FOXF2-DT

Chr 6

FOXF2 divergent transcript

Also known as: LINC01394, TCONS_00012639

NCBI Gene: 105374880ENSG00000261730
101
ClinVar variants
28
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— FOXF2-DT
📋
ClinVar Variants
28 Pathogenic / Likely Pathogenic· 59 VUS of 101 total submissions

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

101 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic25
Likely Pathogenic3
VUS59
Likely Benign12
Benign2
25
Pathogenic
3
Likely Pathogenic
59
VUS
12
Likely Benign
2
Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
25
0
25
Likely Pathogenic
0
0
3
0
3
VUS
0
56
3
0
59
Likely Benign
0
3
3
6
12
Benign
0
0
2
0
2
Total059366101

LoF = frameshift, stop gained/lost, canonical splice · Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

FOXF2-DT · protein map & ClinVar variants

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

OMIM — Genotype-Phenotype

OMIM

No OMIM entries found.

Clinical Literature
Landmark / reviewRecent case evidence

No publications found for FOXF2-DT

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →

External Resources

Links to major genomics databases and tools