Cul7 Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Cul7^{tm1a(EUCOMM)Wtsi}/Cul7⁺ Not Specified	abnormal bone mineralization	J:165965
	decreased body weight	J:165965
	decreased bone mineral density	J:165965
Cul7^tm1Jdec/Cul7^tm1Jdec 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
Cul7^tm1Zqp/Cul7^tm1Zqp 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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