MYO15A (myosin XVA)

2014-11-01  

Identity

HGNC
LOCATION
17p11.2
LOCUSID
ALIAS
DFNB3,MYO15
FUSION GENES

Other Information

Locus ID:

NCBI: 51168
MIM: 602666
HGNC: 7594
Ensembl: ENSG00000091536

Variants:

dbSNP: 51168
ClinVar: 51168
TCGA: ENSG00000091536
COSMIC: MYO15A

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000091536ENST00000418233Q9UKN7
ENSG00000091536ENST00000556535G3V4G3
ENSG00000091536ENST00000557655G3V4Q3
ENSG00000091536ENST00000578472K7EQV1
ENSG00000091536ENST00000578575K7EMS7
ENSG00000091536ENST00000579848K7EL45
ENSG00000091536ENST00000615845A0A087WYA1
ENSG00000091536ENST00000644795A0A2R8Y712
ENSG00000091536ENST00000647165Q9UKN7
ENSG00000091536ENST00000651088A0A494C1B3

Expression (GTEx)

0
10
20
30
40
50
60
70
80

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
381673202024Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss.0
381673202024Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss.0
371892002023Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families.2
371892002023Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families.2
343740742022PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India.4
343882532022Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees.1
349744752022Hearing Features and Cochlear Implantation Outcomes in Patients With Pathogenic MYO15A Variants: a Multicenter Observational Study.2
353461932022Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients.1
361502422022Exosomal microRNA-1 and MYO15A as a target for therapy and diagnosis in renal cell carcinoma.9
362172622022Identification of novel compound heterozygous mutations of the MYO15A gene with autosomal recessive non-syndromic hearing loss.2
343740742022PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India.4
343882532022Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees.1
349744752022Hearing Features and Cochlear Implantation Outcomes in Patients With Pathogenic MYO15A Variants: a Multicenter Observational Study.2
353461932022Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients.1
361502422022Exosomal microRNA-1 and MYO15A as a target for therapy and diagnosis in renal cell carcinoma.9

Citation

Dessen P

MYO15A (myosin XVA)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/70625/favicon/js/_common.js