LZTR1

leucine zipper like transcription regulator 1
OMIM: 600574
PanelMode of inheritanceDetails
8 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Noonan syndrome
R-numbers: R221
Signed-off version 2.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
R-numbers: R21, R412
Signed-off version 4.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Fetal hydrops, Noonan syndrome 10, 616564
R-numbers: R147
Signed-off version 3.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Noonan syndrome 10, increased nuchal translucency, Prenatal hydrops, cardiac findings
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 6.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Noonan syndrome 10, Prenatal hydrops, increased nuchal translucency, cardiac findings
Component of the following Super Panels:
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R135
Signed-off version 4.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Schwannomatosis-2, susceptibility to 615670, Noonan syndrome 10 616564
R-numbers: R236
Signed-off version 3.0
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 3.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Schwannomatosis-2, susceptibility to 615670, Noonan syndrome 10 616564