Cnih2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cnih2
cornichon family AMPA receptor auxiliary protein 2
MGI:1277225

12 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cnih2^tm1.1Ran/Cnih2^tm1.1Ran involves: 129S6/SvEvTac * C57BL/6NTac	no abnormal phenotype detected	J:197912
Cnih2^tm1.1Ran/Cnih2^tm1.1Ran involves: 129S6/SvEvTac * C57BL/6NTac	abnormal AMPA-mediated synaptic currents	J:197912
	abnormal miniature excitatory postsynaptic currents	J:197912
	normal nervous system phenotype	J:197912
	reduced AMPA-mediated synaptic currents	J:197912
Cnih2^tm1.1Ran/Cnih2^tm1.1Ran Neurod6^tm1(cre)Kan/Neurod6⁺ involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6NTac	normal nervous system phenotype	J:197912
	reduced AMPA-mediated synaptic currents	J:197912
Cnih2^{tm1b(KOMP)Wtsi}/Cnih2^{tm1b(KOMP)Wtsi} B6N(Cg)-Cnih2^{tm1b(KOMP)Wtsi}/J	abnormal bone structure	J:211773
	abnormal locomotor behavior	J:211773
	decreased circulating calcium level	J:211773
	hyperactivity	J:211773
	increased circulating alkaline phosphatase level	J:211773
	increased exploration in new environment	J:211773
	increased vertical activity	J:211773

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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