SENP3-EIF4A1

Chr 17

SENP3-EIF4A1 readthrough (NMD candidate)

This locus represents naturally occurring read-through transcription between the neighboring SUMO1/sentrin/SMT3 specific peptidase 3 (SENP3) and eukaryotic translation initiation factor 4A1 (EIF4A1) genes on chromosome 17. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Mar 2011]

79
ClinVar variants
8
Pathogenic / LP
pLI score
0
Active trials
Clinical SummarySENP3-EIF4A1
📋
ClinVar Variants
8 Pathogenic / Likely Pathogenic· 67 VUS of 79 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

79 submitted variants in ClinVar

Classification Summary

Pathogenic7
Likely Pathogenic1
VUS67
Likely Benign3
Benign1
7
Pathogenic
1
Likely Pathogenic
67
VUS
3
Likely Benign
1
Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
7
0
7
Likely Pathogenic
0
0
1
0
1
VUS
0
64
3
0
67
Likely Benign
0
1
0
2
3
Benign
0
0
0
1
1
Total06511379

LoF = frameshift, stop gained/lost, canonical splice · Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SENP3-EIF4A1 · protein map & ClinVar variants

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

OMIM — Genotype-Phenotype

No OMIM entries found.

Clinical Literature
Landmark / reviewRecent case evidence
Key Publications
Landmark & review papers · by relevance
PubMed
Top 10 resultsSearch PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

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