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ZNF781 zinc finger protein 781 [ Homo sapiens (human) ]

Gene ID: 163115, updated on 23-Nov-2021

Summary

Official Symbol
ZNF781provided by HGNC
Official Full Name
zinc finger protein 781provided by HGNC
Primary source
HGNC:HGNC:26745
See related
Ensembl:ENSG00000196381
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Ubiquitous expression in ovary (RPKM 1.4), endometrium (RPKM 1.3) and 23 other tissues See more
Orthologs
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Genomic context

See ZNF781 in Genome Data Viewer
Location:
19q13.12
Exon count:
6
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 19 NC_000019.10 (37667751..37692315, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (38158652..38183216, complement)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene ZNF571 antisense RNA 1 Neighboring gene zinc finger protein 540 Neighboring gene zinc finger protein 571 Neighboring gene MT-CO1 pseudogene 41 Neighboring gene ZFP30 zinc finger protein Neighboring gene selenoprotein K pseudogene 1 Neighboring gene zinc finger protein 607

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

Homology

Clone Names

  • FLJ37549, MGC131783

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables DNA binding IEA
Inferred from Electronic Annotation
more info
 
enables metal ion binding IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
located_in nucleus 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_173329.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC093227
  2. NR_173330.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC093227
  3. NR_173331.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC093227
  4. NR_173332.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC093227

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_000019.10 Reference GRCh38.p13 Primary Assembly

    Range
    37667751..37692315 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_152605.4: Suppressed sequence

    Description
    NM_152605.4: This RefSeq was removed because currently there is support for the transcript but not for the protein.
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