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  2. ADGRL1 - adhesion G protein-coupled receptor L1 Gene

ADGRL1 - adhesion G protein-coupled receptor L1 Gene

Homo sapiens

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

Gene ID: 22859 | Gene type: protein coding

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

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