Transcobalamin Ii Deficiency Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A vitamin B12 deficiency that is characterized by a lack of vitamin B12 intestinal absorption resulting from a deficiency in the B12 transport protein TCII. (Human Disease Ontology, DOID_0050818)
External Link https://www.disgenet.org/browser/0/1/0/C0342701
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Genes

5 genes associated with the disease Transcobalamin Ii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
GIF gastric intrinsic factor (vitamin B synthesis)
MMUT methylmalonyl-CoA mutase
PPBP pro-platelet basic protein (chemokine (C-X-C motif) ligand 7)
TCN1 transcobalamin I (vitamin B12 binding protein, R binder family)
TCN2 transcobalamin II