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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Wdr45
WD repeat domain 45
MGI:1859606
56 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Wdr45em1(IMPC)J/Y
C57BL/6NJ-Wdr45em1(IMPC)J/J
abnormal auditory brainstem response J:211773
abnormal bone structure J:211773
abnormal startle reflex J:211773
hyperactivity J:211773
increased circulating HDL cholesterol level J:211773
Wdr45em1(IMPC)J/Wdr45em1(IMPC)J
C57BL/6NJ-Wdr45em1(IMPC)J/J
decreased bone mineral content J:211773
decreased bone mineral density J:211773
increased circulating alkaline phosphatase level J:211773
Wdr45em1Wrst/Y
involves: C57BL/6N * FVB
abnormal cerebellar Purkinje cell layer J:307284
abnormal mitochondrial ATP synthesis coupled electron transport J:307284
abnormal social recognition J:307284
anisocytosis J:307284
astrocytosis J:307284
decreased circulating amylase level J:307284
decreased circulating lactate level J:307284
decreased circulating serum albumin level J:307284
decreased circulating total protein level J:307284
decreased circulating triglyceride level J:307284
decreased circulating unsaturated transferrin level J:307284
decreased cornea thickness J:307284
decreased dopaminergic neuron number J:307284
homeostasis/metabolism phenotype J:307284
normal homeostasis/metabolism phenotype J:307284
impaired coordination J:307284
impaired hearing J:307284
increased alkaline phosphatase activity J:307284
increased body weight J:307284
increased circulating aspartate transaminase level J:307284
increased circulating glucose level J:307284
increased circulating iron level J:307284
increased circulating lactate dehydrogenase level J:307284
increased erythrocyte cell number J:307284
increased eye anterior chamber depth J:307284
increased hemoglobin content J:307284
increased leukocyte cell number J:307284
increased locomotor activity J:307284
increased or absent threshold for auditory brainstem response J:307284
limb grasping J:307284
lipofuscinosis J:307284
neurodegeneration J:307284
retina degeneration J:307284
tremors J:307284
Wdr45em1Wrst/Wdr45+
involves: C57BL/6N * FVB
impaired coordination J:307284
increased locomotor activity J:307284
increased or absent threshold for auditory brainstem response J:307284
Wdr45em1Wrst/Wdr45em1Wrst
involves: C57BL/6N * FVB
abnormal cerebellar Purkinje cell layer J:307284
abnormal mitochondrial ATP synthesis coupled electron transport J:307284
anisocytosis J:307284
astrocytosis J:307284
decreased circulating lactate level J:307284
decreased cornea thickness J:307284
decreased dopaminergic neuron number J:307284
decreased total retina thickness J:307284
hematopoietic system phenotype J:307284
normal homeostasis/metabolism phenotype J:307284
impaired coordination J:307284
impaired glucose tolerance J:307284
impaired hearing J:307284
increased alkaline phosphatase activity J:307284
increased body weight J:307284
increased circulating aspartate transaminase level J:307284
increased circulating glucose level J:307284
increased circulating iron level J:307284
increased circulating lactate dehydrogenase level J:307284
increased eye anterior chamber depth J:307284
increased locomotor activity J:307284
increased or absent threshold for auditory brainstem response J:307284
limb grasping J:307284
lipofuscinosis J:307284
neurodegeneration J:307284
retina degeneration J:307284
tremors J:307284
Wdr45tm1Beij/Wdr45+
Tg(Nes-cre)1Kln/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL
axonal spheroids J:281235
impaired autophagy J:281235
Wdr45tm1Beij/Y
Tg(Nes-cre)1Kln/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL
abnormal excitatory postsynaptic potential J:281235
abnormal spatial working memory J:281235
astrocytosis J:281235
axon degeneration J:281235
axonal spheroids J:281235
normal behavior/neurological phenotype J:281235
brain vacuoles J:281235
demyelination J:281235
impaired autophagy J:281235
impaired contextual conditioning behavior J:281235
impaired coordination J:281235
impaired spatial learning J:281235
reduced long-term potentiation J:281235
Wdr45tm1Beij/Wdr45tm1Beij
Tg(Nes-cre)1Kln/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL
axonal spheroids J:281235
impaired autophagy J:281235

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
04/23/2024
MGI 6.23
The Jackson Laboratory