Gene Gene information from NCBI Gene database.
Entrez ID 23266
Gene name Adhesion G protein-coupled receptor L2
Gene symbol ADGRL2
Synonyms (NCBI Gene)
CIRL2CL2LEC1LPHH1LPHN2
Chromosome 1
Chromosome location 1p31.1
Summary This gene encodes a member of the latrophilin subfamily of G-protein coupled receptors. The encoded protein participates in the regulation of exocytosis. The proprotein is thought to be further cleaved within a cysteine-rich G-protein-coupled receptor pro
miRNA miRNA information provided by mirtarbase database.
134
miRTarBase ID miRNA Experiments Reference
MIRT740666 hsa-miR-1277-5p HITS-CLIP 21572407
MIRT740667 hsa-miR-5011-5p HITS-CLIP 21572407
MIRT740668 hsa-miR-656-3p HITS-CLIP 21572407
MIRT740669 hsa-miR-190a-3p HITS-CLIP 21572407
MIRT740670 hsa-miR-3924 HITS-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
21
GO ID Ontology Definition Evidence Reference
GO:0004888 Function Transmembrane signaling receptor activity IEA
GO:0004930 Function G protein-coupled receptor activity IBA
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0004930 Function G protein-coupled receptor activity TAS 15203201
GO:0005886 Component Plasma membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607018 18582 ENSG00000117114
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O95490
Protein name Adhesion G protein-coupled receptor L2 (Calcium-independent alpha-latrotoxin receptor 2) (CIRL-2) (Latrophilin homolog 1) (Latrophilin-2) (Lectomedin-1)
Protein function Orphan adhesion G-protein coupled receptor (aGPCR), which mediates synapse specificity (By similarity). Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the ac
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02140 Gal_Lectin 49 129 Galactose binding lectin domain Domain
PF02191 OLF 140 392 Olfactomedin-like domain Family
PF02793 HRM 466 524 Hormone receptor domain Family
PF16489 GAIN 538 760 GPCR-Autoproteolysis INducing (GAIN) domain Domain
PF01825 GPS 786 830 GPCR proteolysis site, GPS, motif Motif
PF00002 7tm_2 844 1080 7 transmembrane receptor (Secretin family) Family
PF02354 Latrophilin 1100 1459 Latrophilin Cytoplasmic C-terminal region Family
Tissue specificity TISSUE SPECIFICITY: Expressed very widely in all normal tissues tested. Expression is variable in tumor cell lines, apparently elevated in some lines and absent or markedly reduced in others. {ECO:0000269|PubMed:10030676}.
Sequence
MVSSGCRMRSLWFIIVISFLPNTEGFSRAALPFGLVRRELSCEGYSIDLRCPGSDVIMIE
SANYGRTDDKICDADPFQMENTDCYLPDAFKIMTQRCNNRTQCIVVTGSDVFPDPCPGTY
KYLEVQYEC
VPYIFVCPGTLKAIVDSPCIYEAEQKAGAWCKDPLQAADKIYFMPWTPYRT
DTLIEYASLEDFQNSRQTTTYKLPNRVDGTGFVVYDGAVFFNKERTRNIVKFDLRTRIKS
GEAIINYANYHDTSPYRWGGKTDIDLAVDENGLWVIYATEQNNGMIVISQLNPYTLRFEA
TWETVYDKRAASNAFMICGVLYVVRSVYQDNESETGKNSIDYIYNTRLNRGEYVDVPFPN
QYQYIAAVDYNPRDNQLYVWNNNFILRYSLEF
GPPDPAQVPTTAVTITSSAELFKTIIST
TSTTSQKGPMSTTVAGSQEGSKGTKPPPAVSTTKIPPITNIFPLPERFCEALDSKGIKWP
QTQRGMMVERPCPKGTRGTASYLCMISTGTWNPKGPDLSNCTSH
WVNQLAQKIRSGENAA
SLANELAKHTKGPVFAGDVSSSVRLMEQLVDILDAQLQELKPSEKDSAGRSYNKLQKREK
TCRAYLKAIVDTVDNLLRPEALESWKHMNSSEQAHTATMLLDTLEEGAFVLADNLLEPTR
VSMPTENIVLEVAVLSTEGQIQDFKFPLGIKGAGSSIQLSANTVKQNSRNGLAKLVFIIY
RSLGQFLSTENATIKLGADFIGRNSTIAVNSHVISVSINK
ESSRVYLTDPVLFTLPHIDP
DNYFNANCSFWNYSERTMMGYWSTQGCKLVDTNKTRTTCACSHLTNFAILMAHREIAYKD
GVHELLLTVITWVGIVISLVCLAICIFTFCFFRGLQSDRNTIHKNLCINLFIAEFIFLIG
IDKTKYAIACPIFAGLLHFFFLAAFAWMCLEGVQLYLMLVEVFESEYSRKKYYYVAGYLF
PATVVGVSAAIDYKSYGTEKACWLHVDNYFIWSFIGPVTFIILLNIIFLVITLCKMVKHS
NTLKPDSSRLENIKSWVLGAFALLCLLGLTWSFGLLFINEETIVMAYLFTIFNAFQGVFI

FIFHCALQKKVRKEYGKCFRHSYCCGGLPTESPHSSVKASTTRTSARYSSGTQSRIRRMW
NDTVRKQSESSFISGDINSTSTLNQGMTGNYLLTNPLLRPHGTNNPYNTLLAETVVCNAP
SAPVFNSPGHSLNNARDTSAMDTLPLNGNFNNSYSLHKGDYNDSVQVVDCGLSLNDTAFE
KMIISELVHNNLRGSSKTHNLELTLPVKPVIGGSSSEDDAIVADASSLMHSDNPGLELHH
KELEAPLIPQRTHSLLYQPQKKVKSEGTDSYVSQLTAEAEDHLQSPNRDSLYTSMPNLRD
SPYPESSPDMEEDLSPSRRSENEDIYYKSMPNLGAGHQLQMCYQISRGNSDGYIIPINKE
GCIPEGDVREGQMQLVTSL
Sequence length 1459
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
33
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
ADGRL2-related disorder Uncertain significance; Likely benign; Benign rs142415541, rs149165038, rs150187776, rs201068501, rs757239872, rs41292984, rs368142284, rs372868281, rs74098542, rs774334338, rs183237089, rs764749995, rs148181687, rs72719419, rs142267708
View all (14 more)
RCV003918956
RCV003966342
RCV003906714
RCV003921897
RCV003911741
RCV003914232
RCV003909668
RCV003947340
RCV003919392
RCV003931646
RCV003941707
RCV003959385
RCV003944510
RCV003924437
RCV003936918
RCV003937168
RCV003922091
RCV003942230
RCV003949129
RCV003937385
RCV003964314
RCV003976940
RCV003971622
RCV003971779
RCV003976693
RCV003966821
RCV003981347
RCV003926115
RCV003916221
Cholangiocarcinoma Likely benign rs141656433 RCV005933466
Colon adenocarcinoma Likely benign rs141656433 RCV005933463
Gastric cancer Likely benign rs141656433 RCV005933465
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 22479588
Colonic Neoplasms Associate 26511811
Depressive Disorder Associate 34972135
Dyspepsia Associate 29143724
Emphysema Associate 28459279
Gastrointestinal Neoplasms Associate 26511811
Inflammation Associate 30332657
Neoplasms Associate 26511811
Orofacial Cleft 1 Associate 26868259
Stomach Neoplasms Associate 26511811