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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Vax1
ventral anterior homeobox 1
MGI:1277163
55 phenotypes from 3 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Vax1tm1b(KOMP)Mbp/Vax1+
C57BL/6N-Vax1tm1b(KOMP)Mbp/J
abnormal sinus arrhythmia J:211773
decreased circulating glucose level J:211773
increased circulating alkaline phosphatase level J:211773
Vax1tm1b(KOMP)Mbp/Vax1tm1b(KOMP)Mbp
C57BL/6N-Vax1tm1b(KOMP)Mbp/J
preweaning lethality, incomplete penetrance J:211773
Vax1tm1Grl/Vax1tm1Grl
involves: 129S1/Sv
coloboma J:98488
Vax1tm1Grl/Vax1tm1Grl
involves: 129S1/Sv * C57BL/6
abnormal axon guidance J:58996
abnormal ependyma morphology J:96805
abnormal eye development J:58996
abnormal lateral ganglionic eminence morphology J:96805
abnormal neuron differentiation J:96805
abnormal olfactory bulb development J:96805
abnormal olfactory bulb morphology J:96805
abnormal optic nerve innervation J:58996
abnormal optic nerve morphology J:58996
abnormal postnatal subventricular zone morphology J:96805
abnormal rostral migratory stream morphology J:96805
absent corpus callosum J:58996
cleft palate J:58996
coloboma J:58996
neonatal lethality, incomplete penetrance J:58996
Vax1tm1Pgr/Vax1tm1Pgr
either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * NMRI)
abnormal anterior commissure morphology J:58997
abnormal corpus callosum morphology J:58997
abnormal forebrain development J:58997
abnormal hypothalamus morphology J:58997
abnormal optic nerve innervation J:58997
abnormal optic nerve morphology J:58997
abnormal telencephalon development J:58997
abnormal upper incisor morphology J:58997
absent optic chiasm J:58997
cleft palate J:58997
coloboma J:58997
fused upper incisors J:58997
holoprosencephaly J:58997
lethality at weaning, incomplete penetrance J:58997
perinatal lethality, incomplete penetrance J:58997
premature death J:58997
Vax1tm1Pgr/Vax1tm1Pgr
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal cranium morphology J:257247
abnormal frontonasal mesenchyme morphology J:257247
abnormal lateral ventricle morphology J:257247
abnormal maxilla morphology J:257247
abnormal midface morphology J:257247
abnormal nasal cavity morphology J:257247
abnormal pituitary gland morphology J:257247
abnormal premaxilla morphology J:257247
abnormal presphenoid bone morphology J:257247
abnormal upper incisor morphology J:257247
abnormal vomeronasal cartilage morphology J:257247
absent nasal septum J:257247
absent palatine bone horizontal plate J:257247
absent presphenoid bone J:257247
cleft palate J:257247
decreased forebrain size J:257247
lobar holoprosencephaly J:257247
maxillary retrognathia J:257247
maxillary shelf hypoplasia J:257247
midface hypoplasia J:257247
palatal shelves fail to meet at midline J:257247
palatine bone hypoplasia J:257247
presphenoid bone hypoplasia J:257247
small cranium J:257247
small mandible J:257247
vomer bone hypoplasia J:257247

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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
04/16/2024
MGI 6.23
The Jackson Laboratory