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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.

Frequently observed phenotypes

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

Swelling caused by excess lymph fluid under skin
 3 (50.0%)
Lymphedema
 2 (33.3%)
Atrial septal defect
 1 (16.7%)
Tetralogy of fallot
 1 (16.7%)
Edema of dorsum of feet
 1 (16.7%)
FLT4 - Gene browser | 3billion