DISEASES

Disease-gene associations mined from literature

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Literature associating MYOT and autosomal recessive limb-girdle muscular dystrophy type 2Q

MYOT [ENSP00000239926]

Myofibrillar titin-like Ig domains protein; Component of a complex of multiple actin cross-linking proteins. Involved in the control of myofibril assembly and stability at the Z lines in muscle cells; I-set domain containing

Synonyms:  MYOT,  B4DT68,  Q9UBF9,  B4DT68p,  hB4DT68 ...

Linkouts:  STRING  Pharos  UniProt  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.