ORF » Species Summary » Homo sapiens » Reactome » Defects in vitamin and cofactor metabolism

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以下のような検索ワードを入力できます：

  • Entrez Gene ID (e.g. 7157)
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  • gene name (e.g. tumor protein p53)
  • gene synonyms (e.g. FLJ92943)
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Homo sapiens (human) Defects in vitamin and cofactor metabolism (provided by Reactome)

Browse by Letter Index, Genomic Locus

18 gene

The longest variant of each gene is displayed. Click the see gene variants link to see all gene variants.


Gene Symbol Full Name
PC pyruvate carboxylase
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
LOC107986404 uncharacterized LOC107986404
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
MMADHC methylmalonic aciduria and homocystinuria, cblD type
CD320 CD320 molecule
GIF gastric intrinsic factor
MMAA methylmalonic aciduria (cobalamin deficiency) cblA type
MCCC2 methylcrotonoyl-CoA carboxylase 2
AMN amnion associated transmembrane protein
PCCB propionyl-CoA carboxylase beta subunit
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
PCCA propionyl-CoA carboxylase alpha subunit
MCCC1 methylcrotonoyl-CoA carboxylase 1
TCN2 transcobalamin 2
MUT methylmalonyl-CoA mutase
ACACA acetyl-CoA carboxylase alpha
CUBN cubilin
ORF
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