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ST20-AS1 ST20 antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 283687, updated on 24-Jul-2021

Summary

Official Symbol
ST20-AS1provided by HGNC
Official Full Name
ST20 antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:27521
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
C15orf37
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Genomic context

See ST20-AS1 in Genome Data Viewer
Location:
15q25.1
Exon count:
1
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 15 NC_000015.10 (79922771..79924854)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (80215113..80217196)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene RNA, U6 small nuclear 667, pseudogene Neighboring gene ST20-MTHFS readthrough Neighboring gene methenyltetrahydrofolate synthetase Neighboring gene suppressor of tumorigenicity 20 Neighboring gene farnesyl diphosphate synthase pseudogene 9 Neighboring gene BCL2 related protein A1

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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_028330.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    BC016975, BC101202, BG677098

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000015.10 Reference GRCh38.p13 Primary Assembly

    Range
    79922771..79924854
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_175898.2: Suppressed sequence

    Description
    NM_175898.2: This RefSeq was permanently suppressed because it is now thought that this gene does not encode a protein.
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