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    C10orf126 chromosome 10 open reading frame 126 [ Homo sapiens (human) ]

    Gene ID: 283080, updated on 17-Sep-2024

    Summary

    Official Symbol
    C10orf126provided by HGNC
    Official Full Name
    chromosome 10 open reading frame 126provided by HGNC
    Primary source
    HGNC:HGNC:28693
    See related
    Ensembl:ENSG00000232624 AllianceGenome:HGNC:28693
    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
    bA492M23.1
    Expression
    Low expression observed in reference dataset See more
    Orthologs
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    Genomic context

    See C10orf126 in Genome Data Viewer
    Location:
    10p12.1
    Exon count:
    5
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (28846408..28881898)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (28878333..28913800)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (29135337..29170827)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 1517 Neighboring gene RNA, U6 small nuclear 270, pseudogene Neighboring gene long intergenic non-protein coding RNA 837 Neighboring gene heart enhancer 23 Neighboring gene RNA, 5S ribosomal pseudogene 308 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr10:29194458-29195657 Neighboring gene ribosomal protein L21 pseudogene 93 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:29214143-29214841 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr10:29274071-29275270 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr10:29279785-29280984 Neighboring gene NANOG hESC enhancer GRCh37_chr10:29299789-29300329 Neighboring gene uncharacterized LOC107984174

    Genomic regions, transcripts, and products

    Expression

    • Project title: 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

    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_164114.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL390248
      Related
      ENST00000375520.4

    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
      28846408..28881898
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060934.1 Alternate T2T-CHM13v2.0

      Range
      28878333..28913800
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001278522.1: Suppressed sequence

      Description
      NM_001278522.1: This RefSeq was removed because it is now thought that this gene does not encode a protein.
    2. NM_173577.1: Suppressed sequence

      Description
      NM_173577.1: This RefSeq record was removed by NCBI staff. Contact [email protected] for further information.