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p23-ST1
Gene Detail
 Symbol
Name
ID
p23-ST1
p23-ST1
MGI:4439296
Feature Type heritable phenotypic marker
Genetic Map
Chromosome 4
Syntenic
Mutations,
alleles, and
phenotypes
All mutations/alleles(1) : Chemically induced (ENU)(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)
Disease annotation references (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/09/2014
MGI 5.19
The Jackson Laboratory