Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2863
Gene name Gene Name - the full gene name approved by the HGNC.
G protein-coupled receptor 39
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GPR39
Synonyms (NCBI Gene) Gene synonyms aliases
ZnR
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q21.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene is a member of the ghrelin receptor family and encodes a rhodopsin-type G-protein-coupled receptor (GPCR). The encoded protein is involved in zinc-dependent signaling in epithelial tissue in intestines, prostate and salivary glands. The protein
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT029962 hsa-miR-26b-5p Microarray 19088304
MIRT736805 hsa-miR-1914-3p Luciferase reporter assay, Western blotting, Immunohistochemistry (IHC) 31576658
MIRT1031367 hsa-miR-1252 CLIP-seq
MIRT1031368 hsa-miR-1260 CLIP-seq
MIRT1031369 hsa-miR-1260b CLIP-seq
Transcription factors
Transcription factor Regulation Reference
HNF1A Unknown 17488974
HNF4A Unknown 17488974
SP1 Unknown 17488974
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0005515 Function Protein binding IPI 26365466
GO:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane TAS 9441746
GO:0007186 Process G protein-coupled receptor signaling pathway TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602886 4496 ENSG00000183840
Protein
UniProt ID O43194
Protein name G-protein coupled receptor 39
Protein function Zinc-sensing receptor that can sense changes in extracellular Zn(2+), mediate Zn(2+) signal transmission, and participates in the regulation of numerous physiological processes including glucose homeostasis regulation, gastrointestinal mobility,
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 47 344 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Expressed in many tissues, including the stomach, intestine and hypothalamus. {ECO:0000269|PubMed:9441746}.
Sequence
Sequence length 453
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Class A/1 (Rhodopsin-like receptors)
G alpha (q) signalling events
G alpha (s) signalling events
ADORA2B mediated anti-inflammatory cytokines production
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Hypertension Hypertensive disease rs13306026 21626137
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 29802348
Carcinoma Squamous Cell Associate 37839873
Diabetes Mellitus Type 2 Inhibit 17371481
Hepatitis B Associate 32784555
Hypertension Associate 21626137
Inflammation Inhibit 31237151
Lymphatic Metastasis Associate 37839873
Migraine Disorders Associate 31842742
Muscular Atrophy Associate 33687156
Neoplasms Associate 19696931, 26716511, 29802348