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    CASC17 cancer susceptibility 17 [ Homo sapiens (human) ]

    Gene ID: 101928165, updated on 10-Oct-2023

    Summary

    Official Symbol
    CASC17provided by HGNC
    Official Full Name
    cancer susceptibility 17provided by HGNC
    Primary source
    HGNC:HGNC:43911
    See related
    Ensembl:ENSG00000260785 AllianceGenome:HGNC:43911
    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
    LINC00600
    Expression
    Restricted expression toward testis (RPKM 1.2) See more
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    Genomic context

    Location:
    17q24.3
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (71097774..71202179, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (71970472..72074817, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (69093915..69198320, complement)

    Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124904104 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr17:68983705-68984206 Neighboring gene VISTA enhancer hs1467 Neighboring gene SERPINE1 mRNA binding protein 1 pseudogene Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr17:69028546-69029302 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr17:69029303-69030057 Neighboring gene SOX9 enhancer cre1 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr17:69067578-69068777 Neighboring gene enhancer upstream of SOX9 Neighboring gene H3K27ac hESC enhancer GRCh37_chr17:69297407-69297907 Neighboring gene H3K27ac hESC enhancer GRCh37_chr17:69300220-69300720 Neighboring gene H3K27ac hESC enhancer GRCh37_chr17:69300721-69301221 Neighboring gene U6 spliceosomal RNA Neighboring gene RNA, U7 small nuclear 155 pseudogene

    Genomic regions, transcripts, and products

    Phenotypes

    EBI GWAS Catalog

    Description
    Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control selection on genetic association studies.
    EBI GWAS Catalog
    Genome-wide association study identifies new prostate cancer susceptibility loci.
    EBI GWAS Catalog
    Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.
    EBI GWAS Catalog
    Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.
    EBI GWAS Catalog
    Multiple newly identified loci associated with prostate cancer susceptibility.
    EBI GWAS Catalog
    Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes.
    EBI GWAS Catalog

    General gene information

    Other Names

    • cancer susceptibility 17 (non-protein coding)
    • cancer susceptibility candidate 17 (non-protein coding)
    • long intergenic non-protein coding RNA 600

    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_104152.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC005273, BC039327, BI459971
      Related
      ENST00000569074.1

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000017.11 Reference GRCh38.p14 Primary Assembly

      Range
      71097774..71202179 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060941.1 Alternate T2T-CHM13v2.0

      Range
      71970472..72074817 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)