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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Park7
Parkinson disease (autosomal recessive, early onset) 7
MGI:2135637
6 phenotypes from multigenic genotypes
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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

Contributing Projects:
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
04/16/2024
MGI 6.23
The Jackson Laboratory