Gene: HSPB8 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26353
Gene Symbol: HSPB8
HSPB8 		0.100 GeneticVariation phenotype CLINVAR Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy. 29029362 2018
Entrez Id: 26353
Gene Symbol: HSPB8
HSPB8 		0.100 GeneticVariation phenotype CLINVAR HSPB8 haploinsufficiency causes dominant adult-onset axial and distal myopathy. 28501893 2017
Entrez Id: 26353
Gene Symbol: HSPB8
HSPB8 		0.100 GeneticVariation phenotype CLINVAR Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathy. 26976520 2016