1. Genes and Genomic Entities
  2. POC5

POC5

POC5 centriolar protein
Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels
Green POC5 in Rhabdomyolysis and metabolic muscle disorders


Level 2: Neurology
Version 6.9
Latest signed off version: v6.8 (12 Aug 2026)

Component of the following Super Panels:

  • Hypotonic infant
  • Other rare neuromuscular disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Retinal dystrophy
    • diabetes mellitus
    • lipodystrophy
    • renal failure
    • abnormal muscle physiology
    • muscle cramps
    Tags
    • gene-checked
    Amber POC5 in Severe insulin resistance and lipodystrophy syndromes


    Level 2: Endocrinology
    Version 5.4
    Latest signed off version: v5.2 (12 Aug 2026)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Retinal dystrophy
    • diabetes mellitus
    • lipodystrophy
    • renal failure
    • abnormal muscle physiology
    Tags
    • Q3_25_promote_green
    • gene-checked
    Amber POC5 in Monogenic diabetes


    Level 2: Endocrinology
    Version 3.27
    Latest signed off version: v3.26 (12 Aug 2026)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Retinal dystrophy
    • diabetes mellitus
    • lipodystrophy
    • renal failure
    • abnormal muscle physiology
    Tags
    • Q3_25_promote_green
    • gene-checked
    Green POC5 in Retinal disorders


    Level 2: Ophthalmology
    Version 9.19
    Latest signed off version: v9.14 (12 Aug 2026)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    • RetNet
    Phenotypes
    • Retinal dystrophy
    • diabetes mellitus
    • lipodystrophy
    • renal failure
    • abnormal muscle physiology
    Tags
    • gene-checked
    Green POC5 in Ophthalmological ciliopathies


    Level 2: Ophthalmology
    Version 6.2
    Latest signed off version: v6.1 (12 Aug 2026)

    Component of the following Super Panels:

  • Paediatric disorders
  • Rare multisystem ciliopathy Super panel

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    • Literature
    Phenotypes
    • Retinal dystrophy
    • diabetes mellitus
    • lipodystrophy
    • renal failure
    • abnormal muscle physiology
    Tags
    • gene-checked
    Amber POC5 in Acute rhabdomyolysis


    Level 2: Neurology
    Version 3.1
    Latest signed off version: v3.0 (12 Aug 2026)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Retinal dystrophy
    • diabetes mellitus
    • lipodystrophy
    • renal failure
    • abnormal muscle physiology
    • muscle cramps
    Tags
    • gene-checked
    • Q3_25_promote_green