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ME3-DT

Chr 11

ME3 divergent transcript

I cannot provide a clinical summary for ME3-DT as no functional or clinical information was provided in the data below the gene name. ME3-DT appears to be a long non-coding RNA or transcript variant, but without details about its function, associated diseases, or inheritance patterns, I cannot write an accurate clinical summary following the strict rules to use only the provided information.

Clinical SummaryME3-DT
📋
ClinVar Variants
4 unique Pathogenic / Likely Pathogenic· 1 VUS of 5 total submissions
Some data sources returned errors (2)

ensembl: Error: Ensembl fetch failed: 400 for https://rest.ensembl.org/lookup/symbol/homo_sapiens/ME3-DT?content-type=application/json&expand=1

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

5 submitted variants in ClinVar

Classification Summary

Pathogenic4
VUS1
4
Pathogenic
1
VUS

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
4
Likely Pathogenic
0
VUS
1
Likely Benign
0
Benign
0
Total5

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

ME3-DT · 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 →
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found