SDHD
Protein-coding gene in the species Homo sapiens / From Wikipedia, the free encyclopedia
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Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial (CybS), also known as succinate dehydrogenase complex subunit D (SDHD), is a protein that in humans is encoded by the SDHD gene. Names previously used for SDHD were PGL and PGL1. Succinate dehydrogenase is an important enzyme in both the citric acid cycle and the electron transport chain.[5][6][7] Hereditary PGL-PCC syndrome is caused by a parental imprint of the SDHD gene. Screening can begin by 6 years of age.
Quick Facts Identifiers, Aliases ...
SDHD | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | SDHD, CBT1, CII-4, CWS3, PGL, PGL1, QPs3, SDH4, cybS, succinate dehydrogenase complex subunit D, MC2DN3 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 602690 MGI: 1914175 HomoloGene: 37718 GeneCards: SDHD | ||||||||||||||||||||||||||||||||||||||||||||||||||
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