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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Plxnc1
plexin C1
MGI:1890127
14 phenotypes from 2 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Plxnc1em1(IMPC)Mbp/Plxnc1em1(IMPC)Mbp
C57BL/6N-Plxnc1em1(IMPC)Mbp/MbpMmucd 		abnormal kidney morphology J:211773
abnormal spleen morphology J:211773
enlarged kidney J:211773
increased circulating calcium level J:211773
increased circulating cholesterol level J:211773
increased circulating HDL cholesterol level J:211773
increased circulating total protein level J:211773
increased vertical activity J:211773
small kidney J:211773
small spleen J:211773
Plxnc1tm1Alk/Plxnc1tm1Alk
B6.129-Plxnc1tm1Alk 		no abnormal phenotype detected J:87191
Plxnc1tm1Alk/Plxnc1tm1Alk
involves: 129 		normal vision/eye phenotype J:172268
Plxnc1tm1Alk/Plxnc1tm1Alk
involves: 129/Sv * C57BL/6 		abnormal neuron morphology J:120909
abnormal neuronal migration J:120909
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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Send questions and comments to User Support. 		last database update
04/09/2024
MGI 6.23 		The Jackson Laboratory