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CASC6 cancer susceptibility 6 [ Homo sapiens (human) ]

Gene ID: 101929083, updated on 10-Oct-2023

Summary

Official Symbol
CASC6provided by HGNC
Official Full Name
cancer susceptibility 6provided by HGNC
Primary source
HGNC:HGNC:49076
See related
AllianceGenome:HGNC:49076
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
Low expression observed in reference dataset See more
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Genomic context

Location:
6q15
Exon count:
4
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (91629040..91690428, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (92840790..92902152, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (92338758..92400146, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107986624 Neighboring gene Sharpr-MPRA regulatory region 15648 Neighboring gene MPRA-validated peak5963 silencer Neighboring gene ATAC-STARR-seq lymphoblastoid active region 24837 Neighboring gene microRNA 4643 Neighboring gene NANOG hESC enhancer GRCh37_chr6:92363967-92364476 Neighboring gene uncharacterized LOC105377894 Neighboring gene MT-ATP6 pseudogene 25 Neighboring gene MT-ND4L pseudogene 19 Neighboring gene MT-CO1 pseudogene 56

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

General gene information

Other Names

  • cancer susceptibility 6 (non-protein coding)
  • cancer susceptibility candidate 6 (non-protein coding)

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_104154.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL132766, BC037927

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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    91629040..91690428 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    92840790..92902152 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)