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Symbol
Name
ID

Aldh1a3
aldehyde dehydrogenase family 1, subfamily A3
MGI:1861722

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Hypoplastic optic chiasm	Optic nerve hypoplasia	Retinal coloboma	Retinal detachment	Anophthalmia	True anophthalmia	Microphthalmia
Disease(s) Associated with ALDH1A3
isolated microphthalmia 8

Mouse Phenotypes		decreased periocular mesenchyme apoptosis	abnormal periocular mesenchyme morphology	ventral rotation of lens	persistent hyperplastic primary vitreous	microphthalmia	absent nasolacrimal duct	increased total retina thickness	decreased ventral retina size	abnormal vitreous body morphology
Availability	Mouse Genotype	decreased periocular mesenchyme apoptosis	abnormal periocular mesenchyme morphology	ventral rotation of lens	persistent hyperplastic primary vitreous	microphthalmia	absent nasolacrimal duct	increased total retina thickness	decreased ventral retina size	abnormal vitreous body morphology
	Aldh1a3^tm1.1Pcn/Aldh1a3^tm1.1Pcn
	Aldh1a3^{tm1b(KOMP)Wtsi}/Aldh1a3^{tm1b(KOMP)Wtsi}
	Aldh1a3^tm1Gdu/Aldh1a3^tm1Gdu

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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