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CASC20 cancer susceptibility 20 [ Homo sapiens (human) ]

Gene ID: 101929244, updated on 29-May-2022

Summary

Official Symbol
CASC20provided by HGNC
Official Full Name
cancer susceptibility 20provided by HGNC
Primary source
HGNC:HGNC:49477
See related
Ensembl:ENSG00000229876 AllianceGenome:HGNC:49477
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

See CASC20 in Genome Data Viewer
Location:
20p12.3
Exon count:
4
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 20 NC_000020.11 (6426732..6528459)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 20 NC_060944.1 (6467898..6569576)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (6407379..6509106)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene fibroblast growth factor receptor 3 pseudogene 3 Neighboring gene uncharacterized LOC124904866 Neighboring gene Sharpr-MPRA regulatory region 10991 Neighboring gene long intergenic non-protein coding RNA 1713

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 20 (non-protein coding)
  • cancer susceptibility candidate 20 (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_109953.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL121911, AL162504, AY007089
    Related
    ENST00000415932.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000020.11 Reference GRCh38.p14 Primary Assembly

    Range
    6426732..6528459
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060944.1 Alternate T2T-CHM13v2.0

    Range
    6467898..6569576
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)