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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ntrk2
neurotrophic tyrosine kinase, receptor, type 2
MGI:97384
14 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Bdnftm1Jae/Bdnftm2(Ntf5)Jae
Ntrk2tm1Kln/Ntrk2tm1Kln
involves: 129S4/SvJae
decreased sensory neuron number J:61340
head bobbing J:61340
hyperactivity J:61340
spinning J:61340
Bdnftm1Par/Bdnf+
Ntrk2tm1.1Tes/Ntrk2+
B6.129S1-Bdnftm1Par Ntrk2tm1.1Tes
increased aggression towards male mice J:144845
Bdnftm1Par/Bdnf+
Ntrk2tm1.1Tes/Ntrk2tm1.1Tes
B6.129S1-Bdnftm1Par Ntrk2tm1.1Tes
increased aggression towards male mice J:144845
increased body weight J:144845
Bdnftm2(Ntf5)Jae/Bdnftm2(Ntf5)Jae
Ntrk2tm1Kln/Ntrk2tm1Kln
involves: 129S4/SvJae
hyperactivity J:61340
Mirc35tm1.1Pern/Mirc35tm1.1Pern
Ntrk2tm1.1(cre/ERT2)Pern/Ntrk2+
involves: 129S2/SvPas * C57BL/6J * CBA/J
abnormal mechanoreceptor morphology J:270955
Ntrk2tm1.1Tes/Ntrk2+
Rb(12.Ts171665Dn)2Cje/0
involves: 129S1/Sv * C3H/HeSnJ * C57BL/6JEi
normal nervous system phenotype J:110478
Ntrk2tm1Kln/Ntrk2tm1Kln
Ntrk3tm1Kln/Ntrk3tm1Kln
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal cochlear nerve morphology J:75365
decreased sensory neuron number J:75365
Ntrk2tm2Kln/Ntrk2tm2Kln
Slc1a3tm1(cre/ERT2)Mgoe/?
Gt(ROSA)26Sortm1Sor/?
involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6 * SJL
abnormal dendrite morphology J:143452
abnormal neuron differentiation J:143452
decreased locomotor activity J:143452
increased thigmotaxis J:143452
reduced long-term potentiation J:143452
Ntrk2tm2Kln/Ntrk2tm2Kln
Slc1a3tm1(cre/ERT2)Mgoe/?
Tg(CAG-Bgeo/GFP)21Lbe/?
involves: 129/Sv * C57BL/6 * SJL
normal nervous system phenotype J:143452

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
04/09/2024
MGI 6.23
The Jackson Laboratory