Non-syndromic hypotrichosis
Gene: C3orf52
Comment on list classification: 2 cases, but may not be relevant to the panel (localized hypotrichosis)Created: 7 Oct 2020, 3:20 p.m. | Last Modified: 7 Oct 2020, 3:20 p.m.
Panel Version: 1.4
PMID: 32336749 - Malki et al 2020 - identified homozygous variants in C3ORF52 in four individuals with Localized autosomal recessive hypotrichosis (LAH) (2 families). C3ORF52 was found to be coexpressed with lipase H in the inner root sheath of the hair follicle and the two proteins were found to directly interact. The variants were associated with decreased C3ORF52 expression and resulted in markedly reduced lipase H-mediated LPA biosynthesis. Abstract only accessed.
Although localized hypotrichosis is an exclusion criteria for this gene, it has been added to this panel as Amber as maybe useful information in the future.
Sources: LiteratureCreated: 7 Oct 2020, 3:19 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Localized hypotrichosis
Publications
Phenotypes for gene: C3orf52 were changed from Localized hypotrichosis to Hypotrichosis 15, OMIM:620177
Gene: c3orf52 has been classified as Amber List (Moderate Evidence).
gene: C3orf52 was added gene: C3orf52 was added to Non-syndromic hypotrichosis. Sources: Literature Mode of inheritance for gene: C3orf52 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: C3orf52 were set to 32336749 Phenotypes for gene: C3orf52 were set to Localized hypotrichosis Review for gene: C3orf52 was set to AMBER