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
-
- Hydrocephalus
- Cerebellar hypoplasia
- Malformations of cortical development
- Fetal anomalies
- Cerebral vascular malformations
- Likely inborn error of metabolism
- Congenital muscular dystrophy
- Dystonia, chorea or related movement disorder, childhood onset
- Undiagnosed metabolic disorders
- Intellectual disability
- Ataxia and cerebellar anomalies - childhood onset
- Structural eye disease
- Early onset or syndromic epilepsy
- Congenital disorders of glycosylation
- Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies
- Clefting
- DDG2P
- Arthrogryposis
- Bilateral congenital or childhood onset cataracts
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