Gene: MYO15A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51168
Gene Symbol: MYO15A
MYO15A 		0.430 Biomarker phenotype BEFREE Yet again, these results endorse the importance of MYO15 screening in hearing impaired populations, particularly in Iran. 30579064 2019
Entrez Id: 51168
Gene Symbol: MYO15A
MYO15A 		0.430 GeneticVariation phenotype BEFREE The majority of MYO15A variants are associated with a congenital severe-to-profound hearing loss phenotype, except for MYO15A variants in exon 2, which cause a milder auditory phenotype, suggesting a genotype-phenotype correlation of MYO15A. 30953472 2019
Entrez Id: 51168
Gene Symbol: MYO15A
MYO15A 		0.430 Biomarker phenotype BEFREE In particular 5 novel alleles were identified in the following genes LOXHD1, TMPRSS3, TECTA and MYO15A already associated with hearing impairment. 24657061 2014
Entrez Id: 51168
Gene Symbol: MYO15A
MYO15A 		0.430 Biomarker phenotype GENOMICS_ENGLAND Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. 9603736 1998
Entrez Id: 51168
Gene Symbol: MYO15A
MYO15A 		0.430 GeneticVariation phenotype CLINVAR
Entrez Id: 51168
Gene Symbol: MYO15A
MYO15A 		0.430 CausalMutation phenotype CLINVAR