Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 59344
MIM: 607206
HGNC: 13743
Ensembl: ENSG00000179148
Variants:
dbSNP: 59344
ClinVar: 59344
TCGA: ENSG00000179148
COSMIC: ALOXE3
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000179148 | ENST00000318227 | Q9BYJ1 |
| ENSG00000179148 | ENST00000380149 | J3KPH2 |
| ENSG00000179148 | ENST00000448843 | Q9BYJ1 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33435499 | 2021 | Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients. | 11 |
| 33581311 | 2021 | The ALOXE3 gene variants from patients with Dravet syndrome decrease gene expression and enzyme activity. | 0 |
| 33435499 | 2021 | Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients. | 11 |
| 33581311 | 2021 | The ALOXE3 gene variants from patients with Dravet syndrome decrease gene expression and enzyme activity. | 0 |
| 31883158 | 2020 | Variants in NIPAL4 and ALOXE3 cause autosomal recessive congenital ichthyosis in Pakistani families. | 1 |
| 32618001 | 2020 | Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis. | 0 |
| 31883158 | 2020 | Variants in NIPAL4 and ALOXE3 cause autosomal recessive congenital ichthyosis in Pakistani families. | 1 |
| 32618001 | 2020 | Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis. | 0 |
| 29935003 | 2019 | Identification and association of recurrent ALOXE3 mutation with non-bullous congenital ichthyosiform erythroderma in two ethnically distinct Pakistani families. | 0 |
| 30678711 | 2019 | The associations of DNA methylation alterations in oxidative stress-related genes with cancer incidence and mortality outcomes: a population-based cohort study. | 12 |
| 29935003 | 2019 | Identification and association of recurrent ALOXE3 mutation with non-bullous congenital ichthyosiform erythroderma in two ethnically distinct Pakistani families. | 0 |
| 30678711 | 2019 | The associations of DNA methylation alterations in oxidative stress-related genes with cancer incidence and mortality outcomes: a population-based cohort study. | 12 |
| 27868147 | 2017 | Congenital Ichthyosis and Recurrent Eczema Associated with a Novel ALOXE3 Mutation. | 0 |
| 27868147 | 2017 | Congenital Ichthyosis and Recurrent Eczema Associated with a Novel ALOXE3 Mutation. | 0 |
| 26578203 | 2016 | Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosis. | 6 |
Citation
Dessen P
ALOXE3 (arachidonate lipoxygenase 3)
Atlas Genet Cytogenet Oncol Haematol. 2019-08-01
Online version: http://atlasgeneticsoncology.org/gene/58154/aloxe3-(arachidonate-lipoxygenase-3)
