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MCHR1 (melanin concentrating hormone receptor 1)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2847
Gene nameGene Name - the full gene name approved by the HGNC.
Melanin concentrating hormone receptor 1
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
MCHR1
SynonymsGene synonyms aliases
GPR24, MCH-1R, MCH1R, SLC-1, SLC1
ChromosomeChromosome number
22
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q13.2
SummarySummary 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
miRNAmiRNA 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 21873635
GO:0005102 Function Signaling receptor binding IEA
GO:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane IBA 21873635
GO:0005929 Component Cilium IDA 28154160
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
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
Sequence
Sequence length 422
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
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
Causal
Disease name Disease term dbSNP ID References
Schizophrenia Schizophrenia rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 22081064, 19502010, 16741940
Unknown
Disease name Disease term dbSNP ID References
Bipolar disorder Bipolar Disorder 16741940, 19502010
Mental depression Mental Depression, Depressive disorder rs587778876, rs587778877 16934771, 22209364, 16230605, 19182070, 17655875, 16934771, 19182070, 17655875, 16230605, 22209364
Mood disorder Mood Disorders 16934771, 19418262

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