Gene: MYH14 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79784
Gene Symbol: MYH14
MYH14 		0.710 Biomarker disease GENOMICS_ENGLAND Molecular diagnosis of inherited peripheral neuropathies by targeted next-generation sequencing: molecular spectrum delineation. 30373780 2018
Entrez Id: 79784
Gene Symbol: MYH14
MYH14 		0.710 Biomarker disease GENOMICS_ENGLAND Variable phenotypic expression and onset in MYH14 distal hereditary motor neuropathy phenotype in a large, multigenerational North American family. 27875632 2017
Entrez Id: 79784
Gene Symbol: MYH14
MYH14 		0.710 CausalMutation disease CLINVAR Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy. 26257172 2015
Entrez Id: 79784
Gene Symbol: MYH14
MYH14 		0.710 Biomarker disease GENOMICS_ENGLAND A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14. 21480433 2011
Entrez Id: 79784
Gene Symbol: MYH14
MYH14 		0.710 CausalMutation disease CLINVAR A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14. 21480433 2011
Entrez Id: 79784
Gene Symbol: MYH14
MYH14 		0.710 GeneticVariation disease BEFREE A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14. 21480433 2011
Entrez Id: 79784
Gene Symbol: MYH14
MYH14 		0.710 GeneticVariation disease UNIPROT A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14. 21480433 2011
Entrez Id: 79784
Gene Symbol: MYH14
MYH14 		0.710 GermlineCausalMutation disease ORPHANET A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14. 21480433 2011
Entrez Id: 79784
Gene Symbol: MYH14
MYH14 		0.710 Biomarker disease CTD_human