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    CCAR1 cell division cycle and apoptosis regulator 1 [ Homo sapiens (human) ]

    Gene ID: 55749, updated on 10-Dec-2024

    Summary

    Official Symbol
    CCAR1provided by HGNC
    Official Full Name
    cell division cycle and apoptosis regulator 1provided by HGNC
    Primary source
    HGNC:HGNC:24236
    See related
    Ensembl:ENSG00000060339 MIM:612569; AllianceGenome:HGNC:24236
    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
    Also known as
    uc.285+
    Summary
    Enables RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; nuclear receptor coactivator activity; and transcription corepressor activity. Involved in positive regulation of cell migration and positive regulation of cell population proliferation. Acts upstream of or within positive regulation of apoptotic process. Located in nuclear envelope lumen. [provided by Alliance of Genome Resources, Dec 2024]
    Expression
    Ubiquitous expression in lymph node (RPKM 17.5), appendix (RPKM 15.2) and 25 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See CCAR1 in Genome Data Viewer
    Location:
    10q21.3
    Exon count:
    25
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (68721239..68792377)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (69590457..69661544)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (70480996..70552134)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene tet methylcytosine dioxygenase 1 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3468 Neighboring gene RPS3A pseudogene 37 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_16818 Neighboring gene uncharacterized LOC124902592 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_16833 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2421 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_16857 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_16866 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_16874 Neighboring gene small nucleolar RNA, C/D box 98 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_16884 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_16893 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_16897 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_16901 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_16907 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_16918 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2422 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2423 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2424 Neighboring gene RNA, U6 small nuclear 697, pseudogene Neighboring gene storkhead box 1 Neighboring gene MPRA-validated peak1002 silencer Neighboring gene NANOG hESC enhancer GRCh37_chr10:70637959-70638530 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3469 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3470 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3471 Neighboring gene RNA, U6 small nuclear 571, pseudogene Neighboring gene DExD-box helicase 50

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    HIV-1 interactions

    Replication interactions

    Interaction Pubs
    Knockdown of cell division cycle and apoptosis regulator 1 (CCAR1) by shRNA library screening inhibits HIV-1 replication in cultured Jurkat T-cells PubMed
    Knockdown of cell division cycle and apoptosis regulator 1 (CCAR1) by siRNA inhibits the early stages of HIV-1 replication in 293T cells infected with VSV-G pseudotyped HIV-1 PubMed

    Go to the HIV-1, Human Interaction Database

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Clone Names

    • MGC44628

    Gene Ontology Provided by GOA

    Component Evidence Code Pubs
    located_in nuclear envelope lumen IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in nucleoplasm TAS
    Traceable Author Statement
    more info
     
    is_active_in nucleus IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in perinuclear region of cytoplasm IEA
    Inferred from Electronic Annotation
    more info
     

    General protein information

    Preferred Names
    cell division cycle and apoptosis regulator protein 1
    Names
    cell cycle and apoptosis regulatory protein 1
    death inducer with SAP domain

    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_001282959.2NP_001269888.1  cell division cycle and apoptosis regulator protein 1 isoform b

      See identical proteins and their annotated locations for NP_001269888.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) uses an alternate splice site in the 5' UTR and lacks an alternate in-frame exon in the 5' coding region compared to variant 1. This results in a shorter protein (isoform b), compared to isoform a. Variants 2 and 3 encode the same isoform (b).
      Source sequence(s)
      AK298004, AK299307, AY249140, BC132725, BU617955, DB636717
      Consensus CDS
      CCDS60547.1
      UniProtKB/TrEMBL
      A0A0C4DGG8
      Related
      ENSP00000445254.1, ENST00000543719.5
      Conserved Domains (5) summary
      smart00513
      Location:622655
      SAP; Putative DNA-binding (bihelical) motif predicted to be involved in chromosomal organisation
      PHA03356
      Location:266298
      PHA03356; tegument protein UL11; Provisional
      pfam14443
      Location:467586
      DBC1; DBC1
      pfam14444
      Location:137189
      S1-like; S1-like
      cl23720
      Location:10211100
      RILP-like; Rab interacting lysosomal protein-like 1 and 2 (Rilpl1 and Rilpl2)
    2. NM_001282960.2NP_001269889.1  cell division cycle and apoptosis regulator protein 1 isoform b

      See identical proteins and their annotated locations for NP_001269889.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) lacks an alternate in-frame exon in the 5' coding region compared to variant 1. This results in a shorter protein (isoform b), compared to isoform a. Variants 2 and 3 encode the same isoform (b).
      Source sequence(s)
      AK299307, AY249140, BC132725, BU617955, DA511293, DB636717
      Consensus CDS
      CCDS60547.1
      UniProtKB/TrEMBL
      A0A0C4DGG8
      Related
      ENSP00000439252.1, ENST00000539539.5
      Conserved Domains (5) summary
      smart00513
      Location:622655
      SAP; Putative DNA-binding (bihelical) motif predicted to be involved in chromosomal organisation
      PHA03356
      Location:266298
      PHA03356; tegument protein UL11; Provisional
      pfam14443
      Location:467586
      DBC1; DBC1
      pfam14444
      Location:137189
      S1-like; S1-like
      cl23720
      Location:10211100
      RILP-like; Rab interacting lysosomal protein-like 1 and 2 (Rilpl1 and Rilpl2)
    3. NM_018237.4NP_060707.2  cell division cycle and apoptosis regulator protein 1 isoform a

      See identical proteins and their annotated locations for NP_060707.2

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longest transcript and encodes the longer isoform (a).
      Source sequence(s)
      AY249140, BC132725, BU617955, DA511293, DB636717
      Consensus CDS
      CCDS7282.1
      UniProtKB/Swiss-Prot
      A0JLT7, A1L4P7, A8K9D4, B4DNP8, B4DRK8, Q32NE3, Q5EBM3, Q5VUP6, Q6PIZ0, Q6X935, Q8IX12, Q9H8N4, Q9NVA7, Q9NVQ0, Q9NWM6
      UniProtKB/TrEMBL
      A0A0C4DGG8
      Related
      ENSP00000265872.6, ENST00000265872.11
      Conserved Domains (5) summary
      smart00513
      Location:637670
      SAP; Putative DNA-binding (bihelical) motif predicted to be involved in chromosomal organisation
      PHA03356
      Location:281313
      PHA03356; tegument protein UL11; Provisional
      pfam14443
      Location:482601
      DBC1; DBC1
      pfam14444
      Location:152204
      S1-like; S1-like
      cl23720
      Location:10361115
      RILP-like; Rab interacting lysosomal protein-like 1 and 2 (Rilpl1 and Rilpl2)

    RNA

    1. NR_104262.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (4) uses an alternate splice site 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, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AY249140, BC144118, BU617955, DA511293, DB636717
      Related
      ENST00000630771.2

    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_000010.11 Reference GRCh38.p14 Primary Assembly

      Range
      68721239..68792377
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060934.1 Alternate T2T-CHM13v2.0

      Range
      69590457..69661544
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)