PRRT1B

Chr 9

proline rich transmembrane protein 1B

Also known as: DSPD2, IFITMD8

Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]

0
Active trials
17
Pathogenic / LP
17
ClinVar variants
4
Pubs (1 yr)
Missense Z
LOEUF
Clinical SummaryPRRT1B
📋
ClinVar Variants
17 Pathogenic / Likely Pathogenic of 17 total submissions
Some data sources returned errors (1)

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

DN
0.5674th %ile
GOF
0.80top 10%
LOF
0.2873th %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

17 submitted variants in ClinVar

Classification Summary

Pathogenic17
17
Pathogenic

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
17
Likely Pathogenic
0
VUS
0
Likely Benign
0
Benign
0
Total17

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

PRRT1B · 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
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found