LNCEGFL7OS

Chr 9

lncRNA EGFL7 opposite strand

Also known as: HSPC324

I cannot write a clinical summary for LNCEGFL7OS because no information about this gene was provided below your instructions. To create an accurate clinical summary following your strict rules about using only provided information, I would need data about the protein function, associated diseases, inheritance patterns, and pathogenic mechanisms for this gene.

Clinical SummaryLNCEGFL7OS
📋
ClinVar Variants
46 unique Pathogenic / Likely Pathogenic of 46 total submissions
Some data sources returned errors (1)

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

46 submitted variants in ClinVar

Classification Summary

Pathogenic45
Likely Pathogenic1
45
Pathogenic
1
Likely Pathogenic

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
45
Likely Pathogenic
1
VUS
0
Likely Benign
0
Benign
0
Total46

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

LNCEGFL7OS · 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 5 full-text resultsSearch PubTator3 ↗
Key Publications
Landmark & review papers · by relevance
PubMed
Top 1 results · since 2015Search PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found