DISEASES

Disease-gene associations mined from literature

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Human genes for transcobalamin II deficiency

Transcobalamin II deficiency [DOID:0050818]

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.

Synonyms:  transcobalamin II deficiency,  DOID:0050818,  transcobalamin II deficiencies,  TCN2 deficiency

Linkouts:  OMIM

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.