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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Wdr81
WD repeat domain 81
MGI:2681828
18 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Wdr81em1(IMPC)J/Wdr81+
C57BL/6NJ-Wdr81em1(IMPC)J/J
decreased grip strength J:211773
increased blood urea nitrogen level J:211773
Wdr81em1(IMPC)J/Wdr81em1(IMPC)J
C57BL/6NJ-Wdr81em1(IMPC)J/J
preweaning lethality, complete penetrance J:211773
Wdr81m1Btlr/Wdr81m1Btlr
C57BL/6J-Wdr81m1Btlr
ataxia J:267697
decreased body weight J:267697
Wdr81nur5/Wdr81nur5
involves: C57BL/6J
abnormal gait J:196651
abnormal neuron mitochondrial morphology J:196651
abnormal Purkinje cell dendrite morphology J:196651
ataxia J:196651
decreased cerebellar granule cell number J:196651
decreased Purkinje cell number J:196651
decreased retina photoreceptor cell number J:196651
decreased total retina thickness J:196651
disorganized mitochondrial cristae J:196651
impaired coordination J:196651
increased mitochondrial size J:196651
short stride length J:196651
tremors J:85113, J:196651
weight loss J:196651

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