinGen
gnomAD
rs763530854
CA6002793
235 E>K No ClinGen
ExAC
TOPMed
gnomAD
COSM4165836
CA6002792
rs758461358
236 R>C kidney [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
CA380542682
rs758461358
236 R>G No ClinGen
ExAC
TOPMed
gnomAD
rs199589565
CA6002790
236 R>H Variant assessed as Somatic; 0.0005552 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
rs199589565
CA6002791
236 R>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs777114356
CA6002789
237 I>V No ClinGen
ExAC
gnomAD
rs745562987
CA6002787
238 E>K No ClinGen
ExAC
gnomAD
CA6002785
rs373939726
239 G>C No ClinGen
ESP
ExAC
gnomAD
rs1446138644
CA380542666
239 G>D Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs373939726
CA6002786
239 G>S No ClinGen
ESP
ExAC
gnomAD
rs1164709176
CA380542663
240 L>M No ClinGen
TOPMed
CA6002782
rs139313864
COSM1289575
241 R>Q Variant assessed as Somatic; 0.0 impact. haematopoietic_and_lymphoid_tissue [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA6002783
rs150001803
241 R>W No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA6002780
rs781106110
242 K>R No ClinGen
ExAC
TOPMed
gnomAD
rs751878030
CA6002778
243 R>P No ClinGen
ExAC
TOPMed
gnomAD
rs751878030
CA222673782
243 R>Q No ClinGen
ExAC
TOPMed
gnomAD
rs755123915
CA6002779
243 R>W No ClinGen
ExAC
TOPMed
gnomAD
rs150819843
CA6002777
244 R>C No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA6002776
rs758486436
244 R>H No ClinGen
ExAC
TOPMed
gnomAD
rs373852614
CA6002775
245 R>Q No ClinGen
ESP
ExAC
gnomAD
CA380542641
rs1181111316
245 R>W No ClinGen
gnomAD
CA6002774
rs765646849
248 S>I No ClinGen
ExAC
gnomAD
rs376442198
CA6002770
251 V>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs376442198
CA6002771
251 V>M No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1590544659
CA380542597
252 V>G No ClinGen
Ensembl
CA380542587
rs1590544646
254 V>G No ClinGen
Ensembl
CA380542590
rs761642013
254 V>L No ClinGen
gnomAD
rs761642013
CA222673714
254 V>M No ClinGen
gnomAD
rs1590544645
CA380542581
255 V>G No ClinGen
Ensembl
CA222673698
rs998772870
256 T>A No ClinGen
TOPMed
gnomAD
rs770578460
CA6002768
256 T>I No ClinGen
ExAC
gnomAD
CA380542572
rs1233100457
257 F>S No ClinGen
TOPMed
CA380542564
rs1296027554
258 A>G No ClinGen
gnomAD
CA6002767
rs762395563
258 A>S No ClinGen
ExAC
TOPMed
TCGA novel 260 C>* Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 262 M>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs772839486
CA6002766
264 Y>H No ClinGen
ExAC
TOPMed
rs192803923
CA6002764
266 L>V No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA380542502
rs1590544597
267 V>G No ClinGen
Ensembl
rs140178173
COSM1746337
CA6002761
269 T>M urinary_tract [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
TOPMed
gnomAD
rs780827696
CA6002762
269 T>S No ClinGen
ExAC
gnomAD
CA380542480
rs1444551373
271 Y>D No ClinGen
TOPMed
gnomAD
CA380542470
rs1216211812
272 M>I No ClinGen
TOPMed
gnomAD
rs953514421
CA222673625
272 M>L No ClinGen
TOPMed
CA222673622
rs953514421
272 M>V No ClinGen
TOPMed
COSM1509128
CA380542462
rs1288189384
274 G>S lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
CA6002755
rs757679361
275 S>N No ClinGen
ExAC
gnomAD
CA380542444
rs754319102
277 L>M No ClinGen
ExAC
gnomAD
rs754319102
CA6002754
277 L>V No ClinGen
ExAC
gnomAD
CA222673607
rs759267329
278 H>Y No ClinGen
TOPMed
CA380542420
rs1565194211
280 P>L No ClinGen
Ensembl
rs764535445
CA6002753
280 P>S No ClinGen
ExAC
gnomAD
rs373559419
CA6002751
282 D>E No ClinGen
ESP
ExAC
gnomAD
rs143772778
CA6002752
282 D>Y No ClinGen
ESP
ExAC
TOPMed
rs1590544516
CA380542393
284 D>A No ClinGen
Ensembl
CA6002750
rs766005445
284 D>H No ClinGen
ExAC
TOPMed
gnomAD
rs1275880431
CA380542388
285 L>F No ClinGen
gnomAD
CA380542383
rs1356693715
286 F>L No ClinGen
TOPMed
rs762662661
CA6002749
286 F>S No ClinGen
ExAC
gnomAD
rs1360794864
CA380542375
287 L>F No ClinGen
gnomAD
CA6002747
rs769396825
290 I>V No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 292 P>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1029675040
CA222673518
294 C>Y No ClinGen
Ensembl
rs200012705
CA6002742
295 T>I No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs200012705
CA6002741
295 T>N No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA380542318
rs746785866
295 T>P No ClinGen
ExAC
gnomAD
CA6002743
rs746785866
295 T>S No ClinGen
ExAC
gnomAD
CA380542316
rs1193417962
296 C>S No ClinGen
gnomAD
CA380542305
rs1478236158
297 I>N No ClinGen
gnomAD
CA678577390
rs1277723533
COSM399639
299 Y>* lung [Cosmic] No ClinGen
cosmic curated
Ensembl
CA222673470
rs187940540
299 Y>H No ClinGen
1000Genomes
COSM1354726
CA6002739
VAR_049375
RCV000967201
rs7943508
300 V>I large_intestine [Cosmic] No ClinGen
cosmic curated
ClinVar
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
TCGA novel 302 S>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1020310646
CA222673440
303 C>G No ClinGen
Ensembl
CA380542254
rs1208391519
304 L>P No ClinGen
TOPMed
rs749336314
CA6002737
306 P>S No ClinGen
ExAC
TOPMed
gnomAD
CA6002738
rs749336314
306 P>T No ClinGen
ExAC
TOPMed
gnomAD
CA6002736
rs778198836
308 L>V No ClinGen
ExAC
gnomAD
CA380542216
rs1192010648
310 A>G No ClinGen
TOPMed
rs1478425596
CA380542219
310 A>T No ClinGen
Ensembl
CA380542212
rs1217801777
311 F>L No ClinGen
gnomAD
rs1371023630
CA380542204
312 F>L No ClinGen
TOPMed
rs1590544456
CA380542195
313 D>A No ClinGen
Ensembl
CA6002733
rs767911833
313 D>H No ClinGen
ExAC
gnomAD
CA6002731
rs764829178
314 P>S No ClinGen
ExAC
TOPMed
gnomAD
CA6002730
rs764829178
314 P>T No ClinGen
ExAC
TOPMed
gnomAD
CA6002728
rs137997556
COSM928532
315 R>C endometrium central_nervous_system [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
TOPMed
gnomAD
rs137997556
CA6002729
315 R>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs760732461
CA6002726
315 R>H Variant assessed as Somatic; 4.623e-05 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs760732461
CA6002727
315 R>L No ClinGen
ExAC
gnomAD
CA380542183
rs1170323244
316 F>I No ClinGen
gnomAD
CA6002725
COSM1354725
rs777561476
317 R>C large_intestine [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
COSM192516
CA6002724
rs200854787
317 R>H Variant assessed as Somatic; 4.624e-05 impact. large_intestine breast [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
TCGA novel 319 A>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA380542155
rs1324943024
320 C>S No ClinGen
TOPMed
rs771075684
CA6002721
321 T>I No ClinGen
ExAC
gnomAD
CA380542150
rs1590544407
321 T>P No ClinGen
Ensembl
TCGA novel 323 M>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA6002720
rs749377510
324 L>R No ClinGen
ExAC
gnomAD
rs377391271
CA222673362
326 C>Y No ClinGen
ESP
TOPMed
CA380542096
rs1318397404
329 S>G No ClinGen
gnomAD
rs748705793
CA6002717
330 R>G No ClinGen
ExAC
gnomAD
CA6002716
rs755331397
330 R>K No ClinGen
ExAC
gnomAD
rs755331397
CA6002715
330 R>M Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs1590544368
CA380542084
331 C>G No ClinGen
Ensembl
CA380542075
rs764929700
332 A>S No ClinGen
ExAC
TOPMed
gnomAD
CA6002713
rs764929700
332 A>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs140133715
CA6002711
333 G>D No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs140133715
CA6002710
333 G>V No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1590544343
CA380542067
334 T>P No ClinGen
Ensembl
CA6002708
rs775524444
336 H>L No ClinGen
ExAC
gnomAD
rs767562498
CA6002707
337 S>G No ClinGen
ExAC
gnomAD
rs759321946
CA6002706
338 S>G No ClinGen
ExAC
TOPMed
gnomAD
CA222673328
rs1003344965
339 S>C No ClinGen
TOPMed
rs1590544308
CA380542019
341 E>G No ClinGen
Ensembl
rs866459668
CA222673326
341 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
Ensembl
NCI-TCGA
rs544631342
CA6002704
343 S>A No ClinGen
1000Genomes
ExAC
gnomAD
CA380542001
rs1278754872
344 A>T No ClinGen
gnomAD
CA380541996
rs1174323988
344 A>V No ClinGen
gnomAD
CA222673286
rs899069343
345 S>G No ClinGen
Ensembl
CA380541976
rs1565194104
347 S>C No ClinGen
Ensembl
CA6002702
rs369393051
348 S>L Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA380541973
rs1378380084
348 S>P No ClinGen
gnomAD
CA6002700
rs748258607
351 S>R No ClinGen
ExAC
TOPMed
gnomAD
CA6002699
rs781612967
352 Q>E No ClinGen
ExAC
gnomAD
TCGA novel 352 Q>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1382995541
CA380541935
354 P>S No ClinGen
TOPMed
CA222673271
rs987154596
355 G>S No ClinGen
TOPMed
gnomAD
CA222673268
rs1048402746
COSM1509129
356 P>T lung Variant assessed as Somatic; impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
NCI-TCGA
TOPMed
CA380541909
rs1309136222
358 M>L No ClinGen
gnomAD
CA6002695
rs146062493
360 K>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs753489933
CA6002694
361 G>S No ClinGen
ExAC
TOPMed
gnomAD
CA6002693
rs777596520
364 Q>E No ClinGen
ExAC
gnomAD
CA380541855
rs1336454338
365 M>I No ClinGen
TOPMed
gnomAD
rs1359961228
CA380541860
365 M>K No ClinGen
gnomAD
CA380541848
rs142294759
366 H>Q No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs755614745
CA6002692
366 H>Y No ClinGen
ExAC
gnomAD
CA6002690
rs767481092
COSM96302
367 E>K lung Variant assessed as Somatic; 0.0 impact. skin [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
CA380541833
rs1213912764
368 K>N Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
CA380541824
rs1252038071
370 I>F No ClinGen
TOPMed
rs1375964948
CA380541814
371 P>L No ClinGen
TOPMed
gnomAD
CA380541815
rs1375964948
371 P>R No ClinGen
TOPMed
gnomAD
CA380541799
rs1410072622
373 S>R No ClinGen
TOPMed
gnomAD
rs375912159
CA222673230
374 Q>* No ClinGen
ESP
TOPMed
CA380541796
rs375912159
374 Q>E No ClinGen
ESP
TOPMed
CA380541794
rs1179892614
374 Q>R No ClinGen
gnomAD
TCGA novel 375 E>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA380541786
rs1472375388
375 E>G No ClinGen
gnomAD
TCGA novel 376 T>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1237677209
CA380541773
377 L>P No ClinGen
gnomAD
CA6002687
rs766139270
379 V>G No ClinGen
ExAC
gnomAD

No associated diseases with P35414

1 regional properties for P35414

Type Name Position InterPro Accession
domain GPCR, rhodopsin-like, 7TM 63 - 358 IPR017452

Functions

Description
EC Number
Subcellular Localization
  • Cell membrane
  • After exposure to apelin (APLN), internalized from the cell surface into an endosomal recycling compartment, from where it is recycled to the cell membrane (By similarity)
  • After exposure to apelin receptor early endogenous ligand (APELA), internalized from the cell surface into an endosomal recycling compartment, from where it is recycled to the cell membrane (PubMed:25639753)
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

2 GO annotations of cellular component

Name Definition
integral component of plasma membrane The component of the plasma membrane consisting of the gene products and protein complexes having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane.
plasma membrane The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins.

3 GO annotations of molecular function

Name Definition
apelin receptor activity Combining with the peptide apelin to initiate a change in cell activity.
G protein-coupled receptor activity Combining with an extracellular signal and transmitting the signal across the membrane by activating an associated G-protein; promotes the exchange of GDP for GTP on the alpha subunit of a heterotrimeric G-protein complex.
signaling receptor activity Receiving a signal and transmitting it in the cell to initiate a change in cell activity. A signal is a physical entity or change in state that is used to transfer information in order to trigger a response.

27 GO annotations of biological process

Name Definition
adult heart development The process whose specific outcome is the progression of the adult heart over time, from its formation to the mature structure.
angiogenesis Blood vessel formation when new vessels emerge from the proliferation of pre-existing blood vessels.
aorta development The progression of the aorta over time, from its initial formation to the mature structure. An aorta is an artery that carries blood from the heart to other parts of the body.
apelin receptor signaling pathway A G protein-coupled receptor signaling pathway initiated by apelin binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process.
atrioventricular valve development The progression of the atrioventricular valve over time, from its formation to the mature structure.
blood vessel development The process whose specific outcome is the progression of a blood vessel over time, from its formation to the mature structure. The blood vessel is the vasculature carrying blood.
coronary vasculature development The process whose specific outcome is the progression of the blood vessels of the heart over time, from its formation to the mature structure.
endocardial cushion formation The developmental process pertaining to the initial formation of an endocardial cushion. The endocardial cushion is a specialized region of mesenchymal cells that will give rise to the heart septa and valves.
G protein-coupled receptor signaling pathway The series of molecular signals initiated by a ligand binding to its receptor, in which the activated receptor promotes the exchange of GDP for GTP on the alpha-subunit of an associated heterotrimeric G-protein complex. The GTP-bound activated alpha-G-protein then dissociates from the beta- and gamma-subunits to further transmit the signal within the cell. The pathway begins with receptor-ligand interaction, and ends with regulation of a downstream cellular process. The pathway can start from the plasma membrane, Golgi or nuclear membrane.
gastrulation A complex and coordinated series of cellular movements that occurs at the end of cleavage during embryonic development of most animals. The details of gastrulation vary from species to species, but usually result in the formation of the three primary germ layers, ectoderm, mesoderm and endoderm.
heart development The process whose specific outcome is the progression of the heart over time, from its formation to the mature structure. The heart is a hollow, muscular organ, which, by contracting rhythmically, keeps up the circulation of the blood.
heart looping The tube morphogenesis process in which the primitive heart tube loops asymmetrically. This looping brings the primitive heart chambers into alignment preceding their future integration. Heart looping begins with dextral-looping and ends when the main regional divisions of the mature heart and primordium of the great arterial trunks become established preceeding septation.
negative regulation of cAMP-mediated signaling Any process which stops, prevents, or reduces the frequency, rate or extent of cAMP-mediated signaling.
negative regulation of gene expression Any process that decreases 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 angiogenesis Any process that activates or increases angiogenesis.
positive regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis Any process that activates or increases the frequency, rate or extent of blood vessel endothelial cell proliferation involved in sprouting angiogenesis.
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 inhibitory G protein-coupled receptor phosphorylation Any process that activates or increases the frequency, rate or extent of inhibitory G protein-coupled receptor phosphorylation.
positive regulation of release of sequestered calcium ion into cytosol Any process that activates or increases the frequency, rate or extent of the release into the cytosolic compartment of calcium ions sequestered in the endoplasmic reticulum or mitochondria.
regulation of body fluid levels Any process that modulates the levels of body fluids.
regulation of gap junction assembly Any process that modulates the frequency, rate or extent of gap junction assembly.
regulation of gene expression Any process that modulates 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).
vascular associated smooth muscle cell differentiation The process in which a relatively unspecialized cell acquires specialized features of a vascular smooth muscle cell.
vasculature development The process whose specific outcome is the progression of the vasculature over time, from its formation to the mature structure. The vasculature is an interconnected tubular multi-tissue structure that contains fluid that is actively transported around the organism.
vasculogenesis The differentiation of endothelial cells from progenitor cells during blood vessel development, and the de novo formation of blood vessels and tubes.
venous blood vessel development The progression of the venous blood vessel over time from its initial formation to the mature structure. Venous blood vessels carry blood back to the heart after the capillary bed.
ventricular septum morphogenesis The developmental process in which a ventricular septum is generated and organized. A ventricular septum is an anatomical structure that separates the lower chambers (ventricles) of the heart from one another.

120 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
Q2YDN1 GPR161 G protein-coupled receptor 161 Bos taurus (Bovine) PR
Q0GBZ5 HCRTR1 Orexin/Hypocretin receptor type 1 Bos taurus (Bovine) PR
Q17QD8 GPR37L1 G-protein coupled receptor 37-like 1 Bos taurus (Bovine) PR
Q8SPN1 PROKR2 Prokineticin receptor 2 Bos taurus (Bovine) PR
P46626 ADRB3 Beta-3 adrenergic receptor Bos taurus (Bovine) PR
O46639 TRHR Thyrotropin-releasing hormone receptor Bos taurus (Bovine) PR
Q8SPN2 PROKR1 Prokineticin receptor 1 Bos taurus (Bovine) PR
B9VR26 CMLKR1 Chemerin-like receptor 1 Bos taurus (Bovine) PR
P18130 ADRA1A Alpha-1A adrenergic receptor Bos taurus (Bovine) PR
B4XF06 GPR39 G-protein coupled receptor 39 Bos taurus (Bovine) PR
O18913 OPN1LW Long-wave-sensitive opsin 1 Felis catus (Cat) (Felis silvestris catus) PR
P28683 PRA1 Green-sensitive opsin Gallus gallus (Chicken) PR
Q9N298 HTR1A 5-hydroxytryptamine receptor 1A Pan troglodytes (Chimpanzee) PR
P08099 Rh2 Opsin Rh2 Drosophila melanogaster (Fruit fly) PR
P06002 ninaE Opsin Rh1 Drosophila melanogaster (Fruit fly) PR
Q4LBB9 Octbeta2R Octopamine receptor beta-2R Drosophila melanogaster (Fruit fly) PR
Q8NFJ6 PROKR2 Prokineticin receptor 2 Homo sapiens (Human) PR
Q9BZJ6 GPR63 Probable G-protein coupled receptor 63 Homo sapiens (Human) PR
Q9H3N8 HRH4 Histamine H4 receptor Homo sapiens (Human) PR
P28336 NMBR Neuromedin-B receptor Homo sapiens (Human) PR
Q9Y5Y3 GPR45 Probable G-protein coupled receptor 45 Homo sapiens (Human) PR
P08913 ADRA2A Alpha-2A adrenergic receptor Homo sapiens (Human) PR
P41597 CCR2 C-C chemokine receptor type 2 Homo sapiens (Human) PR
P51681 CCR5 C-C chemokine receptor type 5 Homo sapiens (Human) PR
Q8TCW9 PROKR1 Prokineticin receptor 1 Homo sapiens (Human) PR
Q99788 CMKLR1 Chemerin-like receptor 1 Homo sapiens (Human) PR
P08908 HTR1A 5-hydroxytryptamine receptor 1A Homo sapiens (Human) PR
P30559 OXTR Oxytocin receptor Homo sapiens (Human) PR
P32239 CCKBR Gastrin/cholecystokinin type B receptor Homo sapiens (Human) PR
O60883 GPR37L1 G-protein coupled receptor 37-like 1 Homo sapiens (Human) PR
Q8TDU9 RXFP4 Relaxin-3 receptor 2 Homo sapiens (Human) PR
P04000 OPN1LW Long-wave-sensitive opsin 1 Homo sapiens (Human) PR
Q6U736 OPN5 Opsin-5 Homo sapiens (Human) PR
P34972 CNR2 Cannabinoid receptor 2 Homo sapiens (Human) PR
P24530 EDNRB Endothelin receptor type B Homo sapiens (Human) PR
P35348 ADRA1A Alpha-1A adrenergic receptor Homo sapiens (Human) PR
Q6W5P4 NPSR1 Neuropeptide S receptor Homo sapiens (Human) PR
O43613 HCRTR1 Orexin/Hypocretin receptor type 1 Homo sapiens (Human) PR
P61073 CXCR4 C-X-C chemokine receptor type 4 Homo sapiens (Human) PR
Q9BXC0 HCAR1 Hydroxycarboxylic acid receptor 1 Homo sapiens (Human) PR
Q15761 NPY5R Neuropeptide Y receptor type 5 Homo sapiens (Human) PR
Q8N6U8 GPR161 G-protein coupled receptor 161 Homo sapiens (Human) PR
Q6DWJ6 GPR139 Probable G-protein coupled receptor 139 Homo sapiens (Human) PR
P21462 FPR1 fMet-Leu-Phe receptor Homo sapiens (Human) PR
P46091 CMKLR2 Chemerin-like receptor 2 Homo sapiens (Human) PR
P32745 SSTR3 Somatostatin receptor type 3 Homo sapiens (Human) PR
P41439 FOLR3 Folate receptor gamma Homo sapiens (Human) PR
P30556 AGTR1 Type-1 angiotensin II receptor Homo sapiens (Human) PR
Q13585 GPR50 Melatonin-related receptor Homo sapiens (Human) PR
P30411 BDKRB2 B2 bradykinin receptor Homo sapiens (Human) PR
P19973 Lsp1 Lymphocyte-specific protein 1 Mus musculus (Mouse) PR
O54799 Nmbr Neuromedin-B receptor Mus musculus (Mouse) PR
Q64264 Htr1a 5-hydroxytryptamine receptor 1A Mus musculus (Mouse) PR
P51675 Ccr1 C-C chemokine receptor type 1 Mus musculus (Mouse) PR
Q5U431 Gpr39 G-protein coupled receptor 39 Mus musculus (Mouse) PR
Q99JG2 Gpr37l1 G-protein coupled receptor 37-like 1 Mus musculus (Mouse) PR
P97295 Npy2r Neuropeptide Y receptor type 2 Mus musculus (Mouse) PR
O08786 Cckar Cholecystokinin receptor type A Mus musculus (Mouse) PR
P56481 Cckbr Gastrin/cholecystokinin type B receptor Mus musculus (Mouse) PR
P30731 Gpr83 G-protein coupled receptor 83 Mus musculus (Mouse) PR
P97468 Cmklr1 Chemerin-like receptor 1 Mus musculus (Mouse) PR
P21761 Trhr Thyrotropin-releasing hormone receptor Mus musculus (Mouse) PR
Q5QD16 Taar3 Trace amine-associated receptor 3 Mus musculus (Mouse) PR
P97292 Hrh2 Histamine H2 receptor Mus musculus (Mouse) PR
Q9EQQ3 Gpr63 Probable G-protein coupled receptor 63 Mus musculus (Mouse) PR
Q924H0 Npffr2 Neuropeptide FF receptor 2 Mus musculus (Mouse) PR
P34971 Adrb1 Beta-1 adrenergic receptor Mus musculus (Mouse) PR
Q91ZY2 Hrh4 Histamine H4 receptor Mus musculus (Mouse) PR
O88416 Gpr33 Probable G-protein coupled receptor 33 Mus musculus (Mouse) PR
Q8K087 Cmklr2 Chemerin-like receptor 2 Mus musculus (Mouse) PR
P70658 Cxcr4 C-X-C chemokine receptor type 4 Mus musculus (Mouse) PR
P97718 Adra1a Alpha-1A adrenergic receptor Mus musculus (Mouse) PR
Q8BZP8 Npsr1 Neuropeptide S receptor Mus musculus (Mouse) PR
Q8K458 Prokr2 Prokineticin receptor 2 Mus musculus (Mouse) PR
P58308 Hcrtr2 Orexin receptor type 2 Mus musculus (Mouse) PR
Q7TQP3 Gpr119 Glucose-dependent insulinotropic receptor Mus musculus (Mouse) PR
Q8BGE9 Rxfp3 Relaxin-3 receptor 1 Mus musculus (Mouse) PR
Q6VZZ7 Opn5 Opsin-5 Mus musculus (Mouse) PR
Q8CIM5 Gpr84 G-protein coupled receptor 84 Mus musculus (Mouse) PR
P25962 Adrb3 Beta-3 adrenergic receptor Mus musculus (Mouse) PR
Q80UC8 Gpr139 Probable G-protein coupled receptor 139 Mus musculus (Mouse) PR
P0C5I1 Gpr25 Probable G-protein coupled receptor 25 Mus musculus (Mouse) PR
P47936 Cnr2 Cannabinoid receptor 2 Mus musculus (Mouse) PR
Q5QD13 Taar6 Trace amine-associated receptor 6 Mus musculus (Mouse) PR
P35846 Folr1 Folate receptor alpha Mus musculus (Mouse) PR
P58307 Hcrtr1 Orexin/Hypocretin receptor type 1 Mus musculus (Mouse) PR
Q8C131 Hcar1 Hydroxycarboxylic acid receptor 1 Mus musculus (Mouse) PR
Q9EQQ4 Gpr45 Probable G-protein coupled receptor 45 Mus musculus (Mouse) PR
B2RPY5 Gpr161 G-protein coupled receptor 161 Mus musculus (Mouse) PR
Q9WV08 Aplnr Apelin receptor Mus musculus (Mouse) PR
Q764M9 CXCR4 C-X-C chemokine receptor type 4 Sus scrofa (Pig) PR
Q9EQD2 Npffr2 Neuropeptide FF receptor 2 Rattus norvegicus (Rat) PR
O08565 Cxcr4 C-X-C chemokine receptor type 4 Rattus norvegicus (Rat) PR
Q01717 Trhr Thyrotropin-releasing hormone receptor Rattus norvegicus (Rat) PR
P30936 Sstr3 Somatostatin receptor type 3 Rattus norvegicus (Rat) PR
P43140 Adra1a Alpha-1A adrenergic receptor Rattus norvegicus (Rat) PR
P19327 Htr1a 5-hydroxytryptamine receptor 1A Rattus norvegicus (Rat) PR
P56719 Hcrtr2 Orexin receptor type 2 Rattus norvegicus (Rat) PR
P28564 Htr1b 5-hydroxytryptamine receptor 1B Rattus norvegicus (Rat) PR
P56718 Hcrtr1 Orexin/Hypocretin receptor type 1 Rattus norvegicus (Rat) PR
P28647 Adora3 Adenosine receptor A3 Rattus norvegicus (Rat) PR
P25102 Hrh2 Histamine H2 receptor Rattus norvegicus (Rat) PR
P23944 Adra1d Alpha-1D adrenergic receptor Rattus norvegicus (Rat) PR
Q8R415 Prokr2 Prokineticin receptor 2 Rattus norvegicus (Rat) PR
Q5QD24 Taar3 Trace amine-associated receptor 3 Rattus norvegicus (Rat) PR
P0C0W8 Gpr139 Probable G-protein coupled receptor 139 Rattus norvegicus (Rat) PR
P35370 Oprl1 Nociceptin receptor Rattus norvegicus (Rat) PR
P46090 Cmklr2 Chemerin-like receptor 2 Rattus norvegicus (Rat) PR
Q9JHG3 Aplnr Apelin receptor Rattus norvegicus (Rat) PR
O97664 CMKLR2 Chemerin-like receptor 2 Macaca mulatta (Rhesus macaque) PR
Q56H79 NPSR1 Neuropeptide S receptor Macaca mulatta (Rhesus macaque) PR
O97666 APLNR Apelin receptor Macaca mulatta (Rhesus macaque) PR
Q18904 npr-8 Probable G-protein coupled receptor npr-8 Caenorhabditis elegans PR
Q09388 gar-2 Muscarinic acetylcholine receptor gar-2 Caenorhabditis elegans PR
B3DM66 gpr161 G-protein coupled receptor 161 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
Q9W6A6 opn1mw4 Green-sensitive opsin-4 Danio rerio (Zebrafish) (Brachydanio rerio) PR
Q9W6A5 opn1mw1 Green-sensitive opsin-1 Danio rerio (Zebrafish) (Brachydanio rerio) PR
Q8AYM7 opn1mw3 Green-sensitive opsin-3 Danio rerio (Zebrafish) (Brachydanio rerio) PR
Q8AYN0 opn1lw2 Red-sensitive opsin-2 Danio rerio (Zebrafish) (Brachydanio rerio) PR
Q90X46 gpr161 G-protein coupled receptor 161 Danio rerio (Zebrafish) (Brachydanio rerio) PR
10 20 30 40 50 60
MEEGGDFDNY YGADNQSECE YTDWKSSGAL IPAIYMLVFL LGTTGNGLVL WTVFRSSREK
70 80 90 100 110 120
RRSADIFIAS LAVADLTFVV TLPLWATYTY RDYDWPFGTF FCKLSSYLIF VNMYASVFCL
130 140 150 160 170 180
TGLSFDRYLA IVRPVANARL RLRVSGAVAT AVLWVLAALL AMPVMVLRTT GDLENTTKVQ
190 200 210 220 230 240
CYMDYSMVAT VSSEWAWEVG LGVSSTTVGF VVPFTIMLTC YFFIAQTIAG HFRKERIEGL
250 260 270 280 290 300
RKRRRLLSII VVLVVTFALC WMPYHLVKTL YMLGSLLHWP CDFDLFLMNI FPYCTCISYV
310 320 330 340 350 360
NSCLNPFLYA FFDPRFRQAC TSMLCCGQSR CAGTSHSSSG EKSASYSSGH SQGPGPNMGK
370
GGEQMHEKSI PYSQETLVVD