1. Genes and Genomic Entities
  2. C4orf26

C4orf26

odontogenesis associated phosphoprotein
OMIM: 614829, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Green C4orf26 in Amelogenesis imperfecta


Level 2: Musculoskeletal
Version 4.26
Latest signed off version: v4.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • UKGTN
  • Radboud University Medical Center, Nijmegen
  • Eligibility statement prior genetic testing
Phenotypes
  • Amelogenesis imperfecta, type IIA4, 614832
  • Amelogenesis Imperfecta, Type IIA4, 614832
  • hypomineralized amelogenesis imperfecta
Tags
  • new-gene-name
Red C4orf26 in Fetal anomalies


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

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • PAGE DD-Gene2Phenotype
Phenotypes
  • Amelogenesis imperfecta, type IIA4, 614832
Tags
  • new-gene-name
Green C4orf26 in DDG2P


Version 6.424
Latest signed off version: v6.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • AMYELOGENESIS 614832
    Tags
    • new-gene-name
    Red C4orf26 in Intellectual disability


    Level 2: Developmental disorders
    Version 9.279
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • BRIDGE study SPEED NEURO Tier1 Gene
    Phenotypes
    • Amelogenesis imperfecta type, IIA4, 614832
    Tags
    • new-gene-name