PanelApp
  1. Genes and Genomic Entities
  2. FLT4

FLT4

fms related tyrosine kinase 4
OMIM: 136352, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green FLT4 in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 0.430

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Congenital heart defects, multiple types, 7, MIM#618780

Green FLT4 in Hydrops fetalis


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.324

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Lymphatic malformation 1, MIM# 153100

Green FLT4 in Lymphoedema_nonsyndromic


Level 2: Cardiovascular disorders
Version 0.44

Component of the following Super Panels:

  • Vascular Malformations SuperPanel

    		•  review Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green FLT4 in Mendeliome


    Version 1.2374

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Congenital heart defects, multiple types, 7, MIM# 618780
    • Lymphatic malformation 1, MIM# 153100

    Green FLT4 in Fetal anomalies


    Version 1.314

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Congenital heart defects, multiple types, 7, MIM# 618780
    • Lymphatic malformation 1, MIM# 153100