DISEASES

Disease-gene associations mined from literature

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Literature associating LMOD3 and nemaline myopathy 2

LMOD3 [ENSP00000414670]

Leiomodin, fetal form; Essential for the organization of sarcomeric actin thin filaments in skeletal muscle. Increases the rate of actin polymerization; Belongs to the tropomodulin family.

Synonyms:  LMOD3,  LMOD3p,  hLMOD3,  Q0VAK6,  Q0VAK6p ...

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.