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ZNF22-AS1 ZNF22 antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 220979, updated on 23-Nov-2021

Summary

Official Symbol
ZNF22-AS1provided by HGNC
Official Full Name
ZNF22 antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:23509
See related
Ensembl:ENSG00000165511
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
C10orf25
Expression
Ubiquitous expression in appendix (RPKM 9.1), fat (RPKM 8.9) and 25 other tissues See more
Orthologs
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Genomic context

See ZNF22-AS1 in Genome Data Viewer
Location:
10q11.21
Exon count:
4
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (44993932..45000803, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (45489380..45496251, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene Ras association domain family member 4 Neighboring gene uncharacterized LOC105378281 Neighboring gene Sharpr-MPRA regulatory region 8316 Neighboring gene DEPP1 autophagy regulator Neighboring gene zinc finger protein 22 Neighboring gene double homeobox A pseudogene 4

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

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Homology

Other Names

  • uncharacterized protein C10orf25

Clone Names

  • FLJ18393, FLJ30567

Gene Ontology Provided by GOA

Component Evidence Code Pubs
located_in extracellular region IEA
Inferred from Electronic Annotation
more info
 

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_126421.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL353801
  2. NR_164113.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL353801
    Related
    ENST00000625168.1

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_000010.11 Reference GRCh38.p13 Primary Assembly

    Range
    44993932..45000803 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001039380.3: Suppressed sequence

    Description
    NM_001039380.3: This RefSeq was removed because it is now thought that this gene does not encode a protein.
  2. NM_145022.1: Suppressed sequence

    Description
    NM_145022.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.
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