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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Gtpbp2
GTP binding protein 2
MGI:1860138
19 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Gtpbp2nmf205/Gtpbp2+
n-TRtct5m1J/n-TRtct5m1J
C57BL/6J-Gtpbp2nmf205/J
no abnormal phenotype detected J:211326
Gtpbp2nmf205/Gtpbp2nmf205
n-TRtct5m1J/n-TRtct5+
involves: 129S1/SvImJ * C57BL/6J
no abnormal phenotype detected J:211326
Gtpbp2nmf205/Gtpbp2nmf205
n-TRtct5m1J/n-TRtct5+
involves: A/J * C57BL/6J
no abnormal phenotype detected J:211326
Gtpbp2nmf205/Gtpbp2nmf205
n-TRtct5m1J/n-TRtct5+
involves: AKR/J * C57BL/6J
no abnormal phenotype detected J:211326
Gtpbp2nmf205/Gtpbp2nmf205
n-TRtct5m1J/n-TRtct5+
involves: C57BL/6J * C57BL/6NJ
no abnormal phenotype detected J:211326
Gtpbp2nmf205/Gtpbp2nmf205
n-TRtct5m1J/n-TRtct5+
involves: C57BL/6J * CBA/J
no abnormal phenotype detected J:211326
Gtpbp2nmf205/Gtpbp2nmf205
n-TRtct5m1J/n-TRtct5+
involves: C57BL/6J * DBA/2J
no abnormal phenotype detected J:211326
Gtpbp2nmf205/Gtpbp2nmf205
n-TRtct5m1J/n-TRtct5+
involves: C57BL/6J * MA/MyJ
no abnormal phenotype detected J:211326
Gtpbp2nmf205/Gtpbp2nmf205
n-TRtct5m1J/n-TRtct5+
involves: C57BL/6J * NOD/ShiLtJ
no abnormal phenotype detected J:211326
Gtpbp2nmf205/Gtpbp2nmf205
n-TRtct5m1J/n-TRtct5m1J
C57BL/6J-Gtpbp2nmf205/J
abnormal cerebellar layer morphology J:211326
abnormal cerebellum morphology J:211326
abnormal dentate gyrus morphology J:211326
abnormal hippocampus CA2 region morphology J:211326
abnormal motor capabilities/coordination/movement J:82238
abnormal retina horizontal cell morphology J:211326
abnormal retina morphology J:211326
abnormal ribosomal stalling J:211326
amacrine cell degeneration J:211326
ataxia J:211326
decreased cerebellar granule cell number J:211326
increased neuron apoptosis J:211326
premature death J:211326
retina degeneration J:211326
retina ganglion cell degeneration J:211326
retina photoreceptor degeneration J:211326
Gtpbp2nmf205/Gtpbp2nmf205
n-TRtct5m1J/n-TRtct5m1J
Tg(n-TRtct1)516Slac/0
C57BL/6J-Gtpbp2nmf205 Tg(n-TRtct1)516Slac
normal nervous system phenotype J:297745
Gtpbp2nmf205/Gtpbp2nmf205
n-TRtct5m1J/n-TRtct5m1J
Tg(n-TRtct2)557Slac/0
C57BL/6J-Gtpbp2nmf205 Tg(n-TRtct2)557Slac
normal nervous system phenotype J:297745
Gtpbp2nmf205/Gtpbp2nmf205
Tg(n-TRtct5)574Slac/0
involves: C57BL/6J
abnormal cerebellum morphology J:211326
Gtpbp2nmf205/Gtpbp2nmf205
Tg(n-TRtct5)609Slac/0
C57BL/6J-Gtpbp2nmf205 Tg(n-TRtct5)609Slac
abnormal cerebellum morphology J:211326
Gtpbp2nmf205/Gtpbp2tm1Ynim
n-TRtct5m1J/n-TRtct5m1J
(C57BL/6J-Gtpbp2nmf205/J x B6.Cg-Gtpbp2tm1Ynim)F1
abnormal cerebellum morphology J:211326
neurodegeneration J:211326
Gtpbp2tm1Ynim/Gtpbp2tm1Ynim
n-TRtct5m1J/n-TRtct5m1J
B6.Cg-Gtpbp2tm1Ynim
abnormal cerebellar layer morphology J:211326
abnormal cerebellum morphology J:211326
increased neuron apoptosis J:211326
neurodegeneration J:211326

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
12/10/2024
MGI 6.24
The Jackson Laboratory