DISEASES

Disease-gene associations mined from literature

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Human genes for PSAT deficiency

PSAT deficiency [DOID:0050723]

A serine deficiency that has_material_basis_in deficiency of phosphoserine aminotransferase and is characterized by low concentartions of serine and flycine in plasma and cerebrospinal fluid.

Synonyms:  PSAT deficiency,  DOID:0050723,  PSAT deficiencies,  Phosphoserine aminotransferase deficiency,  Phosphoserine aminotransferase deficiencies

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.