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    GALNT9-AS1 GALNT9 antisense RNA 1 [ Homo sapiens (human) ]

    Gene ID: 100130238, updated on 10-Dec-2024

    Summary

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    Official Symbol
    GALNT9-AS1provided by HGNC
    Official Full Name
    GALNT9 antisense RNA 1provided by HGNC
    Primary source
    HGNC:HGNC:56353
    See related
    AllianceGenome:HGNC:56353
    Gene type
    ncRNA
    RefSeq status
    PREDICTED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Expression
    Biased expression in spleen (RPKM 3.3), thyroid (RPKM 1.6) and 2 other tissues See more
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    Genomic context

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    See GALNT9-AS1 in Genome Data Viewer
    Location:
    12q24.33
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (132275391..132280900)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (132328533..132334042)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (132851977..132857486)

    Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5114 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5115 Neighboring gene long intergenic non-protein coding RNA 2361 Neighboring gene uncharacterized LOC105370091 Neighboring gene polypeptide N-acetylgalactosaminyltransferase 9 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:132703817-132704677 Neighboring gene MS43a minisatellite repeat instability region Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr12:132831859-132832379 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:132832380-132832899 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:132849568-132850462 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:132850463-132851355 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:132852165-132852941 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:132854851-132855501 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:132860363-132861016 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:132861671-132862324 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr12:132863043-132864242 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:132899827-132900476 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr12:132903614-132904813 Neighboring gene uncharacterized LOC101928416 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr12:132920815-132922014 Neighboring gene ReSE screen-validated silencer GRCh37_chr12:132949478-132949627 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:132982751-132983387 Neighboring gene ReSE screen-validated silencer GRCh37_chr12:132991529-132991667 Neighboring gene uncharacterized LOC105370092 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:133005261-133005795 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5116

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • 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

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    Related articles in PubMed

    1. Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing. Fei T, et al. Proc Natl Acad Sci U S A, 2017 Jun 27. PMID 28611215, Free PMC Article
    2. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. Kimura K, et al. Genome Res, 2006 Jan. PMID 16344560, Free PMC Article
    3. Normalization and subtraction: two approaches to facilitate gene discovery. Bonaldo MF, et al. Genome Res, 1996 Sep. PMID 8889548

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Review eQTL and phenotype association data in this region using PheGenI

    Variation

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    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    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_024563.1 RNA Sequence

      Status: PREDICTED

      Source sequence(s)
      AC148477, AK123118, BM984287, DA121414, DA629674

    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
      132275391..132280900
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 PATCHES

    Genomic

    1. NW_021160007.1 Reference GRCh38.p14 PATCHES

      Range
      181751..187260
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060936.1 Alternate T2T-CHM13v2.0

      Range
      132328533..132334042
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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