Identity
HGNC
LOCATION
17p11.2
LOCUSID
ALIAS
DFNB3,MYO15
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 51168
MIM: 602666
HGNC: 7594
Ensembl: ENSG00000091536
Variants:
dbSNP: 51168
ClinVar: 51168
TCGA: ENSG00000091536
COSMIC: MYO15A
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38167320 | 2024 | Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss. | 0 |
| 38167320 | 2024 | Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss. | 0 |
| 37189200 | 2023 | Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families. | 2 |
| 37189200 | 2023 | Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families. | 2 |
| 34374074 | 2022 | PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India. | 4 |
| 34388253 | 2022 | Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees. | 1 |
| 34974475 | 2022 | Hearing Features and Cochlear Implantation Outcomes in Patients With Pathogenic MYO15A Variants: a Multicenter Observational Study. | 2 |
| 35346193 | 2022 | Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients. | 1 |
| 36150242 | 2022 | Exosomal microRNA-1 and MYO15A as a target for therapy and diagnosis in renal cell carcinoma. | 9 |
| 36217262 | 2022 | Identification of novel compound heterozygous mutations of the MYO15A gene with autosomal recessive non-syndromic hearing loss. | 2 |
| 34374074 | 2022 | PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India. | 4 |
| 34388253 | 2022 | Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees. | 1 |
| 34974475 | 2022 | Hearing Features and Cochlear Implantation Outcomes in Patients With Pathogenic MYO15A Variants: a Multicenter Observational Study. | 2 |
| 35346193 | 2022 | Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients. | 1 |
| 36150242 | 2022 | Exosomal 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/myo15a-(myosin-xva)
