Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
552
Gene name Gene Name - the full gene name approved by the HGNC.
Arginine vasopressin receptor 1A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
AVPR1A
Synonyms (NCBI Gene) Gene synonyms aliases
AVPR V1a, AVPR1, V1aR
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q14.2
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene acts as receptor for arginine vasopressin. This receptor belongs to the subfamily of G-protein coupled receptors which includes AVPR1B, V2R and OXT receptors. Its activity is mediated by G proteins which stimulate a phosph
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT620542 hsa-miR-1276 HITS-CLIP 23824327
MIRT620541 hsa-miR-508-5p HITS-CLIP 23824327
MIRT620540 hsa-miR-1273g-3p HITS-CLIP 23824327
MIRT620539 hsa-miR-6849-3p HITS-CLIP 23824327
MIRT620538 hsa-miR-221-5p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001992 Process Regulation of systemic arterial blood pressure by vasopressin IBA
GO:0001992 Process Regulation of systemic arterial blood pressure by vasopressin IEA
GO:0002125 Process Maternal aggressive behavior IEA
GO:0003084 Process Positive regulation of systemic arterial blood pressure IEA
GO:0004930 Function G protein-coupled receptor activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600821 895 ENSG00000166148
Protein
UniProt ID P37288
Protein name Vasopressin V1a receptor (V1aR) (AVPR V1a) (Antidiuretic hormone receptor 1a) (Vascular/hepatic-type arginine vasopressin receptor)
Protein function Receptor for arginine vasopressin. The activity of this receptor is mediated by G proteins which activate a phosphatidyl-inositol-calcium second messenger system. Has been involved in social behaviors, including affiliation and attachment. {ECO:
PDB 1YTV
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 68 348 7 transmembrane receptor (rhodopsin family) Family
PF08983 DUF1856 372 418 Domain of unknown function (DUF1856) Domain
Sequence
Sequence length 418
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Calcium signaling pathway
Phospholipase D signaling pathway
Neuroactive ligand-receptor interaction
Hormone signaling
Vascular smooth muscle contraction
  Vasopressin-like receptors
G alpha (q) signalling events
Defective AVP does not bind AVPR1A,B and causes neurohypophyseal diabetes insipidus (NDI)
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Autism Spectrum Disorder autism spectrum disorder N/A N/A GenCC
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Acute Pain Associate 31710639
Anemia Sickle Cell Associate 31710639
Autism Spectrum Disorder Associate 27027249, 28808521, 29309996
Autistic Disorder Associate 18490926, 22764113, 28808521
Carcinoma Non Small Cell Lung Associate 16043261
Carcinoma Small Cell Associate 9357056
Communication Disorders Associate 24849541
Depressive Disorder Associate 24373571
Dyslexia Acquired Associate 24849541
Essential Hypertension Associate 12358153