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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Alx3
aristaless-like homeobox 3
MGI:1277097
37 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Alx1tm1Crm/Alx1tm1Crm
Alx3tm1Hubr/Alx3tm1Hubr
involves: 129P2/OlaHsd * 129S7/SvEvBrd
abnormal scapula morphology J:101708
Alx3tm1Hubr/Alx3tm1Hubr
Alx4lst-J/Alx4lst-J
involves: 129P2/OlaHsd * C3H * C57BL/6J * FVB/N
abnormal basicranium morphology J:71880
abnormal clavicle morphology J:71880
abnormal craniofacial bone morphology J:71880
abnormal cranium morphology J:71880
abnormal mandible morphology J:71880
abnormal maxilla morphology J:71880
abnormal maxillary frontal process morphology J:71880
abnormal nasal capsule morphology J:71880
abnormal nasal cavity morphology J:71880
abnormal neurocranium morphology J:71880
abnormal premaxilla morphology J:71880
abnormal pterygoid process morphology J:71880
abnormal viscerocranium morphology J:71880
absent deltoid tuberosity J:71880
absent facial bone J:71880
absent gastric milk in neonates J:71880
absent nasal septum J:71880
bifid nasal tip J:71880
bifid nose J:71880
cleft palate J:71880
decreased cranium height J:71880
exophthalmos J:71880
eyelids open at birth J:71880
increased cranium width J:71880
large fontanelles J:71880
meteorism J:71880
midline facial cleft J:71880
neonatal lethality, complete penetrance J:71880
preaxial polydactyly J:71880
short facial bone J:71880
short temporal bone squamous part J:71880
small alisphenoid bone J:71880
small frontal bone J:71880
small nasal bone J:71880
small parietal bone J:71880
Alx3tm1Hubr/Alx3tm1Hubr
Alx4lst-J/Alx4lst-J
involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J
small pubis J:101708

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
11/12/2024
MGI 6.24
The Jackson Laboratory