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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Khdrbs2
KH domain containing, RNA binding, signal transduction associated 2
MGI:2159649
20 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Khdrbs1tm1Rchd/Khdrbs1tm1Rchd
Khdrbs2tm1.1Schei/Khdrbs2tm1.1Schei
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * BALB/cJ
decreased brain size J:208331
delaminated Purkinje cell layer J:208331
infertility J:208331
reduced cerebellar foliation J:208331
small cerebellum J:208331
Khdrbs2Tg(LRRK2*R1441G)135Cjli/Khdrbs2+
FVB-Khdrbs2Tg(LRRK2*R1441G)135Cjli
abnormal axon morphology J:149135
abnormal dopaminergic neuron morphology J:149135
abnormal locomotor activation J:149135
akinesia J:149135
decreased dopamine level J:149135
decreased locomotor activity J:149135
normal nervous system phenotype J:149135
tau protein deposits J:149135
Khdrbs2Tg(LRRK2*R1441G)135Cjli/Khdrbs2+
FVB/N-Khdrbs2Tg(LRRK2*R1441G)135Cjli/J
abnormal autophagy J:194153
abnormal digestive system physiology J:204940
abnormal locomotor activation J:204940
alpha-synuclein inclusion body J:194153
normal behavior/neurological phenotype J:204940
constipation J:204940
decreased locomotor activity J:204940
decreased vertical activity J:204940
diarrhea J:204940

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
11/19/2024
MGI 6.24
The Jackson Laboratory