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    FGF13-AS1 FGF13 antisense RNA 1 [ Homo sapiens (human) ]

    Gene ID: 100129662, updated on 17-Sep-2024

    Summary

    Official Symbol
    FGF13-AS1provided by HGNC
    Official Full Name
    FGF13 antisense RNA 1provided by HGNC
    Primary source
    HGNC:HGNC:44264
    See related
    Ensembl:ENSG00000226031 MIM:301087; AllianceGenome:HGNC:44264
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Expression
    Broad expression in fat (RPKM 1.6), bone marrow (RPKM 0.4) and 16 other tissues See more
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    Genomic context

    See FGF13-AS1 in Genome Data Viewer
    Location:
    Xq26.3
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (138712107..138716605)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (137022600..137027098)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (137794269..137798767)

    Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene H2A.Q variant histone 1, pseudogene Neighboring gene fibroblast growth factor 13 Neighboring gene microRNA 504 Neighboring gene NANOG hESC enhancer GRCh37_chrX:137842490-137843019 Neighboring gene MED14-independent group 3 enhancer GRCh37_chrX:137859976-137861175 Neighboring gene tropomyosin 2 pseudogene Neighboring gene NFE2L2 motif-containing MPRA enhancer 215 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:138226529-138226732 Neighboring gene uncharacterized LOC124905222

    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_038405.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      BC023610, Z82193
      Related
      ENST00000438238.1

    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_000023.11 Reference GRCh38.p14 Primary Assembly

      Range
      138712107..138716605
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060947.1 Alternate T2T-CHM13v2.0

      Range
      137022600..137027098
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)