Vti1b Phenotype Annotations - Multigenic Genotypes

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

Allelic Composition Genetic Background	Annotated Term	Reference
Vti1a^tm1Gfvm/Vti1a^tm1Gfvm Vti1b^tm1Gfvm/Vti1b^tm1Gfvm 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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