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SP2-AS1 SP2 antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 100506325, updated on 13-May-2022

Summary

Official Symbol
SP2-AS1provided by HGNC
Official Full Name
SP2 antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:51341
See related
Ensembl:ENSG00000234494 AllianceGenome:HGNC:51341
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 SP2-AS1 in Genome Data Viewer
Location:
17q21.32
Exon count:
3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (47898386..47941404, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (48760176..48803194, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (45975752..46018770, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene CRISPRi-validated cis-regulatory element chr17.3283 Neighboring gene SP2 divergent transcript Neighboring gene Sp2 transcription factor Neighboring gene Sharpr-MPRA regulatory region 5948 Neighboring gene pyridoxamine 5'-phosphate oxidase Neighboring gene proline rich 15 like

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

Markers

Clone Names

  • AC003665.1

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_103856.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    AC018521, HY111832
    Related
    ENST00000411573.7
  2. NR_103857.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) uses different splice sites at the 5' and 3' exons, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    AC018521, BM804969, BX097765, HY111832
    Related
    ENST00000451140.6

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_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    47898386..47941404 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    48760176..48803194 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)