Rare genetic inflammatory skin disorders
Gene: MVDEnsemblGeneIds (GRCh38): ENSG00000167508
EnsemblGeneIds (GRCh37): ENSG00000167508
OMIM: 603236, Gene2Phenotype
MVD is in 3 panels
2 reviews
Tom Cullup (Great Ormond Street Hospital)
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
POROKERATOSIS 7, MULTIPLE TYPES; POROK7
Publications
Catherine Snow (Genomics England)
Following discussion with the Genomics England clinical team it was agreed that genes associated with Familial disseminated superficial actinic porokeratosis should be included on this panel. Therefore added to panel as a Green gene.Created: 2 Dec 2019, 3:48 p.m. | Last Modified: 2 Dec 2019, 3:48 p.m.
Panel Version: 0.17
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Green
- Expert Review
- Phenotypes
-
- Porokeratosis 7, multiple types, OMIM:614714
- OMIM
- 603236
- Clinvar variants
- Variants in MVD
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Set Phenotypes
Arina Puzriakova (Genomics England Curator)Phenotypes for gene: MVD were changed from POROKERATOSIS 7, MULTIPLE TYPES, OMIM:614714 to Porokeratosis 7, multiple types, OMIM:614714
Set Phenotypes
Ivone Leong (Genomics England Curator)Phenotypes for gene: MVD were changed from POROKERATOSIS 7, MULTIPLE TYPES; POROK7 to POROKERATOSIS 7, MULTIPLE TYPES, OMIM:614714
Set Phenotypes, Set publications
Catherine Snow (Genomics England)Added phenotypes POROKERATOSIS 7, MULTIPLE TYPES; POROK7 for gene: MVD Publications for gene MVD were changed from to 26202976
Added New Source, Status Update
Catherine Snow (Genomics England)Source Expert Review Green was added to MVD. Rating Changed from Red List (low evidence) to Green List (high evidence)
Created, Added New Source, Set mode of inheritance
Catherine Snow (Genomics England)gene: MVD was added gene: MVD was added to Rare genetic inflammatory skin disorders. Sources: Expert Review Mode of inheritance for gene: MVD was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown