Scube2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Scube2
signal peptide, CUB domain, EGF-like 2
MGI:1928765

20 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Scube2^tm1.1Rbya/Scube2^tm1.1Rbya B6.129-Scube2^tm1.1Rbya	abnormal bone ossification	J:226676
	abnormal chondrocyte differentiation	J:226676
	abnormal endochondral bone ossification	J:226676
	abnormal long bone epiphyseal plate proliferative zone	J:226676
	abnormal long bone hypertrophic chondrocyte zone	J:226676
	abnormal skeleton development	J:226676
	abnormal trabecular bone morphology	J:226676
	decreased body height	J:226676
	decreased body length	J:226676
	decreased body size	J:226676
	decreased body weight	J:226676
	decreased bone trabecula number	J:226676
	decreased chondrocyte proliferation	J:226676
	decreased compact bone thickness	J:226676
	decreased osteoblast cell number	J:226676
	decreased trabecular bone thickness	J:226676
	decreased trabecular bone volume	J:226676
	decreased volumetric bone mineral density	J:226676
	short femur	J:226676
	short tibia	J:226676
Scube2^tm1Rbya/Scube2^tm1Rbya involves: 129S1/Sv * 129X1/SvJ	abnormal skeleton development	J:226676

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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