ETFDH

Protein sydd yn cael eu codio yn y corff dynol gan y genyn ETFDH yw ETFDH a elwir hefyd yn Electron transfer flavoprotein-ubiquinone oxidoreductase, mitochondr

ETFDH
ETFDH
Enghraifft o:genyn Edit this on Wikidata
Mathgenyn codio-protein Edit this on Wikidata
Dynodwyr
OMIM231675 edit this on wikidata
Patrwm mynegiad y genyn yma

Protein sydd yn cael eu codio yn y corff dynol gan y genyn ETFDH yw ETFDH a elwir hefyd yn Electron transfer flavoprotein-ubiquinone oxidoreductase, mitochondrial ac Electron transfer flavoprotein dehydrogenase (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 4, band 4q32.1.

Cyfystyron

Yn 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 mae'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 ETFDH.

  • MADD
  • ETFQO

Llyfryddiaeth

  • "Neurite growth could be impaired by ETFDH mutation but restored by mitochondrial cofactors. ". Muscle Nerve. 2017. PMID 27935074.
  • "[Clinical features and gene mutations in a patient with multiple aeyl-CoA dehydrogenase deficiency with severe fatty liver]. ". Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID 27060313.
  • "Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency. ". Neurol Sci. 2016. PMID 27000805.
  • "Severe sensory neuropathy in patients with adult-onset multiple acyl-CoA dehydrogenase deficiency. ". Neuromuscul Disord. 2016. PMID 26821934.
  • "Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.". J Inherit Metab Dis. 2014. PMID 24357026.

Cyfeiriadau

ETFDH - Cronfa NCBI

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