Genopathy
Gene-Disorder Association · Article
Gene
PRKAR1A
Protein Kinase CAMP-Dependent Type I Regulatory Subunit Alpha
Disorder
Adrenocortical Carcinoma
First reported 2005
Supporting publications 2
Key publication · gene–disorder Molecular genetics of adrenocortical tumours, from familial to sporadic diseases.European journal of endocrinology · 2005
Key publication · disorder Steroid excretion in a case of adrenocortical carcinoma. V. delta 5-Pregnenetriol-3 beta, 17 alpha, 20 alpha.The Journal of biological chemistry · 1950
Manually curated
Association Review

In brief

The association between PRKAR1A (Protein Kinase CAMP-Dependent Type I Regulatory Subunit Alpha) and Adrenocortical Carcinoma is a manually-curated gene–disease association, drawing on a single expert-curated source, which records causative variation.

Sources 1
Clinical variants 0
Symptoms 33
Compounds 0
Trials 0
Publications 2
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
PRKAR1A

The gene

2 source summaries

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

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04
Adrenocortical Carcinoma

The disorder

9 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

29 clinical features

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

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06
Mechanism overlap

Shared mechanisms

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

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07
Literature

Reading

2 publications

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

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08
Provenance

References & sources

8 references

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

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