Varaico: Literature-Extracted Genetic Variants

Gene:ABCA12
Variant:p.E1539K
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ABCA12

NM_173076.3:p.E1539K

Associated Papers

Compound heterozygous ABCA12 variants identified in a Chinese patient with congenital ichthyosiform erythroderma: Advancing genotype-phenotype correlations and literature review.

Liu JW et al.

Molecular Genetics & Genomic Medicine, 2024

38702946 (PubMed )
Supplement: MGG3-12-e2431-s001.docx

Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis.

Hotz A et al.

Genes, 2023

Congenital ichthyosiform erythroderma with a novel variant in ABCA12 in a Chinese patient.

Yang Z et al.

Pediatric Investigation, 2020

A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype-phenotype correlations.

Montalván-Suárez M et al.

Molecular Genetics & Genomic Medicine, 2019

Summary of mutations underlying autosomal recessive congenital ichthyoses (ARCI) in Arabs with four novel mutations in ARCI-related genes from the United Arab Emirates.

Bastaki F et al.

International Journal of Dermatology, 2017

Rare ER protein misfolding-mistrafficking disorders: Therapeutic developments.

Hegde RN et al.

Tissue & Cell, 2017

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis.

Walsh DM et al.

Scientifica, 2012

24278723 (PubMed )
Supplement: 649090.f1.pdf

First- and second-shell metal binding residues in human proteins are disproportionately associated with disease-related SNPs.

Levy R et al.

Human Mutation, 2011

21898656 (PubMed )
Supplement: supplement_1.pdf

Phenotype prediction of non-synonymous single-nucleotide polymorphisms in human ATP-binding cassette transporter genes.

Wang LL et al.

Basic & Clinical Pharmacology & Toxicology, 2011

Functional hot spots in human ATP-binding cassette transporter nucleotide binding domains.

Kelly L et al.

Protein Science : a Publication of the Protein Society, 2010

ABCA12 mutations and autosomal recessive congenital ichthyosis: a review of genotype/phenotype correlations and of pathogenetic concepts.

Akiyama M

Human Mutation, 2010

Recent advances in the genetics and management of harlequin ichthyosis.

Ahmed H et al.

Pediatric Dermatology, 0

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