GPR161 (G protein-coupled receptor 161) - Rat Genome Database

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Gene: GPR161 (G protein-coupled receptor 161) Homo sapiens
Analyze
Symbol: GPR161
Name: G protein-coupled receptor 161
RGD ID: 1607069
HGNC Page HGNC:23694
Description: Predicted to enable G protein-coupled receptor activity. Predicted to be involved in adenylate cyclase-activating G protein-coupled receptor signaling pathway and negative regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning. Predicted to be located in cilium. Predicted to be active in plasma membrane and recycling endosome. Implicated in medulloblastoma.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: FLJ33952; G-protein coupled receptor 161; G-protein coupled receptor RE2; RE2
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381168,079,542 - 168,137,667 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1168,079,542 - 168,137,667 (-)EnsemblGRCh38hg38GRCh38
GRCh371168,048,780 - 168,106,905 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361166,320,621 - 166,372,248 (-)NCBINCBI36Build 36hg18NCBI36
Celera1141,162,980 - 141,214,616 (-)NCBICelera
Cytogenetic Map1q24.2NCBI
HuRef1139,293,385 - 139,351,133 (-)NCBIHuRef
CHM1_11169,470,990 - 169,529,180 (-)NCBICHM1_1
T2T-CHM13v2.01167,431,007 - 167,489,154 (-)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
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9932290   PMID:11959142   PMID:11987825   PMID:12477932   PMID:14702039   PMID:15489334   PMID:16710414   PMID:18250320   PMID:18755178   PMID:19064610   PMID:19536175   PMID:21873635  
PMID:22658674   PMID:23455922   PMID:24599592   PMID:26186194   PMID:26831064   PMID:27002170   PMID:27357676   PMID:27731925   PMID:28298427   PMID:28514442   PMID:29117863   PMID:29222391  
PMID:29386106   PMID:30021884   PMID:30256984   PMID:31609649   PMID:32238831   PMID:32296183   PMID:32707033   PMID:33961781  


Genomics

Comparative Map Data
GPR161
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381168,079,542 - 168,137,667 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1168,079,542 - 168,137,667 (-)EnsemblGRCh38hg38GRCh38
GRCh371168,048,780 - 168,106,905 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361166,320,621 - 166,372,248 (-)NCBINCBI36Build 36hg18NCBI36
Celera1141,162,980 - 141,214,616 (-)NCBICelera
Cytogenetic Map1q24.2NCBI
HuRef1139,293,385 - 139,351,133 (-)NCBIHuRef
CHM1_11169,470,990 - 169,529,180 (-)NCBICHM1_1
T2T-CHM13v2.01167,431,007 - 167,489,154 (-)NCBIT2T-CHM13v2.0
Gpr161
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391165,108,760 - 165,154,314 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1165,123,358 - 165,154,314 (+)EnsemblGRCm39 Ensembl
GRCm381165,281,184 - 165,326,747 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1165,295,789 - 165,326,745 (+)EnsemblGRCm38mm10GRCm38
MGSCv371167,225,897 - 167,251,982 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361167,132,441 - 167,161,079 (+)NCBIMGSCv36mm8
Celera1167,740,027 - 167,766,443 (+)NCBICelera
Cytogenetic Map1H2.2NCBI
cM Map172.64NCBI
Gpr161
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21377,578,257 - 77,623,661 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1377,577,739 - 77,619,613 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.01383,530,389 - 83,576,117 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1383,531,018 - 83,571,505 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01388,409,782 - 88,455,575 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41381,053,624 - 81,074,896 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1377,290,655 - 77,336,787 (+)NCBICelera
Cytogenetic Map13q23NCBI
Gpr161
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554628,981,157 - 9,028,946 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554628,981,729 - 9,034,009 (+)NCBIChiLan1.0ChiLan1.0
GPR161
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1181,295,579 - 81,354,170 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01143,566,775 - 143,625,357 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11147,293,355 - 147,351,510 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1147,299,350 - 147,350,451 (-)Ensemblpanpan1.1panPan2
GPR161
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1730,364,999 - 30,411,038 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl730,366,068 - 30,407,268 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha729,895,733 - 29,948,158 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0730,176,808 - 30,229,264 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl730,182,446 - 30,224,803 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1730,016,737 - 30,069,149 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0730,047,700 - 30,100,163 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0730,285,703 - 30,338,184 (+)NCBIUU_Cfam_GSD_1.0
Gpr161
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024409344100,250,949 - 100,284,605 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493648118,097,692 - 18,129,873 (+)EnsemblSpeTri2.0
SpeTri2.0NW_00493648118,097,704 - 18,130,023 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
GPR161
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl482,844,941 - 82,905,534 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1482,844,944 - 82,909,329 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2490,518,333 - 90,577,014 (+)NCBISscrofa10.2Sscrofa10.2susScr3
GPR161
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12560,908,741 - 60,965,168 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2560,940,047 - 60,959,181 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605562,633,696 - 62,690,375 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Gpr161
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248266,089,127 - 6,134,127 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248266,089,127 - 6,135,076 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in GPR161
41 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1q23.1-25.1(chr1:157747246-176021247)x3 copy number gain See cases [RCV000051854] Chr1:157747246..176021247 [GRCh38]
Chr1:157717036..175990383 [GRCh37]
Chr1:155983660..174257006 [NCBI36]
Chr1:1q23.1-25.1		 pathogenic
GRCh38/hg38 1q23.3-25.2(chr1:164922655-180061589)x3 copy number gain See cases [RCV000051856] Chr1:164922655..180061589 [GRCh38]
Chr1:164891892..180030724 [GRCh37]
Chr1:163158516..178297347 [NCBI36]
Chr1:1q23.3-25.2		 pathogenic
GRCh38/hg38 1q23.3-24.2(chr1:160789732-168617494)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053913]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053913]|See cases [RCV000053913] Chr1:160789732..168617494 [GRCh38]
Chr1:160759522..168586732 [GRCh37]
Chr1:159026146..166853356 [NCBI36]
Chr1:1q23.3-24.2		 pathogenic
GRCh38/hg38 1q23.3-25.1(chr1:161740907-173965154)x1 copy number loss See cases [RCV000053914] Chr1:161740907..173965154 [GRCh38]
Chr1:161710697..173934292 [GRCh37]
Chr1:159977321..172200915 [NCBI36]
Chr1:1q23.3-25.1		 pathogenic
GRCh38/hg38 1q23.3-24.3(chr1:164036599-171252077)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053916]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053916]|See cases [RCV000053916] Chr1:164036599..171252077 [GRCh38]
Chr1:164005836..171221216 [GRCh37]
Chr1:162272460..169487840 [NCBI36]
Chr1:1q23.3-24.3		 pathogenic
GRCh38/hg38 1q24.1-25.1(chr1:166762832-175327423)x1 copy number loss See cases [RCV000053917] Chr1:166762832..175327423 [GRCh38]
Chr1:166732069..175296559 [GRCh37]
Chr1:164998693..173563182 [NCBI36]
Chr1:1q24.1-25.1		 pathogenic
NM_153832.2(GPR161):c.93C>T (p.Phe31=) single nucleotide variant Malignant melanoma [RCV000064296] Chr1:168104758 [GRCh38]
Chr1:168073996 [GRCh37]
Chr1:166340620 [NCBI36]
Chr1:1q24.2		 not provided
GRCh38/hg38 1q23.3-25.1(chr1:163382523-175877022)x1 copy number loss See cases [RCV000143292] Chr1:163382523..175877022 [GRCh38]
Chr1:163352313..175846158 [GRCh37]
Chr1:161618937..174112781 [NCBI36]
Chr1:1q23.3-25.1		 pathogenic
GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3 copy number gain See cases [RCV000143515] Chr1:149854269..180267197 [GRCh38]
Chr1:149825831..180236332 [GRCh37]
Chr1:148092455..178502955 [NCBI36]
Chr1:1q21.2-25.2		 pathogenic
NM_001375883.1(GPR161):c.-5T>A single nucleotide variant Pituitary stalk interruption syndrome [RCV000202520]|not provided [RCV000157613] Chr1:168104855 [GRCh38]
Chr1:168074093 [GRCh37]
Chr1:1q24.2		 likely pathogenic|uncertain significance|not provided
NM_001375883.1(GPR161):c.-45+395dup duplication not provided [RCV001729481]|not specified [RCV000238808] Chr1:168136343..168136344 [GRCh38]
Chr1:168105581..168105582 [GRCh37]
Chr1:1q24.2		 benign|likely benign
GRCh37/hg19 1q23.2-25.1(chr1:160369890-175796325) copy number loss not provided [RCV000767779] Chr1:160369890..175796325 [GRCh37]
Chr1:1q23.2-25.1		 pathogenic
GRCh37/hg19 1q23.3-25.3(chr1:161676893-184071723)x1 copy number loss See cases [RCV000447098] Chr1:161676893..184071723 [GRCh37]
Chr1:1q23.3-25.3		 pathogenic
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_001375883.1(GPR161):c.239T>C (p.Val80Ala) single nucleotide variant Inborn genetic diseases [RCV003262678] Chr1:168104612 [GRCh38]
Chr1:168073850 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.1469C>T (p.Thr490Ile) single nucleotide variant Inborn genetic diseases [RCV003262517] Chr1:168085652 [GRCh38]
Chr1:168054890 [GRCh37]
Chr1:1q24.2		 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
NM_001375883.1(GPR161):c.-45+481A>T single nucleotide variant not provided [RCV001730383]|not specified [RCV001730384] Chr1:168136258 [GRCh38]
Chr1:168105496 [GRCh37]
Chr1:1q24.2		 benign|likely benign
GRCh37/hg19 1q23.2-25.2(chr1:159815642-177026983)x1 copy number loss not provided [RCV000736717] Chr1:159815642..177026983 [GRCh37]
Chr1:1q23.2-25.2		 pathogenic
NM_001375883.1(GPR161):c.243G>C (p.Leu81=) single nucleotide variant not provided [RCV000972368] Chr1:168104608 [GRCh38]
Chr1:168073846 [GRCh37]
Chr1:1q24.2		 benign
NM_001375883.1(GPR161):c.1491C>T (p.Gly497=) single nucleotide variant not provided [RCV000970425] Chr1:168085630 [GRCh38]
Chr1:168054868 [GRCh37]
Chr1:1q24.2		 likely benign
NM_001375883.1(GPR161):c.1396T>C (p.Leu466=) single nucleotide variant not provided [RCV000970426] Chr1:168085725 [GRCh38]
Chr1:168054963 [GRCh37]
Chr1:1q24.2		 benign
NM_001375883.1(GPR161):c.384T>C (p.Ala128=) single nucleotide variant not provided [RCV000899298] Chr1:168097223 [GRCh38]
Chr1:168066461 [GRCh37]
Chr1:1q24.2		 benign
NM_001375883.1(GPR161):c.828C>T (p.Leu276=) single nucleotide variant not provided [RCV000974871] Chr1:168096779 [GRCh38]
Chr1:168066017 [GRCh37]
Chr1:1q24.2		 benign
NM_001375883.1(GPR161):c.1077C>T (p.Phe359=) single nucleotide variant not provided [RCV000925547] Chr1:168096530 [GRCh38]
Chr1:168065768 [GRCh37]
Chr1:1q24.2		 likely benign
NM_001375883.1(GPR161):c.-42G>A single nucleotide variant not provided [RCV000961912] Chr1:168104892 [GRCh38]
Chr1:168074130 [GRCh37]
Chr1:1q24.2		 benign
NM_001375883.1(GPR161):c.594C>T (p.Leu198=) single nucleotide variant not provided [RCV000946523] Chr1:168097013 [GRCh38]
Chr1:168066251 [GRCh37]
Chr1:1q24.2		 benign
NM_001375883.1(GPR161):c.1413G>A (p.Glu471=) single nucleotide variant not provided [RCV000972658] Chr1:168085708 [GRCh38]
Chr1:168054946 [GRCh37]
Chr1:1q24.2		 benign
NM_001375883.1(GPR161):c.885C>G (p.Leu295=) single nucleotide variant not provided [RCV000920126] Chr1:168096722 [GRCh38]
Chr1:168065960 [GRCh37]
Chr1:1q24.2		 likely benign
NM_001375883.1(GPR161):c.66C>T (p.Gly22=) single nucleotide variant not provided [RCV000961911] Chr1:168104785 [GRCh38]
Chr1:168074023 [GRCh37]
Chr1:1q24.2		 benign
NM_001375883.1(GPR161):c.1048G>T (p.Val350Leu) single nucleotide variant Inborn genetic diseases [RCV003248470] Chr1:168096559 [GRCh38]
Chr1:168065797 [GRCh37]
Chr1:1q24.2		 uncertain significance
GRCh37/hg19 1q23.3-24.2(chr1:163093021-168991239)x1 copy number loss not provided [RCV000849156] Chr1:163093021..168991239 [GRCh37]
Chr1:1q23.3-24.2		 pathogenic
NM_001375883.1(GPR161):c.638G>A (p.Arg213His) single nucleotide variant Inborn genetic diseases [RCV003240844] Chr1:168096969 [GRCh38]
Chr1:168066207 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.486C>T (p.Pro162=) single nucleotide variant not provided [RCV000961910] Chr1:168097121 [GRCh38]
Chr1:168066359 [GRCh37]
Chr1:1q24.2		 benign
NM_001375883.1(GPR161):c.75C>T (p.Gly25=) single nucleotide variant not provided [RCV000909491] Chr1:168104776 [GRCh38]
Chr1:168074014 [GRCh37]
Chr1:1q24.2		 benign
NM_001375883.1(GPR161):c.1410T>C (p.Ile470=) single nucleotide variant not provided [RCV000912730] Chr1:168085711 [GRCh38]
Chr1:168054949 [GRCh37]
Chr1:1q24.2		 likely benign
GRCh37/hg19 1q24.2-25.1(chr1:167430471-174635618)x1 copy number loss not provided [RCV001005149] Chr1:167430471..174635618 [GRCh37]
Chr1:1q24.2-25.1		 pathogenic
GRCh37/hg19 1q23.3-24.2(chr1:164608682-169216098)x1 copy number loss not provided [RCV001258478] Chr1:164608682..169216098 [GRCh37]
Chr1:1q23.3-24.2		 likely pathogenic
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44		 uncertain significance
NM_001375883.1(GPR161):c.1196A>G (p.Gln399Arg) single nucleotide variant Medulloblastoma [RCV002254837] Chr1:168090572 [GRCh38]
Chr1:168059810 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.1502del (p.Gly501fs) deletion Medulloblastoma [RCV002254861] Chr1:168085619 [GRCh38]
Chr1:168054857 [GRCh37]
Chr1:1q24.2		 uncertain significance
GRCh37/hg19 1q24.2(chr1:167741130-168188082)x1 copy number loss not provided [RCV001834167] Chr1:167741130..168188082 [GRCh37]
Chr1:1q24.2		 uncertain significance
GRCh37/hg19 1q24.2-24.3(chr1:167391422-171843613) copy number loss not specified [RCV002053691] Chr1:167391422..171843613 [GRCh37]
Chr1:1q24.2-24.3		 pathogenic
GRCh37/hg19 1q23.3-24.3(chr1:162330810-171532331) copy number loss not specified [RCV002053680] Chr1:162330810..171532331 [GRCh37]
Chr1:1q23.3-24.3		 pathogenic
NM_001375883.1(GPR161):c.695A>G (p.Glu232Gly) single nucleotide variant not provided [RCV002211121] Chr1:168096912 [GRCh38]
Chr1:168066150 [GRCh37]
Chr1:1q24.2		 uncertain significance
NC_000001.10:g.(?_167400918)_(168282240_?)dup duplication Immunodeficiency 25 [RCV003113961] Chr1:167400918..168282240 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.1231T>C (p.Tyr411His) single nucleotide variant Medulloblastoma [RCV002292417] Chr1:168087678 [GRCh38]
Chr1:168056916 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.487_488del (p.Leu163fs) deletion Medulloblastoma [RCV002291250] Chr1:168097119..168097120 [GRCh38]
Chr1:168066357..168066358 [GRCh37]
Chr1:1q24.2		 pathogenic
NM_001375883.1(GPR161):c.1559A>G (p.Glu520Gly) single nucleotide variant Predisposition to medulloblastoma [RCV002292261] Chr1:168085562 [GRCh38]
Chr1:168054800 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.1445A>C (p.Glu482Ala) single nucleotide variant Medulloblastoma [RCV002292416] Chr1:168085676 [GRCh38]
Chr1:168054914 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.682G>T (p.Val228Phe) single nucleotide variant Medulloblastoma [RCV002292418] Chr1:168096925 [GRCh38]
Chr1:168066163 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.1212T>A (p.Asp404Glu) single nucleotide variant Inborn genetic diseases [RCV002906964] Chr1:168087697 [GRCh38]
Chr1:168056935 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.764C>T (p.Ala255Val) single nucleotide variant Inborn genetic diseases [RCV002879538] Chr1:168096843 [GRCh38]
Chr1:168066081 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.1409T>C (p.Ile470Thr) single nucleotide variant Inborn genetic diseases [RCV002777863] Chr1:168085712 [GRCh38]
Chr1:168054950 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.838A>C (p.Met280Leu) single nucleotide variant Inborn genetic diseases [RCV002951717] Chr1:168096769 [GRCh38]
Chr1:168066007 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.758G>A (p.Arg253Lys) single nucleotide variant Inborn genetic diseases [RCV002799702] Chr1:168096849 [GRCh38]
Chr1:168066087 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.257C>T (p.Thr86Met) single nucleotide variant Inborn genetic diseases [RCV002707518] Chr1:168104594 [GRCh38]
Chr1:168073832 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.196G>A (p.Val66Ile) single nucleotide variant Inborn genetic diseases [RCV002813624] Chr1:168104655 [GRCh38]
Chr1:168073893 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.1265C>T (p.Thr422Ile) single nucleotide variant Inborn genetic diseases [RCV002920170] Chr1:168087644 [GRCh38]
Chr1:168056882 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.947G>T (p.Ser316Ile) single nucleotide variant Inborn genetic diseases [RCV002944618] Chr1:168096660 [GRCh38]
Chr1:168065898 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.713G>C (p.Gly238Ala) single nucleotide variant Medulloblastoma [RCV003154598] Chr1:168096894 [GRCh38]
Chr1:168066132 [GRCh37]
Chr1:1q24.2		 uncertain significance
NM_001375883.1(GPR161):c.1235C>T (p.Thr412Met) single nucleotide variant Medulloblastoma [RCV003325255] Chr1:168087674 [GRCh38]
Chr1:168056912 [GRCh37]
Chr1:1q24.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2999
Count of miRNA genes:691
Interacting mature miRNAs:812
Transcripts:ENST00000271357, ENST00000361697, ENST00000367835, ENST00000367836, ENST00000367838, ENST00000478868, ENST00000485232, ENST00000493800, ENST00000537209, ENST00000539777, ENST00000546300
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.

Markers in Region
D1S2799  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371168,092,680 - 168,092,880UniSTSGRCh37
Build 361166,359,304 - 166,359,504RGDNCBI36
Celera1141,201,672 - 141,201,872RGD
Cytogenetic Map1q24.2UniSTS
HuRef1139,336,916 - 139,337,108UniSTS
Marshfield Genetic Map1183.19RGD
Marshfield Genetic Map1183.19UniSTS
Genethon Genetic Map1188.5UniSTS
deCODE Assembly Map1169.68UniSTS
Whitehead-YAC Contig Map1 UniSTS
RH98556  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371168,053,970 - 168,054,109UniSTSGRCh37
Build 361166,320,594 - 166,320,733RGDNCBI36
Celera1141,162,953 - 141,163,092RGD
Cytogenetic Map1q24.2UniSTS
HuRef1139,298,575 - 139,298,714UniSTS
GeneMap99-GB4 RH Map1607.52UniSTS
SHGC-83134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371168,084,095 - 168,084,371UniSTSGRCh37
Build 361166,350,719 - 166,350,995RGDNCBI36
Celera1141,193,087 - 141,193,363RGD
Cytogenetic Map1q24.2UniSTS
HuRef1139,328,331 - 139,328,607UniSTS
TNG Radiation Hybrid Map177077.0UniSTS
GPR161_2270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371168,053,859 - 168,054,610UniSTSGRCh37
Build 361166,320,483 - 166,321,234RGDNCBI36
Celera1141,162,842 - 141,163,593RGD
HuRef1139,298,464 - 139,299,215UniSTS
A004N15  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371168,048,803 - 168,048,973UniSTSGRCh37
Build 361166,315,427 - 166,315,597RGDNCBI36
Celera1141,157,786 - 141,157,956RGD
Cytogenetic Map1q24.2UniSTS
HuRef1139,293,408 - 139,293,578UniSTS
GeneMap99-GB4 RH Map1608.14UniSTS
D11S3114  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map10q11.1-q24UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic MapXq13.1-q21.1UniSTS
Cytogenetic Map20pter-q12UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map9p23UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map6p12UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map22q12.3-q13.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map19q11UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map1p32.2-p32.1UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map4q13.2UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map14q24.2UniSTS
D1S1425  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map2p23-p22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic Map2p11.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map3q11.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map15q11-q12UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map4q31.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map10p15-p14UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6q16UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic MapXq21.1UniSTS
WI-13488  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q24.2UniSTS
GeneMap99-GB4 RH Map1607.58UniSTS
Whitehead-RH Map1750.1UniSTS
NCBI RH Map11486.6UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 798 384 13 7 24 9 287 521 112 40 490 112 4 8 193
Low 1612 1781 1340 265 604 108 3534 1078 3551 300 959 1482 165 1196 2062 3
Below cutoff 27 800 363 343 1189 340 535 597 65 78 9 19 5 1 533 2 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_053052 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001267609 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001267610 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001267611 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001267612 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001267613 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001267614 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001349632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001349633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001349634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001349635 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375883 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375884 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375885 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381909 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_153832 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA662800 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF091890 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK026059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056040 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK095302 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK122656 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298797 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298850 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL033532 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY275468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC028163 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000271357   ⟹   ENSP00000271357
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1168,079,543 - 168,137,573 (-)Ensembl
RefSeq Acc Id: ENST00000367835   ⟹   ENSP00000356809
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1168,085,278 - 168,137,583 (-)Ensembl
RefSeq Acc Id: ENST00000367836   ⟹   ENSP00000356810
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1168,085,269 - 168,136,383 (-)Ensembl
RefSeq Acc Id: ENST00000367838   ⟹   ENSP00000356812
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1168,084,759 - 168,136,386 (-)Ensembl
RefSeq Acc Id: ENST00000478868
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1168,085,266 - 168,089,565 (-)Ensembl
RefSeq Acc Id: ENST00000485232
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1168,118,601 - 168,135,037 (-)Ensembl
RefSeq Acc Id: ENST00000493800
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1168,090,446 - 168,104,909 (-)Ensembl
RefSeq Acc Id: ENST00000537209   ⟹   ENSP00000441039
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1168,079,543 - 168,137,667 (-)Ensembl
RefSeq Acc Id: ENST00000539777   ⟹   ENSP00000437576
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1168,079,543 - 168,136,707 (-)Ensembl
RefSeq Acc Id: ENST00000546300   ⟹   ENSP00000444348
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1168,079,543 - 168,137,573 (-)Ensembl
RefSeq Acc Id: ENST00000682931   ⟹   ENSP00000506967
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1168,079,542 - 168,136,930 (-)Ensembl
RefSeq Acc Id: NM_001267609   ⟹   NP_001254538
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,137,667 (-)NCBI
GRCh371168,048,780 - 168,106,905 (-)NCBI
HuRef1139,293,385 - 139,351,133 (-)NCBI
CHM1_11169,470,990 - 169,529,180 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,489,154 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001267610   ⟹   NP_001254539
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,137,434 (-)NCBI
GRCh371168,048,780 - 168,106,905 (-)NCBI
HuRef1139,293,385 - 139,351,133 (-)NCBI
CHM1_11169,470,990 - 169,529,180 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,488,921 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001267611   ⟹   NP_001254540
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,137,573 (-)NCBI
GRCh371168,048,780 - 168,106,905 (-)NCBI
HuRef1139,293,385 - 139,351,133 (-)NCBI
CHM1_11169,470,990 - 169,529,086 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,489,060 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001267612   ⟹   NP_001254541
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,136,930 (-)NCBI
GRCh371168,048,780 - 168,106,905 (-)NCBI
HuRef1139,293,385 - 139,351,133 (-)NCBI
CHM1_11169,470,990 - 169,527,996 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,488,417 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001267613   ⟹   NP_001254542
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,136,707 (-)NCBI
GRCh371168,048,780 - 168,106,905 (-)NCBI
HuRef1139,293,385 - 139,351,133 (-)NCBI
CHM1_11169,470,990 - 169,528,267 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,488,194 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001267614   ⟹   NP_001254543
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,137,573 (-)NCBI
GRCh371168,048,780 - 168,106,905 (-)NCBI
HuRef1139,293,385 - 139,351,133 (-)NCBI
CHM1_11169,470,990 - 169,529,086 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,489,060 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001349632   ⟹   NP_001336561
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,137,667 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,489,154 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001349633   ⟹   NP_001336562
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,137,667 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,489,154 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001349634   ⟹   NP_001336563
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,137,573 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,489,060 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001349635   ⟹   NP_001336564
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,137,667 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,489,154 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001375883   ⟹   NP_001362812
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,136,930 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,488,417 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001375884   ⟹   NP_001362813
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,136,930 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,488,417 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001375885   ⟹   NP_001362814
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,136,930 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,488,417 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001381909   ⟹   NP_001368838
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,136,930 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,488,417 (-)NCBI
Sequence:
RefSeq Acc Id: NM_153832   ⟹   NP_722561
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,079,542 - 168,136,930 (-)NCBI
GRCh371168,048,780 - 168,106,905 (-)NCBI
Build 361166,320,621 - 166,372,248 (-)NCBI Archive
Celera1141,162,980 - 141,214,616 (-)RGD
HuRef1139,293,385 - 139,351,133 (-)NCBI
CHM1_11169,470,990 - 169,528,267 (-)NCBI
T2T-CHM13v2.01167,431,007 - 167,488,417 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001254538 (Get FASTA)   NCBI Sequence Viewer  
  NP_001254539 (Get FASTA)   NCBI Sequence Viewer  
  NP_001254540 (Get FASTA)   NCBI Sequence Viewer  
  NP_001254541 (Get FASTA)   NCBI Sequence Viewer  
  NP_001254542 (Get FASTA)   NCBI Sequence Viewer  
  NP_001254543 (Get FASTA)   NCBI Sequence Viewer  
  NP_001336561 (Get FASTA)   NCBI Sequence Viewer  
  NP_001336562 (Get FASTA)   NCBI Sequence Viewer  
  NP_001336563 (Get FASTA)   NCBI Sequence Viewer  
  NP_001336564 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362812 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362813 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362814 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368838 (Get FASTA)   NCBI Sequence Viewer  
  NP_722561 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC61598 (Get FASTA)   NCBI Sequence Viewer  
  AAH28163 (Get FASTA)   NCBI Sequence Viewer  
  AAP32300 (Get FASTA)   NCBI Sequence Viewer  
  BAC03624 (Get FASTA)   NCBI Sequence Viewer  
  BAG51611 (Get FASTA)   NCBI Sequence Viewer  
  BAG53646 (Get FASTA)   NCBI Sequence Viewer  
  BAH12873 (Get FASTA)   NCBI Sequence Viewer  
  BAH12884 (Get FASTA)   NCBI Sequence Viewer  
  BAH13082 (Get FASTA)   NCBI Sequence Viewer  
  EAW90818 (Get FASTA)   NCBI Sequence Viewer  
  EAW90819 (Get FASTA)   NCBI Sequence Viewer  
  Q8N6U8 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_722561   ⟸   NM_153832
- Peptide Label: isoform 2
- UniProtKB: Q5TGK1 (UniProtKB/Swiss-Prot),   Q5TGK0 (UniProtKB/Swiss-Prot),   O75963 (UniProtKB/Swiss-Prot),   F5H6J7 (UniProtKB/Swiss-Prot),   F5GXD6 (UniProtKB/Swiss-Prot),   B7Z5Z6 (UniProtKB/Swiss-Prot),   B7Z5E8 (UniProtKB/Swiss-Prot),   B7Z5D7 (UniProtKB/Swiss-Prot),   B3KV34 (UniProtKB/Swiss-Prot),   Q5TGK2 (UniProtKB/Swiss-Prot),   Q8N6U8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001254539   ⟸   NM_001267610
- Peptide Label: isoform 2
- UniProtKB: Q5TGK1 (UniProtKB/Swiss-Prot),   Q5TGK0 (UniProtKB/Swiss-Prot),   O75963 (UniProtKB/Swiss-Prot),   F5H6J7 (UniProtKB/Swiss-Prot),   F5GXD6 (UniProtKB/Swiss-Prot),   B7Z5Z6 (UniProtKB/Swiss-Prot),   B7Z5E8 (UniProtKB/Swiss-Prot),   B7Z5D7 (UniProtKB/Swiss-Prot),   B3KV34 (UniProtKB/Swiss-Prot),   Q5TGK2 (UniProtKB/Swiss-Prot),   Q8N6U8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001254538   ⟸   NM_001267609
- Peptide Label: isoform 1
- UniProtKB: Q8N6U8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001254543   ⟸   NM_001267614
- Peptide Label: isoform 6
- UniProtKB: Q8N6U8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001254540   ⟸   NM_001267611
- Peptide Label: isoform 3
- UniProtKB: A0A0A0MQW8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001254542   ⟸   NM_001267613
- Peptide Label: isoform 5
- UniProtKB: Q8N6U8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001254541   ⟸   NM_001267612
- Peptide Label: isoform 4
- UniProtKB: Q8N6U8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001336564   ⟸   NM_001349635
- Peptide Label: isoform 4
- Sequence:
RefSeq Acc Id: NP_001336562   ⟸   NM_001349633
- Peptide Label: isoform 2
- UniProtKB: Q8N6U8 (UniProtKB/Swiss-Prot),   Q5TGK1 (UniProtKB/Swiss-Prot),   Q5TGK0 (UniProtKB/Swiss-Prot),   O75963 (UniProtKB/Swiss-Prot),   F5H6J7 (UniProtKB/Swiss-Prot),   F5GXD6 (UniProtKB/Swiss-Prot),   B7Z5Z6 (UniProtKB/Swiss-Prot),   B7Z5E8 (UniProtKB/Swiss-Prot),   B7Z5D7 (UniProtKB/Swiss-Prot),   B3KV34 (UniProtKB/Swiss-Prot),   Q5TGK2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001336561   ⟸   NM_001349632
- Peptide Label: isoform 2
- UniProtKB: Q8N6U8 (UniProtKB/Swiss-Prot),   Q5TGK1 (UniProtKB/Swiss-Prot),   Q5TGK0 (UniProtKB/Swiss-Prot),   O75963 (UniProtKB/Swiss-Prot),   F5H6J7 (UniProtKB/Swiss-Prot),   F5GXD6 (UniProtKB/Swiss-Prot),   B7Z5Z6 (UniProtKB/Swiss-Prot),   B7Z5E8 (UniProtKB/Swiss-Prot),   B7Z5D7 (UniProtKB/Swiss-Prot),   B3KV34 (UniProtKB/Swiss-Prot),   Q5TGK2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001336563   ⟸   NM_001349634
- Peptide Label: isoform 2
- UniProtKB: Q8N6U8 (UniProtKB/Swiss-Prot),   Q5TGK1 (UniProtKB/Swiss-Prot),   Q5TGK0 (UniProtKB/Swiss-Prot),   O75963 (UniProtKB/Swiss-Prot),   F5H6J7 (UniProtKB/Swiss-Prot),   F5GXD6 (UniProtKB/Swiss-Prot),   B7Z5Z6 (UniProtKB/Swiss-Prot),   B7Z5E8 (UniProtKB/Swiss-Prot),   B7Z5D7 (UniProtKB/Swiss-Prot),   B3KV34 (UniProtKB/Swiss-Prot),   Q5TGK2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001362812   ⟸   NM_001375883
- Peptide Label: isoform 2
- UniProtKB: Q8N6U8 (UniProtKB/Swiss-Prot),   Q5TGK1 (UniProtKB/Swiss-Prot),   Q5TGK0 (UniProtKB/Swiss-Prot),   O75963 (UniProtKB/Swiss-Prot),   F5H6J7 (UniProtKB/Swiss-Prot),   F5GXD6 (UniProtKB/Swiss-Prot),   B7Z5Z6 (UniProtKB/Swiss-Prot),   B7Z5E8 (UniProtKB/Swiss-Prot),   B7Z5D7 (UniProtKB/Swiss-Prot),   B3KV34 (UniProtKB/Swiss-Prot),   Q5TGK2 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001362813   ⟸   NM_001375884
- Peptide Label: isoform 2
- UniProtKB: Q8N6U8 (UniProtKB/Swiss-Prot),   Q5TGK1 (UniProtKB/Swiss-Prot),   Q5TGK0 (UniProtKB/Swiss-Prot),   O75963 (UniProtKB/Swiss-Prot),   F5H6J7 (UniProtKB/Swiss-Prot),   F5GXD6 (UniProtKB/Swiss-Prot),   B7Z5Z6 (UniProtKB/Swiss-Prot),   B7Z5E8 (UniProtKB/Swiss-Prot),   B7Z5D7 (UniProtKB/Swiss-Prot),   B3KV34 (UniProtKB/Swiss-Prot),   Q5TGK2 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001362814   ⟸   NM_001375885
- Peptide Label: isoform 2
- UniProtKB: Q8N6U8 (UniProtKB/Swiss-Prot),   Q5TGK1 (UniProtKB/Swiss-Prot),   Q5TGK0 (UniProtKB/Swiss-Prot),   O75963 (UniProtKB/Swiss-Prot),   F5H6J7 (UniProtKB/Swiss-Prot),   F5GXD6 (UniProtKB/Swiss-Prot),   B7Z5Z6 (UniProtKB/Swiss-Prot),   B7Z5E8 (UniProtKB/Swiss-Prot),   B7Z5D7 (UniProtKB/Swiss-Prot),   B3KV34 (UniProtKB/Swiss-Prot),   Q5TGK2 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001368838   ⟸   NM_001381909
- Peptide Label: isoform 2
- UniProtKB: Q8N6U8 (UniProtKB/Swiss-Prot),   Q5TGK1 (UniProtKB/Swiss-Prot),   Q5TGK0 (UniProtKB/Swiss-Prot),   O75963 (UniProtKB/Swiss-Prot),   F5H6J7 (UniProtKB/Swiss-Prot),   F5GXD6 (UniProtKB/Swiss-Prot),   B7Z5Z6 (UniProtKB/Swiss-Prot),   B7Z5E8 (UniProtKB/Swiss-Prot),   B7Z5D7 (UniProtKB/Swiss-Prot),   B3KV34 (UniProtKB/Swiss-Prot),   Q5TGK2 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: ENSP00000444348   ⟸   ENST00000546300
RefSeq Acc Id: ENSP00000271357   ⟸   ENST00000271357
RefSeq Acc Id: ENSP00000441039   ⟸   ENST00000537209
RefSeq Acc Id: ENSP00000356810   ⟸   ENST00000367836
RefSeq Acc Id: ENSP00000356809   ⟸   ENST00000367835
RefSeq Acc Id: ENSP00000356812   ⟸   ENST00000367838
RefSeq Acc Id: ENSP00000437576   ⟸   ENST00000539777
RefSeq Acc Id: ENSP00000506967   ⟸   ENST00000682931
Protein Domains
G-protein coupled receptors family 1 profile

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8N6U8-F1-model_v2 AlphaFold Q8N6U8 1-529 view protein structure

Promoters
RGD ID:6785676
Promoter ID:HG_KWN:6065
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   NB4
Transcripts:NM_153832,   UC001GFB.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361166,372,376 - 166,372,876 (-)MPROMDB
RGD ID:6858036
Promoter ID:EPDNEW_H2183
Type:initiation region
Name:GPR161_1
Description:G protein-coupled receptor 161
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381168,137,684 - 168,137,744EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:23694 AgrOrtholog
COSMIC GPR161 COSMIC
Ensembl Genes ENSG00000143147 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000271357 ENTREZGENE
  ENSP00000271357.6 UniProtKB/TrEMBL
  ENSP00000356809 ENTREZGENE
  ENSP00000356809.1 UniProtKB/Swiss-Prot
  ENSP00000356810 ENTREZGENE
  ENSP00000356810.1 UniProtKB/Swiss-Prot
  ENSP00000356812 ENTREZGENE
  ENSP00000356812.1 UniProtKB/Swiss-Prot
  ENSP00000437576 ENTREZGENE
  ENSP00000437576.1 UniProtKB/Swiss-Prot
  ENSP00000441039 ENTREZGENE
  ENSP00000441039.1 UniProtKB/Swiss-Prot
  ENSP00000444348 ENTREZGENE
  ENSP00000444348.1 UniProtKB/Swiss-Prot
  ENSP00000506967 ENTREZGENE
  ENSP00000506967.1 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000271357 ENTREZGENE
  ENST00000271357.9 UniProtKB/TrEMBL
  ENST00000367835 ENTREZGENE
  ENST00000367835.1 UniProtKB/Swiss-Prot
  ENST00000367836 ENTREZGENE
  ENST00000367836.5 UniProtKB/Swiss-Prot
  ENST00000367838 ENTREZGENE
  ENST00000367838.5 UniProtKB/Swiss-Prot
  ENST00000537209 ENTREZGENE
  ENST00000537209.5 UniProtKB/Swiss-Prot
  ENST00000539777 ENTREZGENE
  ENST00000539777.5 UniProtKB/Swiss-Prot
  ENST00000546300 ENTREZGENE
  ENST00000546300.5 UniProtKB/Swiss-Prot
  ENST00000682931 ENTREZGENE
  ENST00000682931.1 UniProtKB/Swiss-Prot
Gene3D-CATH Rhodopsin 7-helix transmembrane proteins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000143147 GTEx
HGNC ID HGNC:23694 ENTREZGENE
Human Proteome Map GPR161 Human Proteome Map
InterPro GPCR_Rhodpsn UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_Rhodpsn_7TM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:23432 UniProtKB/Swiss-Prot
NCBI Gene 23432 ENTREZGENE
OMIM 612250 OMIM
PANTHER G PROTEIN-COUPLED RECEPTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  G-PROTEIN COUPLED RECEPTOR 161 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam 7tm_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134931474 PharmGKB
PRINTS GPCRRHODOPSN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE G_PROTEIN_RECEP_F1_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  G_PROTEIN_RECEP_F1_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROKAR_LIPOPROTEIN UniProtKB/TrEMBL
Superfamily-SCOP Family A G protein-coupled receptor-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0A0MQW8 ENTREZGENE, UniProtKB/TrEMBL
  B3KV34 ENTREZGENE
  B7Z5D7 ENTREZGENE
  B7Z5E8 ENTREZGENE
  B7Z5Z6 ENTREZGENE
  F5GXD6 ENTREZGENE
  F5H6J7 ENTREZGENE
  GP161_HUMAN UniProtKB/Swiss-Prot
  O75963 ENTREZGENE
  Q5TGK0 ENTREZGENE
  Q5TGK1 ENTREZGENE
  Q5TGK2 ENTREZGENE
  Q8N6U8 ENTREZGENE
UniProt Secondary B3KV34 UniProtKB/Swiss-Prot
  B7Z5D7 UniProtKB/Swiss-Prot
  B7Z5E8 UniProtKB/Swiss-Prot
  B7Z5Z6 UniProtKB/Swiss-Prot
  F5GXD6 UniProtKB/Swiss-Prot
  F5H6J7 UniProtKB/Swiss-Prot
  O75963 UniProtKB/Swiss-Prot
  Q5TGK0 UniProtKB/Swiss-Prot
  Q5TGK1 UniProtKB/Swiss-Prot
  Q5TGK2 UniProtKB/Swiss-Prot