1. Genes and Genomic Entities
  2. MYO15A

MYO15A

myosin XVA
OMIM: 602666, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
No list MYO15A in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.140
Latest signed off version: v6.0 (30 Apr 2025)

review Not set
Sources
  • Expert Review Removed
Green MYO15A in Monogenic hearing loss


Level 2: Audiology
Version 5.57
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert
    • Radboud University Medical Center, Nijmegen
    • Emory Genetics Laboratory
    • UKGTN
    • Illumina TruGenome Clinical Sequencing Services
    Phenotypes
    • Deafness, autosomal recessive 3 OMIM:600316
    • autosomal recessive nonsyndromic deafness 3 MONDO:0010860