MCC (gene)

Colorectal mutant cancer protein is a protein that in humans is encoded by the MCC gene.[5][6]

MCC
Identifiers
Aliases	MCC, MCC1, mutated in colorectal cancers, WNT signaling pathway regulator, MCC regulator of WNT signaling pathway
External IDs	OMIM: 159350 MGI: 96930 HomoloGene: 20539 GeneCards: MCC
Gene location (Human) Chr. Chromosome 5 (human)[1] Band 5q22.2 Start 113,022,099 bp[1] End 113,488,823 bp[1]
Gene location (Mouse) Chr. Chromosome 18 (mouse)[2] Band 18 B3|18 23.74 cM Start 44,425,060 bp[2] End 44,812,182 bp[2]
RNA expression pattern More reference expression data
Gene ontology Molecular function • GO:0001948 protein binding • signaling receptor activity Cellular component • cytoplasm • cell membrane • cell projection • membrane • cell nucleus • lamellipodium • nucleoplasm • cytosol Biological process • establishment of protein localization • negative regulation of epithelial cell proliferation • negative regulation of epithelial cell migration • Wnt signaling pathway • negative regulation of canonical Wnt signaling pathway • signal transduction Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	4163	328949
Ensembl	ENSG00000171444	ENSMUSG00000071856
UniProt	P23508	n/a
RefSeq (mRNA)	NM_001085377 NM_002387	NM_001033406 NM_001085373 NM_001085374
RefSeq (protein)	NP_001078846 NP_002378	n/a
Location (UCSC)	Chr 5: 113.02 – 113.49 Mb	Chr 18: 44.43 – 44.81 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

This gene is a candidate colorectal tumor suppressor gene that is thought to negatively regulate cell cycle progression. The orthologous gene in the mouse expresses a phosphoprotein associated with the plasma membrane and membrane organelles, and overexpression of the mouse protein inhibits entry into S phase. Multiple transcript variants encoding different isoforms have been found for this gene.[6]

References

1. GRCh38: Ensembl release 89: ENSG00000171444 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000071856 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. Kinzler KW, Nilbert MC, Vogelstein B, Bryan TM, Levy DB, Smith KJ, Preisinger AC, Hamilton SR, Hedge P, Markham A, et al. (Apr 1991). "Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers". Science. 251 (4999): 1366–70. doi:10.1126/science.1848370. PMID 1848370.
6. "Entrez Gene: MCC mutated in colorectal cancers".

Further reading

• Lindgren V, Bryke CR, Ozcelik T, et al. (1992). "Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis". Am. J. Hum. Genet. 50 (5): 988–97. PMC 1682619. PMID 1315124.
• Nishisho I, Nakamura Y, Miyoshi Y, et al. (1991). "Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients". Science. 253 (5020): 665–9. doi:10.1126/science.1651563. PMID 1651563.
• Hoshino Y, Horikawa I, Oshimura M, Yuasa Y (1991). "Normal human chromosome 5, on which a familial adenomatous polyposis gene is located, has tumor suppressive activity". Biochem. Biophys. Res. Commun. 174 (1): 298–304. doi:10.1016/0006-291X(91)90520-H. PMID 1846539.
• Curtis LJ, Bubb VJ, Gledhill S, et al. (1994). "Loss of heterozygosity of MCC is not associated with mutation of the retained allele in sporadic colorectal cancer". Hum. Mol. Genet. 3 (3): 443–6. doi:10.1093/hmg/3.3.443. PMID 8012355.
• Matsumine A, Senda T, Baeg GH, et al. (1996). "MCC, a cytoplasmic protein that blocks cell cycle progression from the G0/G1 to S phase". J. Biol. Chem. 271 (17): 10341–6. doi:10.1074/jbc.271.17.10341. PMID 8626604.
• Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
• Hartley JL, Temple GF, Brasch MA (2001). "DNA Cloning Using In Vitro Site-Specific Recombination". Genome Res. 10 (11): 1788–95. doi:10.1101/gr.143000. PMC 310948. PMID 11076863.
• Wiemann S, Weil B, Wellenreuther R, et al. (2001). "Toward a Catalog of Human Genes and Proteins: Sequencing and Analysis of 500 Novel Complete Protein Coding Human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072. PMID 11230166.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Bouwmeester T, Bauch A, Ruffner H, et al. (2004). "A physical and functional map of the human TNF-alpha/NF-kappa B signal transduction pathway". Nat. Cell Biol. 6 (2): 97–105. doi:10.1038/ncb1086. PMID 14743216.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Wiemann S, Arlt D, Huber W, et al. (2004). "From ORFeome to Biology: A Functional Genomics Pipeline". Genome Res. 14 (10B): 2136–44. doi:10.1101/gr.2576704. PMC 528930. PMID 15489336.
• Mehrle A, Rosenfelder H, Schupp I, et al. (2006). "The LIFEdb database in 2006". Nucleic Acids Res. 34 (Database issue): D415–8. doi:10.1093/nar/gkj139. PMC 1347501. PMID 16381901.
• Ewing RM, Chu P, Elisma F, et al. (2007). "Large-scale mapping of human protein–protein interactions by mass spectrometry". Mol. Syst. Biol. 3 (1): 89. doi:10.1038/msb4100134. PMC 1847948. PMID 17353931.