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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Fbxw8
F-box and WD-40 domain protein 8
MGI:1923041
28 phenotypes from 3 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Fbxw8Gt(RRT057)Byg/Fbxw8Gt(RRT057)Byg
involves: 129P2/OlaHsd * C57BL/6
abnormal brain size J:130238
atelectasis J:130238
cyanosis J:130238
decreased body weight J:130238
decreased embryo size J:130238
decreased fetal size J:130238
decreased placenta weight J:130238
decreased survivor rate J:130238
neonatal lethality, incomplete penetrance J:130238
respiratory distress J:130238
normal skeleton phenotype J:130238
slow postnatal weight gain J:130238
Fbxw8tm1b(EUCOMM)Hmgu/Fbxw8+
C57BL/6N-Fbxw8tm1b(EUCOMM)Hmgu/Nju
decreased lymphocyte cell number J:211773
increased basophil cell number J:211773
increased blood urea nitrogen level J:211773
increased circulating creatinine level J:211773
increased eosinophil cell number J:211773
increased neutrophil cell number J:211773
Fbxw8tm1b(EUCOMM)Hmgu/Fbxw8tm1b(EUCOMM)Hmgu
C57BL/6N-Fbxw8tm1b(EUCOMM)Hmgu/Nju
preweaning lethality, incomplete penetrance J:211773
Fbxw8tm1Kei/Fbxw8tm1Kei
involves: C57BL/6
abnormal placenta labyrinth morphology J:111403
abnormal placenta morphology J:111403
abnormal placental labyrinth vasculature morphology J:111403
abnormal spongiotrophoblast layer morphology J:111403
decreased embryo size J:111403
embryonic growth retardation J:111403
embryonic lethality during organogenesis, incomplete penetrance J:111403
lethality throughout fetal growth and development, incomplete penetrance J:111403
normal respiratory system phenotype J:111403
Fbxw8tm1Kei/Fbxw8tm1Kei
Not Specified
normal cellular phenotype J:183656

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
04/16/2024
MGI 6.23
The Jackson Laboratory