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Symbol
Name
ID

Rax
retina and anterior neural fold homeobox
MGI:109632

Phenotype annotations related to craniofacial

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Ankyloblepharon
Disease(s) Associated with RAX	Ankyloblepharon
isolated microphthalmia 3

Mouse Phenotypes		craniofacial phenotype	absent optic pit	abnormal palate morphology	cleft palate
Availability	Mouse Genotype	craniofacial phenotype	absent optic pit	abnormal palate morphology	cleft palate
	Rax^tm1.2Lwd/Rax^tm1.2Lwd
	Rax^tm1Lwd/Rax^tm1Lwd
	Rax^tm1Mjam/Rax^tm1Mjam
	Rax^tm1.1Lwd/Rax^tm1.1Lwd Tg(rx3-icre)1Mjam/0 (conditional)	*

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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