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H1-10-AS1 H1-10 antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 339942, updated on 25-Nov-2025
Official Symbol
H1-10-AS1provided by HGNC
Official Full Name
H1-10 antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:27953
See related
AllianceGenome:HGNC:27953
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
C3orf47; H1FX-AS1
Expression
Ubiquitous expression in fat (RPKM 3.5), prostate (RPKM 1.9) and 23 other tissues See more
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See H1-10-AS1 in Genome Data Viewer
Location:
3q21.3
Exon count:
5
Annotation release Status Assembly Chr Location
RS_2025_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (129316271..129324569)
RS_2025_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (132061069..132069367)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (129035114..129043412)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene coat protein complex I subunit gamma 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14719 Neighboring gene microRNA 6826 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14720 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20508 Neighboring gene 5-hydroxymethylcytosine binding, ES cell specific Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:129024401-129024985 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20509 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14721 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14722 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14723 Neighboring gene H1.10 linker histone Neighboring gene nucleoporin 210 pseudogene 3 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20510 Neighboring gene MARK2 pseudogene 3 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:129063241-129064068 Neighboring gene MARK2 pseudogene 19

  • 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
Products Interactant Other Gene Complex Source Pubs Description

Markers

Other Names

  • H1FX antisense RNA 1 (non-protein coding)

Clone Names

  • FLJ34151, MGC126788

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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_026991.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC137695, AL040547, AL353963, BC093941, BM709882, BU732259, DA883170

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2025_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    129316271..129324569
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    132061069..132069367
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001025468.1: Suppressed sequence

    Description
    NM_001025468.1: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein and the transcript is a nonsense-mediated mRNA decay (NMD) candidate.