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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Uchl1
ubiquitin carboxy-terminal hydrolase L1
MGI:103149
21 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Tg(PDGFB-UCHL1*I93M)HWada/?
involves: C57BL/6J
abnormal nervous system morphology J:128045
abnormal striatum morphology J:128045
decreased dopamine level J:128045
decreased dopaminergic neuron number J:128045
hyperactivity J:128045
hypoactivity J:128045
Tg(PDGFB-UCHL1*I93M)LWada/0
involves: C57BL/6J
increased susceptibility to dopaminergic neuron neurotoxicity J:128045
normal nervous system phenotype J:128045
Tg(Thy1-Snca)1S13Putt/0
Uchl1tm1Dgen/Uchl1tm1Dgen
involves: 129P2/OlaHsd * C57BL/6
alpha-synuclein inclusion body J:207278
astrocytosis J:207278
decreased grip strength J:207278
impaired coordination J:207278
premature death J:207278
Uchl1gad/Uchl1gad
Uchl3tm1Tilg/Uchl3tm1Tilg
involves: 129S1/Sv * C57BL/6J * CBA/Nga * RFM/Nga
abnormal dorsal root ganglion morphology J:71819
abnormal gait J:71819
ataxia J:71819
axon degeneration J:71819
axonal dystrophy J:71819
decreased body weight J:71819
dysphagia J:71819
paralysis J:71819
premature death J:71819

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
01/07/2020
MGI 6.14
The Jackson Laboratory