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NCKAP5-AS2 NCKAP5 antisense RNA 2 [ Homo sapiens (human) ]

Gene ID: 101928161, updated on 23-Nov-2021

Summary

Official Symbol
NCKAP5-AS2provided by HGNC
Official Full Name
NCKAP5 antisense RNA 2provided by HGNC
Primary source
HGNC:HGNC:54065
See related
Ensembl:ENSG00000226953
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 NCKAP5-AS2 in Genome Data Viewer
Location:
2q21.2
Exon count:
5
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (133266195..133284758)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (134023767..134042330)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene NCK associated protein 5 Neighboring gene uncharacterized LOC112268439 Neighboring gene NCKAP5 antisense RNA 1 Neighboring gene RNA, U6 small nuclear 579, pseudogene Neighboring gene RN7SK pseudogene 154

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

Phenotypes

EBI GWAS Catalog

Description
Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.
EBI GWAS Catalog

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_110294.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC010890
    Related
    ENST00000432414.5

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p13 Primary Assembly

    Range
    133266195..133284758
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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