TRGJP

Chr 7

T cell receptor gamma joining P

Also known as: JP, TCRGJP

0
Active trials
7
Pathogenic / LP
9
ClinVar variants
0
Pubs (1 yr)
Missense Z
LOEUF
Clinical SummaryTRGJP
📋
ClinVar Variants
7 Pathogenic / Likely Pathogenic of 9 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

GOF
DN
0.5869th %ile
GOF
0.78top 25%
LOF
0.4627th %ile

The highest-scoring mechanism for this gene is gain-of-function.

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

9 submitted variants in ClinVar

Classification Summary

Pathogenic7
Likely Benign1
Benign1
7
Pathogenic
1
Likely Benign
1
Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
7
Likely Pathogenic
0
VUS
0
Likely Benign
1
Benign
1
Total9

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

TRGJP · protein map & ClinVar variants

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

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Landmark / reviewRecent case evidence