DSTYK

dual serine/threonine and tyrosine protein kinase
OMIM: 612666
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, CAKUT1 610805, Autosomal Recessive Complicated Spastic Paraparesis SPG23
R-numbers: R21
Signed-off version 1.92
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, CAKUT1
R-numbers: R257
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Renal hypodysplasia, {Congenital anomalies of kidney and urinary tract, susceptibility to}, CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, CAKUT1, ureteropelvic junction obstruction, {Congenital anomalies of kidney and urinary tract, susceptibility to}, 610805, vesicoureteric reflux