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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Plod1
procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
MGI:99907
12 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Plod1tm1b(EUCOMM)Hmgu/Plod1tm1b(EUCOMM)Hmgu
C57BL/6N-Plod1tm1b(EUCOMM)Hmgu/Tcp
decreased bone mineral content J:211773
decreased bone mineral density J:211773
decreased grip strength J:211773
Plod1tm1Soin/Plod1tm1Soin
involves: 129S6/SvEvTac * C57BL/6
abnormal aorta smooth muscle morphology J:120891
abnormal aorta wall morphology J:120891
abnormal cutaneous collagen fibril morphology J:120891
abnormal motor capabilities/coordination/movement J:120891
aortic dissection J:120891
hemorrhage J:120891
hypotonia J:120891
paralysis J:120891
premature death J:120891

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
08/06/2019
MGI 6.14
The Jackson Laboratory