cobalamin metabolic process Gene Set

Dataset GO Biological Process Annotations
Category structural or functional annotations
Type biological process
Description The chemical reactions and pathways involving cobalamin (vitamin B12), a water-soluble vitamin characterized by possession of a corrin nucleus containing a cobalt atom. (Gene Ontology, GO_0009235)
External Link http://amigo.geneontology.org/amigo/term/GO:0009235
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Genes

19 genes participating in the cobalamin metabolic process biological process from the curated GO Biological Process Annotations dataset.

Symbol Name
ABCC1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1
ABCD4 ATP-binding cassette, sub-family D (ALD), member 4
AMN amnion associated transmembrane protein
CD320 CD320 molecule
CTRB2 chymotrypsinogen B2
CUBN cubilin (intrinsic factor-cobalamin receptor)
GIF gastric intrinsic factor (vitamin B synthesis)
LMBRD1 LMBR1 domain containing 1
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
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
MUT methylmalonyl CoA mutase
PRSS1 protease, serine, 1 (trypsin 1)
PRSS3 protease, serine, 3
TCN1 transcobalamin I (vitamin B12 binding protein, R binder family)
TCN2 transcobalamin II