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    C11orf40 chromosome 11 putative open reading frame 40 [ Homo sapiens (human) ]

    Gene ID: 143501, updated on 17-Sep-2024

    Summary

    Official Symbol
    C11orf40provided by HGNC
    Official Full Name
    chromosome 11 putative open reading frame 40provided by HGNC
    Primary source
    HGNC:HGNC:23986
    See related
    Ensembl:ENSG00000171987 AllianceGenome:HGNC:23986
    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
    NOV1
    Orthologs
    NEW
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    Genomic context

    See C11orf40 in Genome Data Viewer
    Location:
    11p15.4
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (4571423..4577820, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (4636704..4643108, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (4592653..4599050, complement)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene olfactory receptor family 52 subfamily M member 2 pseudogene Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr11:4544619-4545119 Neighboring gene olfactory receptor family 52 subfamily M member 1 Neighboring gene ReSE screen-validated silencer GRCh37_chr11:4590598-4590803 Neighboring gene olfactory receptor family 52 subfamily I member 2 Neighboring gene olfactory receptor family 52 subfamily I member 1

    Genomic regions, transcripts, and products

    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_172945.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC090719
      Related
      ENST00000668205.1

    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_000011.10 Reference GRCh38.p14 Primary Assembly

      Range
      4571423..4577820 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      4636704..4643108 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_144663.1: Suppressed sequence

      Description
      NM_144663.1: This RefSeq was removed because it is now thought that this gene does encode a protein.