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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Vps35
VPS35 retromer complex component
MGI:1890467
31 phenotypes from 6 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Vps35em1(IMPC)H/Vps35+
C57BL/6N-Vps35em1(IMPC)H/H
abnormal gait J:211773
abnormal retina morphology J:211773
Vps35em1(IMPC)H/Vps35em1(IMPC)H
C57BL/6N-Vps35em1(IMPC)H/H
preweaning lethality, complete penetrance J:211773
Vps35Gt(RRK261)Byg/Vps35+
B6.129P2-Vps35Gt(RRK261)Byg
abnormal dopaminergic neuron morphology J:225806
abnormal lysosome morphology J:225806
alpha-synuclein inclusion body J:225806
decreased dopamine level J:225806
decreased locomotor activity J:225806
decreased vertical activity J:225806
loss of dopaminergic neurons J:225806
Vps35Gt(RRK261)Byg/Vps35Gt(RRK261)Byg
B6.129P2-Vps35Gt(RRK261)Byg
embryonic lethality, complete penetrance J:178937
Vps35tm1.1Hckn/Vps35tm1.1Hckn
Tg(Vil1-cre/ERT2)23Syr/0
involves: 129P2/OlaHsd * C57BL/6 * DBA/2
abnormal small intestinal crypt cell proliferation J:223191
normal digestive/alimentary phenotype J:223191
Vps35tm1.1Hlw/Vps35+
involves: 129S/SvEv * C57BL/6J
abnormal mitochondrial shape J:329507
abnormal substantia nigra pars compacta morphology J:329507
bradykinesia J:329507
decreased locomotor activity J:329507
decreased mitochondrial size J:329507
normal nervous system phenotype J:329507
oxidative stress J:329507
slow movement J:329507
Vps35tm1.1Mjff/Vps35+
B6.Cg-Vps35tm1.1Mjff
abnormal nervous system dopamine level J:274797
Vps35tm1.1Mjff/Vps35tm1.1Mjff
B6.Cg-Vps35tm1.1Mjff
abnormal axon morphology J:303283
abnormal dopaminergic neuron morphology J:303283
abnormal mitochondrial physiology J:303283
abnormal mitochondrial shape J:303283
abnormal nervous system dopamine level J:274797
alpha-synuclein inclusion body J:303283
astrocytosis J:303283
normal behavior/neurological phenotype J:303283
decreased dopaminergic neuron number J:303283
decreased locomotor activity J:303283
impaired coordination J:303283
lipofuscinosis J:303283
microgliosis J:303283
neurodegeneration J:303283
Vps35tm1.2Mjff/Vps35+
involves: C57BL/6
no abnormal phenotype detected J:101977

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