Format

Send to:

Choose Destination

ZMIZ1-AS1 ZMIZ1 antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 283050, updated on 23-Nov-2021

Summary

Official Symbol
ZMIZ1-AS1provided by HGNC
Official Full Name
ZMIZ1 antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:27433
See related
Ensembl:ENSG00000224596
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
Broad expression in testis (RPKM 1.8), skin (RPKM 1.0) and 21 other tissues See more
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See ZMIZ1-AS1 in Genome Data Viewer
Location:
10q22.3
Exon count:
10
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (78943326..79067448, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (80703083..80827205, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene VISTA enhancer hs1491 Neighboring gene uncharacterized LOC105378379 Neighboring gene uncharacterized LOC112268062 Neighboring gene HNF1 motif-containing MPRA enhancer 157 Neighboring gene Sharpr-MPRA regulatory region 11789 Neighboring gene zinc finger MIZ-type containing 1

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

Associated conditions

Description Tests
Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk.
GeneReviews: Not available

General gene information

Markers

Clone Names

  • FLJ44323, MGC125551

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_015429.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) lacks two internal exons in the 5' region, as compared to variant 1.
    Source sequence(s)
    AK098249, BC102001, BX116874, CB306489
  2. NR_024429.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) lacks two internal exons in the 5' and 3' regions respectively, as compared to variant 1.
    Source sequence(s)
    AK097923, AK098249, BC105703, CB306489
  3. NR_024431.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) is the longest transcript.
    Source sequence(s)
    AK098249, AL356753, AL450398, CB306489
    Related
    ENST00000456353.5

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_000010.11 Reference GRCh38.p13 Primary Assembly

    Range
    78943326..79067448 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center