LZTR1

leucine zipper like transcription regulator 1
OMIM: 600574
PanelMode of inheritanceDetails
6 panels
R-numbers: R135
Signed-off version 1.4
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Schwannomatosis-2, susceptibility to 615670, Noonan syndrome 10 616564
R-numbers: R21
Signed-off version 1.92
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Fetal hydrops, Noonan syndrome 10, 616564
R-numbers: R147
Signed-off version 1.4
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Noonan syndrome 10, increased nuchal translucency, Prenatal hydrops, cardiac findings
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 3.2
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Noonan syndrome 10, Prenatal hydrops, increased nuchal translucency, cardiac findings
R-numbers: R236
Signed-off version 1.4
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
NOONAN SYNDROME 10, NS2, NS10, NOONAN SYNDROME 2, Schwannomatosis-2, susceptibility to 615670, Noonan syndrome 10 616564
R-numbers: R136
Signed-off version 2.2
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Schwannomatosis-2, susceptibility to 615670, Noonan syndrome 10 616564