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    XACT X active specific transcript [ Homo sapiens (human) ]

    Gene ID: 105463123, updated on 10-Dec-2024

    Summary

    Official Symbol
    XACTprovided by HGNC
    Official Full Name
    X active specific transcriptprovided by HGNC
    Primary source
    HGNC:HGNC:45056
    See related
    MIM:300901; AllianceGenome:HGNC:45056
    Gene type
    ncRNA
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Summary
    This gene produces a spliced long non-coding RNA that is thought to play a role in the control of X-chromosome inactivation (XCI). This transcript has been shown to specifically coat the active X chromosome in human pluripotent cells. [provided by RefSeq, Mar 2015]
    Annotation information
    Annotation category: partial on reference assembly
    Expression
    Low expression observed in reference dataset See more
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    Genomic context

    See XACT in Genome Data Viewer
    Location:
    Xq23
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (113616300..113618153, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (112069011..112070863, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (112859587..112861440, complement)

    Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC101928437 Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:112331023-112331523 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:112351918-112352418 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:112352419-112352919 Neighboring gene MED14-independent group 3 enhancer GRCh37_chrX:112516938-112518137 Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:112549954-112550454 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:112644353-112645154 Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:112646849-112647350 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:112782802-112783585 Neighboring gene peptidylprolyl isomerase H pseudogene 2 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:112963371-112963912 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:113040105-113040748 Neighboring gene uncharacterized LOC124905236 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:113172117-113172792 Neighboring gene small nucleolar RNA U3 Neighboring gene queuine tRNA-ribosyltransferase catalytic subunit 1 pseudogene 1

    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

    General gene information

    Other Names

    • X active coating transcript
    • X active specific transcript (non-protein coding)

    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_131204.1 RNA Sequence

      Status: REVIEWED

      Source sequence(s)
      AC236668, BQ010753

    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_000023.11 Reference GRCh38.p14 Primary Assembly

      Range
      113616300..113618153 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060947.1 Alternate T2T-CHM13v2.0

      Range
      112069011..112070863 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)