p23-ST1
Gene Detail

Symbol Name ID

p23-ST1 p23-ST1 MGI:4439296

Feature Type

heritable phenotypic marker

Genetic Map

Chromosome 4
Syntenic

Alleles and phenotypes

All alleles(1) : Chemically induced(1)
 

Mice homozygous for the ENU mutation exhibit normal-pressure hydrocephalus with astrocytosis, microgliosis, impaired coordination, abnormal urination, and deficits in short-term and long-term memory.

 
Human Diseases Modeled Using Mouse p23-ST1 (1)    Alleles Annotated to Human Diseases(1)   

References

(Earliest) J:87589 Wu JY, et al., ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease. J Clin Invest. 2004 Feb;113(3):434-40
(Latest) J:158278 Lee MJ, et al., Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus. PLoS One. 2009;4(11):e7868
All references(2)