Vitamin B12 disorders Gene Set
Genes
13 proteins participating in the Vitamin B12 disorders pathway from the WikiPathways Pathways 2024 dataset.
| Symbol |
Name |
|
AMN
|
amnion associated transmembrane protein
|
|
CBLIF
|
cobalamin binding intrinsic factor
|
|
CD320
|
CD320 molecule
|
|
CUBN
|
cubilin (intrinsic factor-cobalamin receptor)
|
|
MMAA
|
methylmalonic aciduria (cobalamin deficiency) cblA type
|
|
MMAB
|
methylmalonic aciduria (cobalamin deficiency) cblB type
|
|
MMACHC
|
methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
|
|
MMADHC
|
methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
|
|
MMUT
|
methylmalonyl-CoA mutase
|
|
MTR
|
5-methyltetrahydrofolate-homocysteine methyltransferase
|
|
MTRR
|
5-methyltetrahydrofolate-homocysteine methyltransferase reductase
|
|
TCN1
|
transcobalamin I (vitamin B12 binding protein, R binder family)
|
|
TCN2
|
transcobalamin II
|
