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    HOXC13-AS HOXC13 antisense RNA [ Homo sapiens (human) ]

    Gene ID: 100874366, updated on 10-Dec-2024

    Summary

    Official Symbol
    HOXC13-ASprovided by HGNC
    Official Full Name
    HOXC13 antisense RNAprovided by HGNC
    Primary source
    HGNC:HGNC:43753
    See related
    Ensembl:ENSG00000249641 AllianceGenome:HGNC:43753
    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
    HOXC-AS5
    Expression
    Biased expression in skin (RPKM 2.1), placenta (RPKM 0.1) and 1 other tissue See more
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    Genomic context

    See HOXC13-AS in Genome Data Viewer
    Location:
    12q13.13
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (53935328..53939643, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (53900850..53905165, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (54329112..54333427, complement)

    Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105378250 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:54141521-54142049 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:54142050-54142577 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:54144138-54144726 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4517 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4518 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 6429 Neighboring gene chondrogenesis-associated transcript Neighboring gene RN7SK pseudogene 289 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr12:54242057-54243256 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_29403 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr12:54261991-54263190 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_29464 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_29460 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:54321787-54322624 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:54345326-54345913 Neighboring gene uncharacterized LOC105369775 Neighboring gene homeobox C13 Neighboring gene ReSE screen-validated silencer GRCh37_chr12:54355207-54355431 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:54360165-54361069 Neighboring gene NUP98-HOXC11 recombination region Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:54368136-54368730 Neighboring gene homeobox C12 Neighboring gene HOX transcript antisense RNA Neighboring gene homeobox C11

    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?

    General gene information

    Other Names

    • HOXC cluster antisense RNA 5 (non-protein coding)

    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.

    RNA

    1. NR_047507.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      BE905258, BX097788, BX363129, CN364530
      Related
      ENST00000512916.3

    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_000012.12 Reference GRCh38.p14 Primary Assembly

      Range
      53935328..53939643 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060936.1 Alternate T2T-CHM13v2.0

      Range
      53900850..53905165 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)