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Symbol
Name
ID

Ash1l
ASH1 like histone lysine methyltransferase
MGI:2183158

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Astigmatism	Deeply set eye	Hypertelorism	Strabismus	Horizontal nystagmus	Hypermetropia
Disease(s) Associated with ASH1L
autosomal dominant intellectual developmental disorder 52

Mouse Phenotypes		impaired pupillary reflex	absent Meibomian glands	blepharitis	abnormal cornea epithelium morphology
Availability	Mouse Genotype	impaired pupillary reflex	absent Meibomian glands	blepharitis	abnormal cornea epithelium morphology
	Ash1l^{Gt(AL0395)Wtsi}/Ash1l^{Gt(AL0395)Wtsi}
	Ash1l^{tm2b(EUCOMM)Hmgu}/Ash1l⁺

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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