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ZNF236-DT ZNF236 divergent transcript [ Homo sapiens (human) ]

Gene ID: 100131655, updated on 13-May-2022

Summary

Official Symbol
ZNF236-DTprovided by HGNC
Official Full Name
ZNF236 divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:53779
See related
Ensembl:ENSG00000264278 AllianceGenome:HGNC:53779
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 ZNF236-DT in Genome Data Viewer
Location:
18q23
Exon count:
3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 18 NC_000018.10 (76794732..76822295, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 18 NC_060942.1 (77023557..77051067, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (74506688..74534251, complement)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene cyclin D3 pseudogene 2 Neighboring gene uncharacterized LOC124904327 Neighboring gene RNA, U6 small nuclear 346, pseudogene Neighboring gene zinc finger protein 236 Neighboring gene uncharacterized LOC105372214 Neighboring gene ribosomal protein L26 pseudogene 35

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

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_040024.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC027575, BC032908
    Related
    ENST00000585258.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000018.10 Reference GRCh38.p14 Primary Assembly

    Range
    76794732..76822295 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060942.1 Alternate T2T-CHM13v2.0

    Range
    77023557..77051067 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)