About Help FAQ

Symbol
Name
ID

Alx4
aristaless-like homeobox 4
MGI:108359

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes

Shallow orbits

Optic nerve hypoplasia

Blue sclerae

Hypertelorism

Hypotelorism

Proptosis

Microphthalmia

Strabismus

Horizontal nystagmus

Rotary nystagmus

Vertical nystagmus

Hypermetropia

Myopia

Visual field defect

Decreased lacrimation

Ptosis

Disease(s) Associated with ALX4

craniosynostosis

frontonasal dysplasia 2

parietal foramina

Mouse Phenotypes		cataract	failure of eyelid fusion	ocular hypertelorism	eyelids open at birth
Availability	Mouse Genotype	cataract	failure of eyelid fusion	ocular hypertelorism	eyelids open at birth
	Alx4^Lst-2J/Alx4^Lst-2J
	Alx4^M1Yzcm/Alx4^M1Yzcm
	Alx4^Lst-2J/Alx4^lst-J

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