Muscular dystrophy and myopathy_Paediatric
Gene: COL6A2
GeneReviews PMID:20301676
AD variants typically occur near the N terminal of the triple helical (TH) domain, which contains a critical region of 10 to 15 Gly-X-Y triplets; in-frame exon-skipping variants and glycine substitutions in this region tend to result in more severe phenotypes
AR variants are usually nonsense or fs, or biallelic variants located near the C-terminal end of the TH domain, where they will be excluded from assembly
COL6A2 accounts for 44-46% of Collagen VI-Related Dystrophies casesCreated: 4 May 2022, 1:12 a.m. | Last Modified: 4 May 2022, 1:13 a.m.
Panel Version: 0.13673
Mode of inheritance
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes
Bethlem myopathy 1 MIM#158810; Ullrich congenital muscular dystrophy 1 MIM#254090
Publications
Variants in this GENE are reported as part of current diagnostic practice
Well established gene.
Sources: Expert listCreated: 12 Jun 2020, 10:35 a.m.
Mode of inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Bethlem myopathy 1, MIM# 158810; Ullrich congenital muscular dystrophy 1, MIM# 254090
Publications
gene: COL6A2 was added gene: COL6A2 was added to Muscular dystrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: COL6A2 was set to Unknown