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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cul7
cullin 7
MGI:1913765
13 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cul7tm1a(EUCOMM)Wtsi/Cul7+
Not Specified
abnormal bone mineralization J:165965
decreased body weight J:165965
decreased bone mineral density J:165965
Cul7tm1Jdec/Cul7tm1Jdec
involves: C57BL/6 * CD-1
abnormal placenta development J:85161
abnormal vascular development J:85161
decreased embryo size J:85161
decreased trophoblast giant cell number J:85161
hemorrhage J:85161
neonatal lethality, complete penetrance J:85161
respiratory distress J:85161
Cul7tm1Zqp/Cul7tm1Zqp
involves: 129S/SvEv * C57BL/6J
early cellular replicative senescence J:137062
fetal growth retardation J:137062
lethality throughout fetal growth and development, complete penetrance J:137062

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