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    INIP INTS3 and NABP interacting protein [ Homo sapiens (human) ]

    Gene ID: 58493, updated on 28-Oct-2024

    Summary

    Official Symbol
    INIPprovided by HGNC
    Official Full Name
    INTS3 and NABP interacting proteinprovided by HGNC
    Primary source
    HGNC:HGNC:24994
    See related
    Ensembl:ENSG00000148153 MIM:613273; AllianceGenome:HGNC:24994
    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
    MISE; SOSSC; SSBIP1; C9orf80; HSPC043; hSSBIP1
    Summary
    The protein encoded by this gene is a subunit of single-stranded DNA binding complexes that are important for maintaining genome stability. These complexes are involved in G2/M checkpoint control and homologous recombination repair. [provided by RefSeq, Jul 2016]
    Expression
    Ubiquitous expression in lymph node (RPKM 8.2), colon (RPKM 6.8) and 25 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See INIP in Genome Data Viewer
    Location:
    9q32
    Exon count:
    7
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (112683926..112718117, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (124855150..124889339, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (115446206..115480397, complement)

    Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:115141971-115142570 Neighboring gene hydroxysteroid dehydrogenase like 2 Neighboring gene HSDL2 antisense RNA 1 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28825 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20192 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20193 Neighboring gene KIAA1958 Neighboring gene Sharpr-MPRA regulatory region 4745 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:115309395-115309946 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr9:115309947-115310499 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:115310500-115311051 Neighboring gene Sharpr-MPRA regulatory region 8480 Neighboring gene NANOG hESC enhancer GRCh37_chr9:115313867-115314374 Neighboring gene ReSE screen-validated silencer GRCh37_chr9:115357836-115358025 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:115380828-115381410 Neighboring gene MPRA-validated peak7319 silencer Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28826 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20194 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28827 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28828 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:115512887-115513808 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:115513809-115514728 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr9:115516859-115517473 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:115518123-115518802 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:115517474-115518087 Neighboring gene SNX30 divergent transcript Neighboring gene Sharpr-MPRA regulatory region 12854 Neighboring gene sorting nexin family member 30 Neighboring gene OCT4-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:115565661-115566288 Neighboring gene OCT4-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:115566289-115566914 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:115572830-115573740 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20196 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28830 Neighboring gene MPRA-validated peak7321 silencer Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20197 Neighboring gene NANOG hESC enhancer GRCh37_chr9:115608506-115609059 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:115609080-115609580 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:115610366-115610938 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:115628995-115629496 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28831 Neighboring gene solute carrier family 46 member 2

    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

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in DNA damage response IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in DNA repair IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in DNA repair IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in double-strand break repair via homologous recombination IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in mitotic G2/M transition checkpoint IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in response to ionizing radiation IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    part_of SOSS complex IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    part_of SOSS complex IDA
    Inferred from Direct Assay
    more info
    PubMed 
    part_of SOSS complex IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    is_active_in nucleoplasm IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in nucleoplasm IDA
    Inferred from Direct Assay
    more info
     
    located_in nucleus IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in site of double-strand break IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    SOSS complex subunit C
    Names
    SSB-interacting protein 1
    hSSB-interacting protein 1
    minute INTS3/hSSB-associated element
    sensor of single-strand DNA complex subunit C
    sensor of ssDNA subunit C
    single-stranded DNA-binding protein-interacting protein 1

    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_001329585.2NP_001316514.1  SOSS complex subunit C isoform b

      Status: REVIEWED

      Source sequence(s)
      AL390067
      Conserved Domains (1) summary
      pfam15925
      Location:1598
      SOSSC; SOSS complex subunit C
    2. NM_001329586.2NP_001316515.1  SOSS complex subunit C isoform c

      Status: REVIEWED

      Source sequence(s)
      AL390067
    3. NM_001329587.2NP_001316516.1  SOSS complex subunit C isoform d

      Status: REVIEWED

      Source sequence(s)
      AL390067
    4. NM_001329588.2NP_001316517.1  SOSS complex subunit C isoform e

      Status: REVIEWED

      Description
      Transcript Variant: This variant (5), as well as variants 6 and 7, encodes isoform e.
      Source sequence(s)
      AL390067
      Consensus CDS
      CCDS87676.1
      UniProtKB/TrEMBL
      X6R8P6
      Conserved Domains (1) summary
      pfam15925
      Location:471
      SOSSC; SOSS complex subunit C
    5. NM_001329589.2NP_001316518.1  SOSS complex subunit C isoform e

      Status: REVIEWED

      Description
      Transcript Variant: This variant (6), as well as variants 5 and 7, encodes isoform e.
      Source sequence(s)
      AL390067
      Consensus CDS
      CCDS87676.1
      UniProtKB/TrEMBL
      X6R8P6
      Related
      ENSP00000363353.1, ENST00000374236.5
      Conserved Domains (1) summary
      pfam15925
      Location:471
      SOSSC; SOSS complex subunit C
    6. NM_001329590.2NP_001316519.1  SOSS complex subunit C isoform e

      Status: REVIEWED

      Description
      Transcript Variant: This variant (7), as well as variants 5 and 6, encodes isoform e.
      Source sequence(s)
      AL390067
      Consensus CDS
      CCDS87676.1
      UniProtKB/TrEMBL
      X6R8P6
      Conserved Domains (1) summary
      pfam15925
      Location:471
      SOSSC; SOSS complex subunit C
    7. NM_021218.3NP_067041.1  SOSS complex subunit C isoform a

      See identical proteins and their annotated locations for NP_067041.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) encodes the longest isoform (a).
      Source sequence(s)
      AL390067, BC065210, BQ219222
      Consensus CDS
      CCDS6785.1
      UniProtKB/Swiss-Prot
      Q5VWJ7, Q96E04, Q9NRY2, Q9P090
      Related
      ENSP00000363360.3, ENST00000374242.9
      Conserved Domains (1) summary
      pfam15925
      Location:18101
      SOSSC; SOSS complex subunit C

    RNA

    1. NR_138054.2 RNA Sequence

      Status: REVIEWED

      Source sequence(s)
      AL390067
    2. NR_138055.2 RNA Sequence

      Status: REVIEWED

      Source sequence(s)
      AL390067
    3. NR_138056.2 RNA Sequence

      Status: REVIEWED

      Source sequence(s)
      AL390067

    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_000009.12 Reference GRCh38.p14 Primary Assembly

      Range
      112683926..112718117 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060933.1 Alternate T2T-CHM13v2.0

      Range
      124855150..124889339 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)