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BLOC1S6 biogenesis of lysosomal organelles complex 1 subunit 6 [ Homo sapiens (human) ]

Gene ID: 26258, updated on 2-Nov-2024

Summary

Official Symbol
BLOC1S6provided by HGNC
Official Full Name
biogenesis of lysosomal organelles complex 1 subunit 6provided by HGNC
Primary source
HGNC:HGNC:8549
See related
Ensembl:ENSG00000104164 MIM:604310; AllianceGenome:HGNC:8549
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
PA; HPS9; PLDN; BLOS6; PALLID
Summary
The protein encoded by this gene may play a role in intracellular vesicle trafficking. It interacts with Syntaxin 13 which mediates intracellular membrane fusion. Mutations in this gene cause symptoms associated with Hermansky-Pudlak syndrome-9. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the X chromosome. [provided by RefSeq, Aug 2015]
Expression
Ubiquitous expression in thyroid (RPKM 21.0), prostate (RPKM 17.5) and 25 other tissues See more
Orthologs
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Genomic context

See BLOC1S6 in Genome Data Viewer
Location:
15q21.1
Exon count:
7
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (45587123..45609716)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (43395284..43417878)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (45879321..45901914)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene high mobility group nucleosomal binding domain 2 pseudogene 46 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:45839047-45839548 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:45839549-45840048 Neighboring gene small nucleolar RNA, H/ACA box 41B Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr15:45840653-45841852 Neighboring gene MPRA-validated peak2326 silencer Neighboring gene developmental pluripotency associated 5 pseudogene 2 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9362 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9363 Neighboring gene H3K27ac hESC enhancer GRCh37_chr15:45880103-45880723 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9364 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:45926371-45927366 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9365 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9366 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9367 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9368 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9369 Neighboring gene sulfide quinone oxidoreductase Neighboring gene uncharacterized LOC124903484

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Pathways from PubChem

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables actin filament binding IDA
Inferred from Direct Assay
more info
PubMed 
enables identical protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
enables molecular adaptor activity IEA
Inferred from Electronic Annotation
more info
 
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
enables protein homodimerization activity IDA
Inferred from Direct Assay
more info
PubMed 
enables protein homodimerization activity IPI
Inferred from Physical Interaction
more info
PubMed 
enables syntaxin binding TAS
Traceable Author Statement
more info
PubMed 
Process Evidence Code Pubs
involved_in ATP metabolic process IEA
Inferred from Electronic Annotation
more info
 
involved_in actin filament bundle assembly IEA
Inferred from Electronic Annotation
more info
 
involved_in adenosine metabolic process IEA
Inferred from Electronic Annotation
more info
 
involved_in anterograde axonal transport ISS
Inferred from Sequence or Structural Similarity
more info
 
involved_in anterograde synaptic vesicle transport ISS
Inferred from Sequence or Structural Similarity
more info
 
involved_in blood coagulation IEA
Inferred from Electronic Annotation
more info
 
involved_in bradykinin biosynthetic process IEA
Inferred from Electronic Annotation
more info
 
involved_in cellular response to epidermal growth factor stimulus IEA
Inferred from Electronic Annotation
more info
 
involved_in cilium assembly IEA
Inferred from Electronic Annotation
more info
 
involved_in circadian sleep/wake cycle IEA
Inferred from Electronic Annotation
more info
 
involved_in dentate gyrus development IEA
Inferred from Electronic Annotation
more info
 
involved_in endosome to melanosome transport IDA
Inferred from Direct Assay
more info
PubMed 
involved_in endothelium development IEA
Inferred from Electronic Annotation
more info
 
involved_in gene expression IEA
Inferred from Electronic Annotation
more info
 
involved_in glutamate metabolic process IEA
Inferred from Electronic Annotation
more info
 
involved_in glutamine metabolic process IEA
Inferred from Electronic Annotation
more info
 
involved_in homeostasis of number of cells IEA
Inferred from Electronic Annotation
more info
 
involved_in hypothalamus development IEA
Inferred from Electronic Annotation
more info
 
involved_in intracellular nitric oxide homeostasis IEA
Inferred from Electronic Annotation
more info
 
involved_in intracellular transport IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in kidney development IEA
Inferred from Electronic Annotation
more info
 
involved_in lipid homeostasis IEA
Inferred from Electronic Annotation
more info
 
involved_in lung alveolus development IEA
Inferred from Electronic Annotation
more info
 
involved_in melanocyte differentiation IEA
Inferred from Electronic Annotation
more info
 
involved_in melanosome organization NAS
Non-traceable Author Statement
more info
PubMed 
involved_in melanosome transport IDA
Inferred from Direct Assay
more info
PubMed 
involved_in membrane fusion IEA
Inferred from Electronic Annotation
more info
 
involved_in memory IEA
Inferred from Electronic Annotation
more info
 
involved_in multicellular organism growth IEA
Inferred from Electronic Annotation
more info
 
involved_in neuron projection development ISS
Inferred from Sequence or Structural Similarity
more info
 
involved_in phospholipid metabolic process IEA
Inferred from Electronic Annotation
more info
 
involved_in positive regulation of natural killer cell activation IEA
Inferred from Electronic Annotation
more info
 
involved_in positive regulation of pigment cell differentiation IDA
Inferred from Direct Assay
more info
PubMed 
involved_in protein targeting IEA
Inferred from Electronic Annotation
more info
 
involved_in protein transmembrane transport IEA
Inferred from Electronic Annotation
more info
 
involved_in respiratory system process IEA
Inferred from Electronic Annotation
more info
 
involved_in response to acetylcholine IEA
Inferred from Electronic Annotation
more info
 
involved_in response to activity IEA
Inferred from Electronic Annotation
more info
 
involved_in response to xenobiotic stimulus IEA
Inferred from Electronic Annotation
more info
 
involved_in secretion of lysosomal enzymes IEA
Inferred from Electronic Annotation
more info
 
involved_in synaptic vesicle docking NAS
Non-traceable Author Statement
more info
PubMed 
involved_in vasodilation IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
part_of BLOC-1 complex IBA
Inferred from Biological aspect of Ancestor
more info
 
part_of BLOC-1 complex IDA
Inferred from Direct Assay
more info
PubMed 
part_of BLOC-1 complex IPI
Inferred from Physical Interaction
more info
PubMed 
part_of SNARE complex IDA
Inferred from Direct Assay
more info
PubMed 
located_in axon cytoplasm IEA
Inferred from Electronic Annotation
more info
 
located_in cell-cell contact zone IEA
Inferred from Electronic Annotation
more info
 
located_in contractile ring IEA
Inferred from Electronic Annotation
more info
 
located_in cytoplasm IDA
Inferred from Direct Assay
more info
PubMed 
located_in cytosol TAS
Traceable Author Statement
more info
 
located_in endosome IEA
Inferred from Electronic Annotation
more info
 
part_of filamentous actin IEA
Inferred from Electronic Annotation
more info
 
located_in focal adhesion IEA
Inferred from Electronic Annotation
more info
 
located_in membrane-bounded organelle IDA
Inferred from Direct Assay
more info
PubMed 
located_in microvesicle IEA
Inferred from Electronic Annotation
more info
 
located_in presynapse IEA
Inferred from Electronic Annotation
more info
 
located_in ruffle IEA
Inferred from Electronic Annotation
more info
 
located_in stress fiber IEA
Inferred from Electronic Annotation
more info
 
is_active_in transport vesicle IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in transport vesicle IDA
Inferred from Direct Assay
more info
PubMed 

General protein information

Preferred Names
biogenesis of lysosome-related organelles complex 1 subunit 6
Names
BLOC-1 subunit 6
BLOC-1 subunit pallidin
biogenesis of lysosomal organelles complex-1, subunit 5, pallidin
biogenesis of lysosomal organelles complex-1, subunit 6, pallidin
pallid protein homolog
syntaxin 13 binding protein 1
syntaxin 13-interacting protein pallid

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_028194.2 RefSeqGene

    Range
    4905..27498
    Download
    GenBank, FASTA, Sequence Viewer (Graphics), LRG_883

mRNA and Protein(s)

  1. NM_001311255.1NP_001298184.1  biogenesis of lysosome-related organelles complex 1 subunit 6 isoform 1

    Status: REVIEWED

    Source sequence(s)
    AK128626, AL596952, BC026289, BP423071, DA230439
    Consensus CDS
    CCDS81878.1
    UniProtKB/TrEMBL
    B2RDK7, H3BST1
    Related
    ENSP00000456851.1, ENST00000565323.6
    Conserved Domains (1) summary
    pfam14712
    Location:55145
    Snapin_Pallidin; Snapin/Pallidin
  2. NM_001311256.1NP_001298185.1  biogenesis of lysosome-related organelles complex 1 subunit 6 isoform 3

    Status: REVIEWED

    Description
    Transcript Variant: This variant (12) lacks an alternate exon in the central coding region, which results in a frameshift and an early stop codon, compared to variant 1. It encodes isoform 3, which has a shorter and distinct C-terminus, compared to isoform 1.
    Source sequence(s)
    AK128626, BC026289, BP423071, DA226593, DA230439, DA523523
    UniProtKB/TrEMBL
    B3KY40
    Conserved Domains (1) summary
    pfam14712
    Location:5680
    Snapin_Pallidin; Snapin/Pallidin
  3. NM_012388.4NP_036520.1  biogenesis of lysosome-related organelles complex 1 subunit 6 isoform 2

    See identical proteins and their annotated locations for NP_036520.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) differs in the 5' UTR and 5' coding region and initiates translation at an alternate start codon, compared to variant 1. It encodes isoform 2, which has a shorter and distinct N-terminus, compared to isoform 1.
    Source sequence(s)
    AF080470, AK128626, BC026289
    Consensus CDS
    CCDS10126.1
    UniProtKB/Swiss-Prot
    Q9UL45
    UniProtKB/TrEMBL
    B2RDK7
    Related
    ENSP00000220531.4, ENST00000220531.9
    Conserved Domains (1) summary
    pfam14712
    Location:51140
    Snapin_Pallidin; Snapin/Pallidin

RNA

  1. NR_132350.1 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (3) includes an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AK128626, BC026289, BP423071, DA230439
    Related
    ENST00000568816.5
  2. NR_132351.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (4) contains an alternate 5' terminal exon and uses an alternate splice site in an internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 2, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AK057545, AK128626, BC026289
  3. NR_132352.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (5) contains an alternate 5' terminal exon and lacks an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AF080470, AK128626, BC026289, DA247079
  4. NR_132353.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AK128626, BC026289, BP423071, DA468279, DB212570
  5. NR_132354.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AF080470, AK128626, BC026289, BP423071, DA468279, DA798595
  6. NR_132355.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (8) contains an alternate 5' exon and lacks two alternate internal exons, compared to variant 1. This variant is represented as non-coding because the predicted protein does not meet RefSeq quality criteria.
    Source sequence(s)
    AK128626, BC026289, DB287075
  7. NR_132356.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (9) contains an alternate 5' exon compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AK128626, BC026289, DA237963, DB289156
  8. NR_132357.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (10) contains an alternate 5' exon and lacks an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the predicted protein does not meet RefSeq quality criteria.
    Source sequence(s)
    AK128626, BC026289, DA237963, DA859617
  9. NR_132358.1 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (11) lacks two alternate internal exons compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AK128626, BC026289, BP423071, DA226593, DA230439
  10. NR_132359.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (13) contains an alternate 5' terminal exon and lacks two alternate internal exons, compared to variant 1. This variant is represented as non-coding because the predicted protein does not meet RefSeq quality criteria.
    Source sequence(s)
    AK128626, BC026289, DA233328, DA237963

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000015.10 Reference GRCh38.p14 Primary Assembly

    Range
    45587123..45609716
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060939.1 Alternate T2T-CHM13v2.0

    Range
    43395284..43417878
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)