Bos taurus Gene: MC1R
Summary
InnateDB Gene IDBG-647150.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MC1R
Gene Name Melanocyte-stimulating hormone receptor
Synonyms MC1-R; MSHR
Species Bos taurus
Ensembl Gene ENSBTAG00000023731
Encoded Proteins
Melanocyte-stimulating hormone receptor
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000258839:
This intronless gene encodes the receptor protein for melanocyte-stimulating hormone (MSH). The encoded protein, a seven pass transmembrane G protein coupled receptor, controls melanogenesis. Two types of melanin exist: red pheomelanin and black eumelanin. Gene mutations that lead to a loss in function are associated with increased pheomelanin production, which leads to lighter skin and hair color. Eumelanin is photoprotective but pheomelanin may contribute to UV-induced skin damage by generating free radicals upon UV radiation. Binding of MSH to its receptor activates the receptor and stimulates eumelanin synthesis. This receptor is a major determining factor in sun sensitivity and is a genetic risk factor for melanoma and non-melanoma skin cancer. Over 30 variant alleles have been identified which correlate with skin and hair color, providing evidence that this gene is an important component in determining normal human pigment variation. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 18:14757332-14759082
Strand Forward strand
Band
Transcripts
ENSBTAT00000032494 ENSBTAP00000055607
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 5 interaction(s) predicted by orthology.
Predicted by orthology
Total 5 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004871 signal transducer activity
GO:0004930 G-protein coupled receptor activity
GO:0004977 melanocortin receptor activity
GO:0004980 melanocyte-stimulating hormone receptor activity
GO:0005515 protein binding
GO:0031625 ubiquitin protein ligase binding
Biological Process
GO:0007165 signal transduction
GO:0007186 G-protein coupled receptor signaling pathway
GO:0010739 positive regulation of protein kinase A signaling
GO:0019233 sensory perception of pain
GO:0030819 positive regulation of cAMP biosynthetic process
GO:0032720 negative regulation of tumor necrosis factor production
GO:0035556 intracellular signal transduction
GO:0042438 melanin biosynthetic process
GO:0043473 pigmentation
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0051897 positive regulation of protein kinase B signaling
GO:0070914 UV-damage excision repair
GO:0090037 positive regulation of protein kinase C signaling
Cellular Component
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
Orthologs
Species
Mus musculus
Homo sapiens
Gene ID
Gene Order
Pathways
NETPATH
REACTOME
Peptide ligand-binding receptors pathway
Signaling by GPCR pathway
G alpha (s) signalling events pathway
Signal Transduction pathway
GPCR downstream signaling pathway
GPCR ligand binding pathway
Class A/1 (Rhodopsin-like receptors) pathway
KEGG
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
G alpha (s) signalling events pathway
GPCR downstream signaling pathway
Signaling by GPCR pathway
Class A/1 (Rhodopsin-like receptors) pathway
GPCR ligand binding pathway
Peptide ligand-binding receptors pathway
Signal Transduction pathway
G alpha (s) signalling events pathway
Peptide ligand-binding receptors pathway
Class A/1 (Rhodopsin-like receptors) pathway
Signaling by GPCR pathway
Signal Transduction pathway
GPCR downstream signaling pathway
GPCR ligand binding pathway
KEGG
Melanogenesis pathway
Neuroactive ligand-receptor interaction pathway
Neuroactive ligand-receptor interaction pathway
Melanogenesis pathway
INOH
PID NCI
Cross-References
SwissProt P47798
TrEMBL A9UEA8 H9BEA3 Q95KV8
UniProt Splice Variant
Entrez Gene 281298
UniGene Bt.553
RefSeq NM_174108
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL AJ297819 EU169233 JQ004019 S71017 U39469 Y13957 Y19103
GenPept AAB31361 AAC48590 ABX83565 AFD23451 CAA74291 CAB64818 CAC82612
RNA Seq Atlas 281298