Genopathy
Gene-Disorder Association · Article
Gene
CAPRIN1
Cell Cycle Associated Protein 1
Disorder
Neurodevelopmental Disorder With Language Impairment, Autism, And Attention Deficit-Hyperactivity Disorder
First reported 2023
Supporting publications 1
Key publication · gene–disorder CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASD.Brain : a journal of neurology · 2023
Key publication · disorder Long-term follow-up of children with psychiatric disorders.Hospital & community psychiatry · 1983
Manually curated
Association Review

In brief

The association between CAPRIN1 (Cell Cycle Associated Protein 1) and Neurodevelopmental Disorder With Language Impairment, Autism, And Attention Deficit-Hyperactivity Disorder is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.

Sources 2
Clinical variants 5
Symptoms 53
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

2 sources

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

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03
CAPRIN1

The gene

1 source summary

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

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04
Neurodevelopmental Disorder With Language Impairment, Autism, And Attention Deficit-Hyperactivity Disorder

The disorder

5 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

34 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

5 clinical variants

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

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07
Mechanism overlap

Shared mechanisms

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

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08
Literature

Reading

1 publication

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

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09
Provenance

References & sources

5 references

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

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