Gene: LMOD2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 442721
Gene Symbol: LMOD2
LMOD2 		0.020 GeneticVariation disease BEFREE Exome sequencing in a neonate with severe DCM revealed a homozygous nonsense variant in leiomodin 2 (<i>LMOD2</i>, p.Trp398*). 31517052 2019
Entrez Id: 442721
Gene Symbol: LMOD2
LMOD2 		0.020 GeneticVariation disease BEFREE We suggest that the K15N mutation causes DCM by altering Ca<sup>2+</sup>-dependent thin-filament regulation and that one of the possible HCM-causing mechanisms by the R21H mutation is through alteration of leiomodin's function. 30462572 2019