FOXCUT

Chr 6

FOXC1 upstream transcript

Also known as: LINC01379, TCONS_00011636

35
ClinVar variants
32
Pathogenic / LP
pLI score
0
Active trials
Clinical SummaryFOXCUT
📋
ClinVar Variants
32 Pathogenic / Likely Pathogenic· 3 VUS of 35 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

35 submitted variants in ClinVar

Classification Summary

Pathogenic29
Likely Pathogenic3
VUS3
29
Pathogenic
3
Likely Pathogenic
3
VUS

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
29
Likely Pathogenic
3
VUS
3
Likely Benign
0
Benign
0
Total35

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

FOXCUT · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

OMIM — Genotype-Phenotype Relationships

1 OMIM entry

Clinical Literature
Landmark / reviewRecent case evidence

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →