HPS6 Chromosome 10

HPS6 biogenesis of lysosomal organelles complex 2 subunit 3
105 variants 105 Health Risk

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What This Gene Does
This intronless gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. This protein interacts with Hermansky-Pudlak syndrome 5 protein. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 6. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Biogenesis of lysosomal organelles complex 2
Locus Type
gene with protein product
Location
10q24.32
Ensembl
ENSG00000166189
Associated Conditions (4)
Hermansky-Pudlak syndrome 6
Inborn genetic diseases
HPS6-related disorder
Hermansky-Pudlak syndrome
Key Variants
All Variants (105)
RSID Category Clinical Significance Conditions
RS2540987497 Health Risk Pathogenic/Likely pathogenic
RS281865112 Health Risk Pathogenic/Likely pathogenic Hermansky-Pudlak syndrome 6, Hermansky-Pudlak syndrome 6
RS753804000 Health Risk Pathogenic/Likely pathogenic Hermansky-Pudlak syndrome 6, Hermansky-Pudlak syndrome 6
RS756471925 Health Risk Pathogenic/Likely pathogenic Hermansky-Pudlak syndrome, HPS6-related disorder, Hermansky-Pudlak syndrome
RS764867254 Health Risk Pathogenic/Likely pathogenic Hermansky-Pudlak syndrome 6, Hermansky-Pudlak syndrome 6
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