DISEASES

Disease-gene associations mined from literature

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

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