Muscular dystrophy, limb-girdle, autosomal dominant | Gene-Disease Associations & Pathways | GeDiPNet

eDiPNet

Log in to bookmark this disease

Subtype of: Muscular dystrophy

Pathways column key: KEGG Reactome

Disease terms	Disease ID	Gene Symbol	Classification	References	Source	Pathways
muscular dystrophy, limb-girdle, autosomal dominant	MONDO_0012034 MONDO_0012193 MONDO_0015151 MONDO_0029133	CAPN3	Unknown	9150160 27259757 28881388 31937337 32342993 32557990 32896923 32994280	ClinGen, Open Targets	Cytoskeleton in muscle cells Degradation of the extracellular matrix
muscular dystrophy, limb-girdle, autosomal dominant	MONDO_0012034 MONDO_0012193 MONDO_0015151 MONDO_0029133	DNAJB6	Unknown	22334415 22366786	ClinGen, Open Targets	Regulation of HSF1-mediated heat shock response
muscular dystrophy, limb-girdle, autosomal dominant	MONDO_0012034 MONDO_0012193 MONDO_0015151 MONDO_0029133	HNRNPDL	Unknown	24647604	ClinGen, Open Targets	Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation
muscular dystrophy, limb-girdle, autosomal dominant	MONDO_0012034 MONDO_0012193 MONDO_0015151 MONDO_0029133	TNPO3	Causal	23543484 23667635 31071488 31192305 31465518	ClinGen, Open Targets	Nucleocytoplasmic transport Viral life cycle - HIV-1