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Merck

MMAB

methylmalonic aciduria (cobalamin deficiency) cblB type

同義詞:
ATR, cblB, cob
物種:
UniProtKB ID:
基因 ID:
  • Human(326625) Summary: This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group. Alternatively spliced transcript variants have been found. [provided by RefSeq, Apr 2011]
  • Mouse(77697) methylmalonic aciduria (cobalamin deficiency) type B homolog (human)
  • Rat(687861) methylmalonic aciduria (cobalamin deficiency) cblB type
  • cow(617636) methylmalonic aciduria (cobalamin deficiency) cblB type
  • domestic cat(101093552) methylmalonic aciduria (cobalamin deficiency) cblB type
  • sheep(101114057) methylmalonic aciduria (cobalamin deficiency) cblB type
  • dog(486310) methylmalonic aciduria (cobalamin deficiency) cblB type
  • Zebrafish(557077) methylmalonic aciduria (cobalamin deficiency) cblB type
  • naked mole-rat(101708163) methylmalonic aciduria (cobalamin deficiency) cblB type
  • chicken(426287) methylmalonic aciduria (cobalamin deficiency) cblB type
  • domestic guinea pig(100714062) methylmalonic aciduria (cobalamin deficiency) cblB type

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