NDUFA2
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn NDUFA2 yw NDUFA2 a elwir hefyd yn NADH:ubiquinone oxidoreductase subunit A2 (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn ôl o gromosom dynol 5, band 5q31.3.[2]
NDUFA2 | |||||||||||||||||
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Dynodwyr | |||||||||||||||||
Cyfenwau | NDUFA2, B8, CD14, CIB8, NADH:ubiquinone oxidoreductase subunit A2, MC1DN13 | ||||||||||||||||
Dynodwyr allanol | OMIM: 602137 HomoloGene: 37628 GeneCards: NDUFA2 | ||||||||||||||||
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Species | Bod dynol | Llygoden | |||||||||||||||
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RefSeq (protein) |
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Lleoliad (UCSC) | n/a | n/a | |||||||||||||||
PubMed search | [1] | n/a | |||||||||||||||
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Cyfystyron
golyguYn aml mae gan enynnau lawer o gyfystyron. Mae hyn oherwydd eu bod yn aml yn cael eu darganfod gan nifer o bobl mewn cyd-destunau gwahanol heb wybod mai'r un genynnau oeddyn nhw. Hefyd mae gan wahanol gymunedau gwyddonol safonau gwahanol ar gyfer enwi genynnau. Dyma restr o gyfystyron ar gyfer y genyn NDUFA2.
- B8
- CD14
- CIB8
Llyfryddiaeth
golygu- "Subunits of mitochondrial complex I exist as part of matrix- and membrane-associated subcomplexes in living cells. ". J Biol Chem. 2008. PMID 18826940.
- "NDUFA2 complex I mutation leads to Leigh disease. ". Am J Hum Genet. 2008. PMID 18513682.
- "The oxidized subunit B8 from human complex I adopts a thioredoxin fold. ". Structure. 2004. PMID 15341729.
- "Internalization and coreceptor expression are critical for TLR2-mediated recognition of lipoteichoic acid in human peripheral blood. ". J Immunol. 2010. PMID 20713893.
- "Mapping of the NDUFA2, NDUFA6, NDUFA7, NDUFB8, and NDUFS8 electron transport chain genes by intron based radiation hybrid mapping.". Cytogenet Cell Genet. 1998. PMID 9763676.