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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Alx4
aristaless-like homeobox 4
MGI:108359
63 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Alx1em1Jian/Alx1em1Jian
Alx4Lst-2J/Alx4+
involves: C57BL/6J * C57BL/6N * CD-1
abnormal lateral nasal prominence morphology J:320497
abnormal premaxilla morphology J:320497
abnormal presphenoid bone morphology J:320497
broad nasal bridge J:320497
depressed nasal bridge J:320497
midline cleft upper lip J:320497
short philtrum J:320497
Alx1em1Jian/Alx1em1Jian
Alx4Lst-2J/Alx4Lst-2J
involves: C57BL/6J * C57BL/6N * CD-1
abnormal lateral nasal prominence morphology J:320497
abnormal medial nasal prominence morphology J:320497
abnormal premaxilla morphology J:320497
midline cleft upper lip J:320497
midline facial cleft J:320497
Alx1tm1Crm/Alx1+
Alx4tm1Rwi/Alx4+
involves: 129S6/SvEvTac * 129S7/SvEvBrd
no abnormal phenotype detected J:51128
Alx1tm1Crm/Alx1+
Alx4tm1Rwi/Alx4tm1Rwi
involves: 129S6/SvEvTac * 129S7/SvEvBrd
abnormal basisphenoid bone morphology J:51128
abnormal nasal septum cartilage morphology J:51128
abnormal neurocranium morphology J:51128
cleft palate J:51128
eyelids open at birth J:51128
herniated abdominal wall J:51128
midline facial cleft J:51128
polydactyly J:51128
short mandible J:51128
short tibia J:51128
small frontal bone J:51128
small mandible J:51128
small occipital bone J:51128
small parietal bone J:51128
small temporal bone J:51128
Alx1tm1Crm/Alx1tm1Crm
Alx4lst-J/Alx4lst-J
involves: 129S7/SvEvBrd * C3HeB/FeJ * C57BL/6J
abnormal clavicle morphology J:101708
abnormal scapula morphology J:101708
abnormal scapular spine morphology J:101708
small acromion J:101708
small pubis J:101708
Alx1tm1Crm/Alx1tm1Crm
Alx4lst-J/Alx4lst-J
Tbx15de-H/Tbx15+
involves: 129S7/SvEvBrd * C3H * C57BL/6J
abnormal scapula morphology J:101708
abnormal scapular spine morphology J:101708
Alx1tm1Crm/Alx1tm1Crm
Alx4lst-J/Alx4lst-J
Tbx15de-H/Tbx15de-H
involves: 129S7/SvEvBrd * C3H * C57BL/6J
absent clavicle J:101708
small scapula J:101708
Alx1tm1Crm/Alx1tm1Crm
Alx4tm1Rwi/Alx4+
involves: 129S6/SvEvTac * 129S7/SvEvBrd
abnormal basisphenoid bone morphology J:51128
abnormal nasal septum cartilage morphology J:51128
exencephaly J:51128
midline facial cleft J:51128
short mandible J:51128
Alx1tm1Crm/Alx1tm1Crm
Alx4tm1Rwi/Alx4tm1Rwi
involves: 129S6/SvEvTac * 129S7/SvEvBrd
asymmetric rib joints J:51128
decreased rib number J:51128
exencephaly J:51128
herniated abdominal wall J:51128
midline facial cleft J:51128
polydactyly J:51128
short tibia J:51128
split sternum J:51128
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
Alx4lst/Alx4+
Grem1ld/Grem1+
Not Specified
normal limbs/digits/tail phenotype J:35172
Alx4lst/Alx4+
Grem1ld-J/Grem1+
involves: CBA/Ca * NHO
normal limbs/digits/tail phenotype J:35172
Alx4lst/Alx4+
Fmn1ld-TgHD/Fmn1+
involves: BALB/c * C57BL/6 * CD-1 * FVB/N
normal limbs/digits/tail phenotype J:17401
Alx4tm1Rwi/Alx4+
Bmp4tm1Blh/Bmp4+
involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6
polydactyly J:42445

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