Genopathy
Gene-Disorder Association · Article
Gene
ALOX12B
Arachidonate 12-Lipoxygenase, 12R Type
Disorder
Ichthyosis, Congenital, Autosomal Recessive 2
First reported 2002
Supporting publications 18
Key publication · gene–disorder Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1.Human molecular genetics · 2002
Key publication · disorder Improved nuclear contour indices for lymphoid morphometry.Analytical and quantitative cytology and histology · 1987
Manually curated
Association Review

In brief

The association between ALOX12B (Arachidonate 12-Lipoxygenase, 12R Type) and Ichthyosis, Congenital, Autosomal Recessive 2 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and causative variation.

Sources 4
Clinical variants 218
Symptoms 41
Compounds 0
Trials 0
Publications 18
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

4 sources

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
ALOX12B

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

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04
Ichthyosis, Congenital, Autosomal Recessive 2

The disorder

10 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Phenotype

Clinical features

22 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
ClinVar and variant evidence

Genetic basis

218 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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07
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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08
Literature

Reading

18 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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09
Provenance

References & sources

14 references

Every source and publication cited across this dossier, as one numbered reference list.

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