Genopathy
Gene-Disorder Association · Article
Gene
LOC130062601
ATAC-STARR-Seq Lymphoblastoid Silent Region 9492
Disorder
Isolated Microphthalmia 3
First reported 2004
Supporting publications 1
Key publication · disorder Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocornea.Human molecular genetics · 2004
Association Review

In brief

The association between LOC130062601 (ATAC-STARR-Seq Lymphoblastoid Silent Region 9492) and Isolated Microphthalmia 3 is supported by expert-curated evidence, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 8
Symptoms 0
Compounds 0
Trials 0
Publications 1
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

1 source

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

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03
LOC130062601

The gene

1 source summary

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

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04
Isolated Microphthalmia 3

The disorder

3 database identifiers

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

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05
ClinVar and variant evidence

Genetic basis

8 clinical variants

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

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06
Literature

Reading

1 publication

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

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07
Provenance

References & sources

3 references

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

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