Genopathy
Gene-Disorder Association · Article
Gene
AIP
AHR Interacting HSP90 Co-Chaperone
Disorder
Pituitary Adenoma 1, Multiple Types
First reported 2006
Supporting publications 7
Key publication · gene–disorder Pituitary adenoma predisposition caused by germline mutations in the AIP gene.Science (New York, N.Y.) · 2006
Key publication · disorder [Chromatography of total 17-ketosteroids in a case of acromegaly due to pituitary adenoma, before, during and after radiotherapy].Folia endocrinologica; mensile di incretologia e incretoterapia · 1955
Manually curated
Association Review

In brief

The association between AIP (AHR Interacting HSP90 Co-Chaperone) and Pituitary Adenoma 1, Multiple Types is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.

Sources 4
Clinical variants 138
Symptoms 28
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

4 sources

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

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03
AIP

The gene

1 source summary

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

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04
Pituitary Adenoma 1, Multiple Types

The disorder

18 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

13 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

138 clinical variants

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

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07
Genomic context

Regulatory context

1 regulatory element

GeneHancer regulatory elements for the pair, with coordinates, score, element type and supporting literature.

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08
Mechanism overlap

Shared mechanisms

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

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09
Literature

Reading

7 publications

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

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10
Provenance

References & sources

15 references

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

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