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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Map1b
microtubule-associated protein 1B
MGI:1306778
48 phenotypes from 3 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Map1bGt(IRESBetageo)2Pgr/Map1bGt(IRESBetageo)2Pgr
involves: 129S1/Sv * 129X1/SvJ * NMRI
abnormal cerebellar foliation J:65509
abnormal cerebellum morphology J:65509
abnormal cerebral cortex morphology J:65509
abnormal corpus callosum morphology J:65509
abnormal dentate gyrus morphology J:65509
abnormal hippocampus morphology J:65509
abnormal limb posture J:65509
abnormal olfactory bulb morphology J:65509
absent subplate J:65509
enlarged lateral ventricles J:65509
enlarged third ventricle J:65509
neonatal lethality, complete penetrance J:65509
unresponsive to tactile stimuli J:65509
Map1btm1Prop/Map1btm1Prop
involves: 129S1/Sv * 129X1/SvJ
abnormal axon extension J:97265
abnormal eye morphology J:213171
blepharoptosis J:213171
Map1btm1Prop/Map1btm1Prop
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal axon morphology J:97423
abnormal cingulate gyrus morphology J:97423
abnormal eye morphology J:97423
abnormal hippocampus morphology J:97423
abnormal myelination J:97423
abnormal nerve conduction J:97423
abnormal parietal lobe morphology J:97423
absent corpus callosum J:97423
absent hippocampal commissure J:97423
decreased body weight J:97423
decreased corpus callosum size J:97423
decreased exploration in new environment J:97423
dehydration J:97423
delayed eyelid opening J:97423
delayed hair appearance J:97423
postnatal lethality, incomplete penetrance J:97423
reduced fertility J:97423
Map1btm1Prop/Map1btm1Prop
Tg(Isl1-EGFP*)1Slp/0
involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6
abnormal oculomotor nerve morphology J:213171
Map1btm1Rak/Map1b+
involves: 129P2/OlaHsd * C57BL/6J
abnormal cerebellum morphology J:31721
abnormal eye development J:31721
abnormal eye morphology J:31721
abnormal gait J:31721
abnormal hindlimb morphology J:31721
abnormal hippocampus morphology J:31721
abnormal olfactory bulb morphology J:31721
abnormal Purkinje cell dendrite morphology J:31721
abnormal Purkinje cell morphology J:31721
abnormal retina outer plexiform layer morphology J:31721
ataxia J:31721
decreased body size J:31721
decreased body weight J:31721
decreased visual acuity J:31721
disorganized retina inner nuclear layer J:31721
disorganized retina outer nuclear layer J:31721
hindlimb paralysis J:31721
lethargy J:31721
premature death J:31721
tremors J:31721
Map1btm1Rak/Map1btm1Rak
involves: 129P2/OlaHsd * C57BL/6J
embryonic lethality between somite formation and embryo turning, complete penetrance J:31721

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