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    PCAT7 prostate cancer associated transcript 7 [ Homo sapiens (human) ]

    Gene ID: 101928099, updated on 10-Dec-2024

    Summary

    Official Symbol
    PCAT7provided by HGNC
    Official Full Name
    prostate cancer associated transcript 7provided by HGNC
    Primary source
    HGNC:HGNC:48824
    See related
    Ensembl:ENSG00000231806 AllianceGenome:HGNC:48824
    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
    PCAN-R2
    Expression
    Biased expression in stomach (RPKM 5.4), testis (RPKM 2.0) and 9 other tissues See more
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    Genomic context

    See PCAT7 in Genome Data Viewer
    Location:
    9q22.32
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (94554599..94574654)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (106723923..106743981)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (97316881..97336936)

    Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene major facilitator superfamily domain containing 14B Neighboring gene yrdC N(6)-threonylcarbamoyltransferase domain containing pseudogene 1 Neighboring gene MPRA-validated peak7296 silencer Neighboring gene uncharacterized LOC107987100 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_110230 Neighboring gene MPRA-validated peak7297 silencer Neighboring gene leishmanolysin like peptidase pseudogene Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_110244 Neighboring gene RNA, U6 small nuclear 669, pseudogene Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_110264 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_110288 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_110294 Neighboring gene uncharacterized LOC124902218 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:97315577-97316239 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:97316904-97317566 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:97320892-97321392 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:97349793-97350294 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:97350295-97350794 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:97353573-97354115 Neighboring gene fructose-bisphosphatase 2 Neighboring gene NANOG hESC enhancer GRCh37_chr9:97370327-97370828 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:97372257-97372756 Neighboring gene fructose-bisphosphatase 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20057 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28632 Neighboring gene Sharpr-MPRA regulatory region 4124 Neighboring gene uncharacterized LOC124902219 Neighboring gene uncharacterized LOC107987101

    Genomic regions, transcripts, and products

    Expression

    • 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

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    General gene information

    Other Names

    • prostate cancer associated transcript 7 (non-protein coding)
    • prostate cancer-associated noncoding RNA 2

    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_121566.3 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728
    2. NR_121567.3 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728
      Related
      ENST00000644721.2
    3. NR_121568.3 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728
    4. NR_121569.3 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728
    5. NR_185898.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728
    6. NR_185899.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728
    7. NR_185900.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728
    8. NR_185901.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728
    9. NR_185902.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728
    10. NR_185903.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728
    11. NR_185904.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728
    12. NR_185905.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728
    13. NR_185906.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728
    14. NR_185907.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL161728

    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_000009.12 Reference GRCh38.p14 Primary Assembly

      Range
      94554599..94574654
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060933.1 Alternate T2T-CHM13v2.0

      Range
      106723923..106743981
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)