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TRN-GTT2-4

Chr 13

tRNA-Asn (anticodon GTT) 2-4

Also known as: TRNAN7

I cannot write a clinical gene summary for TRN-GTT2-4 because no information about this gene's protein function, associated diseases, or inheritance pattern was provided in the data below the prompt. To create an accurate clinical summary following the specified guidelines, I would need details about what protein this gene encodes, what neurological or other conditions result from mutations, and the inheritance pattern observed in affected families.

Clinical SummaryTRN-GTT2-4
📋
ClinVar Variants
20 unique Pathogenic / Likely Pathogenic· 3 VUS of 23 total submissions
Some data sources returned errors (2)

ensembl: Error: Ensembl fetch failed: 400 for https://rest.ensembl.org/lookup/symbol/homo_sapiens/TRN-GTT2-4?content-type=application/json&expand=1

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

23 submitted variants in ClinVar

Classification Summary

Pathogenic20
VUS3
20
Pathogenic
3
VUS

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
20
Likely Pathogenic
0
VUS
3
Likely Benign
0
Benign
0
Total23

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

TRN-GTT2-4 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

3D Protein StructureAlphaFold

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Open Research Assistant →
Full-Text Mentions
NLP-detected gene mentions in article bodies · via PubTator3
PubTator3
Top 1 full-text resultsSearch PubTator3 ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found