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    DCANP1 dendritic cell associated nuclear protein 1 [ Homo sapiens (human) ]

    Gene ID: 140947, updated on 17-Jun-2024

    Summary

    Official Symbol
    DCANP1provided by HGNC
    Official Full Name
    dendritic cell associated nuclear protein 1provided by HGNC
    Primary source
    HGNC:HGNC:24459
    See related
    Ensembl:ENSG00000251380 MIM:609710; AllianceGenome:HGNC:24459
    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
    DCNP1; C5orf20
    Summary
    This intronless gene is specifically expressed in dendritic cells (DCs), which are potent antigen-presenting cells involved in activating naive T cells to initiate antigen-specific immune response. The encoded protein is localized mainly in the perinucleus. One of the alleles (A/T) of this gene, that causes premature translation termination at aa 117, has been associated with an increased prevalence of major depression in humans. [provided by RefSeq, Jul 2008]
    Orthologs
    NEW
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    Genomic context

    See DCANP1 in Genome Data Viewer
    Location:
    5q31.1
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (135444214..135447348, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (135971385..135974519, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (134779904..134783038, complement)

    Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene PITX1 antisense RNA 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr5:134574510-134575316 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr5:134582317-134583516 Neighboring gene long intergenic non-protein coding RNA 2900 Neighboring gene MPRA-validated peak5478 silencer Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr5:134678129-134679328 Neighboring gene macroH2A.1 histone Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23170 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16373 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16374 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16375 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr5:134735167-134735672 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr5:134735673-134736178 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr5:134739095-134739661 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23171 Neighboring gene VISTA enhancer hs1473 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23172 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr5:134784907-134785408 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr5:134785409-134785908 Neighboring gene uncharacterized LOC124901073 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23173 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23174 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16377 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23175 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr5:134820245-134821093 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:134824474-134825331 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:134825332-134826188 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:134826189-134827045 Neighboring gene TIFA inhibitor Neighboring gene MPRA-validated peak5480 silencer Neighboring gene Sharpr-MPRA regulatory region 242 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:134871641-134872156 Neighboring gene neurogenin 1

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Potential readthrough

    Included gene: TIFAB

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables DNA binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in auditory behavior IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in cochlea development IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in cochlea morphogenesis IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in craniofacial suture morphogenesis IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in genitalia development IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in genitalia morphogenesis IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in hard palate morphogenesis IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in inner ear development IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in inner ear morphogenesis IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in learned vocalization behavior IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in mastication IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in negative regulation of relaxation of muscle IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in negative regulation of saliva secretion IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in neuromuscular process controlling balance IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in peristalsis IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in regulation of muscle organ development IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in thorax and anterior abdomen determination IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in trigeminal nerve development IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in vestibulocochlear nerve formation IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in cytoplasm IEA
    Inferred from Electronic Annotation
    more info
     
    located_in nuclear body IDA
    Inferred from Direct Assay
    more info
     
    located_in nucleoplasm IDA
    Inferred from Direct Assay
    more info
     

    General protein information

    Preferred Names
    dendritic cell nuclear protein 1
    Names
    dendritic cell-associated nuclear protein

    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_130848.3NP_570900.1  dendritic cell nuclear protein 1

      See identical proteins and their annotated locations for NP_570900.1

      Status: REVIEWED

      Source sequence(s)
      AC022092
      Consensus CDS
      CCDS4186.1
      UniProtKB/Swiss-Prot
      Q8TF63
      Related
      ENSP00000421871.1, ENST00000503143.3

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000005.10 Reference GRCh38.p14 Primary Assembly

      Range
      135444214..135447348 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060929.1 Alternate T2T-CHM13v2.0

      Range
      135971385..135974519 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)