Gene-Disease Evidence Index

120-association public preview gene page

GRIN2D

glutamate ionotropic receptor NMDA type subunit 2D

Research use only. This page reports source-attributed evidence observed in the included release data. A gene symbol may appear in more than one rendered disease release. This is not medical advice, diagnosis, treatment guidance, patient risk prediction, clinical decision support, or clinical certainty. It covers only associations included in this release's fixed 120-association preview scope; absence from this page is not evidence of absence.
HGNC:4588 primary gene id
3 associations
3 evidence rows
3 releases

Release Packages

Methods and glossary
alzheimer-top120-v0.1.0-preview

release directory Git tag Data dictionary integrity.json ZIP archive

parkinson-top120-v0.1.0-preview

release directory Git tag Data dictionary integrity.json ZIP archive

epilepsy-top120-v0.1.0-preview

release directory Git tag Data dictionary integrity.json ZIP archive

Identity

genes.json
Symbol
GRIN2D
Name
glutamate ionotropic receptor NMDA type subunit 2D
Aliases
none in primary release
Provenance
HGNC, Open Targets Platform

Alzheimer disease

assoc:4588:0004975:052abcb86f21 · epilepsy-top120-v0.1.0-preview

association row
Status
observed unreviewed
Support tier
single source observed
Review
automatic checks only
Max source-reported score
0.614

Source Coverage

Supporting sources: Open Targets Platform

Silent sources: ClinVar

Single supporting source with queried-but-silent release source context.

  • Open Targets Platform: Source-attributed evidence signal; scores are not clinical truth or a combined confidence score. CC0 1.0; citation. Source freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026. Snapshot freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026; api-v4-graphql-2026-06-14-paper120, 120 records. Snapshot freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026; api-v4-graphql-2026-06-14-paper120, 120 records. Snapshot freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026; api-v4-graphql-2026-06-14-paper120, 120 records.

Evidence Rows evidence_rows.jsonl

Source Type Statement Open Targets score
Open Targets Platform OT:ENSG00000105464:MONDO_0004975 target disease association Open Targets reports GRIN2D as associated with Alzheimer disease. 0.614

Open Targets score breakdown

Source-attributed signals reported by Open Targets for OT:ENSG00000105464:MONDO_0004975. Each value is Open Targets' own per-datatype or per-datasource score — not truth, clinical validity, or a combined confidence score. Labels such as clinical and clinical_precedence are Open Targets' own datatype and datasource names, not a clinical-use or clinical-validity signal for this association. The overall score is Open Targets' own aggregate over these datasources; because those datasources can overlap with evidence from other sources, the overall score is not an independent line of corroboration.

By datatype
  • clinical 0.987
  • literature 0.440
By datasource
  • clinical_precedence 0.987
  • europepmc 0.440

Caveats

  • Public-candidate draft; research-use only and not a clinical finding.
  • AI/referee review artifacts are advisory and do not replace human scientific review.
  • Open Targets scores are source-attributed evidence signals, not truth or clinical validity scores.
  • Open Targets target-disease association context is not diagnostic, treatment, or clinical decision-making guidance.
  • Single-source Open Targets evidence has not passed review gates.

Source names identify provenance only and do not imply endorsement by HGNC, MONDO, Open Targets, ClinVar, NCBI, or any upstream source.

Parkinson disease

assoc:4588:0005180:96b8b7aa9fae · epilepsy-top120-v0.1.0-preview

association row
Status
observed unreviewed
Support tier
single source observed
Review
automatic checks only
Max source-reported score
0.605

Source Coverage

Supporting sources: Open Targets Platform

Silent sources: ClinVar

Single supporting source with queried-but-silent release source context.

  • Open Targets Platform: Source-attributed evidence signal; scores are not clinical truth or a combined confidence score. CC0 1.0; citation. Source freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026. Snapshot freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026; api-v4-graphql-2026-06-14-paper120, 120 records. Snapshot freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026; api-v4-graphql-2026-06-14-paper120, 120 records. Snapshot freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026; api-v4-graphql-2026-06-14-paper120, 120 records.

Evidence Rows evidence_rows.jsonl

Source Type Statement Open Targets score
Open Targets Platform OT:ENSG00000105464:MONDO_0005180 target disease association Open Targets reports GRIN2D as associated with Parkinson disease. 0.605

Open Targets score breakdown

Source-attributed signals reported by Open Targets for OT:ENSG00000105464:MONDO_0005180. Each value is Open Targets' own per-datatype or per-datasource score — not truth, clinical validity, or a combined confidence score. Labels such as clinical and clinical_precedence are Open Targets' own datatype and datasource names, not a clinical-use or clinical-validity signal for this association. The overall score is Open Targets' own aggregate over these datasources; because those datasources can overlap with evidence from other sources, the overall score is not an independent line of corroboration.

By datatype
  • clinical 0.990
  • literature 0.121
By datasource
  • clinical_precedence 0.990
  • europepmc 0.121

Caveats

  • Public-candidate draft; research-use only and not a clinical finding.
  • AI/referee review artifacts are advisory and do not replace human scientific review.
  • Open Targets scores are source-attributed evidence signals, not truth or clinical validity scores.
  • Open Targets target-disease association context is not diagnostic, treatment, or clinical decision-making guidance.
  • Single-source Open Targets evidence has not passed review gates.

Source names identify provenance only and do not imply endorsement by HGNC, MONDO, Open Targets, ClinVar, NCBI, or any upstream source.

Epilepsy

assoc:4588:0005027:e6e2f7e6e501 · epilepsy-top120-v0.1.0-preview

association row
Status
observed unreviewed
Support tier
single source observed
Review
automatic checks only
Max source-reported score
0.810

Source Coverage

Supporting sources: Open Targets Platform

Silent sources: ClinVar

Single supporting source with queried-but-silent release source context.

  • Open Targets Platform: Source-attributed evidence signal; scores are not clinical truth or a combined confidence score. CC0 1.0; citation. Source freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026. Snapshot freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026; api-v4-graphql-2026-06-14-paper120, 120 records. Snapshot freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026; api-v4-graphql-2026-06-14-paper120, 120 records. Snapshot freshness: refresh recommended; assessed Jun 9, 2026; next review Jul 9, 2026; api-v4-graphql-2026-06-14-paper120, 120 records.

Evidence Rows evidence_rows.jsonl

Source Type Statement Open Targets score
Open Targets Platform OT:ENSG00000105464:EFO_0000474 target disease association Open Targets reports GRIN2D as associated with epilepsy. 0.810

Open Targets score breakdown

Source-attributed signals reported by Open Targets for OT:ENSG00000105464:EFO_0000474. Each value is Open Targets' own per-datatype or per-datasource score — not truth, clinical validity, or a combined confidence score. Labels such as clinical and clinical_precedence are Open Targets' own datatype and datasource names, not a clinical-use or clinical-validity signal for this association. The overall score is Open Targets' own aggregate over these datasources; because those datasources can overlap with evidence from other sources, the overall score is not an independent line of corroboration.

By datatype
  • clinical 0.899
  • genetic_association 0.840
  • genetic_literature 0.769
  • literature 0.271
By datasource
  • eva 0.924
  • clinical_precedence 0.899
  • genomics_england 0.827
  • uniprot_literature 0.608
  • orphanet 0.608
  • gene2phenotype 0.608
  • uniprot_variants 0.608
  • europepmc 0.271

Caveats

  • Public-candidate draft; research-use only and not a clinical finding.
  • AI/referee review artifacts are advisory and do not replace human scientific review.
  • Open Targets scores are source-attributed evidence signals, not truth or clinical validity scores.
  • Open Targets target-disease association context is not diagnostic, treatment, or clinical decision-making guidance.
  • Single-source Open Targets evidence has not passed review gates.

Source names identify provenance only and do not imply endorsement by HGNC, MONDO, Open Targets, ClinVar, NCBI, or any upstream source.