About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Alx1
ALX homeobox 1
MGI:104621
52 phenotypes from 2 alleles in 5 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Alx1em1Jian/Alx1em1Jian
C57BL/6N-Alx1em1Jian 		abnormal external nares morphology J:320497
abnormal frontonasal mesenchyme morphology J:320497
abnormal lateral nasal prominence morphology J:320497
abnormal maxillary shelf morphology J:320497
abnormal nasal cartilage morphology J:320497
abnormal optic cup morphology J:320497
abnormal optic stalk morphology J:320497
abnormal periocular mesenchyme morphology J:320497
broad nasal bridge J:320497
cleft palate J:320497
depressed nasal bridge J:320497
eyelids open at birth J:320497
increased periocular mesenchyme apoptosis J:320497
microphthalmia J:320497
midface hypoplasia J:320497
midline cleft upper lip J:320497
neonatal lethality, complete penetrance J:320497
normal nervous system phenotype J:320497
premaxilla hypoplasia J:320497
presphenoid bone hypoplasia J:320497
short philtrum J:320497
short snout J:320497
Alx1em1Jian/Alx1em1Jian
involves: 129S6/SvEvTac * C57BL/6N 		abnormal nasal cartilage morphology J:320497
anophthalmia J:320497
cleft palate J:320497
depressed nasal bridge J:320497
exencephaly J:320497
incomplete rostral neuropore closure J:320497
midline cleft upper lip J:320497
Alx1tm1Crm/Alx1tm1Crm
129S7/SvEvBrd-Alx1tm1Crm 		abnormal forebrain morphology J:33716
abnormal nasal capsule morphology J:33716
abnormal nasal cartilage morphology J:33716
abnormal palatine bone morphology J:33716
absent interparietal bone J:33716
absent neurocranium J:33716
absent presphenoid bone J:33716
acrania J:33716
normal craniofacial phenotype J:51128
decreased cranium length J:33716
normal hearing/vestibular/ear phenotype J:33716
meroanencephaly J:33716
neonatal lethality, complete penetrance J:33716
open neural tube J:33716
short mandible J:33716
short maxilla J:33716
short zygomatic bone J:33716
normal skeleton phenotype J:33716
small alisphenoid bone J:33716
small frontal bone J:33716
small parietal bone J:33716
small supraoccipital bone J:33716
small temporal bone squamous part J:33716
Alx1tm1Crm/Alx1tm1Crm
involves: 129S7/SvEvBrd 		abnormal pectoral girdle bone morphology J:101708
Alx1tm1Crm/Alx1tm1Crm
involves: 129S7/SvEvBrd * C57BL/6J 		absent gastric milk in neonates J:33716
acrania J:33716
cyanosis J:33716
eyelids open at birth J:33716
increased embryonic neuroepithelium thickness J:33716
meroanencephaly J:33716
neonatal lethality, complete penetrance J:33716
open neural tube J:33716
short face J:33716
shortened head J:33716
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory