Palmoplantar keratodermas
Gene: ELOVL4EnsemblGeneIds (GRCh38): ENSG00000118402
EnsemblGeneIds (GRCh37): ENSG00000118402
OMIM: 605512, Gene2Phenotype
ELOVL4 is in 14 panels
1 review
Rebecca Foulger (Genomics England curator)
This gene was part of an initial gene list collated by Thomas Cullup, GOSH and Veronica Kinsler, UCL, 25.Jan.2019 on behalf of the GMS Skin Specialist Test Group. Gene Symbol submitted: ELOVL4; Suggested initial gene rating: Green; Evidence for inclusion: none provided; Evidence for exclusion: none provided; Technical notes (e.g. non-coding/CNV mutations requiring coverage?): none provided.Created: 28 Jan 2019, 10:47 a.m.
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- BOTH monoallelic and biallelic, autosomal or pseudoautosomal
- Sources
-
- London North GLH
- NHS GMS
- Expert Review Green
- Phenotypes
-
- Ichthyosis, spastic quadriplegia, mental retardation
- OMIM
- 605512
- Clinvar variants
- Variants in ELOVL4
- Penetrance
- None
- Panels with this gene
-
- DDG2P
- Structural eye disease
- Intellectual disability
- Hereditary ataxia
- Fetal anomalies
- Glaucoma (developmental)
- Adult onset neurodegenerative disorder
- Palmoplantar keratoderma and erythrokeratodermas
- Childhood onset dystonia, chorea or related movement disorder
- Retinal disorders
- Ichthyosis and erythrokeratoderma
- Hereditary ataxia with onset in adulthood
- Palmoplantar keratodermas
- Ataxia and cerebellar anomalies - narrow panel
History Filter Activity
Added New Source
Rebecca Foulger (Genomics England curator)Source London North GLH was added to ELOVL4.
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Rebecca Foulger (Genomics England curator)gene: ELOVL4 was added gene: ELOVL4 was added to Palmoplantar keratodermas. Sources: Expert Review Green,NHS GMS Mode of inheritance for gene: ELOVL4 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Phenotypes for gene: ELOVL4 were set to Ichthyosis, spastic quadriplegia, mental retardation