HPS1 Products

Description

The HPS1 gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. The encoded protein is a component of three different protein complexes termed biogenesis of lysosome-related org

Bioinformatics

Entrez	3257 Human
Uniprot	NP_872577.1 Human NP_000186.2 Human
Product By Gene ID	3257
Alternate Names	Hermansky-Pudlak syndrome type 1 Hermansky-Pudlak syndrome 1 protein MGC5277 Hermansky-Pudlak syndrome HPS Hermansky-Pudlak syndrome 1

Diseases related to HPS1

Discover more about diseases related to HPS1.

Hermanski-pudlak Syndrome
Albinism, Oculocutaneous
Albinism
Hemorrhage
Fibrosis
Pulmonary Fibrosis
Bleeding Tendency
Platelet Storage Pool Deficiency
Hypopigmentation Disorder
Colitis
Crohn's Disease Of Large Bowel
Hereditary Diseases
Mycoplasma Pneumonia
Lung Diseases
Pneumonia
Inflammation
Melanoma
Nystagmus
Lung Diseases, Interstitial

Pathways for HPS1

View related products by pathway and learn more about each of the pathways below.

Pigmentation
Secretion
Transport
Localization
Membrane Fusion
Vesicle Docking
Pathogenesis
Proteolysis
Gluconeogenesis
Platelet Activation
Serotonin Uptake
Spermatogenesis
Inflammatory Response
Platelet Aggregation
Chemokine Secretion
Chemotaxis
Reverse Transcription
Interphase
Response To Nutrient
Hemostasis

PTMs for HPS1

Learn more about PTMs related to HPS1.

Phosphorylation
Nitrosylation
Glycosylation

Bioinformatics Tool for HPS1

Discover related pathways, diseases and genes to HPS1. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.