INKILN

Chr 4

inflammatory MKL1 (MRTFA) interacting lncRNA

I cannot provide a clinical gene summary for INKILN as no information about this gene's protein function, associated diseases, or inheritance pattern has been provided in the data below the instructions. To write an accurate clinical summary following the strict rules specified, I would need details about what the INKILN protein does, what conditions result from mutations in this gene, and the inheritance pattern.

Clinical SummaryINKILN
📋
ClinVar Variants
9 unique Pathogenic / Likely Pathogenic· 1 VUS of 10 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

10 submitted variants in ClinVar

Classification Summary

Pathogenic8
Likely Pathogenic1
VUS1
8
Pathogenic
1
Likely Pathogenic
1
VUS

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
8
Likely Pathogenic
1
VUS
1
Likely Benign
0
Benign
0
Total10

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

INKILN · 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