Symbol Name ID |
Hps1
HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 MGI:2177763 |
Darker colors indicate more annotations |
Human Phenotypes | Bruising susceptibility |
Ecchymosis |
Hypopigmentation of hair |
Albinism |
Freckling |
Freckles in sun-exposed areas |
Hypopigmentation of the skin |
Melanocytic nevus |
Disease(s) Associated with HPS1 | ||||||||
Hermansky-Pudlak syndrome 1 |
Mouse Phenotypes | abnormal ear pigmentation |
decreased ear pigmentation |
diluted coat color |
decreased tail pigmentation |
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Availability | Mouse Genotype | ||||
Hps1ep-7J/Hps1ep-7J | |||||
Hps1ep/Hps1ep | |||||
Hps1ep/Hps1ep-6J |
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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