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    GATA3-AS1 GATA3 antisense RNA 1 [ Homo sapiens (human) ]

    Gene ID: 399717, updated on 10-Dec-2024

    Summary

    Official Symbol
    GATA3-AS1provided by HGNC
    Official Full Name
    GATA3 antisense RNA 1provided by HGNC
    Primary source
    HGNC:HGNC:33786
    See related
    Ensembl:ENSG00000197308 AllianceGenome:HGNC:33786
    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
    Biased expression in kidney (RPKM 1.7), urinary bladder (RPKM 0.9) and 4 other tissues See more
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    Genomic context

    See GATA3-AS1 in Genome Data Viewer
    Location:
    10p14
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (8050450..8053484, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (8051330..8054364, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (8092413..8095447, complement)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene H3K27ac hESC enhancer GRCh37_chr10:7860144-7860662 Neighboring gene H3K27ac hESC enhancer GRCh37_chr10:7860663-7861180 Neighboring gene TATA-box binding protein associated factor 3 Neighboring gene Sharpr-MPRA regulatory region 6244 Neighboring gene ReSE screen-validated silencer GRCh37_chr10:8003953-8004117 Neighboring gene Sharpr-MPRA regulatory region 13617 Neighboring gene uncharacterized LOC105376394 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:8084925-8085676 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:8085677-8086428 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:8086674-8087217 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:8087218-8087760 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2983 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:8091667-8092510 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:8092511-8093354 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:8093355-8094198 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2115 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2116 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2117 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2118 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2984 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:8105038-8105952 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:8115451-8116429 Neighboring gene GATA binding protein 3 Neighboring gene ReSE screen-validated silencer GRCh37_chr10:8127093-8127295 Neighboring gene NANOG hESC enhancer GRCh37_chr10:8128242-8128743 Neighboring gene uncharacterized LOC105376395 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2985 Neighboring gene H3K27ac hESC enhancer GRCh37_chr10:8154631-8155132 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2986 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2987 Neighboring gene PRP38 domain containing A pseudogene 1

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).
    EBI GWAS Catalog
    Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma.
    EBI GWAS Catalog

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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_024256.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) uses the distal promoter and is alternatively spliced, compared to variant 1.
      Source sequence(s)
      AL390294
      Related
      ENST00000355358.1
    2. NR_104327.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) uses the distal promoter in a complex transcribed region.
      Source sequence(s)
      AL390294, BC036297
      Related
      ENST00000458727.1
    3. NR_104328.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (4) uses the proximal promoter and overlaps variant 1.
      Source sequence(s)
      AL390294, BC141936
      Related
      ENST00000420815.5
    4. NR_104329.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (5) uses the proximal promoter and overlaps variant 1. It uses alternate splice sited compared to variant 4.
      Source sequence(s)
      AL390294, BC141937
    5. NR_104330.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (6) uses the proximal promoter and overlaps variant 1. It uses alternate splice sited compared to variant 4.
      Source sequence(s)
      AL390294, BC128075
      Related
      ENST00000438755.1
    6. NR_104336.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) uses the distal promoter and an alternate splice site, compared to variant 1.
      Source sequence(s)
      AL390294, BC036297, BX089350
      Related
      ENST00000417359.2

    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_000010.11 Reference GRCh38.p14 Primary Assembly

      Range
      8050450..8053484 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060934.1 Alternate T2T-CHM13v2.0

      Range
      8051330..8054364 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_207423.1: Suppressed sequence

      Description
      NM_207423.1: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.
    2. NR_024255.1: Suppressed sequence

      Description
      NR_024255.1: This RefSeq was suppressed because it represents use of unsupported non-consensus splice sites.