Symbol Name ID |
Ash1l
ASH1 like histone lysine methyltransferase MGI:2183158 |
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 | ||||
Ash1lGt(AL0395)Wtsi/Ash1lGt(AL0395)Wtsi | |||||
Ash1ltm2b(EUCOMM)Hmgu/Ash1l+ |
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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last database update 08/02/2024 MGI 6.24 |
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