Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23284
Gene name Gene Name - the full gene name approved by the HGNC.
Adhesion G protein-coupled receptor L3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ADGRL3
Synonyms (NCBI Gene) Gene synonyms aliases
CIRL3, CL3, LEC3, LPHN3
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q13.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the latrophilin subfamily of G-protein coupled receptors (GPCR). Latrophilins may function in both cell adhesion and signal transduction. In experiments with non-human species, endogenous proteolytic cleavage within a cystein
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT740396 hsa-miR-7844-5p HITS-CLIP 19536157
MIRT740397 hsa-miR-5683 HITS-CLIP 19536157
MIRT740398 hsa-miR-1245b-3p HITS-CLIP 19536157
MIRT740399 hsa-miR-3682-3p HITS-CLIP 19536157
MIRT740400 hsa-miR-4775 HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001764 Process Neuron migration ISS
GO:0004930 Function G protein-coupled receptor activity IBA 21873635
GO:0004930 Function G protein-coupled receptor activity NAS 10994649
GO:0005509 Function Calcium ion binding IDA 26235030
GO:0005515 Function Protein binding IPI 26235030
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616417 20974 ENSG00000150471
Protein
UniProt ID Q9HAR2
Protein name Adhesion G protein-coupled receptor L3 (Calcium-independent alpha-latrotoxin receptor 3) (CIRL-3) (Latrophilin-3) (Lectomedin-3)
Protein function Orphan adhesion G-protein coupled receptor (aGPCR), which mediates synapse specificity (PubMed:35418682). Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the
PDB 5CMN , 6VHH , 7SF7 , 8DJG
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02140 Gal_Lectin 43 123 Galactose binding lectin domain Domain
PF02191 OLF 139 391 Olfactomedin-like domain Family
PF16489 GAIN 567 775 GPCR-Autoproteolysis INducing (GAIN) domain Domain
PF01825 GPS 803 847 GPCR proteolysis site, GPS, motif Motif
PF00002 7tm_2 861 1097 7 transmembrane receptor (Secretin family) Family
PF02354 Latrophilin 1117 1184 Latrophilin Cytoplasmic C-terminal region Family
PF02354 Latrophilin 1181 1447 Latrophilin Cytoplasmic C-terminal region Family
Sequence
MWPSQLLIFMMLLAPIIHAFSRAPIPMAVVRRELSCESYPIELRCPGTDVIMIESANYGR
TDDKICDSDPAQMENIRCYLPDAYKIMSQRCNNRTQCAVVAGPDVFPDPCPGTYKYLEVQ
YEC
VPYKVEQKVFLCPGLLKGVYQSEHLFESDHQSGAWCKDPLQASDKIYYMPWTPYRTD
TLTEYSSKDDFIAGRPTTTYKLPHRVDGTGFVVYDGALFFNKERTRNIVKFDLRTRIKSG
EAIIANANYHDTSPYRWGGKSDIDLAVDENGLWVIYATEQNNGKIVISQLNPYTLRIEGT
WDTAYDKRSASNAFMICGILYVVKSVYEDDDNEATGNKIDYIYNTDQSKDSLVDVPFPNS
YQYIAAVDYNPRDNLLYVWNNYHVVKYSLDF
GPLDSRSGQAHHGQVSYISPPIHLDSELE
RPSVKDISTTGPLGMGSTTTSTTLRTTTLSPGRSTTPSVSGRRNRSTSTPSPAVEVLDDM
TTHLPSASSQIPALEESCEAVEAREIMWFKTRQGQIAKQPCPAGTIGVSTYLCLAPDGIW
DPQGPDLSNCSSPWVNHITQKLKSGETAANIARELAEQTRNHLNAGDITYSVRAMDQLVG
LLDVQLRNLTPGGKDSAARSLNKAMVETVNNLLQPQALNAWRDLTTSDQLRAATMLLHTV
EESAFVLADNLLKTDIVRENTDNIKLEVARLSTEGNLEDLKFPENMGHGSTIQLSANTLK
QNGRNGEIRVAFVLYNNLGPYLSTENASMKLGTEALSTNHSVIVNSPVITAAINK
EFSNK
VYLADPVVFTVKHIKQSEENFNPNCSFWSYSKRTMTGYWSTQGCRLLTTNKTHTTCSCNH
LTNFAVL
MAHVEVKHSDAVHDLLLDVITWVGILLSLVCLLICIFTFCFFRGLQSDRNTIH
KNLCISLFVAELLFLIGINRTDQPIACAVFAALLHFFFLAAFTWMFLEGVQLYIMLVEVF
ESEHSRRKYFYLVGYGMPALIVAVSAAVDYRSYGTDKVCWLRLDTYFIWSFIGPATLIIM
LNVIFLGIALYKMFHHTAILKPESGCLDNIKSWVIGAIALLCLLGLTWAFGLMYINESTV
IMAYLFTIFNSLQGMFI
FIFHCVLQKKVRKEYGKCLRTHCCSGKSTESSIGSGKTSGSRT
PGRYSTGSQSRIRRMWNDTVRKQSESSFITGDINSSASLN
REGLLNNARDTSVMDTLPLN
GNHGNSYSIASGEYLSNCVQIIDRGYNHNETALEKKILKELTSNYIPSYLNNHERSSEQN
RNLMNKLVNNLGSGREDDAIVLDDATSFNHEESLGLELIHEESDAPLLPPRVYSTENHQP
HHYTRRRIPQDHSESFFPLLTNEHTEDLQSPHRDSLYTSMPTLAGVAATESVTTSTQTEP
PPAKCGDAEDVYYKSMPNLGSRNHVHQLHTYYQLGRGSSDGFIVPPNKDGTPPEGSSKGP
AHLVTSL
Sequence length 1447
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Attention deficit hyperactivity disorder Attention Deficit Disorder, Attention deficit hyperactivity disorder rs786205019 22405201
Diabetes mellitus Diabetes Mellitus, Non-Insulin-Dependent rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
23670970
Unknown
Disease term Disease name Evidence References Source
Ischemic Stroke Ischemic Stroke GWAS
Coronary artery disease Coronary artery disease GWAS
Myocardial Infarction Myocardial Infarction GWAS
Kidney Disease Kidney Disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Astrocytoma Associate 27692237
Attention Deficit and Disruptive Behavior Disorders Associate 30696812
Attention Deficit Disorder with Hyperactivity Associate 20157310, 21040458, 21606926, 22832519, 23190410, 23245769, 25989180, 26598068, 26746237, 27692237, 28624582, 28871191, 30696812, 31426340, 33504901
View all (2 more)
Bicuspid Aortic Valve Disease Associate 21309044
Breast Neoplasms Associate 23317273, 39948777
Breast Neoplasms Inhibit 33247693
Carcinoma Intraductal Noninfiltrating Associate 26718977
Cutis Laxa Autosomal Dominant Associate 21309044
Disruptive Impulse Control and Conduct Disorders Associate 28624582
Dyslexia Associate 23190410