Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2847
Gene name Gene Name - the full gene name approved by the HGNC.
Melanin concentrating hormone receptor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MCHR1
Synonyms (NCBI Gene) Gene synonyms aliases
GPR24, MCH-1R, MCH1R, SLC-1, SLC1
Chromosome Chromosome number
22
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q13.2
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601751 4479 ENSG00000128285
Protein
UniProt ID 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
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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
Bipolar Disorder Bipolar disorder N/A N/A GWAS
Colorectal Cancer Colorectal cancer N/A N/A GWAS
Insomnia Insomnia N/A N/A GWAS
Neuroticism Neuroticism N/A N/A GWAS
Associations from Text Mining Disease 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