About   Help   FAQ
Symbol
Name
ID
Hmx1
H6 homeobox 1
MGI:107178
Phenotype annotations related to craniofacial
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Short mandibular rami
Nasolacrimal duct obstruction
Disease(s) Associated with HMX1
oculoauricular syndrome

Mouse Phenotypes
craniofacial phenotype
abnormal retrotympanic process morphology
enlarged gonial bone
gonial bone hyperplasia
abnormal ear position
lowered ear position
Availability Mouse Genotype
Hmx1dmbo/Hmx1dmbo *
Hmx1mpe/Hmx1mpe

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
04/16/2024
MGI 6.23
The Jackson Laboratory