TMEM251

transmembrane protein 251
Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Amber TMEM251 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 5.1
Latest signed off version: v5.0 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Dysostosis multiplex, Ain-Naz type, OMIM:19345
    • severe short stature
    Tags
    • new-gene-name
    • gene-checked
    Red TMEM251 in Rare syndromic craniosynostosis or isolated multisuture synostosis

    Level 3: Craniosynostosis syndromes
    Level 2: Skeletal disorders
    Version 5.1
    Latest signed off version: v5.0 (1 May 2024)

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    Phenotypes
    • Dysostosis multiplex, Ain-Naz type, OMIM:619345
    • craniosynostosis, MONDO:0015469
    Tags
    • new-gene-name
    • gene-checked
    Green TMEM251 in DDG2P


    Version 4.1
    Latest signed off version: v4.0 (1 May 2024)

    Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • TMEM251-related skeletal dysplasia
    Tags
    • new-gene-name
    • gene-checked