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CNN3-DT CNN3 divergent transcript [ Homo sapiens (human) ]

Gene ID: 729970, updated on 13-May-2022

Summary

Official Symbol
CNN3-DTprovided by HGNC
Official Full Name
CNN3 divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:54176
See related
AllianceGenome:HGNC:54176
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
Ubiquitous expression in adrenal (RPKM 7.4), duodenum (RPKM 5.7) and 23 other tissues See more
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Genomic context

See CNN3-DT in Genome Data Viewer
Location:
1p21.3
Exon count:
5
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (94926360..94963270)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (94774713..94811607)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (95391916..95428826)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene SLC44A3 antisense RNA 1 Neighboring gene Sharpr-MPRA regulatory region 2553 Neighboring gene solute carrier family 44 member 3 Neighboring gene Sharpr-MPRA regulatory region 980 Neighboring gene calponin 3 Neighboring gene uncharacterized LOC124904224 Neighboring gene ALG14 UDP-N-acetylglucosaminyltransferase subunit Neighboring gene uncharacterized LOC105378863

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

Other Names

  • hCG2028352-like

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_033998.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AA861137, BM693804
  2. NR_168376.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC105942
  3. NR_168377.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC105942

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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    94926360..94963270
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    94774713..94811607
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)