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The official name of this gene is “Hermansky-Pudlak syndrome 3.”
HPS3 is the gene's official symbol. The HPS3 gene is also known by other names, listed below.
The HPS3 gene provides instructions for making a protein that forms part of a complex called biogenesis of lysosome-related organelles complex-2 (BLOC-2). Although the specific function of BLOC-2 is not well understood, it plays a role in the formation and movement (trafficking) of a group of cellular structures called lysosome-related organelles (LROs). LROs are very similar to compartments within the cell called lysosomes, which digest and recycle materials. However, LROs perform specialized functions and are found only in certain cell types.
Within pigment cells (melanocytes), LROs called melanosomes produce and distribute melanin, which is the substance that gives skin, hair, and eyes their color. A different type of LRO is found in platelets, the blood cells involved in normal blood clotting. These LROs, called dense granules, release chemical signals that cause platelets to stick together and form a blood clot.
At least 7 mutations in the HPS3 gene have been found to cause Hermansky-Pudlak syndrome type 3, which is a mild form of the condition. These mutations impair the normal function of BLOC-2, disrupting the size, structure, and function of LROs in cells throughout the body.
One common mutation results in a deletion of genetic material within the HPS3 gene. This deletion includes approximately 3,900 DNA building blocks (nucleotides) and is known as the 3.9kb deletion. It is also written as 339_4260del3904. This mutation, which is found in affected individuals from the central region of Puerto Rico, prevents the production of any HPS3 protein.
Another mutation in the HPS3 gene has been found in people with Central and Eastern European (Ashkenazi) Jewish background. This mutation, called a splice-site mutation, disrupts the way the gene's instructions are used to make the protein. This mutation, which is written as 1163+1G>A, results in an abnormally short protein.
People with Hermansky-Pudlak syndrome have abnormally light pigmentation of the skin, hair, and eyes because melanosomes do not distribute melanin properly. The absence of dense granules within platelets leads to bleeding problems in affected individuals.
Cytogenetic Location: 3q24
Molecular Location on chromosome 3: base pairs 148,847,370 to 148,891,304
The HPS3 gene is located on the long (q) arm of chromosome 3 at position 24.
More precisely, the HPS3 gene is located from base pair 148,847,370 to base pair 148,891,304 on chromosome 3.
See How do geneticists indicate the location of a gene? (http://ghr.nlm.nih.gov/handbook/howgeneswork/genelocation) in the Handbook.
You and your healthcare professional may find the following resources about HPS3 helpful.
You may also be interested in these resources, which are designed for genetics professionals and researchers.
See How are genetic conditions and genes named? (http://ghr.nlm.nih.gov/handbook/mutationsanddisorders/naming) in the Handbook.
blood clotting ; cell ; clotting ; deletion ; DNA ; gene ; lysosome ; melanin ; melanocytes ; mutation ; pigment ; pigmentation ; platelets ; protein ; splice-site mutation ; syndrome
You may find definitions for these and many other terms in the Genetics Home Reference Glossary (http://www.ghr.nlm.nih.gov/glossary).
The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.