Genomics England
GMS Panels
Panels
Genes and Entities

COL12A1

collagen type XII alpha 1 chain
OMIM: 120320
PanelMode of inheritanceDetails
5 panels
Green
in Arthrogryposis
R-numbers: R83
Signed-off version 5.21
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Ullrich congenital muscular dystrophy 2, bethlem myopathy 2
Green
in Congenital muscular dystrophy
Component of the following Super Panels:
  • - Hypotonic infant
  • - Other rare neuromuscular disorders
R-numbers: R79
Signed-off version 4.15
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Ullrich congenital muscular dystrophy 2, Bethlem myopathy 2
Green
in Congenital myopathy
Component of the following Super Panels:
  • - Hypotonic infant
  • - Other rare neuromuscular disorders
R-numbers: R81
Signed-off version 4.33
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
EDS/myopathy overlap syndrome
Green
in Ehlers Danlos syndrome with a likely monogenic cause
R-numbers: R101
Signed-off version 3.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Bethlem myopathy 2, OMIM:616471
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 3.122
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Bethlem myopathy 2, 616471, ?Ullrich congenital muscular dystrophy 2, 616470