1. Gene
  2. MCHR1 - melanin concentrating hormone receptor 1 Gene

MCHR1 - melanin concentrating hormone receptor 1 Gene

Homo sapiens

Also known as SLC1; GPR24; MCH1R; SLC-1; MCH-1R

Gene ID: 2847 | Gene type: protein coding

About MCHR1

Cytogenetic location: 22q13.2 Genomic coordinates (GRCh38): 22:40,679,484-40,682,812 (from NCBI)

This gene has 4 transcripts (splice variants), 241 orthologues and 33 paralogues. Biased expression in brain (RPKM 4.7), ovary (RPKM 1.2) and 5 other tissues.

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 flux, and is probably involved in the neuronal regulation of food consumption. Although structurally similar to somatostatin receptors, this protein does not seem to bind somatostatin. [provided by RefSeq, Jul 2008]

MCHR1 Products(1)

mRNA Protein Name
NM_005297.4 NP_005288.4 melanin-concentrating hormone receptor 1

MCHR1 Protein Structure

7tm_1

7tm_1: 7 transmembrane receptor (rhodopsin family) (126 - 380)

  • 0
  • 100
  • 200
  • 300
  • 422 a.a.
Protein Preferred Names Protein Names

melanin-concentrating hormone receptor 1

G protein-coupled receptor 24

MCH receptor 1

somatostatin receptor-like protein

Related Diseases

Diseases Alias
Retinitis Pigmentosa

RP

Rod-Cone Dystrophy

Autosomal Recessive Retinitis Pigmentosa

Non-Syndromic Retinitis Pigmentosa

Pericentral Pigmentary Retinopathy

Pigmentary Retinopathy

Tapetoretinal Degeneration

Rcd

Retinitis Pigmentosa Autosomal Recessive

ARRP

Retinitis Pigmentosa, Autosomal Recessive

Retinitis Pigmentosa 1

Leptin Deficiency Or Dysfunction

Morbid Obesity

Obesity Due To Congenital Leptin Deficiency

LEPD

Congenital Leptin Deficiency

Obesity, Morbid

Obesity, Morbid, Due To Leptin Deficiency

Severe Obesity

Obesity, Morbid, Nonsyndromic 1

Leptin Deficiency

Obesity, Severe, Due To Leptin Deficiency

Morbid Obesity Due To Leptin Deficiency

Obesity Morbid

Leptin Dysfunction

Leptin

Meckel Syndrome, Type 1

Meckel Syndrome

Meckel-Gruber Syndrome

Dysencephalia Splanchnocystica

Meckel Syndrome 1

MKS1

Mks

Gruber Syndrome

Meckel-Gruber Syndrome, Type 1

Mes

Dysencephalia Splachnocystica

Meckel Gruber Syndrome

Meckel Syndrome Type 1

Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1

Vitiligo

VAMAS1

Slev1

Vtlg

Systemic Lupus Erythematosus, Vitiligo-Related

Vitiligo-Associated Multiple Autoimmune Disease 1

Systemic Lupus Erythematosus Vitiligo-Related

Nephronophthisis

Medullary Cystic Disease

Medullary Cystic Kidney

Nph

Nphp

Kidney Disease, Cystic, Medullary

Body Mass Index Quantitative Trait Locus 11

OBESITY

Obesity, Susceptibility To

Leanness, Inherited

Obesity, Susceptibility To, Bmiq11

Obesity, Mild, Early-Onset

Obesity, Association With

Obesity, Early-Onset, Susceptibility To

Obesity, Severe

Obesity, Severe, And Type Ii Diabetes

Obesity, Late-Onset

BMIQ11

Obesity Bmiq11

Obesity, Early-Onset

Obesity , Susceptibility To

Simple Obesity Nos

Excess Fat

Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified

Adiposis

Iminoglycinuria

Iminoglycinuria, Digenic

IG

Bardet-Biedl Syndrome

Bbs

Biedl-Bardet Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta MCHR1 VGNC VGNC:95360
Mus musculus MCHR1 MGD MGI:2180756
Felis catus MCHR1 VGNC VGNC:67422
Rattus norvegicus MCHR1 RGD RGD:619841
Canis familiaris MCHR1 VGNC VGNC:43076
Bos taurus MCHR1 VGNC VGNC:31305