ERVFRD-3

Chr 9

endogenous retrovirus group FRD member 3

I cannot write a clinical summary for ERVFRD-3 because no information about this gene was provided below the instructions. To create an accurate clinical summary following the strict rules, I would need data about the protein function, associated diseases, inheritance patterns, and pathogenic mechanisms for this gene.

Clinical SummaryERVFRD-3
📋
ClinVar Variants
40 unique Pathogenic / Likely Pathogenic· 1 VUS of 44 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

44 submitted variants in ClinVar

Classification Summary

Pathogenic37
Likely Pathogenic3
VUS1
Likely Benign3
37
Pathogenic
3
Likely Pathogenic
1
VUS
3
Likely Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
37
Likely Pathogenic
3
VUS
1
Likely Benign
3
Benign
0
Total44

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

ERVFRD-3 · 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