DISEASES

Disease-gene associations mined from literature

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Literature associating C6orf136 and autosomal recessive spinocerebellar ataxia 8

C6orf136 [ENSP00000293604]

Uncharacterized protein C6orf136; Chromosome 6 open reading frame 136

Synonyms:  C6orf136,  A0A1U9X7F4,  F8WBB4,  F8WC77,  F8WEV2 ...

Linkouts:  STRING  Pharos  UniProt

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.