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Symbol Name ID |
Cenpj
centromere protein J MGI:2684927 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypertelorism |
Strabismus |
| Disease(s) Associated with CENPJ | ||
| primary autosomal recessive microcephaly 6 |
| Mouse Phenotypes | abnormal iridocorneal angle |
abnormal ciliary process morphology |
abnormal iris morphology |
iris synechia |
abnormal Descemet membrane morphology |
abnormal corneal endothelium morphology |
decreased inner canthal distance |
eyelids fail to open |
abnormal retina photoreceptor layer morphology |
anophthalmia |
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| Availability | Mouse Genotype | ||||||||||
| Cenpjtm1a(EUCOMM)Wtsi/Cenpjtm1a(EUCOMM)Wtsi | |||||||||||
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 04/23/2024 MGI 6.23 |
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