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    SIN3B SIN3 transcription regulator family member B [ Homo sapiens (human) ]

    Gene ID: 23309, updated on 27-Nov-2024

    Summary

    Official Symbol
    SIN3Bprovided by HGNC
    Official Full Name
    SIN3 transcription regulator family member Bprovided by HGNC
    Primary source
    HGNC:HGNC:19354
    See related
    Ensembl:ENSG00000127511 MIM:607777; AllianceGenome:HGNC:19354
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Summary
    Predicted to enable transcription corepressor activity. Predicted to be involved in cardiac muscle tissue development; negative regulation of transcription by RNA polymerase II; and skeletal muscle tissue development. Predicted to be located in nucleus. Predicted to be part of Sin3-type complex. [provided by Alliance of Genome Resources, Nov 2024]
    Expression
    Ubiquitous expression in testis (RPKM 19.2), endometrium (RPKM 17.1) and 25 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See SIN3B in Genome Data Viewer
    Location:
    19p13.11
    Exon count:
    20
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (16829398..16880349)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (16964243..17015192)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (16940209..16991160)

    Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 10314 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr19:16772303-16773111 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr19:16790368-16790868 Neighboring gene transmembrane protein 38A Neighboring gene NACHT and WD repeat domain containing 1 Neighboring gene uncharacterized LOC124904648 Neighboring gene ReSE screen-validated silencer GRCh37_chr19:16928291-16928487 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr19:16936141-16936818 Neighboring gene H3K27ac hESC enhancer GRCh37_chr19:16939935-16940436 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 14248 Neighboring gene H3K27ac hESC enhancer GRCh37_chr19:16947461-16947962 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr19:16957617-16958116 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr19:16957115-16957616 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 14249 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr19:16996894-16997394 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:17000485-17001084 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 14250 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 14251 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 14252 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 10316 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 10317 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 10318 Neighboring gene RNA, 7SL, cytoplasmic 835, pseudogene Neighboring gene C3 and PZP like alpha-2-macroglobulin domain containing 8 Neighboring gene F2R like thrombin or trypsin receptor 3

    Genomic regions, transcripts, and products

    Expression

    • Project title: 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

    Clone Names

    • KIAA0700

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables chromatin binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables transcription corepressor activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    Component Evidence Code Pubs
    part_of Sin3-type complex IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    part_of Sin3-type complex NAS
    Non-traceable Author Statement
    more info
    PubMed 
    located_in X chromosome IEA
    Inferred from Electronic Annotation
    more info
     
    located_in XY body IEA
    Inferred from Electronic Annotation
    more info
     
    located_in Y chromosome IEA
    Inferred from Electronic Annotation
    more info
     
    located_in autosome IEA
    Inferred from Electronic Annotation
    more info
     
    located_in chromatin IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in cytoplasm IEA
    Inferred from Electronic Annotation
    more info
     
    located_in nucleoplasm TAS
    Traceable Author Statement
    more info
     
    located_in nucleus ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    located_in nucleus NAS
    Non-traceable Author Statement
    more info
    PubMed 

    General protein information

    Preferred Names
    paired amphipathic helix protein Sin3b
    Names
    SIN3 homolog B, transcriptional regulator
    SIN3 transcription regulator homolog B
    histone deacetylase complex subunit Sin3b
    transcriptional corepressor Sin3b

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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.

    mRNA and Protein(s)

    1. NM_001297595.2NP_001284524.1  paired amphipathic helix protein Sin3b isoform 2

      See identical proteins and their annotated locations for NP_001284524.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) lacks an alternate in-frame exon in the 5' coding region, compared to variant 1. It encodes isoform 2, which lacks an internal segment and is shorter, compared to isoform 1.
      Source sequence(s)
      AB014600, AY706204, HY055983
      Consensus CDS
      CCDS74308.1
      UniProtKB/Swiss-Prot
      O75182
      Related
      ENSP00000248054.4, ENST00000248054.10
      Conserved Domains (3) summary
      pfam02671
      Location:60104
      PAH; Paired amphipathic helix repeat
      pfam08295
      Location:395489
      Sin3_corepress; Sin3 family co-repressor
      pfam16879
      Location:7431043
      Sin3a_C; C-terminal domain of Sin3a protein
    2. NM_001297597.2NP_001284526.1  paired amphipathic helix protein Sin3b isoform 3

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) differs in the 5' UTR, lacks a portion of the 5' coding region and initiates translation at an alternate start codon, compared to variant 1. It encodes isoform 3, which is shorter and has a distinct N-terminus, compared to isoform 1.
      Source sequence(s)
      AB014600, AK295618, AY706204, DC332740
      Consensus CDS
      CCDS77254.1
      UniProtKB/TrEMBL
      B7Z392, M0QYC5
      Related
      ENSP00000469740.1, ENST00000595541.1
      Conserved Domains (2) summary
      pfam08295
      Location:1279
      Sin3_corepress; Sin3 family co-repressor
      pfam16879
      Location:333633
      Sin3a_C; C-terminal domain of Sin3a protein
    3. NM_015260.4NP_056075.1  paired amphipathic helix protein Sin3b isoform 1

      See identical proteins and their annotated locations for NP_056075.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1).
      Source sequence(s)
      AY706204, HY055983
      Consensus CDS
      CCDS32946.1
      UniProtKB/Swiss-Prot
      O75182, Q2NL91, Q68GC2, Q6P4B8, Q8TB34, Q9BSC8
      Related
      ENSP00000369131.1, ENST00000379803.5
      Conserved Domains (3) summary
      pfam02671
      Location:60104
      PAH; Paired amphipathic helix repeat
      pfam08295
      Location:395521
      Sin3_corepress; Sin3 family co-repressor
      pfam16879
      Location:7751075
      Sin3a_C; C-terminal domain of Sin3a protein

    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_000019.10 Reference GRCh38.p14 Primary Assembly

      Range
      16829398..16880349
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_006722704.2XP_006722767.1  paired amphipathic helix protein Sin3b isoform X1

      UniProtKB/TrEMBL
      B7Z392
      Conserved Domains (1) summary
      pfam16879
      Location:258558
      Sin3a_C; C-terminal domain of Sin3a protein

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060943.1 Alternate T2T-CHM13v2.0

      Range
      16964243..17015192
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054320368.1XP_054176343.1  paired amphipathic helix protein Sin3b isoform X1