COX7C
From Wikipedia, the free encyclopedia
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Cytochrome c oxidase subunit VIIc
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| Identifiers | ||||||||||||||
| Symbol(s) | COX7C; | |||||||||||||
| External IDs | OMIM: 603774 MGI: 103226 HomoloGene: 81691 | |||||||||||||
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| RNA expression pattern | ||||||||||||||
| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 1350 | 12867 | ||||||||||||
| Ensembl | ENSG00000127184 | ENSMUSG00000017778 | ||||||||||||
| Uniprot | P15954 | P17665 | ||||||||||||
| Refseq | NM_001867 (mRNA) NP_001858 (protein) |
NM_007749 (mRNA) NP_031775 (protein) |
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| Location | Chr 5: 85.95 - 85.95 Mb | Chr 13: 86.52 - 86.52 Mb | ||||||||||||
| Pubmed search | [1] | [2] | ||||||||||||
Cytochrome c oxidase subunit VIIc, also known as COX7C, is a human gene.[1]
Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes subunit VIIc, which shares 87% and 85% amino acid sequence identity with mouse and bovine COX VIIc, respectively, and is found in all tissues. A pseudogene COX7CP1 has been found on chromosome 13.[1]
[edit] References
[edit] Further reading
- Lenka N, Vijayasarathy C, Mullick J, Avadhani NG (1998). "Structural organization and transcription regulation of nuclear genes encoding the mammalian cytochrome c oxidase complex.". Prog. Nucleic Acid Res. Mol. Biol. 61: 309-44. PMID 9752724.
- Sirchia R, Luparello C (2007). "Mid-region parathyroid hormone-related protein (PTHrP) and gene expression of MDA-MB231 breast cancer cells.". Biol. Chem. 388 (5): 457-65. doi:. PMID 17516841.
- 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:. PMID 15489334.
- 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:. PMID 12477932.
- Hofmann S, Lichtner P, Schuffenhauer S, et al. (1999). "Assignment of the human genes coding for cytochrome c oxidase subunits Va (COX5A), VIc (COX6C) and VIIc (COX7C) to chromosome bands 15q25, 8q22-->q23 and 5q14 and of three pseudogenes (COX5AP1, COX6CP1, COX7CP1) to 14q22, 16p12 and 13q14-->q21 by FISH and radiation hybrid mapping.". Cytogenet. Cell Genet. 83 (3-4): 226-7. PMID 10072584.
- Kaminishi H, Hamatake H, Cho T, et al. (1994). "Activation of blood clotting factors by microbial proteinases.". FEMS Microbiol. Lett. 121 (3): 327-32. PMID 7926688.
- Koga Y, Fabrizi GM, Mita S, et al. (1990). "Sequence of a cDNA specifying subunit VIIc of human cytochrome c oxidase.". Nucleic Acids Res. 18 (3): 684. PMID 2155413.
- Van Kuilenburg AB, Van Beeumen JJ, Van der Meer NM, Muijsers AO (1992). "Subunits VIIa,b,c of human cytochrome c oxidase. Identification of both 'heart-type' and 'liver-type' isoforms of subunit VIIa in human heart.". Eur. J. Biochem. 203 (1-2): 193-9. PMID 1309697.

