ADGRL1 - adhesion G protein-coupled receptor L1 Gene

Also Known as CL1; LEC2; CIRL1; LPHN1; DEDBANP

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 22859

About ADGRL1

Cytogenetic location: 19p13.12 Genomic coordinates (GRCh38): 19:14,147,743-14,206,169 (from NCBI)

This gene has 8 transcripts (splice variants), 1 gene allele, 211 orthologues and 42 paralogues. Broad expression in brain (RPKM 19.5), fat (RPKM 7.9) and 22 other tissues.

Summary

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 cysteine-rich GPS (G-protein-coupled-receptor proteolysis site) domain resulted in two subunits (a large extracellular N-terminal cell adhesion subunit and a subunit with substantial similarity to the secretin/Calcitonin family of GPCRs) being non-covalently bound at the cell membrane. Latrophilin-1 has been shown to recruit the neurotoxin from black widow spider venom, alpha-latrotoxin, to the synapse plasma membrane. Alternative splicing results in multiple variants encoding distinct isoforms.[provided by RefSeq, Oct 2008]

ADGRL1 Products (2)

mRNA Protein Name
NM_001008701.3 NP_001008701.1 adhesion G protein-coupled receptor L1 isoform 1 precursor
NM_014921.5 NP_055736.2 adhesion G protein-coupled receptor L1 isoform 2 precursor
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
21078624 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ADGRL1 Protein Structure

Gal_Lectin

Gal_Lectin: Galactose binding lectin domain (48 - 128)

OLF

OLF: Olfactomedin-like domain (144 - 397)

HRM

HRM: Hormone receptor domain (478 - 534)

(542 - 775)

GPS

GPS: GPCR proteolysis site, GPS, motif (799 - 845)

7tm_2

7tm_2: 7 transmembrane receptor (Secretin family) (859 - 1093)

Latrophilin

Latrophilin: Latrophilin Cytoplasmic C-terminal region (1113 - 1474)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1474 a.a.
Protein Preferred Names Protein Names

adhesion G protein-coupled receptor L1

  • CIRL-1

Related Diseases

Diseases Alias
Developmental Delay, Behavioral Abnormalities, And Neuropsychiatric Disorders
  • DEDBANP

Specific Learning Disability
  • Specific Learning Difficulty

  • Specific Learning Disorder

Attention Deficit-Hyperactivity Disorder
  • Attention Deficit Hyperactivity Disorder

  • ADHD

  • Attention Deficit Disorder

  • Attention Deficit-Hyperactivity Disorder, Susceptibility To

  • Attention Deficit Disorder With Hyperactivity

  • Hyperkinetic Disorder

  • Hyperactivity Of Childhood

  • Attention-Deficit/Hyperactivity Disorder

  • Add

  • Addh

  • Attention Deficit

  • Attention Deficit Disorder Of Childhood With Hyperactivity

  • Attention Deficit Disorder With Hyperactivity Syndrome

  • Hyperkinetic Syndrome

  • Attention-Deficit Hyperactivity Disorder

  • Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type

  • Disturbance Of Activity And Attention

  • Disorder Of Activity And Attention

  • Adhd - [Attention Deficit Hyperactivity Disorder]

  • Hyperkinetic Disorders

  • Disorder Of Activity And Attention With Hyperkinesia

  • Attention Deficit Syndrome With Hyperactivity

Loiasis
  • Loa Loa Filariasis

  • Mansonelliasis

  • African Eye Worm

  • Mansonella Perstans Infections

  • Mansonellosis

  • Eye Worm Disease Of Africa

  • Loa Loa Infestation

  • African Eyeworm Disease

  • Calabar Swelling

Polymicrogyria, Bilateral Frontoparietal
  • Bilateral Frontoparietal Polymicrogyria

  • BFPP

  • Cerebellar Ataxia With Neuronal Migration Defect

Congenital Disorder Of Glycosylation, Type In
  • Congenital Disorder Of Glycosylation

  • CDG1N

  • Congenital Disorders Of Glycosylation

  • Cdg In

  • Cdgin

  • Congenital Disorder Of Glycosylation 1n

  • Carbohydrate-Deficient Glycoprotein Syndrome

  • Cdg

  • Rft1-Cdg

  • Cdg-In

  • Congenital Disorder Of Glycosylation Type In

  • Carbohydrate Deficient Glycoprotein Syndrome

  • Cdg Syndrome

  • Congenital Disorder Of Glycosylation In

  • Carbohydrate-Deficient Glycoprotein Syndromes

  • Cdg Syndrome Type In

  • Carbohydrate Deficient Glycoprotein Syndrome Type In

  • Congenital Disorder Of Glycosylation Type 1n

  • Man5glcnac2-Pp-Dol Flippase Deficiency

  • Glycosylation, Congenital Disorder Of

  • Glycosylation, Congenital Disorder Of, Type In

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus ADGRL1 VGNC VGNC:59638
Mus musculus ADGRL1 MGD MGI:1929461
Rattus norvegicus ADGRL1 RGD RGD:620768
Canis familiaris ADGRL1 VGNC VGNC:37650
Macaca mulatta ADGRL1 VGNC VGNC:69658
Bos taurus ADGRL1 VGNC VGNC:25671
Others ADGRL1 NCBI