DISEASES

Disease-gene associations mined from literature

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Human genes for Charcot-Marie-Tooth disease type 2A1

Charcot-Marie-Tooth disease type 2A1 [DOID:0110154]

A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the KIF1B gene on chromosome 1p36.

Synonyms:  Charcot-Marie-Tooth disease type 2A1,  CharcotMarieTooth disease type 2A1,  DOID:0110154,  autosomal dominant Charcot-Marie-Tooth disease axonal type 2A1,  Charcot-Marie-Tooth disease neuronal type 2A1 ...

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.