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UCHL1-DT UCHL1 divergent transcript [ Homo sapiens (human) ]

Gene ID: 101410542, updated on 25-Jan-2022

Summary

Official Symbol
UCHL1-DTprovided by HGNC
Official Full Name
UCHL1 divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:40600
See related
Ensembl:ENSG00000251173 AllianceGenome:HGNC:40600
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
UCHL1-AS1
Expression
Low expression observed in reference dataset See more
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Genomic context

See UCHL1-DT in Genome Data Viewer
Location:
4p13
Exon count:
3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 4 NC_000004.12 (41220074..41256727, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (41222091..41258744, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene amyloid beta precursor protein binding family B member 2 Neighboring gene RNA, U6 small nuclear 836, pseudogene Neighboring gene RNA, U6 small nuclear 1195, pseudogene Neighboring gene ubiquitin C-terminal hydrolase L1 Neighboring gene LIM and calponin homology domains 1 Neighboring gene ribosomal protein L12 pseudogene 20

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_102709.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC095043, AC096712, DB169394
    Related
    ENST00000507190.1

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_000004.12 Reference GRCh38.p13 Primary Assembly

    Range
    41220074..41256727 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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