Palmoplantar keratodermas
Gene: ALOX12BEnsemblGeneIds (GRCh38): ENSG00000179477
EnsemblGeneIds (GRCh37): ENSG00000179477
OMIM: 603741, Gene2Phenotype
ALOX12B is in 7 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: ALOX12B 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
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- London North GLH
- NHS GMS
- Expert Review Green
- Phenotypes
-
- Autosomal recessive congenital ichthyosis
- OMIM
- 603741
- Clinvar variants
- Variants in ALOX12B
- Penetrance
- None
- Panels with this gene
History Filter Activity
Added New Source
Rebecca Foulger (Genomics England curator)Source London North GLH was added to ALOX12B.
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Rebecca Foulger (Genomics England curator)gene: ALOX12B was added gene: ALOX12B was added to Palmoplantar keratodermas. Sources: Expert Review Green,NHS GMS Mode of inheritance for gene: ALOX12B was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ALOX12B were set to Autosomal recessive congenital ichthyosis