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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Nrn1
neuritin 1
MGI:1915654
14 phenotypes from 1 allele in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Nrn1tm1.2Ndiv/Nrn1tm1.2Ndiv
C57BL/6-Nrn1tm1.2Ndiv
abnormal CNS synapse formation J:178970
abnormal dendrite morphology J:178970
abnormal miniature excitatory postsynaptic currents J:178970
abnormal nervous system development J:178970
abnormal postsynaptic density morphology J:178970
abnormal spatial learning J:178970
abnormal synapse morphology J:178970
decreased body length J:178970
decreased body weight J:178970
delayed axon extension J:178970
delayed CNS synapse formation J:178970
impaired contextual conditioning behavior J:178970
impaired cued conditioning behavior J:178970
normal nervous system phenotype J:178970
Nrn1tm1.2Ndiv/Nrn1tm1.2Ndiv
Tg(Thy1-EGFP)SJrs/0
involves: C57BL/6 * CBA
abnormal CNS synapse formation J:178970

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
04/30/2024
MGI 6.23
The Jackson Laboratory