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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Wbp11
WW domain binding protein 11
MGI:1891823
28 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Wbp11em1Gcha/Wbp11+
involves: C57BL/6J * FVB/N
abnormal cervical rib J:300837
abnormal cervical vertebrae morphology J:300837
abnormal esophagus morphology J:300837
abnormal kidney morphology J:300837
abnormal rib morphology J:300837
abnormal thoracic vertebrae morphology J:300837
abnormal vertebral transverse process morphology J:300837
normal cardiovascular system phenotype J:300837
cerebral edema J:300837
cervical vertebral fusion J:300837
choanal atresia J:300837
cleft palate J:300837
decreased brain size J:300837
decreased fetal weight J:300837
decreased lumbar vertebrae number J:300837
decreased placenta weight J:300837
decreased rib number J:300837
ectopic thymus J:300837
embryonic growth retardation J:300837
hemivertebra J:300837
prenatal lethality, incomplete penetrance J:300837
preweaning lethality, incomplete penetrance J:300837
small kidney J:300837
small liver J:300837
small lung J:300837
sternebra fusion J:300837
thoracic vertebral fusion J:300837
Wbp11em1Gcha/Wbp11em1Gcha
involves: C57BL/6J * FVB/N
embryonic lethality prior to organogenesis, complete penetrance J:300837

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
10/09/2024
MGI 6.24
The Jackson Laboratory