1. Genes and Genomic Entities
  2. SGCG

SGCG

sarcoglycan gamma
OMIM: 608896, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Red SGCG in Arthrogryposis


Level 2: Neurology
Version 9.24
Latest signed off version: v9.0 (30 Apr 2025)

review Not set
Sources
  • Expert Review Red
  • Expert list
Green SGCG in Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies


Level 2: Neurology
Version 5.29
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Hypotonic infant
  • Other rare neuromuscular disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Radboud University Medical Center, Nijmegen
    • Emory Genetics Laboratory
    • Illumina TruGenome Clinical Sequencing Services
    Phenotypes
    • Limb-Girdle Muscular Dystrophy, Recessive
    • Muscular dystrophy, limb-girdle, type 2C, 253700
    • Limb-girdle muscular dystrophy
    Green SGCG 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 Green
    • Expert list
    Phenotypes
    • Muscular dystrophy, limb-girdle, autosomal recessive 5, OMIM:253700
    • Autosomal recessive limb-girdle muscular dystrophy type 2C, MONDO:0009677
    Amber SGCG in Paediatric or syndromic cardiomyopathy


    Level 2: Cardiology
    Version 7.96
    Latest signed off version: v7.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Muscular dystrophy, limb-girdle, autosomal recessive 5, OMIM:253700
    • autosomal recessive limb-girdle muscular dystrophy type 2C, MONDO:0009677
    Tags
    • Q3_25_promote_green