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 		0.420 GeneticVariation group 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 		0.420 Biomarker group BEFREE Mutations in the small heat shock protein B8 gene (HSPB8/HSP22) have been associated with distal hereditary motor neuropathy, Charcot-Marie-Tooth disease, and recently distal myopathy. 28780615 2018
Entrez Id: 26353
Gene Symbol: HSPB8
HSPB8 		0.420 GeneticVariation group CLINVAR HSPB8 haploinsufficiency causes dominant adult-onset axial and distal myopathy. 28501893 2017
Entrez Id: 26353
Gene Symbol: HSPB8
HSPB8 		0.420 GeneticVariation group BEFREE Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathy. 26718575 2016
Entrez Id: 26353
Gene Symbol: HSPB8
HSPB8 		0.420 Biomarker group GENOMICS_ENGLAND Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathy. 26718575 2016
Entrez Id: 26353
Gene Symbol: HSPB8
HSPB8 		0.420 GeneticVariation group CLINVAR Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathy. 26976520 2016