TMEM132E

transmembrane protein 132E
OMIM: 616178, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red TMEM132E in Monogenic hearing loss


Level 2: Audiology
Version 6.35
Latest signed off version: v6.34 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    Phenotypes
    • Nonsyndromic Hearing Loss
    Tags
    • watchlist
    Red TMEM132E in Intellectual disability


    Level 2: Developmental disorders
    Version 11.1
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders
  • review Not set
    Sources
    • Expert Review Red