CPEB2-DT

Chr 4

CPEB2 divergent transcript

Also known as: CPEB2-AS1, DRAIR

I cannot provide a clinical summary for CPEB2-DT as no functional or clinical information has been provided in the data below. A meaningful clinical gene summary requires information about protein function, associated diseases, and inheritance patterns, which are not available for this gene.

0
Active trials
0
Pubs (1 yr)
22
P/LP submissions
P/LP missense
LOEUF
Mechanism
Clinical SummaryCPEB2-DT
📋
ClinVar Variants
22 unique Pathogenic / Likely Pathogenic of 22 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

22 submitted variants in ClinVar

Classification Summary

Pathogenic22
22
Pathogenic

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
22
Likely Pathogenic
0
VUS
0
Likely Benign
0
Benign
0
Total22

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

CPEB2-DT · 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 →
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found