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ZNF667-AS1 ZNF667 antisense RNA 1 (head to head) [ Homo sapiens (human) ]

Gene ID: 100128252, updated on 19-Sep-2021

Summary

Official Symbol
ZNF667-AS1provided by HGNC
Official Full Name
ZNF667 antisense RNA 1 (head to head)provided by HGNC
Primary source
HGNC:HGNC:44321
See related
Ensembl:ENSG00000166770
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
MORT
Expression
Broad expression in thyroid (RPKM 15.6), brain (RPKM 15.5) and 25 other tissues See more
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Genomic context

See ZNF667-AS1 in Genome Data Viewer
Location:
19q13.43
Exon count:
2
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 19 NC_000019.10 (56477874..56495437)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (56989243..57006806)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene ZNF582 divergent transcript Neighboring gene zinc finger protein 583 Neighboring gene zinc finger protein 667 Neighboring gene uncharacterized LOC105372471 Neighboring gene zinc finger protein 471 Neighboring gene ZFP28 divergent transcript Neighboring gene ZFP28 zinc finger protein

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

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Other Names

  • Mortal Obligate RNA Transcript

Clone Names

  • MGC9913, AC004696.2

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_036521.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    AC098795, AW955601, BC110411
    Related
    ENST00000585445.1
  2. NR_036522.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) uses an alternate splice donor site, compared to variant 1.
    Source sequence(s)
    AC004696, AC098795
    Related
    ENST00000669162.1

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_000019.10 Reference GRCh38.p13 Primary Assembly

    Range
    56477874..56495437
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_198879.1: Suppressed sequence

    Description
    NM_198879.1: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.
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