ZNF593OS

Chr 1

ZNF593 opposite strand

Also known as: ZNF593-AS

I cannot provide a clinical summary for ZNF593OS as the available information only describes predicted subcellular localization without any data on protein function, associated diseases, or inheritance patterns. Clinical gene summaries require established disease associations and functional information that are not present in the provided data.

ResearchSummary from RefSeq
Multiplemechanism
Clinical SummaryZNF593OS
📋
ClinVar Variants
2 unique Pathogenic / Likely Pathogenic· 19 VUS of 23 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

DN
0.7327th %ile
GOF
0.83top 10%
LOF
0.2289th %ile

This gene has evidence for multiple mechanisms of pathogenicity (gain-of-function and dominant-negative). Both the Badonyi & Marsh prediction and the broader genomic evidence point to gain-of-function as the predominant mechanism. Different variants in this gene may act through different mechanisms — interpret in context of the specific variant.

GOFprediction above median
DNprediction 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

23 submitted variants in ClinVar

Classification Summary

Pathogenic2
VUS19
2
Pathogenic
19
VUS

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
2
0
2
Likely Pathogenic
0
0
0
0
0
VUS
0
18
1
0
19
Likely Benign
0
0
0
0
0
Benign
0
0
0
0
0
Total0183021

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

View in ClinVar →

Protein Context — Lollipop Plot

ZNF593OS · 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 →
Full-Text Mentions
NLP-detected gene mentions in article bodies · via PubTator3
PubTator3
Top 1 full-text resultsSearch PubTator3 ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found