FGGY-DT

Chr 1

FGGY divergent transcript

I cannot write a clinical gene summary for FGGY-DT as no information about this gene's protein function, associated diseases, or inheritance patterns has been provided in the data below my instructions. To create an accurate clinical summary, I would need specific information about what protein this gene encodes, what phenotypes result from mutations, and the inheritance pattern observed in affected families.

Clinical SummaryFGGY-DT
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ClinVar Variants
8 unique Pathogenic / Likely Pathogenic· 1 VUS of 9 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

9 submitted variants in ClinVar

Classification Summary

Pathogenic6
Likely Pathogenic2
VUS1
6
Pathogenic
2
Likely Pathogenic
1
VUS

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
6
Likely Pathogenic
2
VUS
1
Likely Benign
0
Benign
0
Total9

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

FGGY-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.

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Clinical Literature
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