ORF » Species Summary » Homo sapiens » Reactome » Defects in cobalamin (B12) metabolism
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Browse by Letter Index, Genomic Locus
12 gene
The longest variant of each gene is displayed. Click the see gene variants link to see all gene variants.
Gene Symbol | Full Name |
---|---|
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 |
AMN | amnion associated transmembrane protein |
MTR | 5-methyltetrahydrofolate-homocysteine methyltransferase |
TCN2 | transcobalamin 2 |
MUT | methylmalonyl-CoA mutase |
CUBN | cubilin |