Symbol Name ID |
Hps1
HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 MGI:2177763 |
Darker colors indicate more annotations |
Human Phenotypes | Ocular albinism |
Nystagmus |
Photophobia |
Blindness |
Severely reduced visual acuity |
Disease(s) Associated with HPS1 | |||||
Hermansky-Pudlak syndrome 1 |
Mouse Phenotypes | abnormal choroid pigmentation |
abnormal ciliary body pigmentation |
abnormal iris pigmentation |
decreased eye pigmentation |
abnormal retina morphology |
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Availability | Mouse Genotype | |||||
Hps1ep/Hps1ep |
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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