Symbol Name ID |
Park7
Parkinson disease (autosomal recessive, early onset) 7 MGI:2135637 |
Allelic Composition Genetic Background |
Annotated Term | Reference |
Gpx1tm1Ysh/Gpx1tm1Ysh Prkntm1Shn/Prkntm1Shn Park7tm1Shn/Park7tm1Shn B6.Cg-Park7tm1Shn Gpx1tm1Ysh Prkntm1Shn |
impaired coordination | J:202221 |
increased dopamine level | J:202221 | |
increased serotonin level | J:202221 | |
Park7Gt(XE726)Byg/Park7Gt(XE726)Byg Pink1tm1.1Wrst/Pink1tm1.1Wrst involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6J |
normal cellular phenotype | J:242309 |
Park7Gt(XE726)Byg/Park7Gt(XE726)Byg Pink1tm1.1Wrst/Pink1tm1.1Wrst Rrn3tm1.1Igt/Rrn3tm1.1Igt Tg(Slc6a3-cre/ERT2)1Span/0 involves: 129 * 129P2/OlaHsd * 129S2/SvPas * C57BL/6J |
abnormal cell physiology | J:242309 |
abnormal nucleolus morphology | J:242309 | |
Prkntm1Shn/Prkntm1Shn Park7tm1Shn/Park7tm1Shn B6.Cg-Park7tm1Shn Prkntm1Shn |
impaired coordination | J:202221 |
increased serotonin level | J:202221 |
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 12/17/2024 MGI 6.24 |
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