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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Grin2c
glutamate receptor, ionotropic, NMDA2C (epsilon 3)
MGI:95822
9 phenotypes from 6 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Grin2ctm1Bnno/Grin2ctm1Bnno
involves: 129S6/SvEvTac * FVB/N
no abnormal phenotype detected J:123236
Grin2ctm1Mwa/Grin2ctm1Mwa
involves: C57BL/6 * CBA
no abnormal phenotype detected J:92648
Grin2ctm1Nak/Grin2ctm1Nak
involves: 129S/SvEv
abnormal excitatory postsynaptic currents J:66455
abnormal miniature excitatory postsynaptic currents J:66455
normal behavior/neurological phenotype J:66455
decreased vertical activity J:66455
normal nervous system phenotype J:66455
Grin2ctm1Nts/Grin2ctm1Nts
involves: 129S2/SvPas * C57BL/6J
abnormal CNS synaptic transmission J:34597
abnormal NMDA-mediated synaptic currents J:34597
Grin2ctm1Rsp/Grin2ctm1Rsp
involves: 129S1/Sv * 129X1/SvJ
impaired balance J:45446
Grin2ctm2Rsp/Grin2ctm2Rsp
involves: 129S1/Sv * 129X1/SvJ
impaired balance J:45446

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
04/23/2024
MGI 6.23
The Jackson Laboratory