Autoinflammatory disorders
Gene: MVK
MVK (mevalonate kinase)
EnsemblGeneIds (GRCh38): ENSG00000110921
EnsemblGeneIds (GRCh37): ENSG00000110921
OMIM: 251170, Gene2Phenotype
MVK is in 23 panels
EnsemblGeneIds (GRCh38): ENSG00000110921
EnsemblGeneIds (GRCh37): ENSG00000110921
OMIM: 251170, Gene2Phenotype
MVK is in 23 panels
1 review
Arina Puzriakova (Genomics England Curator)
This gene has been added to the panel on the recommendation of the NHS Genomic Medicine Service and should be rated green.Created: 16 Feb 2022, 11:44 a.m. | Last Modified: 16 Feb 2022, 11:44 a.m.
Panel Version: 0.36
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- NHS GMS
- Expert Review Green
- Phenotypes
-
- Mevalonic aciduria, OMIM:610377
- Hyper-IgD syndrome, OMIM:260920
- OMIM
- 251170
- Clinvar variants
- Variants in MVK
- Penetrance
- None
- Publications
- Panels with this gene
-
- Neonatal cholestasis
- Gastrointestinal epithelial barrier disorders
- Familial disseminated superficial actinic porokeratosis
- Rare genetic inflammatory skin disorders
- Infantile enterocolitis & monogenic inflammatory bowel disease
- Fetal anomalies
- Autoinflammatory disorders
- Cholestasis
- Hereditary ataxia, adult onset
- COVID-19 research
- Undiagnosed metabolic disorders
- Hereditary ataxia
- Neurodegenerative disorders, adult onset
- Fetal hydrops
- Periodic fever syndromes
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Mosaic skin disorders - Deep sequencing
- Ataxia and cerebellar anomalies - childhood onset
- Intellectual disability
- Likely inborn error of metabolism
- Dystonia, chorea or related movement disorder, childhood onset
- Palmoplantar keratodermas
- Retinal disorders
History Filter Activity
19 Jan 2022, Gel status: 3
Added New Source
Arina Puzriakova (Genomics England Curator)Source NHS GMS was added to MVK.
11 Jan 2022, Gel status: 3
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Arina Puzriakova (Genomics England Curator)gene: MVK was added gene: MVK was added to Autoinflammatory disorders. Sources: Expert Review Green Mode of inheritance for gene: MVK was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: MVK were set to 21708801; 16435210; 22038276; 10369261; 19011501 Phenotypes for gene: MVK were set to Mevalonic aciduria, OMIM:610377; Hyper-IgD syndrome, OMIM:260920