Bilateral congenital or childhood onset cataracts
Gene: POMGNT2EnsemblGeneIds (GRCh38): ENSG00000144647
EnsemblGeneIds (GRCh37): ENSG00000144647
OMIM: 614828, Gene2Phenotype
POMGNT2 is in 17 panels
1 review
Ellen McDonagh (Genomics England Curator)
Comment on list classification: We discussed and agreed internally that all genes within the Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) phenotypic series available on OMIM should be demoted to red, as it is unlikely that these conditions would present with cataracts as a main feature.Created: 27 Jun 2016, 4:28 p.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Red
- Other
- Phenotypes
-
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 8
- OMIM
- 614828
- Clinvar variants
- Variants in POMGNT2
- Penetrance
- Complete
- Panels with this gene
-
- Retinal disorders
- Congenital disorders of glycosylation
- Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies
- Cerebellar hypoplasia
- Undiagnosed metabolic disorders
- Childhood onset dystonia, chorea or related movement disorder
- Arthrogryposis
- Structural eye disease
- Intellectual disability
- Hydrocephalus
- Malformations of cortical development
- Bilateral congenital or childhood onset cataracts
- DDG2P
- Likely inborn error of metabolism
- Fetal anomalies
- Congenital muscular dystrophy
- Ataxia and cerebellar anomalies - narrow panel
History Filter Activity
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Created
Ellen McDonagh (Genomics England Curator)POMGNT2 was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)POMGNT2 was added to Cataractspanel. Sources: Other