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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Wsb2
WD repeat and SOCS box-containing 2
MGI:2144041
15 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Wsb2tm1b(EUCOMM)Hmgu/Wsb2tm1b(EUCOMM)Hmgu
C57BL/6N-Wsb2tm1b(EUCOMM)Hmgu/Cnrm
abnormal retina blood vessel morphology J:211773
abnormal retina vasculature morphology J:211773
abnormal tooth morphology J:211773
decreased cardiac muscle contractility J:211773
decreased food intake J:211773
decreased heart rate J:211773
decreased locomotor activity J:211773
decreased respiratory quotient J:211773
decreased total retina thickness J:211773
decreased vertical activity J:211773
female infertility J:211773
hyperactivity J:211773
increased circulating alkaline phosphatase level J:211773
increased grip strength J:211773
male infertility J:211773

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