Bgn Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Bgn
biglycan
MGI:88158

21 phenotypes from 2 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Bgn^{tm1.1(KOMP)Vlcg}/Bgn^{tm1.1(KOMP)Vlcg} C57BL/6N-Bgn^{tm1.1(KOMP)Vlcg}/Wtsi	decreased body length	J:211773
Bgn^tm1Mfy/Y involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	abnormal bone collagen fibril morphology	J:91512
	abnormal cutaneous collagen fibril morphology	J:91512
	abnormal tendon collagen fibril morphology	J:91512
	normal integument phenotype	J:91512
	thin dermal layer	J:91512
Bgn^tm1Mfy/Y involves: 129S4/SvJae * C57BL/6	abnormal bone ossification	J:76203
	abnormal femur morphology	J:49647
	abnormal long bone diaphysis morphology	J:49647
	abnormal long bone epiphysis morphology	J:49647
	abnormal long bone metaphysis morphology	J:49647
	abnormal tendon collagen fibril morphology	J:76203
	abnormal trabecular bone morphology	J:49647
	decreased body weight	J:49647
	decreased bone mineral content	J:49647
	decreased compact bone thickness	J:49647
	decreased osteoblast cell number	J:49647
	osteoarthritis	J:76203
	osteoporosis	J:49647
	short femur	J:49647
Bgn^tm1Mfy/Bgn^tm1Mfy involves: 129S4/SvJae	decreased body weight	J:222369
	decreased collagen level	J:222369
	osteoarthritis	J:222369
	normal skeleton phenotype	J:222369

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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