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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Vti1b
vesicle transport through interaction with t-SNAREs 1B
MGI:1855688
28 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Vti1atm1Gfvm/Vti1atm1Gfvm
Vti1btm1Gfvm/Vti1btm1Gfvm
involves: 129P2/OlaHsd * C57BL/6
abnormal axon extension J:169107
abnormal axon guidance J:169107
abnormal brain commissure morphology J:169107
abnormal cranial ganglia morphology J:169107
abnormal innervation J:169107
abnormal nervous system development J:169107
abnormal optic tract morphology J:169107
abnormal sensory ganglion morphology J:169107
abnormal striatum morphology J:169107
abnormal superior cervical ganglion morphology J:169107
absent anterior commissure J:169107
absent hippocampal commissure J:169107
normal cellular phenotype J:169107
decreased brain size J:169107
decreased corpus callosum size J:169107
decreased optic chiasm size J:169107
dorsal root ganglion degeneration J:169107
enlarged brain ventricles J:169107
enlarged lateral ventricles J:169107
increased neuron apoptosis J:169107
neurodegeneration J:169107
perinatal lethality, complete penetrance J:169107
small geniculate ganglion J:169107
small nodose ganglion J:169107
small petrosal ganglion J:169107
small trigeminal ganglion J:169107
vestibular ganglion degeneration J:169107
vestibular ganglion hypoplasia J:169107

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
11/12/2019
MGI 6.14
The Jackson Laboratory