DISEASES

Disease-gene associations mined from literature

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Human genes for CAKUT2

CAKUT2 [DOID:0080207]

A CAKUT that has_material_basis_in heterozygous mutation in the TBX18 gene on chromosome 6q14.

Synonyms:  CAKUT2,  DOID:0080207,  Congenital anomalies of the kidney and urinary tract 2

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.