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    ZNF252P-AS1 ZNF252P antisense RNA 1 [ Homo sapiens (human) ]

    Gene ID: 286103, updated on 10-Oct-2023

    Summary

    Official Symbol
    ZNF252P-AS1provided by HGNC
    Official Full Name
    ZNF252P antisense RNA 1provided by HGNC
    Primary source
    HGNC:HGNC:27821
    See related
    Ensembl:ENSG00000255559 AllianceGenome:HGNC:27821
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    C8orf77
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    Genomic context

    See ZNF252P-AS1 in Genome Data Viewer
    Location:
    8q24.3
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (145002811..145006046)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (146177956..146181191)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (146228197..146231432)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene zinc finger protein 16 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19717 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28110 Neighboring gene zinc finger protein 252, pseudogene Neighboring gene transmembrane p24 trafficking protein 10 pseudogene 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:146228590-146229166 Neighboring gene endogenous retrovirus group K member 6 Env polyprotein-like Neighboring gene zinc finger with KRAB and SCAN domains 8 pseudogene

    Genomic regions, transcripts, and products

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Other Names

    • ZNF252P antisense RNA 1 (non-protein coding)

    Clone Names

    • MGC141859

    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.

    RNA

    1. NR_026974.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AF235103, AK092777, BC046439, BC122544, BX104600
      Related
      ENST00000527067.1

    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_000008.11 Reference GRCh38.p14 Primary Assembly

      Range
      145002811..145006046
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060932.1 Alternate T2T-CHM13v2.0

      Range
      146177956..146181191
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001039382.1: Suppressed sequence

      Description
      NM_001039382.1: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.
    2. NM_178535.2: Suppressed sequence

      Description
      NM_178535.2: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.