MAGOH-DT

Chr 1

MAGOH divergent transcript

I cannot provide a clinical summary for MAGOH-DT as no information about this gene's protein function, associated diseases, or inheritance patterns has been provided in the data below the instructions. Without supporting evidence about what this gene encodes or its clinical relevance, I cannot write an accurate clinical summary following the specified guidelines.

Clinical SummaryMAGOH-DT
📋
ClinVar Variants
3 unique Pathogenic / Likely Pathogenic of 4 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

4 submitted variants in ClinVar

Classification Summary

Pathogenic1
Likely Pathogenic2
1
Pathogenic
2
Likely Pathogenic

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
1
Likely Pathogenic
2
VUS
0
Likely Benign
0
Benign
0
Total3

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

MAGOH-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 →
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