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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Grin3a
glutamate receptor ionotropic, NMDA3A
MGI:1933206
7 phenotypes from 3 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Grin3atm1b(EUCOMM)Hmgu/Grin3atm1b(EUCOMM)Hmgu
C57BL/6N-Grin3atm1b(EUCOMM)Hmgu/H
abnormal epididymis morphology J:211773
Grin3atm1Lex/Grin3atm1Lex
involves: 129S5/SvEvBrd * C57BL/6J
no abnormal phenotype detected J:103485
Grin3atm1Nnk/Grin3atm1Nnk
either: (involves: 129S/SvEv * 129X1/SvJ) or (involves: 129X1/SvJ * Black Swiss)
abnormal dendrite morphology J:66481
abnormal eye electrophysiology J:85752
abnormal single cell response J:66481
Grin3atm1Nnk/Grin3atm1Nnk
involves: 129X1/SvJ * Black Swiss * C57BL/6
abnormal prepulse inhibition J:102120
normal behavior/neurological phenotype J:102120

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
11/12/2024
MGI 6.24
The Jackson Laboratory