Genopathy
Gene-Disorder Association · Article
Gene
SLC45A2
Solute Carrier Family 45 Member 2
Disorder
Albinism
First reported 2004
Supporting publications 1
Key publication · gene–disorder Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4.Human mutation · 2004
Key publication · disorder [Some mutations affecting the eyes, collected as examples in the canton of Neuchatel and the Jura Bernois (congenital aniridia, universal albinism, congenital anophthalmos, total achromatopsia, oligophrenia associated with keratoconus, with ectopy of the crystalline, with congenital cataract and with atrophy of the optic nerve)].Bulletin der Schweizerischen Akademie der Medizinischen Wissenschaften · 1950
Manually curated
Association Review

In brief

The association between SLC45A2 (Solute Carrier Family 45 Member 2) and Albinism is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
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
SLC45A2

The gene

1 source summary

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

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04
Albinism

The disorder

1 database identifier

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

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05
Literature

Reading

1 publication

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

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06
Provenance

References & sources

3 references

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

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