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Merck
CN

MMADHC

methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria

别名:
C2orf25, CL25022, cblD
物种:
UniProtKB ID:
基因ID:
  • Human(27249) Summary: This gene encodes a mitochondrial protein that is involved in an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans. Mutations in this gene cause methylmalonic aciduria and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X.[provided by RefSeq, Nov 2008]
  • Mouse(109129) methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
  • Rat(362134) methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
  • domestic guinea pig(100730134) methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
  • naked mole-rat(101715098) methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
  • chicken(424311) methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
  • Zebrafish(402886) methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
  • dog(476145) methylmalonic aciduria and homocystinuria type D homolog, mitochondrial-like
  • cow(521533) methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria

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Antibodies

Product Number
说明
物种反应性
应用
Anti-MMADHC antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
物种反应性
human
应用
immunohistochemistry
western blot
Anti-MMADHC antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
物种反应性
human
应用
immunohistochemistry

esiRNA

Product Number
说明
物种
MISSION® esiRNA, targeting mouse Mmadhc,
物种
mouse
MISSION® esiRNA, targeting human MMADHC,
物种
human