FLT4 gene homepage

General information
Gene symbol FLT4
Gene name fms-related tyrosine kinase 4
Chromosome 5
Chromosomal band q34-q35
Imprinted Unknown
Genomic reference NG_011536.1
Transcript reference NM_182925.4
Exon/intron information NM_182925.4 exon/intron table
Associated with diseases LMPH-1A, Hemangioma, capillary infantile
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (4) Pia Ostergaard, Michel van Geel, Élodie Fastré and Pascal Brouillard
Total number of public variants reported 117
Unique public DNA variants reported 72
Individuals with public variants 197
Hidden variants 35
Notes Aliases for FLT4 include VEGFR3, PCL, FLT41, LMPH1A
Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created April 29, 2010
Date last updated January 13, 2018
Version FLT4:180113

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_182925.4.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL http://www.LOVD.nl/FLT4
External URL Orphanet
HGNC 3767
Entrez Gene 2324
PubMed articles FLT4
OMIM - Gene 136352
OMIM - Diseases LMPH-1A (lymphedema, hereditary, type Ia (LMPH-1A, Milroy disease))
Hemangioma, capillary infantile
GeneCards FLT4
GeneTests FLT4

Active transcripts




NCBI ID     

NCBI Protein ID     

00024081 5 transcript variant 1 NM_182925.4 NP_891555.2 117

Copyright & disclaimer
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