Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84539
Gene name Gene Name - the full gene name approved by the HGNC.
Melanin concentrating hormone receptor 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MCHR2
Synonyms (NCBI Gene) Gene synonyms aliases
GPR145, GPRv17, MCH-2R, MCH-R2, MCH2, MCH2R, MCHR-2, SLT
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6q16.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018648 hsa-miR-335-5p Microarray 18185580
MIRT1137155 hsa-miR-3145-5p CLIP-seq
MIRT1137156 hsa-miR-3691-3p CLIP-seq
MIRT1137157 hsa-miR-151-3p CLIP-seq
MIRT1137158 hsa-miR-4662a-5p CLIP-seq
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:0004966 Function Galanin receptor activity IBA
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606111 20867 ENSG00000152034
Protein
UniProt ID Q969V1
Protein name Melanin-concentrating hormone receptor 2 (MCH receptor 2) (MCH-R2) (MCHR-2) (G-protein coupled receptor 145) (GPRv17) (MCH-2R) (MCH2) (MCH2R)
Protein function Receptor for melanin-concentrating hormone, coupled to G proteins that activate phosphoinositide hydrolysis.
PDB 8WST
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 51 306 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Specifically expressed in the brain, with highest levels in cerebral cortex, hippocampus and amygdala. No expression detected in the cerebellum, thalamus or hypothalamus.
Sequence
Sequence length 340
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Neuroactive ligand-receptor interaction
Hormone signaling
  Peptide ligand-binding receptors
G alpha (q) signalling events
G alpha (i) signalling events
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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
Breast Cancer Breast cancer N/A N/A GWAS
Cystitis Cystitis N/A N/A GWAS
Glioblastoma Glioblastoma N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Binge Eating Disorder Associate 37550530
Colorectal Neoplasms Associate 35545337
Depressive Disorder Associate 26461262
Erectile Dysfunction Associate 30583798
Escherichia coli Infections Associate 1639518
Gastrointestinal Diseases Associate 1639518
Hemolytic Uremic Syndrome Associate 1629337
Osteoporosis Associate 38484114