TRANSCOBALAMIN II DEFICIENCY Gene Set

Dataset CTD 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 http://ctdbase.org/detail.go?type=disease&acc=OMIM:275350
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Genes

1 genes/proteins associated with the disease TRANSCOBALAMIN II DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
TCN2 transcobalamin II 2.88009