Clefting
Gene: POMT2EnsemblGeneIds (GRCh38): ENSG00000009830
EnsemblGeneIds (GRCh37): ENSG00000009830
OMIM: 607439, Gene2Phenotype
POMT2 is in 19 panels
1 review
Louise Daugherty (Genomics England Curator)
Comment on publications: Only 1 case clefting. Clefting not a key feature.Created: 31 May 2017, 2:01 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2, 613150
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert list
- Phenotypes
-
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2, 613150
- OMIM
- 607439
- Clinvar variants
- Variants in POMT2
- Penetrance
- Complete
- Publications
- Panels with this gene
-
- Cerebellar hypoplasia
- Likely inborn error of metabolism
- Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies
- DDG2P
- Cerebral vascular malformations
- Ataxia and cerebellar anomalies - narrow panel
- Undiagnosed metabolic disorders
- Childhood onset dystonia, chorea or related movement disorder
- Fetal anomalies
- Early onset or syndromic epilepsy
- Hydrocephalus
- Bilateral congenital or childhood onset cataracts
- Malformations of cortical development
- Arthrogryposis
- Congenital muscular dystrophy
- Congenital disorders of glycosylation
- Intellectual disability
- Structural eye disease
- Clefting
History Filter Activity
panel promoted to version 1
Louise Daugherty (Genomics England Curator)Panel reviews were assessed, and panel was revised according to reviews and further curation 31st May 2017
Set publications
Louise Daugherty (Genomics England Curator)Publications for POMT2 were set to 15894594
Added New Source
Louise Daugherty (Genomics England Curator)POMT2 was added to Cleftingpanel. Sources: Expert list
Created
Louise Daugherty (Genomics England Curator)POMT2 was created by LouiseD