Foxi3 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Foxi3
forkhead box I3
MGI:3511278

50 phenotypes from 5 alleles in 7 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Foxi3^em1Ybz/Foxi3^em1Ybz C57BL/6-Foxi3^em1Ybz	abnormal cranium morphology	J:336768
	abnormal mandible morphology	J:336768
	abnormal neurocranium morphology	J:336768
	abnormal retrotympanic process morphology	J:336768
	abnormal stapes morphology	J:336768
	abnormal temporal bone morphology	J:336768
	abnormal zygomatic bone morphology	J:336768
	absent incus	J:336768
	absent malleus	J:336768
	absent outer ear	J:336768
	absent tympanic ring	J:336768
	cleft palate	J:336768
	craniofacial asymmetry	J:336768
	decreased birth body size	J:336768
	decreased birth weight	J:336768
	decreased mouth size	J:336768
	neonatal lethality, complete penetrance	J:336768
	pterygoid bone hypoplasia	J:336768
	small ears	J:336768
	syngnathia	J:336768
Foxi3^em2Ybz/Foxi3^em2Ybz C57BL/6-Foxi3^em2Ybz	no abnormal phenotype detected	J:336768
Foxi3^em3Akg/Foxi3^em3Akg C57BL/6-Foxi3^em3Akg	no abnormal phenotype detected	J:336768
Foxi3^em3Akg/Foxi3^tm1.2Akg involves: 129X1/SvJ * C57BL/6	abnormal respiration	J:336768
	athymia	J:336768
	normal craniofacial phenotype	J:336768
	decreased body weight	J:336768
	normal hearing/vestibular/ear phenotype	J:336768
	postnatal lethality, complete penetrance	J:336768
Foxi3^tm1.1Akg/Foxi3^tm1.1Akg involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	no abnormal phenotype detected	J:207523
Foxi3^tm1.2Akg/Foxi3^tm1.2Akg involves: 129X1/SvJ	abnormal geniculate ganglion morphology	J:228880
	abnormal nervous system development	J:228880
	abnormal otic placode morphology	J:228880
	abnormal trigeminal ganglion morphology	J:228880
	abnormal vestibulocochlear ganglion morphology	J:228880
	increased embryonic tissue cell apoptosis	J:228880
Foxi3^tm1.2Akg/Foxi3^tm1.2Akg involves: 129X1/SvJ * BALB/c	abnormal facial morphology	J:207523
	abnormal mandible morphology	J:207523
	abnormal maxilla morphology	J:207523
	abnormal Meckel's cartilage morphology	J:207523
	abnormal middle ear morphology	J:207523
	abnormal palatine bone morphology	J:207523
	abnormal pharyngeal pouch morphology	J:207523
	abnormal temporal bone squamous part morphology	J:207523
	absent incus	J:207523
	absent inner ear	J:207523
	absent malleus	J:207523
	absent mouth	J:207523
	absent outer ear	J:207523
	absent pharyngeal arches	J:207523
	absent stapes	J:207523
	absent tympanic ring	J:207523
	absent vibrissae	J:207523
	absent zygomatic bone	J:207523
	cranioschisis	J:207523
	embryonic lethality during organogenesis, incomplete penetrance	J:207523
	increased cranial neural crest cell apoptosis	J:207523
	neonatal lethality, complete penetrance	J:207523
	small face	J:207523
	syngnathia	J:207523

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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