Symbol Name ID |
Prrc2a
proline-rich coiled-coil 2A MGI:1915467 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Polydipsia |
Polyphagia |
Disease(s) Associated with PRRC2A | ||
type 1 diabetes mellitus |
Mouse Phenotypes | nervous system phenotype |
decreased oligodendrocyte progenitor number |
abnormal brain morphology |
abnormal brain development |
increased brain weight |
enlarged lateral ventricles |
abnormal corpus callosum morphology |
decreased astrocyte number |
decreased oligodendrocyte number |
abnormal astrocyte physiology |
dysmyelination |
decreased nerve conduction velocity |
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Availability | Mouse Genotype | ||||||||||||
Prrc2atm1Fcw/Prrc2atm1Fcw Tg(Nes-cre)1Kln/0 (conditional) |
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Prrc2atm1Fcw/Prrc2atm1Fcw Olig2tm2(TVA,cre)Rth/Olig2+ (conditional) |
* | ||||||||||||
Prrc2atm1Fcw/Prrc2atm1Fcw Tg(Gfap-cre)77.6Mvs/0 (conditional) |
* |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/30/2024 MGI 6.23 |
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