Homo sapiens Protein: MC2R
Summary
InnateDB Protein IDBP-1284.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MC2R
Protein Name melanocortin 2 receptor (adrenocorticotropic hormone)
Synonyms ACTHR;
Species Homo sapiens
Ensembl Protein ENSP00000333821
InnateDB Gene IDBG-1282 (MC2R)
Protein Structure
UniProt Annotation
Function Receptor for corticotropin (ACTH). This receptor is mediated by G proteins (G(s)) which activate adenylate cyclase (cAMP). {ECO:0000269PubMed:19329486, ECO:0000269PubMed:20371771}.
Subcellular Localization Cell membrane; Multi-pass membrane protein.
Disease Associations Glucocorticoid deficiency 1 (GCCD1) [MIM:202200]: A rare, potentially lethal, autosomal recessive disorder characterized by resistance to ACTH action on the adrenal cortex, adrenal insufficiency and an inability of the adrenal cortex to produce cortisol. It usually presents in the neonatal period or in early childhood with episodes of hypoglycemia and other symptoms related to cortisol deficiency, including failure to thrive, recurrent illnesses or infections, convulsions, and shock. In a small number of patients hypoglycemia can be sufficiently severe and persistent that it leads to serious long-term neurological damage or death. The diagnosis is readily confirmed with a low plasma cortisol measurement in the presence of an elevated ACTH level, and normal aldosterone and plasma renin measurements. {ECO:0000269PubMed:10971458, ECO:0000269PubMed:12213892, ECO:0000269PubMed:8094489, ECO:0000269PubMed:8227361, ECO:0000269PubMed:8636348}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Melanocytes and corticoadrenal tissue.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 5 [view]
Protein-Protein 5 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004930 G-protein coupled receptor activity
GO:0004977 melanocortin receptor activity
GO:0004978 corticotropin receptor activity
GO:0005515 protein binding
Biological Process
GO:0001890 placenta development
GO:0007186 G-protein coupled receptor signaling pathway
GO:0007187 G-protein coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger
GO:0007218 neuropeptide signaling pathway
GO:0030819 positive regulation of cAMP biosynthetic process
Cellular Component
GO:0005737 cytoplasm
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR000276 G protein-coupled receptor, rhodopsin-like
IPR001168 Adrenocorticotrophin (ACTH) receptor
IPR001671 Melanocortin/ACTH receptor
IPR017452 GPCR, rhodopsin-like, 7TM
IPR019424 7TM GPCR, olfactory receptor/chemoreceptor Srsx
IPR019430 7TM GPCR, serpentine receptor class x (Srx)
PFAM PF00001
PF10320
PF10328
PRINTS PR00237
PR00520
PR00534
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q01718
PhosphoSite PhosphoSite-Q01718
TrEMBL R4GMM0
UniProt Splice Variant
Entrez Gene 4158
UniGene Hs.248144
RefSeq NP_001278840
HUGO HGNC:6930
OMIM 607397
CCDS CCDS11869
HPRD 06304
IMGT
EMBL AB065915 AK289381 AK315319 AP001086 AY225229 BC069074 BC094710 BC104169 BC104170 CH471113 X65633
GenPept AAH69074 AAH94710 AAI04170 AAI04171 AAO67714 BAC06130 BAF82070 BAG37722 CAA46587 EAX01503