Gene Gene information from NCBI Gene database.
Entrez ID 2847
Gene name Melanin concentrating hormone receptor 1
Gene symbol MCHR1
Synonyms (NCBI Gene)
GPR24MCH-1RMCH1RSLC-1SLC1
Chromosome 22
Chromosome location 22q13.2
Summary The protein encoded by this gene, a member of the G protein-coupled receptor family 1, is an integral plasma membrane protein which binds melanin-concentrating hormone. The encoded protein can inhibit cAMP accumulation and stimulate intracellular calcium
miRNA miRNA information provided by mirtarbase database.
32
miRTarBase ID miRNA Experiments Reference
MIRT1137137 hsa-miR-1207-5p CLIP-seq
MIRT1137138 hsa-miR-1270 CLIP-seq
MIRT1137139 hsa-miR-1293 CLIP-seq
MIRT1137140 hsa-miR-146b-3p CLIP-seq
MIRT1137141 hsa-miR-1909 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
30
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IBA
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0004930 Function G protein-coupled receptor activity TAS 10421367
GO:0005102 Function Signaling receptor binding IEA
GO:0005886 Component Plasma membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601751 4479 ENSG00000128285
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q99705
Protein name Melanin-concentrating hormone receptor 1 (MCH receptor 1) (MCH-R1) (MCHR-1) (G-protein coupled receptor 24) (MCH-1R) (MCH1R) (MCHR) (SLC-1) (Somatostatin receptor-like protein)
Protein function Receptor for melanin-concentrating hormone, coupled to both G proteins that inhibit adenylyl cyclase and G proteins that activate phosphoinositide hydrolysis.
PDB 8WSS , 8WWH , 8WWI , 8WWJ , 8WWK , 8WWL , 8WWM , 8WWN , 8YNT
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 126 380 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Highest level in brain, particularly in the frontal cortex and hypothalamus, lower levels in the liver and heart.
Sequence
Sequence length 422
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
BBSome-mediated cargo-targeting to cilium
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
17
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
MCHR1-related disorder Benign; Uncertain significance; Likely benign rs11914085, rs143942609, rs565709738, rs199936867, rs1409004434, rs149149384, rs112405400, rs150069806, rs987667577, rs146628737, rs45439291, rs199847547, rs36115367, rs117372135, rs201321975
View all (2 more)
RCV003976027
RCV003410223
RCV004747259
RCV003417084
RCV003410611
RCV003399564
RCV003974576
RCV003894426
RCV003904664
RCV003982300
RCV003977331
RCV003944083
RCV003939691
RCV003939324
RCV003927030
RCV003957282
RCV003983268
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Anxiety Disorders Associate 22921745
Bipolar Disorder Stimulate 19502010
Bovine Respiratory Disease Complex Associate 24305679
Carcinoma Renal Cell Associate 32788609
Colorectal Neoplasms Associate 39456726
Depressive Disorder Major Inhibit 16230605
Fibrosis Associate 34912333
Hyperphagia Associate 15166293
Neoplasms Associate 39456726
Obesity Associate 15166293, 18198296, 20054173, 21637341, 22921745, 24305679, 32329245