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Symbol
Name
ID

Hoxa1
homeobox A1
MGI:96170

Phenotype annotations related to craniofacial

Darker colors indicate more annotations

Human Phenotypes	Internal carotid artery hypoplasia
Disease(s) Associated with HOXA1	Internal carotid artery hypoplasia
Athabaskan brainstem dysgenesis syndrome

Mouse Phenotypes		abnormal basioccipital bone morphology	abnormal interparietal bone morphology	abnormal exoccipital bone morphology	small malleus	absent stapes	absent middle ear ossicles	small second pharyngeal arch	abnormal outer ear morphology
Availability	Mouse Genotype	abnormal basioccipital bone morphology	abnormal interparietal bone morphology	abnormal exoccipital bone morphology	small malleus	absent stapes	absent middle ear ossicles	small second pharyngeal arch	abnormal outer ear morphology
	Hoxa1^tm1Ipc/Hoxa1^tm1Ipc
	Hoxa1^tm1Mrc/Hoxa1^tm1Mrc
	Hoxa1^tm1Rez/Hoxa1^tm1Rez
	Hoxa1^tm3.1Mrc/Hoxa1^tm3.1Mrc

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 04/09/2024 MGI 6.23