Genopathy
Gene-Disorder Association · Article
Gene
TAP1
Transporter 1, ATP Binding Cassette Subfamily B Member
Disorder
Mhc Class I Deficiency
First reported 1999
Supporting publications 7
Key publication · gene–disorder HLA class I deficiencies due to mutations in subunit 1 of the peptide transporter TAP1.The Journal of clinical investigation · 1999
Key publication · disorder [The bare lymphocyte syndrome. Combined immune deficiency by absence of HLA antigen expression].Presse medicale (Paris, France : 1983) · 1984
Manually curated
Association Review

In brief

The association between TAP1 (Transporter 1, ATP Binding Cassette Subfamily B Member) and Mhc Class I Deficiency is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording pathogenic variants.

Sources 2
Clinical variants 412
Symptoms 0
Compounds 0
Trials 0
Publications 7
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

2 sources

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

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03
TAP1

The gene

1 source summary

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

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04
Mhc Class I Deficiency

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

412 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

7 publications

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

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07
Provenance

References & sources

10 references

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

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