INE2

Chr X

inactivation escape 2

Also known as: NCRNA00011

NCBI Gene: 8551ENSG00000281371OMIM: 300165

I don't have any information provided about the INE2 gene, including its protein function, associated diseases, or inheritance pattern. Without this essential data, I cannot write a clinical gene summary that meets the strict requirement to use only supported information.

OMIMResearch
Clinical Summary— INE2
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Some data sources returned errors (1)

gnomad: Error: Gene not found

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

0 submitted variants in ClinVar

ClinVar

Protein Context — Lollipop Plot

INE2 · 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

ClinicalTrials.gov

No active trials found for this gene.

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Clinical Literature
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Full-Text Mentions
NLP-detected gene mentions in article bodies · via PubTator3
PubTator3
Chromium-Tanned Leather and Microbial Consortia: Identification of Taxa With Biodegradation Potential and Chromium Tolerance
Bonilla-Espadas M et al.·Environ Microbiol Rep
2025
Integrative lncRNA-mRNA co-expression network analysis identifies novel lncRNA E2F3-IT1 for rheumatoid arthritis
Wu LF et al.·Clin Transl Med
2021
Science and beyond science in the reporting of quality of facility-based maternal and newborn care during the COVID-19 pandemic:Authors' reply
Lazzerini M et al.·Lancet Reg Health Eur
2022
The mechanism of internal and external efficacy influences residents' pro-environmental behavior through environmental willingness
Yan QS et al.·PLoS One
2024Functional
Sequence complementarity between human noncoding RNAs and SARS-CoV-2 genes: What are the implications for human health?
Talotta R et al.·Biochim Biophys Acta Mol Basis Dis
2022
Top 5 full-text resultsSearch PubTator3 ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found

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External Resources

Links to major genomics databases and tools

Franklin by Genoox
AI-powered variant curation and clinical analysis
DECIPHER
Genomic variants and phenotypes in rare disease patients