BLOC1S2

Last updated
BLOC1S2
Identifiers
Aliases BLOC1S2 , BLOS2, CEAP, CEAP11, BORCS2, biogenesis of lysosomal organelles complex 1 subunit 2
External IDs OMIM: 609768 MGI: 1920939 HomoloGene: 45479 GeneCards: BLOC1S2
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_028607

RefSeq (protein)

NP_082883

Location (UCSC) Chr 10: 100.27 – 100.29 Mb Chr 19: 44.13 – 44.13 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Biogenesis of lysosome-related organelles complex 1 subunit 2 is a protein that in humans is encoded by the BLOC1S2 gene. [5] [6] [7]

Contents


Interactions

BLOC1S2 has been shown to interact with BLOC1S1, [6] SNAPAP, [6] MUTED, [6] CNO [6] and PLDN. [6]

Related Research Articles

<span class="mw-page-title-main">Hermansky–Pudlak syndrome</span> Medical condition

Heřmanský–Pudlák syndrome is an extremely rare autosomal recessive disorder which results in oculocutaneous albinism, bleeding problems due to a platelet abnormality, and storage of an abnormal fat-protein compound. It is considered to affect around 1 in 500,000 people worldwide, with a significantly higher occurrence in Puerto Ricans, with a prevalence of 1 in 1800. Many of the clinical research studies on the disease have been conducted in Puerto Rico.

<span class="mw-page-title-main">Dysbindin</span> Protein

Dysbindin, short for dystrobrevin-binding protein 1, is a protein constituent of the dystrophin-associated protein complex (DPC) of skeletal muscle cells. It is also a part of BLOC-1, or biogenesis of lysosome-related organelles complex 1. Dysbindin was discovered by the research group of Derek Blake via yeast two-hybrid screening for binding partners of α-dystrobrevin. In addition, dysbindin is found in neural tissue of the brain, particularly in axon bundles and especially in certain axon terminals, notably mossy fiber synaptic terminals in the cerebellum and hippocampus. In humans, dysbindin is encoded by the DTNBP1 gene.

BLOC-1 or biogenesis of lysosome-related organelles complex 1 is a ubiquitously expressed multisubunit protein complex in a group of complexes that also includes BLOC-2 and BLOC-3. BLOC-1 is required for normal biogenesis of specialized organelles of the endosomal-lysosomal system, such as melanosomes and platelet dense granules. These organelles are called LROs which are apparent in specific cell-types, such as melanocytes. The importance of BLOC-1 in membrane trafficking appears to extend beyond such LROs, as it has demonstrated roles in normal protein-sorting, normal membrane biogenesis, as well as vesicular trafficking. Thus, BLOC-1 is multi-purposed, with adaptable function depending on both organism and cell-type.

<span class="mw-page-title-main">AP3B1</span> Protein-coding gene in the species Homo sapiens

AP-3 complex subunit beta-1 is a protein that in humans is encoded by the AP3B1 gene.

<span class="mw-page-title-main">40S ribosomal protein S16</span> Protein-coding gene in the species Homo sapiens

40S ribosomal protein S16' is a protein that in humans is encoded by the RPS16 gene.

<span class="mw-page-title-main">SNAPAP</span> Protein-coding gene in the species Homo sapiens

SNARE-associated protein Snapin is a protein that in humans is encoded by the SNAPIN gene.

<span class="mw-page-title-main">PLDN</span>

Pallidin is a protein that in humans is encoded by the PLDN gene.

<span class="mw-page-title-main">HPS1</span> Protein-coding gene in humans

Hermansky–Pudlak syndrome 1 protein is a protein that in humans is encoded by the HPS1 gene.

<span class="mw-page-title-main">AP3M1</span> Protein-coding gene in the species Homo sapiens

AP-3 complex subunit mu-1 is a protein that in humans is encoded by the AP3M1 gene.

<span class="mw-page-title-main">HPS4</span>

Hermansky–Pudlak syndrome 4 protein is a protein that in humans is encoded by the HPS4 gene.

<span class="mw-page-title-main">AP3S2</span> Protein-coding gene in the species Homo sapiens

AP-3 complex subunit sigma-2 is a protein that in humans is encoded by the AP3S2 gene.

<span class="mw-page-title-main">HPS3</span>

Hermansky–Pudlak syndrome 3 protein is a protein that in humans is encoded by the HPS3 gene.

<span class="mw-page-title-main">HPS5</span>

Hermansky–Pudlak syndrome 5 protein is a protein that in humans is encoded by the HPS5 gene.

<span class="mw-page-title-main">BCKDK</span> Protein-coding gene in the species Homo sapiens

Branched chain ketoacid dehydrogenase kinase (BCKDK) is an enzyme encoded by the BCKDK gene on chromosome 16. This enzyme is part of the mitochondrial protein kinases family and it is a regulator of the valine, leucine, and isoleucine catabolic pathways. BCKDK is found in the mitochondrial matrix and the prevalence of it depends on the type of cell. Liver cells tend to have the lowest concentration of BCKDK, whereas skeletal muscle cells have the highest amount. Abnormal activity of this enzyme often leads to diseases such as maple syrup urine disease and cachexia.

<span class="mw-page-title-main">BLOC1S1</span> Protein-coding gene in the species Homo sapiens

Biogenesis of lysosome-related organelles complex 1 subunit 1 is a protein that in humans is encoded by the BLOC1S1 gene.

<span class="mw-page-title-main">MUTED</span>

Protein Muted homolog is a protein that in humans is encoded by the MUTED gene.

<span class="mw-page-title-main">CNO (gene)</span> Protein-coding gene in the species Homo sapiens

Protein cappuccino homolog is a protein that in humans is encoded by the CNO gene.

<span class="mw-page-title-main">HPS6</span> Protein found in humans

Hermansky–Pudlak syndrome 6 (HPS6), also known as ruby-eye protein homolog (Ru), is a protein that in humans is encoded by the HPS6 gene.

<span class="mw-page-title-main">Dystrobrevin beta</span> Protein-coding gene in the species Homo sapiens

Dystrobrevin beta is a protein which in humans is encoded by the DTNB gene.

BLOC-3 or biogenesis of lysosome-related organelles complex 3 is a ubiquitously expressed multisubunit protein complex.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000196072 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000057506 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Yu Y, Zhang C, Zhou G, Wu S, Qu X, Wei H, Xing G, Dong C, Zhai Y, Wan J, Ouyang S, Li L, Zhang S, Zhou K, Zhang Y, Wu C, He F (Aug 2001). "Gene expression profiling in human fetal liver and identification of tissue- and developmental-stage-specific genes through compiled expression profiles and efficient cloning of full-length cDNAs". Genome Res. 11 (8): 1392–403. doi:10.1101/gr.175501. PMC   311073 . PMID   11483580.
  6. 1 2 3 4 5 6 Starcevic M, Dell'Angelica EC (Jun 2004). "Identification of snapin and three novel proteins (BLOS1, BLOS2, and BLOS3/reduced pigmentation) as subunits of biogenesis of lysosome-related organelles complex-1 (BLOC-1)". J Biol Chem. 279 (27): 28393–401. doi: 10.1074/jbc.M402513200 . PMID   15102850.
  7. "Entrez Gene: BLOC1S2 biogenesis of lysosome-related organelles complex-1, subunit 2".

Further reading