FLT4 - Gene browser

FLT4

fms related receptor tyrosine kinase 4

HCNC Approved Symbol: FLT4 (HGNC:3767)
Genomic Coordinates: 5:180,601,506 - 180,650,298 (5q35.3)
Synonyms: VEGFR3, PCL, VEGFR-3
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

6Patients

In total, 6 patients were diagnosed with a variant in the FLT4 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

06
Patient count

Swelling caused by excess lymph fluid under skin: 3 (50.0%)
Patient Count: 3 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (50.0%)
Lymphedema: 2 (33.3%)
Patient Count: 2 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (33.3%)
Atrial septal defect: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Tetralogy of fallot: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Edema of dorsum of feet: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)