Genomics England
GMS Panels
Panels
Genes and Entities

BGN

biglycan
OMIM: 301870
PanelMode of inheritanceDetails
5 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.48
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
Severe syndromic form of thoracic aortic aneurysm & dissection, X-Linked Spondyloepimetaphyseal Dysplasia
Green
in Ehlers Danlos syndrome with a likely monogenic cause
R-numbers: R101
Signed-off version 3.21
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes
Meester-Loeys syndrome, OMIM:300989
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 5.80
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
Severe syndromic form of thoracic aortic aneurysm & dissection, X-Linked Spondyloepimetaphyseal Dysplasia, Meester-Loeys syndrome, 300989, Spondyloepimetaphyseal dysplasia, X-linked, 300106
Green
in Skeletal dysplasia
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 7.26
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
Spondyloepimetaphyseal dysplasia, X-linked, OMIM:300106
Green
in Thoracic aortic aneurysm or dissection (GMS)
R-numbers: R125
Signed-off version 3.19
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes
X-linked syndromic TAAD, syndromic thoracic aortic aneurysm and dissection