Genopathy
Gene-Disorder Association · Article
Gene
GRIN1
Glutamate Ionotropic Receptor NMDA Type Subunit 1
Disorder
Intellectual Disability, Autosomal Dominant 8
First reported 1998
Supporting publications 27
Key publication · disorder Statistical features of human exons and their flanking regions.Human molecular genetics · 1998
Manually curated
Association Review

In brief

The association between GRIN1 (Glutamate Ionotropic Receptor NMDA Type Subunit 1) and Intellectual Disability, Autosomal Dominant 8 is well established and manually curated, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 950
Symptoms 0
Compounds 0
Trials 0
Publications 27
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
GRIN1

The gene

2 source summaries

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

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04
Intellectual Disability, Autosomal Dominant 8

The disorder

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

950 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

27 publications

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

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07
Provenance

References & sources

11 references

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

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