I cannot write a clinical gene summary for TEX53 because the provided information is insufficient. While you've indicated a predicted gain-of-function mechanism, there is no information provided about the protein's function, associated diseases, inheritance patterns, or clinical manifestations. A clinically useful summary requires these fundamental details to inform pediatric neurologists about the gene's relevance to patient care.

ResearchSummary from Mechanism
Multiplemechanism
Clinical SummaryTEX53
📋
ClinVar Variants
13 unique Pathogenic / Likely Pathogenic· 1 VUS of 15 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

DN
0.85top 10%
GOF
0.84top 5%
LOF
0.3067th %ile

This gene has evidence for multiple mechanisms of pathogenicity (dominant-negative and gain-of-function). Both the Badonyi & Marsh prediction and the broader genomic evidence point to dominant-negative as the predominant mechanism. Different variants in this gene may act through different mechanisms — interpret in context of the specific variant.

DNprediction above median
GOFprediction above median

Note: In-silico variant effect predictors (SIFT, PolyPhen, REVEL, CADD) may underestimate pathogenicity of missense variants in genes with GOF or DN mechanisms. Consider functional evidence and clinical context.

Predictions from Badonyi M, Marsh JA. PLoS ONE. 2024;19(8):e0307312.

ClinVar Variant Classifications

15 submitted variants in ClinVar

Classification Summary

Pathogenic13
VUS1
Benign1
13
Pathogenic
1
VUS
1
Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
13
Likely Pathogenic
0
VUS
1
Likely Benign
0
Benign
1
Total15

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

TEX53 · 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 2 full-text resultsSearch PubTator3 ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found