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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 04/16/2024 MGI 6.23 |
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