mortality/aging
• homozygotes are born alive at the expected frequency (25%) and start suckling but die within 24 hrs after birth
|
renal/urinary system
• mutant kidneys display mesangial cell hypercellularity
|
• newborn homozygotes exhibit microcysts in the kidney cortex
|
• newborn homozygotes exhibit microcysts in the kidney medulla
|
• 24-hr-old homozygotes exhibit a 12% increase in kidney weight relative to wild-type pups; no differences in kidney weight are noted at birth
|
• newborn homozygotes display massive non-selective proteinuria
|
albuminuria
(
J:66970
)
• most of the proteins in the urine of mutant mice are of the size of albumin and smaller proteins; however, some proteins larger than albumin are also detected
|
• mutant kidneys display an enlarged Bowman's space
|
• mutant podocyte foot processes are abnormally low in number and in closer apposition
|
• mutant glomeruli exhibit partial effacement of podocyte foot processes
|
• cellular junctions devoid of slit diaphragms
|
• newborn homozygotes exhibit dilated distal renal tubules
|
• newborn homozygotes exhibit dilated proximal renal tubules
|
homeostasis/metabolism
• newborn homozygotes display massive non-selective proteinuria
|
albuminuria
(
J:66970
)
• most of the proteins in the urine of mutant mice are of the size of albumin and smaller proteins; however, some proteins larger than albumin are also detected
|
nervous system
N |
• newborn homozygotes display neither anatomical nor morphological abnormalities in the brain, despite significant expression in the ventricular zone of the fourth ventricle, the developing spinal cord, cerebellum, hippocampus and olfactory bulb
|
growth/size/body
• newborn homozygotes exhibit microcysts in the kidney cortex
|
• newborn homozygotes exhibit microcysts in the kidney medulla
|
• 24-hr-old homozygotes exhibit a 12% increase in kidney weight relative to wild-type pups; no differences in kidney weight are noted at birth
|
cellular
• mutant kidneys display mesangial cell hypercellularity
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
nephrotic syndrome | DOID:1184 | J:66970 |