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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Wbp2
WW domain binding protein 2
MGI:104709
17 phenotypes from 1 allele in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Wbp2tm2a(EUCOMM)Wtsi/Wbp2tm2a(EUCOMM)Wtsi
C57BL/6N-Wbp2tm2a(EUCOMM)Wtsi/Cnrm
abnormal behavior J:165965
decreased body weight J:165965
hyperactivity J:165965
increased leukocyte cell number J:165965
Wbp2tm2a(EUCOMM)Wtsi/Wbp2tm2a(EUCOMM)Wtsi
C57BL/6N-Wbp2tm2a(EUCOMM)Wtsi/Wtsi
abnormal behavior J:175295
absent pinna reflex J:175295
decreased circulating fructosamine level J:175295
decreased circulating serum albumin level J:175295
hyperactivity J:175295
Wbp2tm2a(EUCOMM)Wtsi/Wbp2tm2a(EUCOMM)Wtsi
involves: C57BL/6N * C57BL/6NTac
abnormal auditory brainstem response waveform shape J:229594
abnormal auditory summating potential J:229594
abnormal cochlear IHC afferent innervation pattern J:229594
abnormal cochlear OHC afferent innervation pattern J:229594
abnormal distortion product otoacoustic emission J:229594
abnormal organ of Corti morphology J:229594
decreased circulating amylase level J:229594
normal hearing/vestibular/ear phenotype J:229594
increased or absent threshold for auditory brainstem response J:229594
sensorineural hearing loss J:229594

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
04/09/2024
MGI 6.23
The Jackson Laboratory