ADGRB2 (adhesion G protein-coupled receptor B2) - Rat Genome Database

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Gene: ADGRB2 (adhesion G protein-coupled receptor B2) Homo sapiens
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Symbol: ADGRB2
Name: adhesion G protein-coupled receptor B2
RGD ID: 1319770
HGNC Page HGNC:944
Description: Enables G protein-coupled receptor activity. Involved in G protein-coupled receptor signaling pathway and calcineurin-NFAT signaling cascade. Located in plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: BAI2; brain-specific angiogenesis inhibitor 2; Brain-specific angiongenesis inhibitor-2
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38131,727,117 - 31,764,340 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl131,727,117 - 31,764,893 (-)EnsemblGRCh38hg38GRCh38
GRCh37132,192,718 - 32,229,941 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36131,965,305 - 32,002,235 (-)NCBINCBI36Build 36hg18NCBI36
Build 34131,861,811 - 31,898,729NCBI
Celera130,461,955 - 30,498,884 (-)NCBICelera
Cytogenetic Map1p35.2NCBI
HuRef130,310,212 - 30,346,996 (-)NCBIHuRef
CHM1_1132,308,513 - 32,345,443 (-)NCBICHM1_1
T2T-CHM13v2.0131,584,757 - 31,621,990 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients. Xiong Y, etal., Emerg Microbes Infect. 2020 Dec;9(1):761-770. doi: 10.1080/22221751.2020.1747363.
Additional References at PubMed
PMID:9533023   PMID:10964907   PMID:12218411   PMID:12477932   PMID:12508107   PMID:12543931   PMID:14697242   PMID:14702039   PMID:15123239   PMID:15203201   PMID:15225653   PMID:16169070  
PMID:16344560   PMID:16412436   PMID:16710414   PMID:20367554   PMID:20677014   PMID:21653829   PMID:21787750   PMID:21873635   PMID:25713288   PMID:28891236   PMID:28986522   PMID:31586073  
PMID:33961781   PMID:35748872  


Genomics

Comparative Map Data
ADGRB2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38131,727,117 - 31,764,340 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl131,727,117 - 31,764,893 (-)EnsemblGRCh38hg38GRCh38
GRCh37132,192,718 - 32,229,941 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36131,965,305 - 32,002,235 (-)NCBINCBI36Build 36hg18NCBI36
Build 34131,861,811 - 31,898,729NCBI
Celera130,461,955 - 30,498,884 (-)NCBICelera
Cytogenetic Map1p35.2NCBI
HuRef130,310,212 - 30,346,996 (-)NCBIHuRef
CHM1_1132,308,513 - 32,345,443 (-)NCBICHM1_1
T2T-CHM13v2.0131,584,757 - 31,621,990 (-)NCBIT2T-CHM13v2.0
Adgrb2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm394129,878,566 - 129,916,426 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl4129,878,663 - 129,916,426 (+)EnsemblGRCm39 Ensembl
GRCm384129,984,773 - 130,022,633 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl4129,984,870 - 130,022,633 (+)EnsemblGRCm38mm10GRCm38
MGSCv374129,662,408 - 129,699,877 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv364129,494,372 - 129,524,652 (+)NCBIMGSCv36mm8
Celera4128,319,684 - 128,357,331 (+)NCBICelera
Cytogenetic Map4D2.2NCBI
cM Map463.43NCBI
Adgrb2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr85147,581,573 - 147,646,726 (+)NCBIGRCr8
mRatBN7.25142,299,190 - 142,362,540 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl5142,331,329 - 142,362,540 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx5145,032,526 - 145,063,767 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.05146,802,347 - 146,833,584 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.05146,799,866 - 146,831,097 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.05148,168,530 - 148,231,587 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl5148,193,710 - 148,231,587 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.05151,888,166 - 151,950,961 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.45149,014,053 - 149,046,244 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.15149,017,386 - 149,056,274 (+)NCBI
Celera5140,800,108 - 140,831,213 (+)NCBICelera
Cytogenetic Map5q36NCBI
Adgrb2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545210,131,371 - 10,167,597 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495545210,131,371 - 10,167,597 (-)NCBIChiLan1.0ChiLan1.0
ADGRB2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21195,065,768 - 195,102,744 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11194,187,456 - 194,224,391 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0131,010,807 - 31,047,780 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1132,028,239 - 32,065,277 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl132,028,554 - 32,060,582 (-)Ensemblpanpan1.1panPan2
ADGRB2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1269,353,425 - 69,389,256 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl269,353,413 - 69,389,225 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha265,932,620 - 65,968,435 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0269,918,691 - 69,954,503 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl269,918,648 - 69,954,496 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1266,754,617 - 66,790,423 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0267,750,754 - 67,786,570 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0268,750,286 - 68,786,095 (+)NCBIUU_Cfam_GSD_1.0
Adgrb2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505849,010,839 - 49,046,033 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493647414,835,602 - 14,870,821 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493647414,835,621 - 14,870,815 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ADGRB2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl688,256,146 - 88,293,330 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1688,256,144 - 88,293,519 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2681,956,153 - 81,986,674 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ADGRB2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.120101,107,561 - 101,144,359 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl20101,081,197 - 101,295,467 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603315,546,820 - 15,583,862 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Adgrb2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462476414,964,480 - 15,001,320 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462476414,964,614 - 15,001,429 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ADGRB2
295 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001364857.2(ADGRB2):c.4393C>T (p.Arg1465Trp) single nucleotide variant Progressive spastic paraparesis [RCV000577924] Chr1:31728621 [GRCh38]
Chr1:32194222 [GRCh37]
Chr1:1p35.2		 likely pathogenic
GRCh38/hg38 1p36.11-35.2(chr1:26963045-32279045)x3 copy number gain See cases [RCV000051801] Chr1:26963045..32279045 [GRCh38]
Chr1:27289536..32744646 [GRCh37]
Chr1:27162123..32517233 [NCBI36]
Chr1:1p36.11-35.2		 pathogenic
GRCh38/hg38 1p35.2-35.1(chr1:31122108-32402160)x3 copy number gain See cases [RCV000051802] Chr1:31122108..32402160 [GRCh38]
Chr1:31594955..32867761 [GRCh37]
Chr1:31367542..32640348 [NCBI36]
Chr1:1p35.2-35.1		 pathogenic
GRCh38/hg38 1p35.2-35.1(chr1:30766758-33359428)x1 copy number loss See cases [RCV000053802] Chr1:30766758..33359428 [GRCh38]
Chr1:31239605..33825029 [GRCh37]
Chr1:31012192..33597616 [NCBI36]
Chr1:1p35.2-35.1		 pathogenic
NM_001294335.1(ADGRB2):c.4482C>T (p.Phe1494=) single nucleotide variant Malignant melanoma [RCV000060173] Chr1:31728212 [GRCh38]
Chr1:32193813 [GRCh37]
Chr1:31966400 [NCBI36]
Chr1:1p35.2		 not provided
NM_001294335.1(ADGRB2):c.3354-52C>T single nucleotide variant Malignant melanoma [RCV000064713] Chr1:31735333 [GRCh38]
Chr1:32200934 [GRCh37]
Chr1:31973521 [NCBI36]
Chr1:1p35.2		 not provided
NM_001294335.1(ADGRB2):c.2086C>T (p.Arg696Cys) single nucleotide variant Malignant melanoma [RCV000064714] Chr1:31740007 [GRCh38]
Chr1:32205608 [GRCh37]
Chr1:31978195 [NCBI36]
Chr1:1p35.2		 not provided
GRCh38/hg38 1p35.3-35.1(chr1:28424867-33122854)x1 copy number loss See cases [RCV000135447] Chr1:28424867..33122854 [GRCh38]
Chr1:28751378..33588455 [GRCh37]
Chr1:28623965..33361042 [NCBI36]
Chr1:1p35.3-35.1		 pathogenic
GRCh38/hg38 1p36.11-34.2(chr1:24381206-41401517)x3 copy number gain See cases [RCV000138891] Chr1:24381206..41401517 [GRCh38]
Chr1:24707696..41886350 [GRCh37]
Chr1:24580283..41658937 [NCBI36]
Chr1:1p36.11-34.2		 pathogenic
GRCh38/hg38 1p35.2(chr1:30864842-32021241)x3 copy number gain See cases [RCV000142920] Chr1:30864842..32021241 [GRCh38]
Chr1:31337689..32486842 [GRCh37]
Chr1:31110276..32259429 [NCBI36]
Chr1:1p35.2		 uncertain significance
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3 copy number loss not provided [RCV000762767] Chr1:20608823..120546301 [GRCh37]
Chr1:1p36.12-12		 likely benign
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
NM_001364857.2(ADGRB2):c.1183C>A (p.Gln395Lys) single nucleotide variant not specified [RCV004316765] Chr1:31742907 [GRCh38]
Chr1:32208508 [GRCh37]
Chr1:1p35.2		 uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p35.2-34.3(chr1:31562164-37421958)x3 copy number gain not provided [RCV000748949] Chr1:31562164..37421958 [GRCh37]
Chr1:1p35.2-34.3		 pathogenic
NM_001364857.2(ADGRB2):c.3702C>T (p.Asn1234=) single nucleotide variant not provided [RCV000914643] Chr1:31732535 [GRCh38]
Chr1:32198136 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.4515+10C>T single nucleotide variant not provided [RCV000971250] Chr1:31728172 [GRCh38]
Chr1:32193773 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.91A>G (p.Thr31Ala) single nucleotide variant not provided [RCV000923670] Chr1:31756746 [GRCh38]
Chr1:32222347 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2558C>T (p.Pro853Leu) single nucleotide variant not provided [RCV000953421] Chr1:31738875 [GRCh38]
Chr1:32204476 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.3663G>A (p.Arg1221=) single nucleotide variant not provided [RCV000961269] Chr1:31732574 [GRCh38]
Chr1:32198175 [GRCh37]
Chr1:1p35.2		 benign
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3 copy number gain Global developmental delay [RCV000787285] Chr1:103343285..103455144 [GRCh37]
Chr1:1p36.22-21.1		 uncertain significance
NM_001364857.2(ADGRB2):c.3373G>C (p.Ala1125Pro) single nucleotide variant not specified [RCV004293984] Chr1:31735262 [GRCh38]
Chr1:32200863 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1012T>C (p.Ser338Pro) single nucleotide variant not provided [RCV001090923]|not specified [RCV004907681] Chr1:31744268 [GRCh38]
Chr1:32209869 [GRCh37]
Chr1:1p35.2		 uncertain significance
GRCh37/hg19 1p35.2(chr1:32090118-32280833)x3 copy number gain not provided [RCV000846698] Chr1:32090118..32280833 [GRCh37]
Chr1:1p35.2		 uncertain significance
GRCh37/hg19 1p35.2-35.1(chr1:30819875-34380419)x3 copy number gain not provided [RCV001005079] Chr1:30819875..34380419 [GRCh37]
Chr1:1p35.2-35.1		 likely pathogenic
GRCh37/hg19 1p35.2-35.1(chr1:32139063-32940848)x4 copy number gain not provided [RCV000846712] Chr1:32139063..32940848 [GRCh37]
Chr1:1p35.2-35.1		 uncertain significance
NM_001364857.2(ADGRB2):c.3292G>A (p.Val1098Ile) single nucleotide variant not specified [RCV004304055] Chr1:31735641 [GRCh38]
Chr1:32201242 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2714G>A (p.Arg905His) single nucleotide variant not specified [RCV004287686] Chr1:31738258 [GRCh38]
Chr1:32203859 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3865C>T (p.Pro1289Ser) single nucleotide variant not provided [RCV003106806] Chr1:31731315 [GRCh38]
Chr1:32196916 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3620G>A (p.Arg1207Gln) single nucleotide variant not specified [RCV004293258] Chr1:31732976 [GRCh38]
Chr1:32198577 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1990C>T (p.Arg664Cys) single nucleotide variant not specified [RCV004292704] Chr1:31740178 [GRCh38]
Chr1:32205779 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3786C>T (p.Cys1262=) single nucleotide variant not provided [RCV000933562] Chr1:31731394 [GRCh38]
Chr1:32196995 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4542G>A (p.Ser1514=) single nucleotide variant not provided [RCV000916284] Chr1:31728055 [GRCh38]
Chr1:32193656 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2619T>C (p.His873=) single nucleotide variant not provided [RCV000963752] Chr1:31738613 [GRCh38]
Chr1:32204214 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.2224A>T (p.Met742Leu) single nucleotide variant not provided [RCV000887647] Chr1:31739579 [GRCh38]
Chr1:32205180 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.342C>A (p.Pro114=) single nucleotide variant not provided [RCV000884857] Chr1:31756495 [GRCh38]
Chr1:32222096 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.4716G>A (p.Glu1572=) single nucleotide variant not provided [RCV000953420] Chr1:31727462 [GRCh38]
Chr1:32193063 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.2848C>T (p.Leu950=) single nucleotide variant not provided [RCV000929447] Chr1:31737680 [GRCh38]
Chr1:32203281 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4554C>G (p.Ala1518=) single nucleotide variant not provided [RCV000891365] Chr1:31728043 [GRCh38]
Chr1:32193644 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.4197G>A (p.Leu1399=) single nucleotide variant not provided [RCV000955695] Chr1:31730983 [GRCh38]
Chr1:32196584 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.4508C>T (p.Thr1503Met) single nucleotide variant not provided [RCV000955694] Chr1:31728189 [GRCh38]
Chr1:32193790 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.3577G>A (p.Ala1193Thr) single nucleotide variant not provided [RCV002770974]|not specified [RCV004064751] Chr1:31733019 [GRCh38]
Chr1:32198620 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.550G>A (p.Glu184Lys) single nucleotide variant not specified [RCV004308250] Chr1:31756287 [GRCh38]
Chr1:32221888 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3309G>A (p.Met1103Ile) single nucleotide variant not provided [RCV001090922] Chr1:31735624 [GRCh38]
Chr1:32201225 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2701G>A (p.Ala901Thr) single nucleotide variant not provided [RCV001963829] Chr1:31738271 [GRCh38]
Chr1:32203872 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2197G>A (p.Ala733Thr) single nucleotide variant not provided [RCV001875026]|not specified [RCV004040576] Chr1:31739606 [GRCh38]
Chr1:32205207 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3353+6G>C single nucleotide variant not provided [RCV001950107] Chr1:31735574 [GRCh38]
Chr1:32201175 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4093G>A (p.Gly1365Ser) single nucleotide variant not provided [RCV001969472]|not specified [RCV004042222] Chr1:31731087 [GRCh38]
Chr1:32196688 [GRCh37]
Chr1:1p35.2		 likely benign|uncertain significance
NM_001364857.2(ADGRB2):c.4327C>T (p.Arg1443Trp) single nucleotide variant not provided [RCV002025685] Chr1:31730853 [GRCh38]
Chr1:32196454 [GRCh37]
Chr1:1p35.2		 uncertain significance
GRCh37/hg19 1p36.11-35.1(chr1:27543877-32819121) copy number gain not specified [RCV002052559] Chr1:27543877..32819121 [GRCh37]
Chr1:1p36.11-35.1		 uncertain significance
NM_001364857.2(ADGRB2):c.536C>T (p.Ala179Val) single nucleotide variant not provided [RCV002039946] Chr1:31756301 [GRCh38]
Chr1:32221902 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2079C>G (p.His693Gln) single nucleotide variant not provided [RCV001886203] Chr1:31740014 [GRCh38]
Chr1:32205615 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4572+1G>A single nucleotide variant not provided [RCV002026430] Chr1:31728024 [GRCh38]
Chr1:32193625 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4555G>A (p.Glu1519Lys) single nucleotide variant not provided [RCV001939911] Chr1:31728042 [GRCh38]
Chr1:32193643 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2645C>T (p.Ala882Val) single nucleotide variant not provided [RCV002016950] Chr1:31738587 [GRCh38]
Chr1:32204188 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1307C>T (p.Ala436Val) single nucleotide variant not provided [RCV001899517] Chr1:31742163 [GRCh38]
Chr1:32207764 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3578C>T (p.Ala1193Val) single nucleotide variant not provided [RCV001875194]|not specified [RCV004040593] Chr1:31733018 [GRCh38]
Chr1:32198619 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.862A>C (p.Lys288Gln) single nucleotide variant not provided [RCV001991671] Chr1:31744708 [GRCh38]
Chr1:32210309 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.971C>T (p.Thr324Met) single nucleotide variant not provided [RCV001935579]|not specified [RCV004907745] Chr1:31744309 [GRCh38]
Chr1:32209910 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2839C>G (p.Leu947Val) single nucleotide variant not provided [RCV001897504] Chr1:31737689 [GRCh38]
Chr1:32203290 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2809G>C (p.Val937Leu) single nucleotide variant not provided [RCV001925924] Chr1:31737719 [GRCh38]
Chr1:32203320 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4685G>A (p.Arg1562Gln) single nucleotide variant not provided [RCV002015087] Chr1:31727493 [GRCh38]
Chr1:32193094 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3352G>A (p.Gly1118Arg) single nucleotide variant not provided [RCV001973006] Chr1:31735581 [GRCh38]
Chr1:32201182 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.271G>A (p.Ala91Thr) single nucleotide variant not provided [RCV002046166]|not specified [RCV004907771] Chr1:31756566 [GRCh38]
Chr1:32222167 [GRCh37]
Chr1:1p35.2		 likely benign|uncertain significance
NM_001364857.2(ADGRB2):c.411G>A (p.Ala137=) single nucleotide variant not provided [RCV002111076] Chr1:31756426 [GRCh38]
Chr1:32222027 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3267+11G>A single nucleotide variant not provided [RCV002106789] Chr1:31735816 [GRCh38]
Chr1:32201417 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.4516-17G>A single nucleotide variant not provided [RCV002124788] Chr1:31728098 [GRCh38]
Chr1:32193699 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.627C>T (p.Gly209=) single nucleotide variant not provided [RCV002111057] Chr1:31756210 [GRCh38]
Chr1:32221811 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3256G>A (p.Val1086Ile) single nucleotide variant not provided [RCV002109384] Chr1:31735838 [GRCh38]
Chr1:32201439 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3201-8C>G single nucleotide variant not provided [RCV002109552] Chr1:31735901 [GRCh38]
Chr1:32201502 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.273A>T (p.Ala91=) single nucleotide variant not provided [RCV002210148] Chr1:31756564 [GRCh38]
Chr1:32222165 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4113G>C (p.Glu1371Asp) single nucleotide variant not provided [RCV002148325] Chr1:31731067 [GRCh38]
Chr1:32196668 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.2877-6C>T single nucleotide variant not provided [RCV002185690] Chr1:31737537 [GRCh38]
Chr1:32203138 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2508C>T (p.Ala836=) single nucleotide variant not provided [RCV002124654] Chr1:31738925 [GRCh38]
Chr1:32204526 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.2168-18A>C single nucleotide variant not provided [RCV002075205] Chr1:31739653 [GRCh38]
Chr1:32205254 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.396G>A (p.Glu132=) single nucleotide variant not provided [RCV002129584] Chr1:31756441 [GRCh38]
Chr1:32222042 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3353+12G>A single nucleotide variant not provided [RCV002132005] Chr1:31735568 [GRCh38]
Chr1:32201169 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.4134G>C (p.Pro1378=) single nucleotide variant not provided [RCV002113306] Chr1:31731046 [GRCh38]
Chr1:31731046..31731047 [GRCh38]
Chr1:32196647 [GRCh37]
Chr1:32196647..32196648 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.4671C>A (p.Pro1557=) single nucleotide variant not provided [RCV002212885] Chr1:31727507 [GRCh38]
Chr1:32193108 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3153C>T (p.Ala1051=) single nucleotide variant not provided [RCV002112480] Chr1:31736368 [GRCh38]
Chr1:32201969 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1179C>G (p.Pro393=) single nucleotide variant not provided [RCV002093683] Chr1:31742911 [GRCh38]
Chr1:32208512 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.525C>T (p.Pro175=) single nucleotide variant not provided [RCV002132193] Chr1:31756312 [GRCh38]
Chr1:32221913 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.3892C>T (p.Leu1298=) single nucleotide variant not provided [RCV002132194] Chr1:31731288 [GRCh38]
Chr1:32196889 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.4551A>G (p.Ala1517=) single nucleotide variant not provided [RCV002117351] Chr1:31728046 [GRCh38]
Chr1:32193647 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.2602-6C>T single nucleotide variant not provided [RCV002165174] Chr1:31738636 [GRCh38]
Chr1:32204237 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2448C>T (p.Ile816=) single nucleotide variant not provided [RCV002090752] Chr1:31739355 [GRCh38]
Chr1:32204956 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.1140C>T (p.Cys380=) single nucleotide variant not provided [RCV002116584] Chr1:31742950 [GRCh38]
Chr1:32208551 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3268-14T>A single nucleotide variant not provided [RCV002133452] Chr1:31735679 [GRCh38]
Chr1:32201280 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3760+11C>T single nucleotide variant not provided [RCV002211990] Chr1:31732104 [GRCh38]
Chr1:32197705 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.3135G>A (p.Leu1045=) single nucleotide variant not provided [RCV002194029] Chr1:31736386 [GRCh38]
Chr1:32201987 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1418-13A>C single nucleotide variant not provided [RCV002115645] Chr1:31741980 [GRCh38]
Chr1:32207581 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.1586-11T>C single nucleotide variant not provided [RCV002119327] Chr1:31741736 [GRCh38]
Chr1:32207337 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3576C>T (p.Ser1192=) single nucleotide variant not provided [RCV002103674] Chr1:31733020 [GRCh38]
Chr1:32198621 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3792G>A (p.Pro1264=) single nucleotide variant not provided [RCV002175411] Chr1:31731388 [GRCh38]
Chr1:32196989 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3353+12dup duplication not provided [RCV002098788] Chr1:31735567..31735568 [GRCh38]
Chr1:32201168..32201169 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.3498C>T (p.Leu1166=) single nucleotide variant not provided [RCV002138363] Chr1:31733098 [GRCh38]
Chr1:32198699 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4515+7G>C single nucleotide variant not provided [RCV002140173] Chr1:31728175 [GRCh38]
Chr1:32193776 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4594C>T (p.Arg1532Cys) single nucleotide variant not provided [RCV002122639] Chr1:31727584 [GRCh38]
Chr1:32193185 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.4461G>A (p.Glu1487=) single nucleotide variant not provided [RCV002202884] Chr1:31728236 [GRCh38]
Chr1:32193837 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3222C>T (p.Gly1074=) single nucleotide variant not provided [RCV002122909] Chr1:31735872 [GRCh38]
Chr1:32201473 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.4730C>T (p.Pro1577Leu) single nucleotide variant not provided [RCV002180065] Chr1:31727448 [GRCh38]
Chr1:32193049 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.3353+11G>C single nucleotide variant not provided [RCV002155514] Chr1:31735569 [GRCh38]
Chr1:32201170 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.1470G>A (p.Thr490=) single nucleotide variant not provided [RCV002083771] Chr1:31741915 [GRCh38]
Chr1:32207516 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1088-16A>T single nucleotide variant not provided [RCV002123539] Chr1:31743018 [GRCh38]
Chr1:32208619 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.772C>T (p.Pro258Ser) single nucleotide variant not provided [RCV002177968] Chr1:31756065 [GRCh38]
Chr1:32221666 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3000T>G (p.Ala1000=) single nucleotide variant not provided [RCV002219774] Chr1:31736703 [GRCh38]
Chr1:32202304 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4275G>A (p.Pro1425=) single nucleotide variant not provided [RCV002123946] Chr1:31730905 [GRCh38]
Chr1:32196506 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.22-4A>G single nucleotide variant not provided [RCV003111995] Chr1:31756819 [GRCh38]
Chr1:32222420 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1121G>A (p.Ser374Asn) single nucleotide variant not specified [RCV004313827] Chr1:31742969 [GRCh38]
Chr1:32208570 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1883G>A (p.Arg628Gln) single nucleotide variant not specified [RCV004134996] Chr1:31740453 [GRCh38]
Chr1:32206054 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1858C>T (p.Arg620Cys) single nucleotide variant not specified [RCV004218016] Chr1:31740478 [GRCh38]
Chr1:32206079 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1688-7C>T single nucleotide variant not provided [RCV002614768] Chr1:31741486 [GRCh38]
Chr1:32207087 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2759C>T (p.Pro920Leu) single nucleotide variant not provided [RCV003546926]|not specified [RCV004196094] Chr1:31738213 [GRCh38]
Chr1:32203814 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1440A>G (p.Pro480=) single nucleotide variant not provided [RCV002975288] Chr1:31741945 [GRCh38]
Chr1:32207546 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2091C>T (p.Val697=) single nucleotide variant not provided [RCV002903395] Chr1:31740002 [GRCh38]
Chr1:32205603 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.3407C>T (p.Ala1136Val) single nucleotide variant not specified [RCV004151477] Chr1:31735228 [GRCh38]
Chr1:32200829 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3705G>T (p.Gly1235=) single nucleotide variant not provided [RCV002730173] Chr1:31732532 [GRCh38]
Chr1:32198133 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.541C>T (p.Arg181Cys) single nucleotide variant not specified [RCV004151605] Chr1:31756296 [GRCh38]
Chr1:32221897 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4322G>A (p.Arg1441His) single nucleotide variant not specified [RCV004120320] Chr1:31730858 [GRCh38]
Chr1:32196459 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2293G>T (p.Val765Leu) single nucleotide variant not specified [RCV004149635] Chr1:31739510 [GRCh38]
Chr1:32205111 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.21+20T>C single nucleotide variant not provided [RCV002618330] Chr1:31757181 [GRCh38]
Chr1:32222782 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4559G>A (p.Arg1520Gln) single nucleotide variant not provided [RCV002618530] Chr1:31728038 [GRCh38]
Chr1:32193639 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4619G>A (p.Arg1540His) single nucleotide variant not specified [RCV004098493] Chr1:31727559 [GRCh38]
Chr1:32193160 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1585+13T>C single nucleotide variant not provided [RCV002690078] Chr1:31741787 [GRCh38]
Chr1:32207388 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2243T>C (p.Met748Thr) single nucleotide variant not specified [RCV004233686] Chr1:31739560 [GRCh38]
Chr1:32205161 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3131-16A>G single nucleotide variant not provided [RCV002975256] Chr1:31736406 [GRCh38]
Chr1:32202007 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3706C>A (p.Gln1236Lys) single nucleotide variant not specified [RCV004121764] Chr1:31732531 [GRCh38]
Chr1:32198132 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2448C>G (p.Ile816Met) single nucleotide variant not specified [RCV004141746] Chr1:31739355 [GRCh38]
Chr1:32204956 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.686C>T (p.Ala229Val) single nucleotide variant not provided [RCV002640670] Chr1:31756151 [GRCh38]
Chr1:32221752 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4573-13G>A single nucleotide variant not provided [RCV002795801] Chr1:31727618 [GRCh38]
Chr1:32193219 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1284G>C (p.Trp428Cys) single nucleotide variant not provided [RCV003039358] Chr1:31742186 [GRCh38]
Chr1:32207787 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1113G>T (p.Gly371=) single nucleotide variant not provided [RCV002795327] Chr1:31742977 [GRCh38]
Chr1:32208578 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4724A>G (p.Glu1575Gly) single nucleotide variant not specified [RCV004118318] Chr1:31727454 [GRCh38]
Chr1:32193055 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.32A>G (p.His11Arg) single nucleotide variant not provided [RCV002795192] Chr1:31756805 [GRCh38]
Chr1:32222406 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1041G>A (p.Gly347=) single nucleotide variant not provided [RCV002976585] Chr1:31744239 [GRCh38]
Chr1:32209840 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2602-8C>T single nucleotide variant not provided [RCV002637051] Chr1:31738638 [GRCh38]
Chr1:32204239 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.1298C>T (p.Thr433Met) single nucleotide variant not specified [RCV004110764] Chr1:31742172 [GRCh38]
Chr1:32207773 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4416+11TG[3] microsatellite not provided [RCV002795461] Chr1:31728580..31728581 [GRCh38]
Chr1:32194181..32194182 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.929C>T (p.Pro310Leu) single nucleotide variant not provided [RCV002999308] Chr1:31744351 [GRCh38]
Chr1:32209952 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4490G>T (p.Arg1497Leu) single nucleotide variant not specified [RCV004122790] Chr1:31728207 [GRCh38]
Chr1:32193808 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4201G>A (p.Val1401Met) single nucleotide variant not specified [RCV004216001] Chr1:31730979 [GRCh38]
Chr1:32196580 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3513C>T (p.Ala1171=) single nucleotide variant not provided [RCV002923706] Chr1:31733083 [GRCh38]
Chr1:32198684 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.982G>A (p.Gly328Ser) single nucleotide variant not specified [RCV004161259] Chr1:31744298 [GRCh38]
Chr1:32209899 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2302C>G (p.Leu768Val) single nucleotide variant not provided [RCV002957896] Chr1:31739501 [GRCh38]
Chr1:32205102 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.94G>A (p.Ala32Thr) single nucleotide variant not specified [RCV004123223] Chr1:31756743 [GRCh38]
Chr1:32222344 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2181G>T (p.Gln727His) single nucleotide variant not specified [RCV004140204] Chr1:31739622 [GRCh38]
Chr1:32205223 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3313C>T (p.Arg1105Cys) single nucleotide variant not provided [RCV003720714]|not specified [RCV004206886] Chr1:31735620 [GRCh38]
Chr1:32201221 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.683A>G (p.Glu228Gly) single nucleotide variant not provided [RCV002917933]|not specified [RCV004066151] Chr1:31756154 [GRCh38]
Chr1:32221755 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4573-12C>T single nucleotide variant not provided [RCV002666764] Chr1:31727617 [GRCh38]
Chr1:32193218 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4439G>A (p.Arg1480Gln) single nucleotide variant not specified [RCV004118962] Chr1:31728258 [GRCh38]
Chr1:32193859 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2553G>T (p.Gln851His) single nucleotide variant not specified [RCV004147731] Chr1:31738880 [GRCh38]
Chr1:32204481 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2980-17A>G single nucleotide variant not provided [RCV002800650] Chr1:31736740 [GRCh38]
Chr1:32202341 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1989+7C>T single nucleotide variant not provided [RCV002928242] Chr1:31740340 [GRCh38]
Chr1:32205941 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2287A>G (p.Lys763Glu) single nucleotide variant not specified [RCV004134162] Chr1:31739516 [GRCh38]
Chr1:32205117 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2646-14C>T single nucleotide variant not provided [RCV002800903] Chr1:31738340 [GRCh38]
Chr1:32203941 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.270C>T (p.Cys90=) single nucleotide variant not provided [RCV002595977] Chr1:31756567 [GRCh38]
Chr1:32222168 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2168-13C>T single nucleotide variant not provided [RCV002576201] Chr1:31739648 [GRCh38]
Chr1:32205249 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2404C>T (p.Arg802Cys) single nucleotide variant not specified [RCV004146358] Chr1:31739399 [GRCh38]
Chr1:32205000 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.922+13C>T single nucleotide variant not provided [RCV002575500] Chr1:31744635 [GRCh38]
Chr1:32210236 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.860C>T (p.Pro287Leu) single nucleotide variant not provided [RCV002932713] Chr1:31744710 [GRCh38]
Chr1:32210311 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1236T>G (p.Ser412Arg) single nucleotide variant not specified [RCV004120409] Chr1:31742854 [GRCh38]
Chr1:32208455 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1650C>T (p.Gly550=) single nucleotide variant not provided [RCV003059035]|not specified [RCV004907813] Chr1:31741661 [GRCh38]
Chr1:32207262 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3351C>T (p.Ala1117=) single nucleotide variant not provided [RCV003085291] Chr1:31735582 [GRCh38]
Chr1:32201183 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.2854G>A (p.Ala952Thr) single nucleotide variant not provided [RCV002667617] Chr1:31737674 [GRCh38]
Chr1:32203275 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2645+12G>A single nucleotide variant not provided [RCV002630400] Chr1:31738575 [GRCh38]
Chr1:32204176 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.350C>T (p.Ala117Val) single nucleotide variant not provided [RCV002966754]|not specified [RCV004068217] Chr1:31756487 [GRCh38]
Chr1:32222088 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.106G>A (p.Ala36Thr) single nucleotide variant not specified [RCV004078743] Chr1:31756731 [GRCh38]
Chr1:32222332 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.414G>T (p.Gly138=) single nucleotide variant not provided [RCV002922921] Chr1:31756423 [GRCh38]
Chr1:32222024 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.3569T>C (p.Phe1190Ser) single nucleotide variant not specified [RCV004174005] Chr1:31733027 [GRCh38]
Chr1:32198628 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3077T>C (p.Ile1026Thr) single nucleotide variant not provided [RCV002962094]|not specified [RCV004068204] Chr1:31736626 [GRCh38]
Chr1:32202227 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1253-19C>T single nucleotide variant not provided [RCV002630399] Chr1:31742236 [GRCh38]
Chr1:32207837 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.932C>T (p.Ala311Val) single nucleotide variant not provided [RCV003011082] Chr1:31744348 [GRCh38]
Chr1:32209949 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.2167+13A>C single nucleotide variant not provided [RCV002580046] Chr1:31739913 [GRCh38]
Chr1:32205514 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4294G>A (p.Ala1432Thr) single nucleotide variant not provided [RCV002966469] Chr1:31730886 [GRCh38]
Chr1:32196487 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1628C>T (p.Thr543Met) single nucleotide variant not provided [RCV002937313] Chr1:31741683 [GRCh38]
Chr1:32207284 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2183G>A (p.Arg728Gln) single nucleotide variant not specified [RCV004171848] Chr1:31739620 [GRCh38]
Chr1:32205221 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2877-12G>A single nucleotide variant not provided [RCV002580432] Chr1:31737543 [GRCh38]
Chr1:32203144 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.3761-19C>G single nucleotide variant not provided [RCV003027799] Chr1:31731438 [GRCh38]
Chr1:32197039 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1351C>T (p.Pro451Ser) single nucleotide variant not provided [RCV002599548] Chr1:31742119 [GRCh38]
Chr1:32207720 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1176G>T (p.Val392=) single nucleotide variant not provided [RCV002832816] Chr1:31742914 [GRCh38]
Chr1:32208515 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1586-14C>T single nucleotide variant not provided [RCV002576605] Chr1:31741739 [GRCh38]
Chr1:32207340 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1049G>A (p.Arg350Gln) single nucleotide variant not provided [RCV003542459]|not specified [RCV004112763] Chr1:31744231 [GRCh38]
Chr1:32209832 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2792C>T (p.Ser931Phe) single nucleotide variant not specified [RCV004118622] Chr1:31737736 [GRCh38]
Chr1:32203337 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1971C>T (p.Pro657=) single nucleotide variant not provided [RCV002962437] Chr1:31740365 [GRCh38]
Chr1:32205966 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3353+12del deletion not provided [RCV002576471] Chr1:31735568 [GRCh38]
Chr1:32201169 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.4615C>T (p.Arg1539Trp) single nucleotide variant not specified [RCV004219488] Chr1:31727563 [GRCh38]
Chr1:32193164 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.11C>T (p.Thr4Ile) single nucleotide variant not provided [RCV002588481]|not specified [RCV004068832] Chr1:31757211 [GRCh38]
Chr1:32222812 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3176C>T (p.Thr1059Met) single nucleotide variant not provided [RCV003730438]|not specified [RCV004253665] Chr1:31736345 [GRCh38]
Chr1:32201946 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4432C>T (p.Arg1478Trp) single nucleotide variant not specified [RCV004260080] Chr1:31728265 [GRCh38]
Chr1:32193866 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.910A>G (p.Met304Val) single nucleotide variant not specified [RCV004267311] Chr1:31744660 [GRCh38]
Chr1:32210261 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.82C>A (p.Arg28Ser) single nucleotide variant not specified [RCV004277470] Chr1:31756755 [GRCh38]
Chr1:32222356 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1115C>T (p.Ser372Phe) single nucleotide variant not provided [RCV003666237] Chr1:31742975 [GRCh38]
Chr1:32208576 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.343G>A (p.Glu115Lys) single nucleotide variant not specified [RCV004342980] Chr1:31756494 [GRCh38]
Chr1:32222095 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4541C>T (p.Ser1514Leu) single nucleotide variant not specified [RCV004338683] Chr1:31728056 [GRCh38]
Chr1:32193657 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1198G>A (p.Ala400Thr) single nucleotide variant not specified [RCV004346716] Chr1:31742892 [GRCh38]
Chr1:32208493 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3328G>A (p.Asp1110Asn) single nucleotide variant not specified [RCV004353927] Chr1:31735605 [GRCh38]
Chr1:32201206 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4679G>A (p.Arg1560Gln) single nucleotide variant not provided [RCV003873782] Chr1:31727499 [GRCh38]
Chr1:32193100 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3353+10G>A single nucleotide variant not provided [RCV003569294] Chr1:31735570 [GRCh38]
Chr1:32201171 [GRCh37]
Chr1:1p35.2		 likely benign
GRCh38/hg38 1p36.33-35.1(chr1:99125-34026935)x3 copy number gain Trisomy 12p [RCV003447845] Chr1:99125..34026935 [GRCh38]
Chr1:1p36.33-35.1		 pathogenic
NM_001364857.2(ADGRB2):c.4516A>C (p.Arg1506=) single nucleotide variant not provided [RCV003406281] Chr1:31728081 [GRCh38]
Chr1:32193682 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3353+6G>A single nucleotide variant not provided [RCV003830260] Chr1:31735574 [GRCh38]
Chr1:32201175 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2114T>C (p.Val705Ala) single nucleotide variant not provided [RCV003576955] Chr1:31739979 [GRCh38]
Chr1:32205580 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.839-17C>T single nucleotide variant not provided [RCV003572578] Chr1:31744748 [GRCh38]
Chr1:32210349 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2760G>A (p.Pro920=) single nucleotide variant not provided [RCV003546282] Chr1:31738212 [GRCh38]
Chr1:32203813 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4067G>A (p.Arg1356Gln) single nucleotide variant not provided [RCV003876212] Chr1:31731113 [GRCh38]
Chr1:32196714 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1381A>G (p.Thr461Ala) single nucleotide variant not provided [RCV003662704] Chr1:31742089 [GRCh38]
Chr1:32207690 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.958G>A (p.Val320Met) single nucleotide variant not provided [RCV003830948] Chr1:31744322 [GRCh38]
Chr1:32209923 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3817C>T (p.Arg1273Cys) single nucleotide variant not provided [RCV003546104] Chr1:31731363 [GRCh38]
Chr1:32196964 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3088C>T (p.Arg1030Cys) single nucleotide variant not provided [RCV003829249] Chr1:31736615 [GRCh38]
Chr1:32202216 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2168-15C>G single nucleotide variant not provided [RCV003661606] Chr1:31739650 [GRCh38]
Chr1:32205251 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1020C>A (p.Pro340=) single nucleotide variant not provided [RCV003715550] Chr1:31744260 [GRCh38]
Chr1:32209861 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1374T>C (p.Gly458=) single nucleotide variant not provided [RCV003717359] Chr1:31742096 [GRCh38]
Chr1:32207697 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2334G>A (p.Gly778=) single nucleotide variant not provided [RCV003549593] Chr1:31739469 [GRCh38]
Chr1:32205070 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1449G>A (p.Ala483=) single nucleotide variant not provided [RCV003835734] Chr1:31741936 [GRCh38]
Chr1:32207537 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2603G>C (p.Gly868Ala) single nucleotide variant not provided [RCV003725829] Chr1:31738629 [GRCh38]
Chr1:32204230 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.417G>A (p.Leu139=) single nucleotide variant not provided [RCV003817354] Chr1:31756420 [GRCh38]
Chr1:32222021 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1974G>A (p.Ser658=) single nucleotide variant not provided [RCV003659148] Chr1:31740362 [GRCh38]
Chr1:32205963 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.509C>T (p.Pro170Leu) single nucleotide variant not provided [RCV003561677] Chr1:31756328 [GRCh38]
Chr1:32221929 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.656C>T (p.Ala219Val) single nucleotide variant not provided [RCV003670093] Chr1:31756181 [GRCh38]
Chr1:32221782 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3025T>G (p.Ser1009Ala) single nucleotide variant not provided [RCV003717131] Chr1:31736678 [GRCh38]
Chr1:32202279 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4515+16G>A single nucleotide variant not provided [RCV003840223] Chr1:31728166 [GRCh38]
Chr1:32193767 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1346C>T (p.Ala449Val) single nucleotide variant not provided [RCV003548443] Chr1:31742124 [GRCh38]
Chr1:32207725 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3353+18G>C single nucleotide variant not provided [RCV003814481] Chr1:31735562 [GRCh38]
Chr1:32201163 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.846G>A (p.Glu282=) single nucleotide variant not provided [RCV003672106] Chr1:31744724 [GRCh38]
Chr1:32210325 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4735G>A (p.Gly1579Ser) single nucleotide variant not provided [RCV003724619] Chr1:31727443 [GRCh38]
Chr1:32193044 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4134G>A (p.Pro1378=) single nucleotide variant not provided [RCV003548209] Chr1:31731046 [GRCh38]
Chr1:32196647 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.707C>G (p.Thr236Ser) single nucleotide variant not provided [RCV003832264] Chr1:31756130 [GRCh38]
Chr1:32221731 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1038C>T (p.Ser346=) single nucleotide variant not provided [RCV003822479] Chr1:31744242 [GRCh38]
Chr1:32209843 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.3789C>A (p.Asn1263Lys) single nucleotide variant not provided [RCV003542228] Chr1:31731391 [GRCh38]
Chr1:32196992 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.904C>A (p.Leu302Ile) single nucleotide variant not provided [RCV003866597] Chr1:31744666 [GRCh38]
Chr1:32210267 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3314G>A (p.Arg1105His) single nucleotide variant not provided [RCV003552799] Chr1:31735619 [GRCh38]
Chr1:32201220 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.637G>A (p.Gly213Ser) single nucleotide variant not provided [RCV003858161] Chr1:31756200 [GRCh38]
Chr1:32221801 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1341C>T (p.Ser447=) single nucleotide variant not provided [RCV003728421] Chr1:31742129 [GRCh38]
Chr1:32207730 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1989+17A>G single nucleotide variant not provided [RCV003542971] Chr1:31740330 [GRCh38]
Chr1:32205931 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2982C>T (p.Gly994=) single nucleotide variant not provided [RCV003729407] Chr1:31736721 [GRCh38]
Chr1:32202322 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4416+10A>G single nucleotide variant not provided [RCV003733131] Chr1:31728588 [GRCh38]
Chr1:32194189 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.357C>T (p.Ala119=) single nucleotide variant not provided [RCV003733248] Chr1:31756480 [GRCh38]
Chr1:32222081 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2087G>A (p.Arg696His) single nucleotide variant not provided [RCV003871330] Chr1:31740006 [GRCh38]
Chr1:32205607 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1990-20A>G single nucleotide variant not provided [RCV003869764] Chr1:31740198 [GRCh38]
Chr1:32205799 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4563C>T (p.Ser1521=) single nucleotide variant not provided [RCV003728940] Chr1:31728034 [GRCh38]
Chr1:32193635 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1060C>T (p.Pro354Ser) single nucleotide variant not provided [RCV003719791] Chr1:31744220 [GRCh38]
Chr1:32209821 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3476T>C (p.Val1159Ala) single nucleotide variant not provided [RCV003868110] Chr1:31733120 [GRCh38]
Chr1:32198721 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.972G>A (p.Thr324=) single nucleotide variant not provided [RCV003551315] Chr1:31744308 [GRCh38]
Chr1:32209909 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.351G>A (p.Ala117=) single nucleotide variant not provided [RCV003719982] Chr1:31756486 [GRCh38]
Chr1:32222087 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4232C>T (p.Ala1411Val) single nucleotide variant not provided [RCV003738572]|not specified [RCV004374274] Chr1:31730948 [GRCh38]
Chr1:32196549 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.363G>A (p.Ala121=) single nucleotide variant not provided [RCV003552441] Chr1:31756474 [GRCh38]
Chr1:32222075 [GRCh37]
Chr1:1p35.2		 benign
NM_001364857.2(ADGRB2):c.267G>A (p.Val89=) single nucleotide variant not provided [RCV003845598] Chr1:31756570 [GRCh38]
Chr1:32222171 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.677C>A (p.Pro226His) single nucleotide variant not provided [RCV003680088] Chr1:31756160 [GRCh38]
Chr1:32221761 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.342C>T (p.Pro114=) single nucleotide variant not provided [RCV003821850] Chr1:31756495 [GRCh38]
Chr1:32222096 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1200C>T (p.Ala400=) single nucleotide variant not provided [RCV003675960] Chr1:31742890 [GRCh38]
Chr1:32208491 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.4281G>A (p.Pro1427=) single nucleotide variant not provided [RCV003843396] Chr1:31730899 [GRCh38]
Chr1:32196500 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.1688-15C>T single nucleotide variant not provided [RCV003563708] Chr1:31741494 [GRCh38]
Chr1:32207095 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.188C>T (p.Ser63Leu) single nucleotide variant not provided [RCV003562631] Chr1:31756649 [GRCh38]
Chr1:32222250 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2144C>T (p.Ser715Phe) single nucleotide variant not provided [RCV003568129] Chr1:31739949 [GRCh38]
Chr1:32205550 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.472G>A (p.Val158Met) single nucleotide variant not provided [RCV003736165] Chr1:31756365 [GRCh38]
Chr1:32221966 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.93C>T (p.Thr31=) single nucleotide variant not provided [RCV003847096] Chr1:31756744 [GRCh38]
Chr1:32222345 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2024C>T (p.Ala675Val) single nucleotide variant not specified [RCV004376861] Chr1:31740144 [GRCh38]
Chr1:32205745 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1019C>G (p.Pro340Arg) single nucleotide variant not specified [RCV004376813] Chr1:31744261 [GRCh38]
Chr1:32209862 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1108T>G (p.Trp370Gly) single nucleotide variant not specified [RCV004376822] Chr1:31742982 [GRCh38]
Chr1:32208583 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1180C>T (p.Pro394Ser) single nucleotide variant not specified [RCV004376828] Chr1:31742910 [GRCh38]
Chr1:32208511 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1369A>T (p.Thr457Ser) single nucleotide variant not specified [RCV004376845] Chr1:31742101 [GRCh38]
Chr1:32207702 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1888A>G (p.Thr630Ala) single nucleotide variant not specified [RCV004376853] Chr1:31740448 [GRCh38]
Chr1:32206049 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2119G>A (p.Asp707Asn) single nucleotide variant not specified [RCV004378938] Chr1:31739974 [GRCh38]
Chr1:32205575 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2595C>G (p.Ile865Met) single nucleotide variant not specified [RCV004378970] Chr1:31738838 [GRCh38]
Chr1:32204439 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3514G>A (p.Val1172Ile) single nucleotide variant not specified [RCV004379027] Chr1:31733082 [GRCh38]
Chr1:32198683 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3859G>A (p.Val1287Met) single nucleotide variant not specified [RCV004379036] Chr1:31731321 [GRCh38]
Chr1:32196922 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4288C>T (p.Pro1430Ser) single nucleotide variant not specified [RCV004379040] Chr1:31730892 [GRCh38]
Chr1:32196493 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.521C>T (p.Ala174Val) single nucleotide variant not specified [RCV004379057] Chr1:31756316 [GRCh38]
Chr1:32221917 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.562A>G (p.Ile188Val) single nucleotide variant not specified [RCV004379064] Chr1:31756275 [GRCh38]
Chr1:32221876 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.848C>T (p.Pro283Leu) single nucleotide variant not specified [RCV004379068] Chr1:31744722 [GRCh38]
Chr1:32210323 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4490G>A (p.Arg1497His) single nucleotide variant not specified [RCV004379048] Chr1:31728207 [GRCh38]
Chr1:32193808 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4150C>T (p.Arg1384Ter) single nucleotide variant Hereditary spastic paraplegia [RCV004586505] Chr1:31731030 [GRCh38]
Chr1:32196631 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2983G>A (p.Val995Met) single nucleotide variant not specified [RCV004378981] Chr1:31736720 [GRCh38]
Chr1:32202321 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3280A>G (p.Ile1094Val) single nucleotide variant not specified [RCV004378994] Chr1:31735653 [GRCh38]
Chr1:32201254 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4669C>G (p.Pro1557Ala) single nucleotide variant not specified [RCV004379055] Chr1:31727509 [GRCh38]
Chr1:32193110 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.859C>G (p.Pro287Ala) single nucleotide variant not specified [RCV004608484] Chr1:31744711 [GRCh38]
Chr1:32210312 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3011A>G (p.His1004Arg) single nucleotide variant not specified [RCV004608604] Chr1:31736692 [GRCh38]
Chr1:32202293 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1289C>T (p.Pro430Leu) single nucleotide variant not specified [RCV004608495] Chr1:31742181 [GRCh38]
Chr1:32207782 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.618G>T (p.Glu206Asp) single nucleotide variant not specified [RCV004608473] Chr1:31756219 [GRCh38]
Chr1:32221820 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3115C>A (p.Leu1039Ile) single nucleotide variant not specified [RCV004608505] Chr1:31736588 [GRCh38]
Chr1:32202189 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4495C>T (p.Arg1499Cys) single nucleotide variant not specified [RCV004608525] Chr1:31728202 [GRCh38]
Chr1:32193803 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1408G>A (p.Glu470Lys) single nucleotide variant not specified [RCV004608546] Chr1:31742062 [GRCh38]
Chr1:32207663 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1096G>A (p.Val366Met) single nucleotide variant not specified [RCV004608556] Chr1:31742994 [GRCh38]
Chr1:32208595 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.345G>T (p.Glu115Asp) single nucleotide variant not specified [RCV004608586] Chr1:31756492 [GRCh38]
Chr1:32222093 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.137G>A (p.Gly46Asp) single nucleotide variant not specified [RCV004608515] Chr1:31756700 [GRCh38]
Chr1:32222301 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1676C>T (p.Pro559Leu) single nucleotide variant not specified [RCV004608534] Chr1:31741635 [GRCh38]
Chr1:32207236 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.407C>T (p.Ala136Val) single nucleotide variant not specified [RCV004608576] Chr1:31756430 [GRCh38]
Chr1:32222031 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2553G>C (p.Gln851His) single nucleotide variant not specified [RCV004608595] Chr1:31738880 [GRCh38]
Chr1:32204481 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.406G>A (p.Ala136Thr) single nucleotide variant not specified [RCV004608566] Chr1:31756431 [GRCh38]
Chr1:32222032 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4358_4359del (p.Thr1453fs) deletion not provided [RCV005052195] Chr1:31730821..31730822 [GRCh38]
Chr1:32196422..32196423 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4558C>T (p.Arg1520Trp) single nucleotide variant not specified [RCV004912779] Chr1:31728039 [GRCh38]
Chr1:32193640 [GRCh37]
Chr1:1p35.2		 likely benign
NM_001364857.2(ADGRB2):c.2408T>G (p.Leu803Arg) single nucleotide variant not specified [RCV004912845] Chr1:31739395 [GRCh38]
Chr1:32204996 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.53C>T (p.Pro18Leu) single nucleotide variant not specified [RCV004912884] Chr1:31756784 [GRCh38]
Chr1:32222385 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4280C>T (p.Pro1427Leu) single nucleotide variant not specified [RCV004912913] Chr1:31730900 [GRCh38]
Chr1:32196501 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.1882C>T (p.Arg628Trp) single nucleotide variant not specified [RCV004912895] Chr1:31740454 [GRCh38]
Chr1:32206055 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.913G>T (p.Ala305Ser) single nucleotide variant not specified [RCV004912902] Chr1:31744657 [GRCh38]
Chr1:32210258 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.331C>T (p.Arg111Trp) single nucleotide variant not specified [RCV004912827] Chr1:31756506 [GRCh38]
Chr1:32222107 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2226G>C (p.Met742Ile) single nucleotide variant not specified [RCV004912835] Chr1:31739577 [GRCh38]
Chr1:32205178 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.608G>A (p.Arg203His) single nucleotide variant not specified [RCV004912747] Chr1:31756229 [GRCh38]
Chr1:32221830 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.3727T>G (p.Phe1243Val) single nucleotide variant not specified [RCV004912817] Chr1:31732148 [GRCh38]
Chr1:32197749 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4211C>T (p.Ser1404Leu) single nucleotide variant not specified [RCV004912741] Chr1:31730969 [GRCh38]
Chr1:32196570 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2225T>C (p.Met742Thr) single nucleotide variant not specified [RCV004912856] Chr1:31739578 [GRCh38]
Chr1:32205179 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4141A>C (p.Thr1381Pro) single nucleotide variant not specified [RCV004912894] Chr1:31731039 [GRCh38]
Chr1:32196640 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.2752G>A (p.Ala918Thr) single nucleotide variant not specified [RCV004912863] Chr1:31738220 [GRCh38]
Chr1:32203821 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4133C>T (p.Pro1378Leu) single nucleotide variant not specified [RCV004912789] Chr1:31731047 [GRCh38]
Chr1:32196648 [GRCh37]
Chr1:1p35.2		 uncertain significance
NM_001364857.2(ADGRB2):c.4571C>T (p.Thr1524Ile) single nucleotide variant not specified [RCV004912874] Chr1:31728026 [GRCh38]
Chr1:32193627 [GRCh37]
Chr1:1p35.2		 uncertain significance
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:7379
Count of miRNA genes:994
Interacting mature miRNAs:1277
Transcripts:ENST00000257070, ENST00000373655, ENST00000373658, ENST00000398538, ENST00000398542, ENST00000398547, ENST00000398556, ENST00000420125, ENST00000436464, ENST00000440175, ENST00000465239, ENST00000465256, ENST00000466109, ENST00000468430, ENST00000473952, ENST00000484002, ENST00000525655, ENST00000527361, ENST00000530134, ENST00000530999, ENST00000533175
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
597227800GWAS1323874_Hself reported educational attainment QTL GWAS1323874 (human)5e-14self reported educational attainment13173349831733499Human
597240666GWAS1336740_Heducational attainment QTL GWAS1336740 (human)2e-09educational attainment13173165631731657Human
597347421GWAS1443495_Hbody fat percentage QTL GWAS1443495 (human)3e-08body fat mass (VT:0010482)body fat percentage (CMO:0000302)13173165631731657Human
597469467GWAS1565541_Hmathematical ability QTL GWAS1565541 (human)4e-08mathematical ability13173908231739083Human
407009678GWAS658654_Hparental longevity QTL GWAS658654 (human)0.000005total life span (VT:0001661)13173165631731657Human
597109978GWAS1206052_Hself reported educational attainment QTL GWAS1206052 (human)1e-08self reported educational attainment13175631231756313Human
597109977GWAS1206051_Hself reported educational attainment QTL GWAS1206051 (human)5e-10self reported educational attainment13174095531740956Human
597344341GWAS1440415_Hsmoking initiation QTL GWAS1440415 (human)3e-08smoking initiation13172948731729488Human
1576329MYI9_HMyocardial infarction susceptibility QTL 9 (human)12Myocardial infarction susceptibilityearly-onset1758550333585503Human
597227213GWAS1323287_Hsmoking status measurement QTL GWAS1323287 (human)4e-09smoking status measurement13173021831730219Human
597145473GWAS1241547_Hself reported educational attainment QTL GWAS1241547 (human)0.000002self reported educational attainment13173104631731047Human
597048461GWAS1144535_Hmetabolic syndrome QTL GWAS1144535 (human)1e-10metabolic syndrome13173165631731657Human
1576325MYI1_HMyocardial infarction susceptibility QTL 1 (human)11.681e-12Myocardial infarction susceptibilityearly-onset1758550333585503Human
597053323GWAS1149397_Hhousehold income QTL GWAS1149397 (human)1e-09household income13173349831733499Human
597309383GWAS1405457_Hbody mass index QTL GWAS1405457 (human)3e-09body mass indexbody mass index (BMI) (CMO:0000105)13174198031741981Human
597395312GWAS1491386_Heducational attainment QTL GWAS1491386 (human)4e-29educational attainment13173908231739083Human
596968254GWAS1087773_Hbody mass index QTL GWAS1087773 (human)3e-09body mass index13174198031741981Human
597345846GWAS1441920_Hcolor vision disorder QTL GWAS1441920 (human)0.000004color vision disorder13173843431738435Human
1643380BW316_HBody weight QTL 316 (human)2.620.0002Body weightBMI1758550333585503Human
597199209GWAS1295283_Hfat body mass QTL GWAS1295283 (human)7e-13body fat mass (VT:0010482)total body fat mass (CMO:0000305)13174238931742390Human
597116771GWAS1212845_Hself reported educational attainment QTL GWAS1212845 (human)9e-14self reported educational attainment13173349831733499Human
597517929GWAS1614003_Hdrug use measurement QTL GWAS1614003 (human)2e-08drug use measurement13173908231739083Human
597029665GWAS1125739_Hself reported educational attainment QTL GWAS1125739 (human)1e-08self reported educational attainment13174238931742390Human
597144610GWAS1240684_Hself reported educational attainment QTL GWAS1240684 (human)4e-12self reported educational attainment13173104631731047Human
597215151GWAS1311225_Hsmoking status measurement QTL GWAS1311225 (human)7e-13smoking status measurement13173021831730219Human
596955309GWAS1074828_Hmetabolic syndrome QTL GWAS1074828 (human)1e-10metabolic syndrome13173165631731657Human
597264672GWAS1360746_HX-12063 measurement QTL GWAS1360746 (human)2e-08X-12063 measurement13174275731742758Human
597232868GWAS1328942_Hmultisite chronic pain QTL GWAS1328942 (human)3e-08multisite chronic pain13173104631731047Human
597225382GWAS1321456_Hsmoking initiation QTL GWAS1321456 (human)6e-09smoking initiation13174238931742390Human

Markers in Region
G06240  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37132,192,721 - 32,192,846UniSTSGRCh37
Build 36131,965,308 - 31,965,433RGDNCBI36
Celera130,461,958 - 30,462,083RGD
Cytogenetic Map1p35UniSTS
HuRef130,310,215 - 30,310,340UniSTS
IB428  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37132,192,733 - 32,193,009UniSTSGRCh37
Build 36131,965,320 - 31,965,596RGDNCBI36
Celera130,461,970 - 30,462,246RGD
Cytogenetic Map1p35UniSTS
HuRef130,310,227 - 30,310,503UniSTS
GeneMap99-GB4 RH Map196.82UniSTS
Whitehead-RH Map1102.1UniSTS
NCBI RH Map1169.7UniSTS
STS-G06240  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37132,192,722 - 32,192,808UniSTSGRCh37
Build 36131,965,309 - 31,965,395RGDNCBI36
Celera130,461,959 - 30,462,045RGD
Cytogenetic Map1p35UniSTS
HuRef130,310,216 - 30,310,302UniSTS
GeneMap99-GB4 RH Map194.68UniSTS
NCBI RH Map1176.5UniSTS
BAI2_3938  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37132,192,730 - 32,193,141UniSTSGRCh37
Build 36131,965,317 - 31,965,728RGDNCBI36
Celera130,461,967 - 30,462,378RGD
HuRef130,310,224 - 30,310,635UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2433 2788 2245 4970 1647 2269 5 544 1831 386 2269 7084 6339 50 3734 1 841 1740 1614 173 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001294335 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001294336 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001364857 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011541848 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011541849 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011541858 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001899 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001900 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001901 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001903 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001905 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001907 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001908 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001909 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001911 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001912 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448673 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426173 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426178 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426179 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426180 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426181 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426182 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426183 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426185 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426186 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426187 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426188 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426189 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426190 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426191 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337863 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337864 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337865 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337866 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337867 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337868 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337870 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337871 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337872 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337873 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337874 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337875 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337876 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337877 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337878 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337879 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337880 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337881 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337882 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337883 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337884 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337885 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337886 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054337890 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737343 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB005298 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB065648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC114488 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI291691 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK123392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294361 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294999 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307805 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL354919 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX646677 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC009035 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC014780 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC136533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BE379230 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA314854 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA494051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000373655   ⟹   ENSP00000362759
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,727,117 - 31,764,035 (-)Ensembl
Ensembl Acc Id: ENST00000373658   ⟹   ENSP00000362762
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,727,117 - 31,764,340 (-)Ensembl
Ensembl Acc Id: ENST00000398538   ⟹   ENSP00000381548
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,727,411 - 31,756,801 (-)Ensembl
Ensembl Acc Id: ENST00000398542   ⟹   ENSP00000381550
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,727,117 - 31,764,340 (-)Ensembl
Ensembl Acc Id: ENST00000398547   ⟹   ENSP00000381555
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,727,117 - 31,763,922 (-)Ensembl
Ensembl Acc Id: ENST00000398556   ⟹   ENSP00000381564
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,727,117 - 31,759,423 (-)Ensembl
Ensembl Acc Id: ENST00000420125   ⟹   ENSP00000410921
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,738,245 - 31,756,815 (-)Ensembl
Ensembl Acc Id: ENST00000436464   ⟹   ENSP00000414758
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,757,217 - 31,761,026 (-)Ensembl
Ensembl Acc Id: ENST00000465256
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,727,118 - 31,736,679 (-)Ensembl
Ensembl Acc Id: ENST00000466109
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,738,200 - 31,739,210 (-)Ensembl
Ensembl Acc Id: ENST00000468430
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,742,108 - 31,743,673 (-)Ensembl
Ensembl Acc Id: ENST00000527361   ⟹   ENSP00000435397
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,727,195 - 31,757,259 (-)Ensembl
Ensembl Acc Id: ENST00000530134
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,739,515 - 31,756,264 (-)Ensembl
Ensembl Acc Id: ENST00000530999
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,727,170 - 31,735,347 (-)Ensembl
Ensembl Acc Id: ENST00000533175   ⟹   ENSP00000437219
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl131,741,800 - 31,764,893 (-)Ensembl
RefSeq Acc Id: NM_001294335   ⟹   NP_001281264
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,764,340 (-)NCBI
CHM1_1132,308,501 - 32,345,459 (-)NCBI
T2T-CHM13v2.0131,584,757 - 31,621,990 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001294336   ⟹   NP_001281265
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,764,340 (-)NCBI
CHM1_1132,308,501 - 32,345,459 (-)NCBI
T2T-CHM13v2.0131,584,757 - 31,621,990 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001364857   ⟹   NP_001351786
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,764,340 (-)NCBI
T2T-CHM13v2.0131,584,757 - 31,621,990 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011541858   ⟹   XP_011540160
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,764,340 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001899   ⟹   XP_016857388
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,764,340 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001900   ⟹   XP_016857389
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,647 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001901   ⟹   XP_016857390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,647 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001902   ⟹   XP_016857391
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,648 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001903   ⟹   XP_016857392
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,648 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001905   ⟹   XP_016857394
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,646 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001906   ⟹   XP_016857395
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,646 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001908   ⟹   XP_016857397
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,646 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001909   ⟹   XP_016857398
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,647 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001910   ⟹   XP_016857399
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,645 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001911   ⟹   XP_016857400
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,646 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001912   ⟹   XP_016857401
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,645 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448673   ⟹   XP_024304441
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,646 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047426173   ⟹   XP_047282129
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,760,981 (-)NCBI
RefSeq Acc Id: XM_047426178   ⟹   XP_047282134
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,764,340 (-)NCBI
RefSeq Acc Id: XM_047426179   ⟹   XP_047282135
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,647 (-)NCBI
RefSeq Acc Id: XM_047426180   ⟹   XP_047282136
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,764,340 (-)NCBI
RefSeq Acc Id: XM_047426181   ⟹   XP_047282137
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,760,981 (-)NCBI
RefSeq Acc Id: XM_047426182   ⟹   XP_047282138
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,646 (-)NCBI
RefSeq Acc Id: XM_047426183   ⟹   XP_047282139
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,647 (-)NCBI
RefSeq Acc Id: XM_047426184   ⟹   XP_047282140
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,648 (-)NCBI
RefSeq Acc Id: XM_047426185   ⟹   XP_047282141
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,648 (-)NCBI
RefSeq Acc Id: XM_047426186   ⟹   XP_047282142
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,764,340 (-)NCBI
RefSeq Acc Id: XM_047426187   ⟹   XP_047282143
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,764,340 (-)NCBI
RefSeq Acc Id: XM_047426188   ⟹   XP_047282144
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,760,579 (-)NCBI
RefSeq Acc Id: XM_047426189   ⟹   XP_047282145
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,647 (-)NCBI
RefSeq Acc Id: XM_047426190   ⟹   XP_047282146
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,727,117 - 31,757,647 (-)NCBI
RefSeq Acc Id: XM_047426191   ⟹   XP_047282147
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,735,575 - 31,757,657 (-)NCBI
RefSeq Acc Id: XM_054337863   ⟹   XP_054193838
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,618,661 (-)NCBI
RefSeq Acc Id: XM_054337864   ⟹   XP_054193839
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,621,990 (-)NCBI
RefSeq Acc Id: XM_054337865   ⟹   XP_054193840
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,297 (-)NCBI
RefSeq Acc Id: XM_054337866   ⟹   XP_054193841
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,296 (-)NCBI
RefSeq Acc Id: XM_054337867   ⟹   XP_054193842
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,297 (-)NCBI
RefSeq Acc Id: XM_054337868   ⟹   XP_054193843
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,298 (-)NCBI
RefSeq Acc Id: XM_054337869   ⟹   XP_054193844
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,298 (-)NCBI
RefSeq Acc Id: XM_054337870   ⟹   XP_054193845
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,621,990 (-)NCBI
RefSeq Acc Id: XM_054337871   ⟹   XP_054193846
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,296 (-)NCBI
RefSeq Acc Id: XM_054337872   ⟹   XP_054193847
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,296 (-)NCBI
RefSeq Acc Id: XM_054337873   ⟹   XP_054193848
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,297 (-)NCBI
RefSeq Acc Id: XM_054337874   ⟹   XP_054193849
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,621,990 (-)NCBI
RefSeq Acc Id: XM_054337875   ⟹   XP_054193850
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,296 (-)NCBI
RefSeq Acc Id: XM_054337876   ⟹   XP_054193851
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,296 (-)NCBI
RefSeq Acc Id: XM_054337877   ⟹   XP_054193852
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,297 (-)NCBI
RefSeq Acc Id: XM_054337878   ⟹   XP_054193853
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,297 (-)NCBI
RefSeq Acc Id: XM_054337879   ⟹   XP_054193854
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,298 (-)NCBI
RefSeq Acc Id: XM_054337880   ⟹   XP_054193855
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,298 (-)NCBI
RefSeq Acc Id: XM_054337881   ⟹   XP_054193856
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,621,990 (-)NCBI
RefSeq Acc Id: XM_054337882   ⟹   XP_054193857
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,295 (-)NCBI
RefSeq Acc Id: XM_054337883   ⟹   XP_054193858
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,621,990 (-)NCBI
RefSeq Acc Id: XM_054337884   ⟹   XP_054193859
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,296 (-)NCBI
RefSeq Acc Id: XM_054337885   ⟹   XP_054193860
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,295 (-)NCBI
RefSeq Acc Id: XM_054337886   ⟹   XP_054193861
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,618,229 (-)NCBI
RefSeq Acc Id: XM_054337887   ⟹   XP_054193862
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,297 (-)NCBI
RefSeq Acc Id: XM_054337888   ⟹   XP_054193863
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,615,297 (-)NCBI
RefSeq Acc Id: XM_054337889   ⟹   XP_054193864
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,584,757 - 31,621,990 (-)NCBI
RefSeq Acc Id: XM_054337890   ⟹   XP_054193865
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0131,593,219 - 31,615,307 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001281264 (Get FASTA)   NCBI Sequence Viewer  
  NP_001281265 (Get FASTA)   NCBI Sequence Viewer  
  NP_001351786 (Get FASTA)   NCBI Sequence Viewer  
  XP_011540160 (Get FASTA)   NCBI Sequence Viewer  
  XP_016857388 (Get FASTA)   NCBI Sequence Viewer  
  XP_016857389 (Get FASTA)   NCBI Sequence Viewer  
  XP_016857390 (Get FASTA)   NCBI Sequence Viewer  
  XP_016857391 (Get FASTA)   NCBI Sequence Viewer  
  XP_016857392 (Get FASTA)   NCBI Sequence Viewer  
  XP_016857394 (Get FASTA)   NCBI Sequence Viewer  
  XP_016857395 (Get FASTA)   NCBI Sequence Viewer  
  XP_016857397 (Get FASTA)   NCBI Sequence Viewer  
  XP_016857398 (Get FASTA)   NCBI Sequence Viewer  
  XP_016857399 (Get FASTA)   NCBI Sequence Viewer  
  XP_016857400 (Get FASTA)   NCBI Sequence Viewer  
  XP_016857401 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304441 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282129 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282134 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282135 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282136 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282137 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282138 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282139 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282140 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282141 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282142 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282143 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282144 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282145 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282146 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282147 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193838 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193839 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193840 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193841 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193842 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193843 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193844 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193845 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193846 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193847 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193848 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193849 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193850 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193851 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193852 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193853 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193854 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193855 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193856 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193857 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193858 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193859 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193860 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193861 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193862 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193863 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193864 (Get FASTA)   NCBI Sequence Viewer  
  XP_054193865 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH09035 (Get FASTA)   NCBI Sequence Viewer  
  AAI36534 (Get FASTA)   NCBI Sequence Viewer  
  BAA25362 (Get FASTA)   NCBI Sequence Viewer  
  BAC05874 (Get FASTA)   NCBI Sequence Viewer  
  BAG57625 (Get FASTA)   NCBI Sequence Viewer  
  BAG58063 (Get FASTA)   NCBI Sequence Viewer  
  BAG59135 (Get FASTA)   NCBI Sequence Viewer  
  CAD69465 (Get FASTA)   NCBI Sequence Viewer  
  EAX07589 (Get FASTA)   NCBI Sequence Viewer  
  EAX07590 (Get FASTA)   NCBI Sequence Viewer  
  EAX07591 (Get FASTA)   NCBI Sequence Viewer  
  EAX07592 (Get FASTA)   NCBI Sequence Viewer  
  EAX07593 (Get FASTA)   NCBI Sequence Viewer  
  EAX07594 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000362759
  ENSP00000362759.2
  ENSP00000362762
  ENSP00000362762.3
  ENSP00000381548
  ENSP00000381548.1
  ENSP00000381550
  ENSP00000381550.1
  ENSP00000381555
  ENSP00000381555.1
  ENSP00000381564
  ENSP00000381564.3
  ENSP00000410921
  ENSP00000410921.1
  ENSP00000435397
  ENSP00000435397.1
  ENSP00000437219.1
GenBank Protein O60241 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001281265   ⟸   NM_001294336
- Peptide Label: isoform 2 preproprotein
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001281264   ⟸   NM_001294335
- Peptide Label: isoform 1 preproprotein
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011540160   ⟸   XM_011541858
- Peptide Label: isoform X26
- UniProtKB: B4DKC3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016857388   ⟸   XM_017001899
- Peptide Label: isoform X1
- UniProtKB: Q8NGW8 (UniProtKB/Swiss-Prot),   Q5T6K0 (UniProtKB/Swiss-Prot),   B9EGK9 (UniProtKB/Swiss-Prot),   Q96GZ9 (UniProtKB/Swiss-Prot),   O60241 (UniProtKB/Swiss-Prot),   A2A3C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016857392   ⟸   XM_017001903
- Peptide Label: isoform X6
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016857391   ⟸   XM_017001902
- Peptide Label: isoform X5
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016857389   ⟸   XM_017001900
- Peptide Label: isoform X2
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016857390   ⟸   XM_017001901
- Peptide Label: isoform X4
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016857398   ⟸   XM_017001909
- Peptide Label: isoform X14
- UniProtKB: A2A3C3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016857394   ⟸   XM_017001905
- Peptide Label: isoform X8
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016857400   ⟸   XM_017001911
- Peptide Label: isoform X21
- UniProtKB: A2A3C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016857397   ⟸   XM_017001908
- Peptide Label: isoform X12
- UniProtKB: A2A3C3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016857395   ⟸   XM_017001906
- Peptide Label: isoform X9
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016857399   ⟸   XM_017001910
- Peptide Label: isoform X19
- UniProtKB: A2A3C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016857401   ⟸   XM_017001912
- Peptide Label: isoform X22
- UniProtKB: A2A3C3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024304441   ⟸   XM_024448673
- Peptide Label: isoform X3
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001351786   ⟸   NM_001364857
- Peptide Label: isoform 3 preproprotein
- UniProtKB: Q8NGW8 (UniProtKB/Swiss-Prot),   Q5T6K0 (UniProtKB/Swiss-Prot),   O60241 (UniProtKB/Swiss-Prot),   B9EGK9 (UniProtKB/Swiss-Prot),   Q96GZ9 (UniProtKB/Swiss-Prot),   A2A3C2 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000381548   ⟸   ENST00000398538
Ensembl Acc Id: ENSP00000381564   ⟸   ENST00000398556
Ensembl Acc Id: ENSP00000381550   ⟸   ENST00000398542
Ensembl Acc Id: ENSP00000381555   ⟸   ENST00000398547
Ensembl Acc Id: ENSP00000362759   ⟸   ENST00000373655
Ensembl Acc Id: ENSP00000362762   ⟸   ENST00000373658
Ensembl Acc Id: ENSP00000437219   ⟸   ENST00000533175
Ensembl Acc Id: ENSP00000410921   ⟸   ENST00000420125
Ensembl Acc Id: ENSP00000435397   ⟸   ENST00000527361
Ensembl Acc Id: ENSP00000414758   ⟸   ENST00000436464
RefSeq Acc Id: XP_047282143   ⟸   XM_047426187
- Peptide Label: isoform X20
- UniProtKB: A2A3C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282142   ⟸   XM_047426186
- Peptide Label: isoform X18
- UniProtKB: A2A3C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282136   ⟸   XM_047426180
- Peptide Label: isoform X11
- UniProtKB: A2A3C3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282134   ⟸   XM_047426178
- Peptide Label: isoform X7
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282137   ⟸   XM_047426181
- Peptide Label: isoform X11
- UniProtKB: A2A3C3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282129   ⟸   XM_047426173
- Peptide Label: isoform X1
- UniProtKB: Q8NGW8 (UniProtKB/Swiss-Prot),   Q5T6K0 (UniProtKB/Swiss-Prot),   O60241 (UniProtKB/Swiss-Prot),   B9EGK9 (UniProtKB/Swiss-Prot),   Q96GZ9 (UniProtKB/Swiss-Prot),   A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282144   ⟸   XM_047426188
- Peptide Label: isoform X23
- UniProtKB: A2A3C1 (UniProtKB/TrEMBL),   A2A3C3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282141   ⟸   XM_047426185
- Peptide Label: isoform X17
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282140   ⟸   XM_047426184
- Peptide Label: isoform X16
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282146   ⟸   XM_047426190
- Peptide Label: isoform X25
- UniProtKB: A2A3C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282145   ⟸   XM_047426189
- Peptide Label: isoform X24
- UniProtKB: A2A3C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282139   ⟸   XM_047426183
- Peptide Label: isoform X15
- UniProtKB: A2A3C3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282135   ⟸   XM_047426179
- Peptide Label: isoform X10
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282138   ⟸   XM_047426182
- Peptide Label: isoform X13
- UniProtKB: A2A3C3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282147   ⟸   XM_047426191
- Peptide Label: isoform X27
- UniProtKB: A2A3C4 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193864   ⟸   XM_054337889
- Peptide Label: isoform X26
- UniProtKB: B4DKC3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193858   ⟸   XM_054337883
- Peptide Label: isoform X20
- UniProtKB: A2A3C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193856   ⟸   XM_054337881
- Peptide Label: isoform X18
- UniProtKB: A2A3C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193849   ⟸   XM_054337874
- Peptide Label: isoform X11
- UniProtKB: A2A3C3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193845   ⟸   XM_054337870
- Peptide Label: isoform X7
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193839   ⟸   XM_054337864
- Peptide Label: isoform X1
- UniProtKB: Q8NGW8 (UniProtKB/Swiss-Prot),   Q5T6K0 (UniProtKB/Swiss-Prot),   O60241 (UniProtKB/Swiss-Prot),   B9EGK9 (UniProtKB/Swiss-Prot),   Q96GZ9 (UniProtKB/Swiss-Prot),   A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193838   ⟸   XM_054337863
- Peptide Label: isoform X1
- UniProtKB: Q8NGW8 (UniProtKB/Swiss-Prot),   Q5T6K0 (UniProtKB/Swiss-Prot),   O60241 (UniProtKB/Swiss-Prot),   B9EGK9 (UniProtKB/Swiss-Prot),   Q96GZ9 (UniProtKB/Swiss-Prot),   A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193861   ⟸   XM_054337886
- Peptide Label: isoform X23
- UniProtKB: A2A3C1 (UniProtKB/TrEMBL),   A2A3C3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193855   ⟸   XM_054337880
- Peptide Label: isoform X17
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193854   ⟸   XM_054337879
- Peptide Label: isoform X16
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193844   ⟸   XM_054337869
- Peptide Label: isoform X6
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193843   ⟸   XM_054337868
- Peptide Label: isoform X5
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193852   ⟸   XM_054337877
- Peptide Label: isoform X14
- UniProtKB: A2A3C3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193863   ⟸   XM_054337888
- Peptide Label: isoform X25
- UniProtKB: A2A3C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193862   ⟸   XM_054337887
- Peptide Label: isoform X24
- UniProtKB: A2A3C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193853   ⟸   XM_054337878
- Peptide Label: isoform X15
- UniProtKB: A2A3C3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193848   ⟸   XM_054337873
- Peptide Label: isoform X10
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193840   ⟸   XM_054337865
- Peptide Label: isoform X2
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193842   ⟸   XM_054337867
- Peptide Label: isoform X4
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193841   ⟸   XM_054337866
- Peptide Label: isoform X3
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193859   ⟸   XM_054337884
- Peptide Label: isoform X21
- UniProtKB: A2A3C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193850   ⟸   XM_054337875
- Peptide Label: isoform X12
- UniProtKB: A2A3C3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193851   ⟸   XM_054337876
- Peptide Label: isoform X13
- UniProtKB: A2A3C3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193846   ⟸   XM_054337871
- Peptide Label: isoform X8
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193847   ⟸   XM_054337872
- Peptide Label: isoform X9
- UniProtKB: A2A3C2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193860   ⟸   XM_054337885
- Peptide Label: isoform X22
- UniProtKB: A2A3C3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193857   ⟸   XM_054337882
- Peptide Label: isoform X19
- UniProtKB: A2A3C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054193865   ⟸   XM_054337890
- Peptide Label: isoform X27
- UniProtKB: A2A3C4 (UniProtKB/TrEMBL)
Protein Domains
Adhesion G protein-coupled receptor B N-terminal   G-protein coupled receptors family 2 profile   GAIN-B   TSP type-1

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O60241-F1-model_v2 AlphaFold O60241 1-1585 view protein structure

Promoters
RGD ID:6854796
Promoter ID:EPDNEW_H563
Type:single initiation site
Name:ADGRB2_2
Description:adhesion G protein-coupled receptor B2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H564  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,758,257 - 31,758,317EPDNEW
RGD ID:6854798
Promoter ID:EPDNEW_H564
Type:initiation region
Name:ADGRB2_1
Description:adhesion G protein-coupled receptor B2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H563  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38131,764,050 - 31,764,110EPDNEW
RGD ID:6784685
Promoter ID:HG_KWN:1776
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000313758
Position:
Human AssemblyChrPosition (strand)Source
Build 36131,982,581 - 31,983,081 (-)MPROMDB
RGD ID:6784686
Promoter ID:HG_KWN:1779
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour
Transcripts:OTTHUMT00000313759
Position:
Human AssemblyChrPosition (strand)Source
Build 36131,999,236 - 31,999,736 (-)MPROMDB
RGD ID:6785204
Promoter ID:HG_KWN:1780
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour
Transcripts:ENST00000257070,   ENST00000398542,   ENST00000398547,   NM_001703
Position:
Human AssemblyChrPosition (strand)Source
Build 36132,002,369 - 32,002,869 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:944 AgrOrtholog
COSMIC ADGRB2 COSMIC
Ensembl Genes ENSG00000121753 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000373655 ENTREZGENE
  ENST00000373655.6 UniProtKB/Swiss-Prot
  ENST00000373658 ENTREZGENE
  ENST00000373658.8 UniProtKB/Swiss-Prot
  ENST00000398538 ENTREZGENE
  ENST00000398538.5 UniProtKB/TrEMBL
  ENST00000398542 ENTREZGENE
  ENST00000398542.5 UniProtKB/TrEMBL
  ENST00000398547 ENTREZGENE
  ENST00000398547.5 UniProtKB/TrEMBL
  ENST00000398556 ENTREZGENE
  ENST00000398556.7 UniProtKB/TrEMBL
  ENST00000420125 ENTREZGENE
  ENST00000420125.5 UniProtKB/TrEMBL
  ENST00000527361 ENTREZGENE
  ENST00000527361.5 UniProtKB/Swiss-Prot
  ENST00000533175.1 UniProtKB/TrEMBL
Gene3D-CATH 1.25.40.610 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.20.100.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.60.220.50 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  4.10.1240.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Rhodopsin 7-helix transmembrane proteins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000121753 GTEx
HGNC ID HGNC:944 ENTREZGENE
Human Proteome Map ADGRB2 Human Proteome Map
InterPro AGRB_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Angio_Inhib/Adhesion_GPCR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GAIN_dom_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GAIN_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_2-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_2_brain_angio_inhib UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_2_extracell_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_2_extracellular_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_2_secretin-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSP1_rpt UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSP1_rpt_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:576 UniProtKB/Swiss-Prot
NCBI Gene 576 ENTREZGENE
OMIM 602683 OMIM
PANTHER ADHESION G PROTEIN-COUPLED RECEPTOR B2 UniProtKB/Swiss-Prot
  ADHESION G PROTEIN-COUPLED RECEPTOR B2 UniProtKB/TrEMBL
  ADHESION G PROTEIN-COUPLED RECEPTOR B2 UniProtKB/TrEMBL
  ADHESION G-PROTEIN COUPLED RECEPTOR UniProtKB/TrEMBL
  ISTHMIN-2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam 7tm_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AGRB_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HRM UniProtKB/TrEMBL
  TSP_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA25248 PharmGKB
PRINTS BAIPRECURSOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCRSECRETIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSP1REPEAT UniProtKB/TrEMBL
PROSITE G_PROTEIN_RECEP_F2_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  G_PROTEIN_RECEP_F2_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSP1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART GPS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HormR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSP1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Family A G protein-coupled receptor-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF82895 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A2A3C1 ENTREZGENE, UniProtKB/TrEMBL
  A2A3C2 ENTREZGENE, UniProtKB/TrEMBL
  A2A3C3 ENTREZGENE, UniProtKB/TrEMBL
  A2A3C4 ENTREZGENE, UniProtKB/TrEMBL
  A2A3C6 ENTREZGENE, UniProtKB/TrEMBL
  AGRB2_HUMAN UniProtKB/Swiss-Prot
  B4DKC3 ENTREZGENE, UniProtKB/TrEMBL
  B9EGK9 ENTREZGENE
  E9PND1_HUMAN UniProtKB/TrEMBL
  O60241 ENTREZGENE
  Q5T6K0 ENTREZGENE
  Q8NGW8 ENTREZGENE
  Q96GZ9 ENTREZGENE
UniProt Secondary B9EGK9 UniProtKB/Swiss-Prot
  Q5T6K0 UniProtKB/Swiss-Prot
  Q8NGW8 UniProtKB/Swiss-Prot
  Q96GZ9 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-03-10 ADGRB2  adhesion G protein-coupled receptor B2  BAI2  brain-specific angiogenesis inhibitor 2  Symbol and/or name change 5135510 APPROVED