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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 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)