ACAD8
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn ACAD8 yw ACAD8 a elwir hefyd yn Acyl-CoA dehydrogenase family member 8 (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn blaen o gromosom dynol 11, band 11q25.[2]
ACAD8 | |||||||||||||||||
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Dynodwyr | |||||||||||||||||
Cyfenwau | ACAD8, ACAD-8, ARC42, acyl-CoA dehydrogenase family member 8, IBDH | ||||||||||||||||
Dynodwyr allanol | OMIM: 604773 HomoloGene: 8662 GeneCards: ACAD8 | ||||||||||||||||
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Species | Bod dynol | Llygoden | |||||||||||||||
Entrez |
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RefSeq (mRNA) |
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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 ACAD8.
- ARC42
- ACAD-8
Llyfryddiaeth
golygu- "Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans. ". Mol Genet Metab. 2002. PMID 12359132.
- "Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism. ". Am J Hum Genet. 2000. PMID 11013134.
- "A novel ACAD8 mutation in asymptomatic patients with isobutyryl-CoA dehydrogenase deficiency and a review of the ACAD8 mutation spectrum. ". Clin Genet. 2015. PMID 24635911.
- "Structures of isobutyryl-CoA dehydrogenase and enzyme-product complex: comparison with isovaleryl- and short-chain acyl-CoA dehydrogenases. ". J Biol Chem. 2004. PMID 14752098.
- "Isolation and characterisation of a cDNA encoding the precursor for a novel member of the acyl-CoA dehydrogenase gene family.". Biochim Biophys Acta. 1999. PMID 10524212.