ADGRL3 (adhesion G protein-coupled receptor L3) - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Gene: ADGRL3 (adhesion G protein-coupled receptor L3) Homo sapiens
Analyze
Symbol: ADGRL3
Name: adhesion G protein-coupled receptor L3
RGD ID: 1353351
HGNC Page HGNC:20974
Description: Enables calcium ion binding activity. Involved in cell-cell adhesion via plasma-membrane adhesion molecules. Located in plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: calcium-independent alpha-latrotoxin receptor 3; CIRL-3; CIRL3; CL3; latrophilin 3; latrophilin homolog 3 (cow); latrophilin-3; LEC3; lectomedin 3; LPHN3
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
GRCh38461,200,326 - 62,078,335 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl461,200,326 - 62,078,335 (+)EnsemblGRCh38hg38GRCh38
GRCh37462,066,044 - 62,944,053 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36462,045,434 - 62,620,763 (+)NCBINCBI36Build 36hg18NCBI36
Build 34462,191,604 - 62,766,933NCBI
Celera459,821,669 - 60,396,265 (+)NCBICelera
Cytogenetic Map4q13.1NCBI
HuRef458,271,407 - 58,846,164 (+)NCBIHuRef
CHM1_1462,398,708 - 62,974,117 (+)NCBICHM1_1
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
17alpha-ethynylestradiol  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-sulfonyldiphenol  (ISO)
6-propyl-2-thiouracil  (ISO)
aflatoxin B1  (EXP)
amitrole  (ISO)
ammonium chloride  (ISO)
antirheumatic drug  (EXP)
aristolochic acid A  (EXP)
arsane  (ISO)
arsenic atom  (ISO)
belinostat  (EXP)
benzo[a]pyrene  (EXP,ISO)
bisphenol A  (ISO)
bisphenol F  (EXP,ISO)
cadmium dichloride  (ISO)
carbon nanotube  (ISO)
CGP 52608  (EXP)
chloroprene  (ISO)
cocaine  (ISO)
coumarin  (EXP)
crocidolite asbestos  (ISO)
Cuprizon  (ISO)
cyclosporin A  (EXP)
dichloroacetic acid  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP)
endosulfan  (ISO)
entinostat  (EXP)
ethanol  (ISO)
fenvalerate  (ISO)
folic acid  (ISO)
fulvestrant  (EXP)
genistein  (EXP)
gentamycin  (ISO)
glyphosate  (ISO)
hexane-1,6-diamine  (EXP)
maneb  (ISO)
methimazole  (ISO)
methylmercury chloride  (EXP)
methylseleninic acid  (EXP)
Monobutylphthalate  (ISO)
N,N-diethyl-m-toluamide  (ISO)
nickel atom  (EXP)
ozone  (ISO)
panobinostat  (EXP)
paraquat  (ISO)
perfluorohexanesulfonic acid  (ISO)
permethrin  (ISO)
pirinixic acid  (ISO)
potassium dichromate  (ISO)
SB 431542  (EXP)
silicon dioxide  (EXP)
silver atom  (ISO)
silver(0)  (ISO)
sotorasib  (EXP)
sulfadimethoxine  (ISO)
sulforaphane  (ISO)
sunitinib  (EXP)
thimerosal  (EXP)
thioacetamide  (ISO)
titanium dioxide  (ISO)
trametinib  (EXP)
tremolite asbestos  (ISO)
trichloroethene  (ISO)
trichostatin A  (EXP)
triptonide  (ISO)
valproic acid  (EXP)
vorinostat  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Involvement of the calcium-independent receptor for alpha-latrotoxin in brain ischemia. Bin Sun H, etal., Brain Res Mol Brain Res. 2002 Aug 15;104(2):246-9.
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
Additional References at PubMed
PMID:7937745   PMID:9847074   PMID:9872452   PMID:10964907   PMID:10994649   PMID:11520923   PMID:12477932   PMID:14702039   PMID:15066411   PMID:15203201   PMID:16344560   PMID:19043545  
PMID:20157310   PMID:20379614   PMID:20522523   PMID:20677014   PMID:21040458   PMID:21107309   PMID:21184580   PMID:21432600   PMID:21606926   PMID:21873635   PMID:22105624   PMID:22405201  
PMID:22486528   PMID:22575564   PMID:22832519   PMID:23245769   PMID:23317273   PMID:25713288   PMID:25871512   PMID:25989180   PMID:26186194   PMID:26235030   PMID:27325752   PMID:27692237  
PMID:28514442   PMID:30021884   PMID:30406846   PMID:30652248   PMID:30696812   PMID:32691279   PMID:32778842   PMID:32787626   PMID:33247693   PMID:33504901   PMID:33914279   PMID:33961781  
PMID:34009035   PMID:34048709   PMID:35013530   PMID:35044719   PMID:35393556   PMID:35741042   PMID:36151371   PMID:36724073   PMID:37224017  


Genomics

Comparative Map Data
ADGRL3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38461,200,326 - 62,078,335 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl461,200,326 - 62,078,335 (+)EnsemblGRCh38hg38GRCh38
GRCh37462,066,044 - 62,944,053 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36462,045,434 - 62,620,763 (+)NCBINCBI36Build 36hg18NCBI36
Build 34462,191,604 - 62,766,933NCBI
Celera459,821,669 - 60,396,265 (+)NCBICelera
Cytogenetic Map4q13.1NCBI
HuRef458,271,407 - 58,846,164 (+)NCBIHuRef
CHM1_1462,398,708 - 62,974,117 (+)NCBICHM1_1
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBIT2T-CHM13v2.0
Adgrl3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39581,167,600 - 81,980,556 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl581,167,985 - 81,972,980 (+)EnsemblGRCm39 Ensembl
GRCm38581,019,085 - 81,827,825 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl581,020,138 - 81,825,133 (+)EnsemblGRCm38mm10GRCm38
MGSCv37581,450,618 - 82,224,755 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36582,096,154 - 82,870,291 (+)NCBIMGSCv36mm8
Celera578,280,126 - 79,039,754 (+)NCBICelera
Cytogenetic Map5D- E1NCBI
cM Map542.62NCBI
Adgrl3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81426,690,891 - 27,458,132 (-)NCBIGRCr8
mRatBN7.21426,336,320 - 27,104,060 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1426,368,277 - 27,105,860 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1426,715,441 - 27,465,812 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01428,027,851 - 28,778,270 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01426,509,623 - 27,260,039 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01428,362,176 - 29,226,085 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1428,393,394 - 28,967,980 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01428,183,727 - 29,040,121 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41428,385,112 - 28,854,677 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11428,385,120 - 28,854,677 (-)NCBI
Celera1425,731,451 - 26,185,004 (-)NCBICelera
Cytogenetic Map14p21NCBI
Adgrl3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554479,943,598 - 10,709,008 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554479,912,679 - 10,708,743 (-)NCBIChiLan1.0ChiLan1.0
ADGRL3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2367,717,238 - 68,578,490 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1467,937,970 - 68,799,235 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0461,876,694 - 62,742,354 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1468,315,996 - 69,183,881 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl468,323,404 - 69,003,093 (-)Ensemblpanpan1.1panPan2
ADGRL3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11352,742,043 - 53,568,184 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1352,909,684 - 53,538,625 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1352,651,031 - 53,476,080 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01353,378,322 - 54,210,364 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1353,378,109 - 54,181,953 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11353,058,300 - 53,887,839 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01352,577,693 - 53,373,845 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01353,501,337 - 54,367,460 (+)NCBIUU_Cfam_GSD_1.0
Adgrl3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440528522,750,332 - 23,528,212 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365825,338,982 - 5,819,018 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365825,313,215 - 6,091,351 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ADGRL3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl860,630,117 - 60,792,899 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1859,988,280 - 60,800,177 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
ADGRL3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.176,726,400 - 7,261,059 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_0236660667,000,551 - 7,860,788 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Adgrl3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247617,242,948 - 7,804,418 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247617,219,269 - 8,101,988 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ADGRL3
52 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_015236.4(ADGRL3):c.56-36681A>G single nucleotide variant Lung cancer [RCV000094957] Chr4:61550546 [GRCh38]
Chr4:62416264 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_015236.4(ADGRL3):c.1196-20300G>A single nucleotide variant Lung cancer [RCV000094958] Chr4:61793509 [GRCh38]
Chr4:62659227 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_015236.4(ADGRL3):c.1277-37904A>T single nucleotide variant Lung cancer [RCV000094959] Chr4:61854752 [GRCh38]
Chr4:62720470 [GRCh37]
Chr4:4q13.1		 uncertain significance
GRCh38/hg38 4p13-q13.1(chr4:44356201-62245882)x3 copy number gain See cases [RCV000050683] Chr4:44356201..62245882 [GRCh38]
Chr4:44358218..63111600 [GRCh37]
Chr4:44052975..62794195 [NCBI36]
Chr4:4p13-q13.1		 pathogenic
GRCh38/hg38 4q12-13.2(chr4:51831622-66991489)x3 copy number gain See cases [RCV000051771] Chr4:51831622..66991489 [GRCh38]
Chr4:52697788..67857207 [GRCh37]
Chr4:52392545..67539802 [NCBI36]
Chr4:4q12-13.2		 pathogenic
GRCh38/hg38 4q12-22.3(chr4:51831622-97505618)x3 copy number gain See cases [RCV000051772] Chr4:51831622..97505618 [GRCh38]
Chr4:52697788..98426769 [GRCh37]
Chr4:52392545..98645792 [NCBI36]
Chr4:4q12-22.3		 pathogenic
GRCh38/hg38 4q12-13.1(chr4:54198601-62270115)x1 copy number loss See cases [RCV000053266] Chr4:54198601..62270115 [GRCh38]
Chr4:55064768..63135833 [GRCh37]
Chr4:54759525..62818428 [NCBI36]
Chr4:4q12-13.1		 pathogenic
NM_015236.4(ADGRL3):c.3747C>T (p.Asn1249=) single nucleotide variant Malignant melanoma [RCV000066471] Chr4:62070245 [GRCh38]
Chr4:62935963 [GRCh37]
Chr4:62618558 [NCBI36]
Chr4:4q13.1		 not provided
GRCh38/hg38 4q13.1(chr4:61178277-62895417)x1 copy number loss See cases [RCV000134981] Chr4:61178277..62895417 [GRCh38]
Chr4:62043995..63761135 [GRCh37]
Chr4:61726590..63443730 [NCBI36]
Chr4:4q13.1		 likely benign
GRCh38/hg38 4q13.1(chr4:61375984-61631530)x1 copy number loss See cases [RCV000137674] Chr4:61375984..61631530 [GRCh38]
Chr4:62241702..62497248 [GRCh37]
Chr4:61924297..62179843 [NCBI36]
Chr4:4q13.1		 uncertain significance
GRCh38/hg38 4q13.1(chr4:61356169-62527994)x3 copy number gain See cases [RCV000142533] Chr4:61356169..62527994 [GRCh38]
Chr4:62221887..63393712 [GRCh37]
Chr4:61904482..63076307 [NCBI36]
Chr4:4q13.1		 likely benign|conflicting data from submitters
NC_000004.12:g.61469401G>A single nucleotide variant Lung cancer [RCV000094956] Chr4:61469401 [GRCh38]
Chr4:62335119 [GRCh37]
Chr4:4q13.1		 uncertain significance
GRCh37/hg19 4q13.1(chr4:62241702-62525578)x3 copy number gain not provided [RCV000762748] Chr4:62241702..62525578 [GRCh37]
Chr4:4q13.1		 likely benign
GRCh37/hg19 4q13.1(chr4:62910103-66106762)x3 copy number gain See cases [RCV000240542] Chr4:62910103..66106762 [GRCh37]
Chr4:4q13.1		 uncertain significance
GRCh37/hg19 4q13.1(chr4:62789165-62881087)x1 copy number loss See cases [RCV000240217] Chr4:62789165..62881087 [GRCh37]
Chr4:4q13.1		 uncertain significance
GRCh37/hg19 4p16.3-q35.2(chr4:12440-190904441)x3 copy number gain See cases [RCV000446653] Chr4:12440..190904441 [GRCh37]
Chr4:4p16.3-q35.2		 pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473) copy number gain See cases [RCV000510453] Chr4:68346..190957473 [GRCh37]
Chr4:4p16.3-q35.2		 pathogenic
GRCh37/hg19 4p16.3-q13.1(chr4:68345-66440622)x3 copy number gain See cases [RCV000511193] Chr4:68345..66440622 [GRCh37]
Chr4:4p16.3-q13.1		 pathogenic
NM_001387552.1(ADGRL3):c.296G>A (p.Arg99His) single nucleotide variant Inborn genetic diseases [RCV003267845] Chr4:61587263 [GRCh38]
Chr4:62452981 [GRCh37]
Chr4:4q13.1		 uncertain significance
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)x3 copy number gain See cases [RCV000512241] Chr4:68346..190957473 [GRCh37]
Chr4:4p16.3-q35.2		 pathogenic
GRCh37/hg19 4q13.1(chr4:62197441-62704852)x3 copy number gain not provided [RCV000682407] Chr4:62197441..62704852 [GRCh37]
Chr4:4q13.1		 uncertain significance
GRCh37/hg19 4q13.1(chr4:62197441-63436758)x3 copy number gain not provided [RCV000682408] Chr4:62197441..63436758 [GRCh37]
Chr4:4q13.1		 likely benign
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190915650)x3 copy number gain not provided [RCV000743155] Chr4:49450..190915650 [GRCh37]
Chr4:4p16.3-q35.2		 pathogenic
GRCh37/hg19 4q12-13.3(chr4:58332294-71587615)x1 copy number loss not provided [RCV000743602] Chr4:58332294..71587615 [GRCh37]
Chr4:4q12-13.3		 pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190963766)x3 copy number gain not provided [RCV000743156] Chr4:49450..190963766 [GRCh37]
Chr4:4p16.3-q35.2		 pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:11525-191028879)x3 copy number gain not provided [RCV000743147] Chr4:11525..191028879 [GRCh37]
Chr4:4p16.3-q35.2		 pathogenic
Single allele deletion Arthrogryphosis [RCV000787451] Chr4:62509484..62818444 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.728C>G (p.Thr243Ser) single nucleotide variant Inborn genetic diseases [RCV003288990] Chr4:61732883 [GRCh38]
Chr4:62598601 [GRCh37]
Chr4:4q13.1		 uncertain significance
Single allele deletion Neurodevelopmental disorder [RCV000787447] Chr4:61605456..68762943 [GRCh37]
Chr4:4q13.1-13.2		 likely pathogenic
NM_001387552.1(ADGRL3):c.2746A>G (p.Thr916Ala) single nucleotide variant Inborn genetic diseases [RCV003291761] Chr4:61948217 [GRCh38]
Chr4:62813935 [GRCh37]
Chr4:4q13.1		 uncertain significance
GRCh37/hg19 4q13.1(chr4:62844407-63436758)x3 copy number gain not provided [RCV001005549] Chr4:62844407..63436758 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.1693A>G (p.Ser565Gly) single nucleotide variant Inborn genetic diseases [RCV003252497] Chr4:61892868 [GRCh38]
Chr4:62758586 [GRCh37]
Chr4:4q13.1		 uncertain significance
GRCh37/hg19 4q13.1(chr4:62859667-62944363)x1 copy number loss not provided [RCV001005550] Chr4:62859667..62944363 [GRCh37]
Chr4:4q13.1		 uncertain significance
GRCh37/hg19 4q13.1(chr4:62385651-62551302)x1 copy number loss not provided [RCV001259263] Chr4:62385651..62551302 [GRCh37]
Chr4:4q13.1		 uncertain significance
GRCh37/hg19 4q13.1(chr4:62646230-63285731)x3 copy number gain not provided [RCV001259264] Chr4:62646230..63285731 [GRCh37]
Chr4:4q13.1		 uncertain significance
GRCh37/hg19 4q13.1(chr4:62131908-62559298)x3 copy number gain not provided [RCV001258647] Chr4:62131908..62559298 [GRCh37]
Chr4:4q13.1		 likely benign
GRCh38/hg38 4q12-21.1(chr4:51891814-76009719)x1 copy number loss Piebaldism [RCV001420508] Chr4:51891814..76009719 [GRCh38]
Chr4:4q12-21.1		 pathogenic
GRCh37/hg19 4q13.1(chr4:62684816-62765507)x1 copy number loss not provided [RCV001829256] Chr4:62684816..62765507 [GRCh37]
Chr4:4q13.1		 uncertain significance
GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3 copy number gain not provided [RCV001827738] Chr4:52866944..143582507 [GRCh37]
Chr4:4q12-31.21		 pathogenic
GRCh37/hg19 4q13.1-13.3(chr4:61867555-74711517) copy number loss not specified [RCV002053422] Chr4:61867555..74711517 [GRCh37]
Chr4:4q13.1-13.3		 pathogenic
NM_001387552.1(ADGRL3):c.2957T>G (p.Ile986Ser) single nucleotide variant Inborn genetic diseases [RCV003304616] Chr4:61979714 [GRCh38]
Chr4:62845432 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.4226A>C (p.Tyr1409Ser) single nucleotide variant Inborn genetic diseases [RCV002772381] Chr4:62070502 [GRCh38]
Chr4:62936220 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.1251G>T (p.Lys417Asn) single nucleotide variant Inborn genetic diseases [RCV002733470] Chr4:61733406 [GRCh38]
Chr4:62599124 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.4550G>T (p.Gly1517Val) single nucleotide variant Inborn genetic diseases [RCV002839968] Chr4:62070826 [GRCh38]
Chr4:62936544 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.4487G>A (p.Gly1496Asp) single nucleotide variant Inborn genetic diseases [RCV002902275] Chr4:62070763 [GRCh38]
Chr4:62936481 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.2451C>A (p.Asn817Lys) single nucleotide variant Inborn genetic diseases [RCV002753258] Chr4:61946945 [GRCh38]
Chr4:62812663 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.2501C>T (p.Thr834Met) single nucleotide variant Inborn genetic diseases [RCV002980466] Chr4:61946995 [GRCh38]
Chr4:62812713 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.358A>G (p.Met120Val) single nucleotide variant Inborn genetic diseases [RCV002823651] Chr4:61587325 [GRCh38]
Chr4:62453043 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.1471T>C (p.Ser491Pro) single nucleotide variant Inborn genetic diseases [RCV002911405] Chr4:61813880 [GRCh38]
Chr4:62679598 [GRCh37]
Chr4:4q13.1		 likely benign
NM_001387552.1(ADGRL3):c.1876A>G (p.Ile626Val) single nucleotide variant Inborn genetic diseases [RCV002701787] Chr4:61895823 [GRCh38]
Chr4:62761541 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.1781T>C (p.Ile594Thr) single nucleotide variant Inborn genetic diseases [RCV002768469] Chr4:61892956 [GRCh38]
Chr4:62758674 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.1739G>A (p.Arg580His) single nucleotide variant Inborn genetic diseases [RCV002984211] Chr4:61892914 [GRCh38]
Chr4:62758632 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.2681G>A (p.Arg894His) single nucleotide variant Inborn genetic diseases [RCV002941684] Chr4:61948152 [GRCh38]
Chr4:62813870 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.1537C>T (p.Arg513Trp) single nucleotide variant Inborn genetic diseases [RCV002940443] Chr4:61892712 [GRCh38]
Chr4:62758430 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.1078C>G (p.Pro360Ala) single nucleotide variant Inborn genetic diseases [RCV002652581] Chr4:61733233 [GRCh38]
Chr4:62598951 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.3002G>A (p.Arg1001Gln) single nucleotide variant Inborn genetic diseases [RCV003196573] Chr4:61979759 [GRCh38]
Chr4:62845477 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.2740C>T (p.His914Tyr) single nucleotide variant Inborn genetic diseases [RCV003221148] Chr4:61948211 [GRCh38]
Chr4:62813929 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.4102G>T (p.Gly1368Cys) single nucleotide variant Inborn genetic diseases [RCV003200674] Chr4:62070378 [GRCh38]
Chr4:62936096 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.3559A>G (p.Ile1187Val) single nucleotide variant Inborn genetic diseases [RCV003186264] Chr4:62031578 [GRCh38]
Chr4:62897296 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.778A>G (p.Ile260Val) single nucleotide variant Inborn genetic diseases [RCV003196609] Chr4:61732933 [GRCh38]
Chr4:62598651 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.4468A>G (p.Lys1490Glu) single nucleotide variant Inborn genetic diseases [RCV003381371] Chr4:62070744 [GRCh38]
Chr4:62936462 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.2923A>G (p.Ser975Gly) single nucleotide variant Inborn genetic diseases [RCV003369968] Chr4:61979680 [GRCh38]
Chr4:62845398 [GRCh37]
Chr4:4q13.1		 uncertain significance
GRCh37/hg19 4q12-13.3(chr4:57584845-72430996)x1 copy number loss not provided [RCV003485417] Chr4:57584845..72430996 [GRCh37]
Chr4:4q12-13.3		 pathogenic
GRCh37/hg19 4q13.1(chr4:62360062-62453209)x1 copy number loss not provided [RCV003485420] Chr4:62360062..62453209 [GRCh37]
Chr4:4q13.1		 uncertain significance
NM_001387552.1(ADGRL3):c.675G>A (p.Ala225=) single nucleotide variant not provided [RCV003439326] Chr4:61732830 [GRCh38]
Chr4:62598548 [GRCh37]
Chr4:4q13.1		 likely benign
GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3 copy number gain not provided [RCV003885507] Chr4:45455621..191003541 [GRCh37]
Chr4:4p12-q35.2		 pathogenic
NM_001387552.1(ADGRL3):c.4390G>A (p.Ala1464Thr) single nucleotide variant Inborn genetic diseases [RCV003340120] Chr4:62070666 [GRCh38]
Chr4:62936384 [GRCh37]
Chr4:4q13.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:7472
Count of miRNA genes:1063
Interacting mature miRNAs:1373
Transcripts:ENST00000502815, ENST00000504896, ENST00000506700, ENST00000506720, ENST00000506746, ENST00000507164, ENST00000507625, ENST00000508078, ENST00000508693, ENST00000508946, ENST00000509089, ENST00000509779, ENST00000509896, ENST00000511324, ENST00000512091, ENST00000514157, ENST00000514591, ENST00000514996, ENST00000545650
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
D4S1600  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,897,648 - 62,897,784UniSTSGRCh37
GRCh37462,897,651 - 62,897,790UniSTSGRCh37
Build 36462,580,246 - 62,580,385RGDNCBI36
Celera460,355,745 - 60,355,881UniSTS
Celera460,355,748 - 60,355,887RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,805,651 - 58,805,788UniSTS
HuRef458,805,648 - 58,805,782UniSTS
Marshfield Genetic Map472.52RGD
Genethon Genetic Map471.5UniSTS
TNG Radiation Hybrid Map434574.0UniSTS
deCODE Assembly Map476.19UniSTS
Stanford-G3 RH Map43582.0UniSTS
Whitehead-YAC Contig Map4 UniSTS
NCBI RH Map4758.1UniSTS
GeneMap99-G3 RH Map43566.0UniSTS
D4S399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,802,559 - 62,802,713UniSTSGRCh37
Celera460,260,641 - 60,260,795UniSTS
HuRef458,710,500 - 58,710,654UniSTS
Marshfield Genetic Map475.2RGD
Marshfield Genetic Map475.2UniSTS
Genethon Genetic Map474.1UniSTS
TNG Radiation Hybrid Map434295.0UniSTS
Whitehead-YAC Contig Map4 UniSTS
SHGC-14245  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,910,625 - 62,910,844UniSTSGRCh37
Build 36462,593,220 - 62,593,439RGDNCBI36
Celera460,368,722 - 60,368,941RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,818,623 - 58,818,842UniSTS
TNG Radiation Hybrid Map434489.0UniSTS
SHGC-59839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,937,105 - 62,937,270UniSTSGRCh37
Build 36462,619,700 - 62,619,865RGDNCBI36
Celera460,395,202 - 60,395,367RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,845,101 - 58,845,266UniSTS
GeneMap99-GB4 RH Map4371.17UniSTS
SHGC-50484  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,777,380 - 62,777,515UniSTSGRCh37
Build 36462,459,975 - 62,460,110RGDNCBI36
Celera460,235,462 - 60,235,597RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,685,321 - 58,685,456UniSTS
TNG Radiation Hybrid Map434384.0UniSTS
G01805  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,382,014 - 62,382,165UniSTSGRCh37
Build 36462,064,609 - 62,064,760RGDNCBI36
Celera459,840,843 - 59,840,993RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,290,585 - 58,290,735UniSTS
SHGC-32352  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,934,995 - 62,935,105UniSTSGRCh37
Build 36462,617,590 - 62,617,700RGDNCBI36
Celera460,393,092 - 60,393,202RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,842,991 - 58,843,101UniSTS
TNG Radiation Hybrid Map434609.0UniSTS
Stanford-G3 RH Map43590.0UniSTS
Whitehead-RH Map4390.9UniSTS
NCBI RH Map4759.6UniSTS
GeneMap99-G3 RH Map43574.0UniSTS
SHGC-51538  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,493,598 - 62,493,700UniSTSGRCh37
Build 36462,176,193 - 62,176,295RGDNCBI36
Celera459,952,443 - 59,952,545RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,402,197 - 58,402,299UniSTS
TNG Radiation Hybrid Map434067.0UniSTS
SHGC-83398  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,804,540 - 62,804,868UniSTSGRCh37
Build 36462,487,135 - 62,487,463RGDNCBI36
Celera460,262,622 - 60,262,950RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,712,481 - 58,712,810UniSTS
TNG Radiation Hybrid Map434345.0UniSTS
RH123343  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,564,503 - 62,564,848UniSTSGRCh37
Build 36462,247,098 - 62,247,443RGDNCBI36
Celera460,022,753 - 60,023,098RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,472,564 - 58,472,909UniSTS
TNG Radiation Hybrid Map434076.0UniSTS
G63159  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,877,964 - 62,878,254UniSTSGRCh37
Build 36462,560,559 - 62,560,849RGDNCBI36
Celera460,336,061 - 60,336,351RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,785,971 - 58,786,261UniSTS
TNG Radiation Hybrid Map434479.0UniSTS
D4S2778E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,571,644 - 62,571,756UniSTSGRCh37
Build 36462,254,239 - 62,254,351RGDNCBI36
Celera460,029,895 - 60,030,007RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,479,706 - 58,479,818UniSTS
D4S2559E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,937,126 - 62,937,344UniSTSGRCh37
Build 36462,619,721 - 62,619,939RGDNCBI36
Celera460,395,223 - 60,395,441RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,845,122 - 58,845,340UniSTS
SHGC-107457  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,466,694 - 62,467,002UniSTSGRCh37
Build 36462,149,289 - 62,149,597RGDNCBI36
Celera459,925,539 - 59,925,847RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,375,295 - 58,375,603UniSTS
TNG Radiation Hybrid Map434073.0UniSTS
SHGC-145295  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,697,722 - 62,698,007UniSTSGRCh37
Build 36462,380,317 - 62,380,602RGDNCBI36
Celera460,155,883 - 60,156,168RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,605,698 - 58,605,983UniSTS
TNG Radiation Hybrid Map434195.0UniSTS
1754  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,571,648 - 62,571,756UniSTSGRCh37
Build 36462,254,243 - 62,254,351RGDNCBI36
Celera460,029,899 - 60,030,007RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,479,710 - 58,479,818UniSTS
GeneMap99-GB4 RH Map4364.72UniSTS
NCBI RH Map4747.5UniSTS
SHGC-59823  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,581,491 - 62,581,659UniSTSGRCh37
Build 36462,264,086 - 62,264,254RGDNCBI36
Celera460,039,774 - 60,039,942RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,489,559 - 58,489,727UniSTS
GeneMap99-GB4 RH Map4367.63UniSTS
G16255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,690,817 - 62,691,003UniSTSGRCh37
Build 36462,373,412 - 62,373,598RGDNCBI36
Celera460,148,978 - 60,149,164RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,598,793 - 58,598,979UniSTS
REN78185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,165,096 - 210,165,196UniSTSGRCh37
GRCh372232,899,799 - 32,900,023UniSTSGRCh37
Build 362209,873,341 - 209,873,441RGDNCBI36
Celera2203,932,934 - 203,933,034RGD
Celera2216,701,971 - 16,702,195UniSTS
HuRef458,542,537 - 58,542,721UniSTS
HuRef2202,011,032 - 202,011,132UniSTS
HuRef2215,856,981 - 15,857,205UniSTS
LPHN3_9332  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,937,408 - 62,938,258UniSTSGRCh37
Build 36462,620,003 - 62,620,853RGDNCBI36
Celera460,395,505 - 60,396,355RGD
HuRef458,845,404 - 58,846,254UniSTS
SHGC-63452  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,937,249 - 62,937,343UniSTSGRCh37
Build 36462,619,844 - 62,619,938RGDNCBI36
Celera460,395,346 - 60,395,440RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,845,245 - 58,845,339UniSTS
TNG Radiation Hybrid Map434609.0UniSTS
D4S586  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,386,843 - 62,387,081UniSTSGRCh37
Build 36462,069,438 - 62,069,676RGDNCBI36
Celera459,845,686 - 59,845,924RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,295,428 - 58,295,666UniSTS
TNG Radiation Hybrid Map434054.0UniSTS
A004G27  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,777,268 - 62,777,427UniSTSGRCh37
Build 36462,459,863 - 62,460,022RGDNCBI36
Celera460,235,350 - 60,235,509RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,685,209 - 58,685,368UniSTS
GeneMap99-GB4 RH Map4364.94UniSTS
RH36109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,938,502 - 62,938,603UniSTSGRCh37
Build 36462,621,097 - 62,621,198RGDNCBI36
Celera460,396,599 - 60,396,700RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,846,498 - 58,846,599UniSTS
GeneMap99-GB4 RH Map4356.54UniSTS
NCBI RH Map4788.9UniSTS
WI-14844  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,777,330 - 62,777,530UniSTSGRCh37
Build 36462,459,925 - 62,460,125RGDNCBI36
Celera460,235,412 - 60,235,612RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,685,271 - 58,685,471UniSTS
GeneMap99-GB4 RH Map4358.88UniSTS
Whitehead-RH Map4403.5UniSTS
D4S1017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,789,709 - 62,789,859UniSTSGRCh37
Build 36462,472,304 - 62,472,454RGDNCBI36
Celera460,247,791 - 60,247,941RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,697,650 - 58,697,800UniSTS
Stanford-G3 RH Map43586.0UniSTS
NCBI RH Map4766.2UniSTS
D4S528  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,493,316 - 62,494,005UniSTSGRCh37
Build 36462,175,911 - 62,176,600RGDNCBI36
Celera459,952,161 - 59,952,850RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,401,915 - 58,402,604UniSTS
D4S472  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,365,539 - 62,365,688UniSTSGRCh37
Build 36462,048,134 - 62,048,283RGDNCBI36
Celera459,824,369 - 59,824,518RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,274,107 - 58,274,256UniSTS
TNG Radiation Hybrid Map433976.0UniSTS
D20S1010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372035,240,586 - 35,240,753UniSTSGRCh37
Build 362034,674,000 - 34,674,167RGDNCBI36
Celera2031,947,660 - 31,947,827RGD
Cytogenetic Map20qUniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map4q13.1UniSTS
HuRef2031,976,633 - 31,976,800UniSTS
GeneMap99-GB4 RH Map20203.6UniSTS
NCBI RH Map20303.0UniSTS
GeneMap99-G3 RH Map201961.0UniSTS
G09520  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,804,296 - 62,804,434UniSTSGRCh37
Build 36462,486,891 - 62,487,029RGDNCBI36
Celera460,262,378 - 60,262,516RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,712,237 - 58,712,375UniSTS
WI-21794  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,764,255 - 62,764,335UniSTSGRCh37
Build 36462,446,850 - 62,446,930RGDNCBI36
Celera460,222,340 - 60,222,420RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,672,203 - 58,672,283UniSTS
GeneMap99-GB4 RH Map4364.63UniSTS
Whitehead-RH Map4403.7UniSTS
NCBI RH Map4764.3UniSTS
SHGC4-1183  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,791,641 - 62,791,776UniSTSGRCh37
Build 36462,474,236 - 62,474,371RGDNCBI36
Celera460,249,723 - 60,249,858RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,699,582 - 58,699,717UniSTS
TNG Radiation Hybrid Map434465.0UniSTS
HUMXT00114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,571,561 - 62,571,732UniSTSGRCh37
Build 36462,254,156 - 62,254,327RGDNCBI36
Celera460,029,812 - 60,029,983RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,479,623 - 58,479,794UniSTS
TNG Radiation Hybrid Map434095.0UniSTS
Stanford-G3 RH Map43565.0UniSTS
GeneMap99-G3 RH Map43549.0UniSTS
D4S3085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,777,382 - 62,777,550UniSTSGRCh37
Build 36462,459,977 - 62,460,145RGDNCBI36
Celera460,235,464 - 60,235,632RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,685,323 - 58,685,491UniSTS
Stanford-G3 RH Map43578.0UniSTS
GeneMap99-GB4 RH Map4363.44UniSTS
Whitehead-RH Map4378.0UniSTS
Whitehead-YAC Contig Map4 UniSTS
NCBI RH Map4757.4UniSTS
GeneMap99-G3 RH Map43562.0UniSTS
SHGC-34181  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37462,943,323 - 62,943,448UniSTSGRCh37
Build 36462,625,918 - 62,626,043RGDNCBI36
Celera460,401,420 - 60,401,545RGD
Cytogenetic Map4q13.1UniSTS
HuRef458,851,319 - 58,851,444UniSTS
TNG Radiation Hybrid Map434609.0UniSTS
Stanford-G3 RH Map43603.0UniSTS
NCBI RH Map4762.0UniSTS
GeneMap99-G3 RH Map43587.0UniSTS
D4S1600  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map4q13.1UniSTS
Marshfield Genetic Map472.52UniSTS
Genethon Genetic Map471.5UniSTS
deCODE Assembly Map476.19UniSTS
Whitehead-YAC Contig Map4 UniSTS
D4S399  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map4q13.1UniSTS
TNG Radiation Hybrid Map434295.0UniSTS


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
High
Medium 15 516 5 2 11 2 930 4 977 21 66 36 131 789
Low 2217 1260 803 105 247 35 2526 1259 2506 165 1066 1106 77 1 952 1270 3
Below cutoff 127 981 836 463 868 373 858 907 229 179 262 380 93 121 729 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_033950 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001322402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371342 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371343 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371344 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371345 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371346 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387522 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387525 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387526 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387527 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387528 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387529 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387531 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387532 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387534 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387535 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387536 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387537 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387538 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387539 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387540 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387543 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387544 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387545 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387546 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387547 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387549 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387552 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_015236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011531788 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011531791 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007929 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007930 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007931 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007932 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007933 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007934 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007935 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007936 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007938 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007940 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007941 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007942 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449934 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449935 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449936 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449938 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449940 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449941 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449942 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449943 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449944 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449945 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349461 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349464 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349467 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349470 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349471 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349472 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349473 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349474 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349475 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349476 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349477 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349478 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349479 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349480 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349481 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054349482 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB018311 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC007511 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC020741 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC092643 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC092663 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC092668 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC096723 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC104813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC108161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC225889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK000781 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK094703 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294689 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299651 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309793 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC039452 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF511741 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA808156 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF457762 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF457763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000502815   ⟹   ENSP00000424402
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,895,741 - 62,072,437 (+)Ensembl
RefSeq Acc Id: ENST00000504896   ⟹   ENSP00000423434
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,497,199 - 62,071,038 (+)Ensembl
RefSeq Acc Id: ENST00000506700   ⟹   ENSP00000424120
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,497,121 - 62,071,138 (+)Ensembl
RefSeq Acc Id: ENST00000506720   ⟹   ENSP00000420931
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,497,294 - 62,071,127 (+)Ensembl
RefSeq Acc Id: ENST00000506746   ⟹   ENSP00000425884
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,497,294 - 62,071,127 (+)Ensembl
RefSeq Acc Id: ENST00000507164   ⟹   ENSP00000421476
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,497,165 - 62,070,993 (+)Ensembl
RefSeq Acc Id: ENST00000507625   ⟹   ENSP00000421372
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,497,188 - 62,071,058 (+)Ensembl
RefSeq Acc Id: ENST00000508078
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,933,843 - 61,947,077 (+)Ensembl
RefSeq Acc Id: ENST00000508693   ⟹   ENSP00000424030
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,497,165 - 62,070,993 (+)Ensembl
RefSeq Acc Id: ENST00000508946   ⟹   ENSP00000421627
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,497,294 - 62,071,127 (+)Ensembl
RefSeq Acc Id: ENST00000509089
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,587,368 - 61,677,392 (+)Ensembl
RefSeq Acc Id: ENST00000509779
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,201,664 - 61,385,769 (+)Ensembl
RefSeq Acc Id: ENST00000509896   ⟹   ENSP00000423787
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,497,121 - 62,071,138 (+)Ensembl
RefSeq Acc Id: ENST00000511324   ⟹   ENSP00000425033
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,497,121 - 62,071,138 (+)Ensembl
RefSeq Acc Id: ENST00000512091   ⟹   ENSP00000423388
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,201,258 - 62,078,335 (+)Ensembl
RefSeq Acc Id: ENST00000514157   ⟹   ENSP00000425201
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,497,199 - 62,071,038 (+)Ensembl
RefSeq Acc Id: ENST00000514591   ⟹   ENSP00000422533
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,202,142 - 62,072,466 (+)Ensembl
RefSeq Acc Id: ENST00000514996   ⟹   ENSP00000424258
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,497,294 - 62,071,127 (+)Ensembl
RefSeq Acc Id: ENST00000683033   ⟹   ENSP00000507980
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl461,200,326 - 62,078,335 (+)Ensembl
RefSeq Acc Id: NM_001322246   ⟹   NP_001309175
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
CHM1_1462,102,609 - 62,980,006 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001322402   ⟹   NP_001309331
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
CHM1_1462,102,609 - 62,980,006 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001371342   ⟹   NP_001358271
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,202,172 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,640,110 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001371343   ⟹   NP_001358272
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001371344   ⟹   NP_001358273
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001371345   ⟹   NP_001358274
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001371346   ⟹   NP_001358275
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387522   ⟹   NP_001374451
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387523   ⟹   NP_001374452
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387524   ⟹   NP_001374453
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387525   ⟹   NP_001374454
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387526   ⟹   NP_001374455
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387527   ⟹   NP_001374456
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387528   ⟹   NP_001374457
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387529   ⟹   NP_001374458
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387530   ⟹   NP_001374459
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,202,172 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,640,110 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387531   ⟹   NP_001374460
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387532   ⟹   NP_001374461
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,202,172 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,640,110 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387533   ⟹   NP_001374462
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387534   ⟹   NP_001374463
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387535   ⟹   NP_001374464
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387536   ⟹   NP_001374465
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387537   ⟹   NP_001374466
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387538   ⟹   NP_001374467
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387539   ⟹   NP_001374468
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,202,172 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,640,110 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387540   ⟹   NP_001374469
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387541   ⟹   NP_001374470
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,202,172 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,640,110 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387542   ⟹   NP_001374471
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387543   ⟹   NP_001374472
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,202,172 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,640,110 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387544   ⟹   NP_001374473
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387545   ⟹   NP_001374474
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387546   ⟹   NP_001374475
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387547   ⟹   NP_001374476
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387548   ⟹   NP_001374477
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387549   ⟹   NP_001374478
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387552   ⟹   NP_001374481
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: NM_015236   ⟹   NP_056051
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,326 - 62,078,335 (+)NCBI
GRCh37462,066,949 - 62,938,168 (+)NCBI
Build 36462,045,434 - 62,620,763 (+)NCBI Archive
HuRef458,271,407 - 58,846,164 (+)ENTREZGENE
CHM1_1462,102,609 - 62,980,006 (+)NCBI
T2T-CHM13v2.0464,638,264 - 65,515,643 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011531791   ⟹   XP_011530093
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017007929   ⟹   XP_016863418
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,251,872 - 62,078,335 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017007930   ⟹   XP_016863419
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,380,175 - 62,078,335 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017007931   ⟹   XP_016863420
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017007933   ⟹   XP_016863422
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017007934   ⟹   XP_016863423
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017007936   ⟹   XP_016863425
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017007937   ⟹   XP_016863426
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,380,175 - 62,078,335 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017007940   ⟹   XP_016863429
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017007941   ⟹   XP_016863430
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047449934   ⟹   XP_047305890
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
RefSeq Acc Id: XM_047449935   ⟹   XP_047305891
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
RefSeq Acc Id: XM_047449936   ⟹   XP_047305892
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
RefSeq Acc Id: XM_047449937   ⟹   XP_047305893
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
RefSeq Acc Id: XM_047449938   ⟹   XP_047305894
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
RefSeq Acc Id: XM_047449939   ⟹   XP_047305895
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
RefSeq Acc Id: XM_047449940   ⟹   XP_047305896
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,202,172 - 62,078,335 (+)NCBI
RefSeq Acc Id: XM_047449941   ⟹   XP_047305897
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,202,172 - 62,078,335 (+)NCBI
RefSeq Acc Id: XM_047449942   ⟹   XP_047305898
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
RefSeq Acc Id: XM_047449943   ⟹   XP_047305899
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,078,335 (+)NCBI
RefSeq Acc Id: XM_047449944   ⟹   XP_047305900
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,047,342 (+)NCBI
RefSeq Acc Id: XM_047449945   ⟹   XP_047305901
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,255,654 - 62,047,342 (+)NCBI
RefSeq Acc Id: XM_054349459   ⟹   XP_054205434
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,818,080 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349460   ⟹   XP_054205435
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,689,803 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349461   ⟹   XP_054205436
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349462   ⟹   XP_054205437
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349463   ⟹   XP_054205438
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349464   ⟹   XP_054205439
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349465   ⟹   XP_054205440
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349466   ⟹   XP_054205441
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349467   ⟹   XP_054205442
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349468   ⟹   XP_054205443
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349469   ⟹   XP_054205444
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349470   ⟹   XP_054205445
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,818,080 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349471   ⟹   XP_054205446
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349472   ⟹   XP_054205447
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349473   ⟹   XP_054205448
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349474   ⟹   XP_054205449
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,640,110 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349475   ⟹   XP_054205450
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,640,110 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349476   ⟹   XP_054205451
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,605 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349477   ⟹   XP_054205452
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349478   ⟹   XP_054205453
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349479   ⟹   XP_054205454
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349480   ⟹   XP_054205455
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,515,643 (+)NCBI
RefSeq Acc Id: XM_054349481   ⟹   XP_054205456
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,484,650 (+)NCBI
RefSeq Acc Id: XM_054349482   ⟹   XP_054205457
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0464,693,601 - 65,484,650 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001309175 (Get FASTA)   NCBI Sequence Viewer  
  NP_001309331 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358271 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358272 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358273 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358274 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358275 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374451 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374452 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374453 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374454 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374455 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374456 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374457 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374458 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374459 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374460 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374461 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374462 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374463 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374464 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374465 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374466 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374467 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374468 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374469 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374470 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374471 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374472 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374473 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374474 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374475 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374476 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374477 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374478 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374481 (Get FASTA)   NCBI Sequence Viewer  
  NP_056051 (Get FASTA)   NCBI Sequence Viewer  
  XP_011530093 (Get FASTA)   NCBI Sequence Viewer  
  XP_016863418 (Get FASTA)   NCBI Sequence Viewer  
  XP_016863419 (Get FASTA)   NCBI Sequence Viewer  
  XP_016863420 (Get FASTA)   NCBI Sequence Viewer  
  XP_016863422 (Get FASTA)   NCBI Sequence Viewer  
  XP_016863423 (Get FASTA)   NCBI Sequence Viewer  
  XP_016863425 (Get FASTA)   NCBI Sequence Viewer  
  XP_016863426 (Get FASTA)   NCBI Sequence Viewer  
  XP_016863429 (Get FASTA)   NCBI Sequence Viewer  
  XP_016863430 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305890 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305891 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305892 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305893 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305894 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305895 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305896 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305897 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305898 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305899 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305900 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305901 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205434 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205435 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205436 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205437 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205438 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205439 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205440 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205441 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205442 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205443 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205444 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205445 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205446 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205447 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205448 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205449 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205450 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205451 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205452 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205453 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205454 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205455 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205456 (Get FASTA)   NCBI Sequence Viewer  
  XP_054205457 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAY40992 (Get FASTA)   NCBI Sequence Viewer  
  BAA34488 (Get FASTA)   NCBI Sequence Viewer  
  BAA91375 (Get FASTA)   NCBI Sequence Viewer  
  BAH11848 (Get FASTA)   NCBI Sequence Viewer  
  BAH13089 (Get FASTA)   NCBI Sequence Viewer  
  EAX05525 (Get FASTA)   NCBI Sequence Viewer  
  EAX05526 (Get FASTA)   NCBI Sequence Viewer  
  EAX05527 (Get FASTA)   NCBI Sequence Viewer  
  EAX05528 (Get FASTA)   NCBI Sequence Viewer  
  EAX05529 (Get FASTA)   NCBI Sequence Viewer  
  EAX05530 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000420931
  ENSP00000420931.1
  ENSP00000421372
  ENSP00000421372.1
  ENSP00000421476
  ENSP00000421476.1
  ENSP00000421627
  ENSP00000421627.1
  ENSP00000422533
  ENSP00000422533.1
  ENSP00000423388
  ENSP00000423388.1
  ENSP00000423434
  ENSP00000423434.1
  ENSP00000423787
  ENSP00000423787.1
  ENSP00000424030.1
  ENSP00000424120
  ENSP00000424120.1
  ENSP00000424258
  ENSP00000424258.1
  ENSP00000424402.1
  ENSP00000425033
  ENSP00000425033.1
  ENSP00000425201.1
  ENSP00000425884.1
  ENSP00000507980
  ENSP00000507980.1
GenBank Protein Q9HAR2 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_056051   ⟸   NM_015236
- Peptide Label: isoform 2 precursor
- UniProtKB: E7EW95 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011530093   ⟸   XM_011531791
- Peptide Label: isoform X12
- UniProtKB: E7ETE3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001309331   ⟸   NM_001322402
- Peptide Label: isoform 1 precursor
- UniProtKB: E7ETE3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001309175   ⟸   NM_001322246
- Peptide Label: isoform 3 precursor
- UniProtKB: E7EMR3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016863418   ⟸   XM_017007929
- Peptide Label: isoform X1
- UniProtKB: E7ETE3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016863420   ⟸   XM_017007931
- Peptide Label: isoform X2
- UniProtKB: E7EUW2 (UniProtKB/TrEMBL),   E7ETE3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016863429   ⟸   XM_017007940
- Peptide Label: isoform X16
- UniProtKB: E7EUP0 (UniProtKB/TrEMBL),   E7EN28 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016863430   ⟸   XM_017007941
- Peptide Label: isoform X18
- UniProtKB: E7ESV6 (UniProtKB/TrEMBL),   E7EX52 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016863422   ⟸   XM_017007933
- Peptide Label: isoform X6
- UniProtKB: E7ETE3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016863425   ⟸   XM_017007936
- Peptide Label: isoform X8
- UniProtKB: E7ETE3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016863423   ⟸   XM_017007934
- Peptide Label: isoform X7
- UniProtKB: E7ETE3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016863419   ⟸   XM_017007930
- Peptide Label: isoform X1
- UniProtKB: E7ETE3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016863426   ⟸   XM_017007937
- Peptide Label: isoform X11
- UniProtKB: E7EW95 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001358272   ⟸   NM_001371343
- Peptide Label: isoform 5 precursor
- UniProtKB: E7ETE3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358273   ⟸   NM_001371344
- Peptide Label: isoform 6 precursor
- UniProtKB: E7EVD6 (UniProtKB/TrEMBL),   E7ETE3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358274   ⟸   NM_001371345
- Peptide Label: isoform 7 precursor
- UniProtKB: E7ETE3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358275   ⟸   NM_001371346
- Peptide Label: isoform 8 precursor
- UniProtKB: E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358271   ⟸   NM_001371342
- Peptide Label: isoform 4 precursor
- UniProtKB: E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000424402   ⟸   ENST00000502815
RefSeq Acc Id: ENSP00000423434   ⟸   ENST00000504896
RefSeq Acc Id: ENSP00000424120   ⟸   ENST00000506700
RefSeq Acc Id: ENSP00000420931   ⟸   ENST00000506720
RefSeq Acc Id: ENSP00000425884   ⟸   ENST00000506746
RefSeq Acc Id: ENSP00000421476   ⟸   ENST00000507164
RefSeq Acc Id: ENSP00000421372   ⟸   ENST00000507625
RefSeq Acc Id: ENSP00000424030   ⟸   ENST00000508693
RefSeq Acc Id: ENSP00000421627   ⟸   ENST00000508946
RefSeq Acc Id: ENSP00000423787   ⟸   ENST00000509896
RefSeq Acc Id: ENSP00000425033   ⟸   ENST00000511324
RefSeq Acc Id: ENSP00000423388   ⟸   ENST00000512091
RefSeq Acc Id: ENSP00000425201   ⟸   ENST00000514157
RefSeq Acc Id: ENSP00000422533   ⟸   ENST00000514591
RefSeq Acc Id: ENSP00000424258   ⟸   ENST00000514996
RefSeq Acc Id: NP_001374481   ⟸   NM_001387552
- Peptide Label: isoform 23 precursor
- UniProtKB: A0A804HKL8 (UniProtKB/TrEMBL),   E7ETE3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374451   ⟸   NM_001387522
- Peptide Label: isoform 6 precursor
- UniProtKB: E7EVD6 (UniProtKB/TrEMBL),   E7ETE3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374452   ⟸   NM_001387523
- Peptide Label: isoform 9 precursor
- UniProtKB: E7ETE3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374453   ⟸   NM_001387524
- Peptide Label: isoform 25 precursor
- UniProtKB: E7ETE3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374463   ⟸   NM_001387534
- Peptide Label: isoform 13 precursor
- UniProtKB: E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374467   ⟸   NM_001387538
- Peptide Label: isoform 15 precursor
- UniProtKB: Q9HAR2 (UniProtKB/Swiss-Prot),   O94867 (UniProtKB/Swiss-Prot),   E9PE04 (UniProtKB/Swiss-Prot),   Q9NWK5 (UniProtKB/Swiss-Prot),   E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374477   ⟸   NM_001387548
- Peptide Label: isoform 21 precursor
- UniProtKB: E7EMR3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374465   ⟸   NM_001387536
- Peptide Label: isoform 14 precursor
- UniProtKB: E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374469   ⟸   NM_001387540
- Peptide Label: isoform 24 precursor
- UniProtKB: E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374473   ⟸   NM_001387544
- Peptide Label: isoform 18
- UniProtKB: E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374474   ⟸   NM_001387545
- Peptide Label: isoform 19 precursor
- UniProtKB: E7EUP0 (UniProtKB/TrEMBL),   E7EN28 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374454   ⟸   NM_001387525
- Peptide Label: isoform 5 precursor
- UniProtKB: E7ETE3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374476   ⟸   NM_001387547
- Peptide Label: isoform 3 precursor
- UniProtKB: E7EMR3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374457   ⟸   NM_001387528
- Peptide Label: isoform 26 precursor
- UniProtKB: E7EW95 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374458   ⟸   NM_001387529
- Peptide Label: isoform 2 precursor
- UniProtKB: E7EW95 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374462   ⟸   NM_001387533
- Peptide Label: isoform 13 precursor
- UniProtKB: E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374466   ⟸   NM_001387537
- Peptide Label: isoform 15 precursor
- UniProtKB: Q9HAR2 (UniProtKB/Swiss-Prot),   O94867 (UniProtKB/Swiss-Prot),   E9PE04 (UniProtKB/Swiss-Prot),   Q9NWK5 (UniProtKB/Swiss-Prot),   E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374455   ⟸   NM_001387526
- Peptide Label: isoform 10 precursor
- UniProtKB: E7EW95 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374460   ⟸   NM_001387531
- Peptide Label: isoform 12 precursor
- UniProtKB: E7EW95 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374456   ⟸   NM_001387527
- Peptide Label: isoform 11 precursor
- UniProtKB: E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374478   ⟸   NM_001387549
- Peptide Label: isoform 22 precursor
- UniProtKB: E7EMR3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374464   ⟸   NM_001387535
- Peptide Label: isoform 14 precursor
- UniProtKB: E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374475   ⟸   NM_001387546
- Peptide Label: isoform 20 precursor
- UniProtKB: E7ENK1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374471   ⟸   NM_001387542
- Peptide Label: isoform 17 precursor
- UniProtKB: E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374468   ⟸   NM_001387539
- Peptide Label: isoform 15 precursor
- UniProtKB: Q9HAR2 (UniProtKB/Swiss-Prot),   O94867 (UniProtKB/Swiss-Prot),   E9PE04 (UniProtKB/Swiss-Prot),   Q9NWK5 (UniProtKB/Swiss-Prot),   E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374461   ⟸   NM_001387532
- Peptide Label: isoform 12 precursor
- UniProtKB: E7EW95 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374459   ⟸   NM_001387530
- Peptide Label: isoform 12 precursor
- UniProtKB: E7EW95 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374472   ⟸   NM_001387543
- Peptide Label: isoform 18
- UniProtKB: E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374470   ⟸   NM_001387541
- Peptide Label: isoform 16
- UniProtKB: E9PBG4 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000507980   ⟸   ENST00000683033
RefSeq Acc Id: XP_047305896   ⟸   XM_047449940
- Peptide Label: isoform X14
RefSeq Acc Id: XP_047305897   ⟸   XM_047449941
- Peptide Label: isoform X15
RefSeq Acc Id: XP_047305891   ⟸   XM_047449935
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047305890   ⟸   XM_047449934
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047305898   ⟸   XM_047449942
- Peptide Label: isoform X17
RefSeq Acc Id: XP_047305899   ⟸   XM_047449943
- Peptide Label: isoform X19
RefSeq Acc Id: XP_047305893   ⟸   XM_047449937
- Peptide Label: isoform X9
RefSeq Acc Id: XP_047305892   ⟸   XM_047449936
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047305894   ⟸   XM_047449938
- Peptide Label: isoform X10
RefSeq Acc Id: XP_047305895   ⟸   XM_047449939
- Peptide Label: isoform X13
RefSeq Acc Id: XP_047305900   ⟸   XM_047449944
- Peptide Label: isoform X20
RefSeq Acc Id: XP_047305901   ⟸   XM_047449945
- Peptide Label: isoform X21
RefSeq Acc Id: XP_054205449   ⟸   XM_054349474
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054205450   ⟸   XM_054349475
- Peptide Label: isoform X15
RefSeq Acc Id: XP_054205435   ⟸   XM_054349460
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054205436   ⟸   XM_054349461
- Peptide Label: isoform X2
- UniProtKB: E7EUW2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054205452   ⟸   XM_054349477
- Peptide Label: isoform X16
- UniProtKB: E7EUP0 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054205454   ⟸   XM_054349479
- Peptide Label: isoform X18
- UniProtKB: E7ESV6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054205440   ⟸   XM_054349465
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054205442   ⟸   XM_054349467
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054205438   ⟸   XM_054349463
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054205446   ⟸   XM_054349471
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054205437   ⟸   XM_054349462
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054205453   ⟸   XM_054349478
- Peptide Label: isoform X17
RefSeq Acc Id: XP_054205441   ⟸   XM_054349466
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054205455   ⟸   XM_054349480
- Peptide Label: isoform X19
RefSeq Acc Id: XP_054205443   ⟸   XM_054349468
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054205439   ⟸   XM_054349464
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054205444   ⟸   XM_054349469
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054205447   ⟸   XM_054349472
- Peptide Label: isoform X22
RefSeq Acc Id: XP_054205448   ⟸   XM_054349473
- Peptide Label: isoform X13
RefSeq Acc Id: XP_054205456   ⟸   XM_054349481
- Peptide Label: isoform X20
RefSeq Acc Id: XP_054205457   ⟸   XM_054349482
- Peptide Label: isoform X21
RefSeq Acc Id: XP_054205451   ⟸   XM_054349476
- Peptide Label: isoform X23
RefSeq Acc Id: XP_054205434   ⟸   XM_054349459
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054205445   ⟸   XM_054349470
- Peptide Label: isoform X11
Protein Domains
G-protein coupled receptors family 2 profile   GPS   Olfactomedin-like   SUEL-type lectin

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9HAR2-F1-model_v2 AlphaFold Q9HAR2 1-1447 view protein structure

Promoters
RGD ID:6867548
Promoter ID:EPDNEW_H6939
Type:initiation region
Name:ADGRL3_3
Description:adhesion G protein-coupled receptor L3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H6940  EPDNEW_H6941  EPDNEW_H6942  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,075 - 61,200,135EPDNEW
RGD ID:6867550
Promoter ID:EPDNEW_H6940
Type:initiation region
Name:ADGRL3_2
Description:adhesion G protein-coupled receptor L3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H6939  EPDNEW_H6941  EPDNEW_H6942  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,710 - 61,200,770EPDNEW
RGD ID:6867552
Promoter ID:EPDNEW_H6941
Type:initiation region
Name:ADGRL3_4
Description:adhesion G protein-coupled receptor L3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H6939  EPDNEW_H6940  EPDNEW_H6942  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,200,912 - 61,200,972EPDNEW
RGD ID:6867554
Promoter ID:EPDNEW_H6942
Type:initiation region
Name:ADGRL3_1
Description:adhesion G protein-coupled receptor L3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H6939  EPDNEW_H6940  EPDNEW_H6941  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38461,201,231 - 61,201,291EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:20974 AgrOrtholog
COSMIC ADGRL3 COSMIC
Ensembl Genes ENSG00000150471 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000502815.1 UniProtKB/TrEMBL
  ENST00000504896 ENTREZGENE
  ENST00000504896.5 UniProtKB/TrEMBL
  ENST00000506700 ENTREZGENE
  ENST00000506700.5 UniProtKB/TrEMBL
  ENST00000506720 ENTREZGENE
  ENST00000506720.5 UniProtKB/TrEMBL
  ENST00000506746.5 UniProtKB/TrEMBL
  ENST00000507164 ENTREZGENE
  ENST00000507164.5 UniProtKB/TrEMBL
  ENST00000507625 ENTREZGENE
  ENST00000507625.5 UniProtKB/TrEMBL
  ENST00000508693.5 UniProtKB/TrEMBL
  ENST00000508946 ENTREZGENE
  ENST00000508946.5 UniProtKB/TrEMBL
  ENST00000509896 ENTREZGENE
  ENST00000509896.5 UniProtKB/TrEMBL
  ENST00000511324 ENTREZGENE
  ENST00000511324.5 UniProtKB/TrEMBL
  ENST00000512091 ENTREZGENE
  ENST00000512091.6 UniProtKB/Swiss-Prot
  ENST00000514157.5 UniProtKB/TrEMBL
  ENST00000514591 ENTREZGENE
  ENST00000514591.5 UniProtKB/Swiss-Prot
  ENST00000514996 ENTREZGENE
  ENST00000514996.5 UniProtKB/TrEMBL
  ENST00000683033 ENTREZGENE
  ENST00000683033.1 UniProtKB/TrEMBL
Gene3D-CATH 1.25.40.610 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.60.120.740 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 ENSG00000150471 GTEx
HGNC ID HGNC:20974 ENTREZGENE
Human Proteome Map ADGRL3 Human Proteome Map
InterPro 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_extracell_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_2_extracellular_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_2_latrophilin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_2_latrophilin_rcpt_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_2_secretin-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_2_secretin-like_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Lectin_gal-bd_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Lectin_gal-bd_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Olfac-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:23284 UniProtKB/Swiss-Prot
NCBI Gene 23284 ENTREZGENE
OMIM 616417 OMIM
PANTHER ADHESION G-PROTEIN COUPLED RECEPTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR12011:SF60 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam 7tm_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Gal_Lectin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HRM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Latrophilin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OLF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134968284 PharmGKB
PRINTS GPCRSECRETIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  LATROPHILIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE G_PROTEIN_RECEP_F2_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  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
  OLF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SUEL_LECTIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART GPS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HormR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OLF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Family A G protein-coupled receptor-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A804HKL8 ENTREZGENE, UniProtKB/TrEMBL
  AGRL3_HUMAN UniProtKB/Swiss-Prot
  B7Z2G2_HUMAN UniProtKB/TrEMBL
  E7EMR3 ENTREZGENE, UniProtKB/TrEMBL
  E7EN28 ENTREZGENE, UniProtKB/TrEMBL
  E7ENK1 ENTREZGENE, UniProtKB/TrEMBL
  E7ES20_HUMAN UniProtKB/TrEMBL
  E7ESV6 ENTREZGENE, UniProtKB/TrEMBL
  E7ETE3 ENTREZGENE, UniProtKB/TrEMBL
  E7EUP0 ENTREZGENE, UniProtKB/TrEMBL
  E7EUW2 ENTREZGENE, UniProtKB/TrEMBL
  E7EVD6 ENTREZGENE, UniProtKB/TrEMBL
  E7EW95 ENTREZGENE, UniProtKB/TrEMBL
  E7EX52 ENTREZGENE, UniProtKB/TrEMBL
  E9PBG4 ENTREZGENE, UniProtKB/TrEMBL
  E9PE04 ENTREZGENE
  H0Y9K5_HUMAN UniProtKB/TrEMBL
  O94867 ENTREZGENE
  Q9HAR2 ENTREZGENE
  Q9NWK5 ENTREZGENE
UniProt Secondary E9PE04 UniProtKB/Swiss-Prot
  O94867 UniProtKB/Swiss-Prot
  Q9NWK5 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-03-10 ADGRL3  adhesion G protein-coupled receptor L3  LPHN3  latrophilin 3  Symbol and/or name change 5135510 APPROVED