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UBE2Q2P1 UBE2Q2 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 388165, updated on 25-Jan-2022

Summary

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Official Symbol
UBE2Q2P1provided by HGNC
Official Full Name
UBE2Q2 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:37439
See related
Ensembl:ENSG00000189136 AllianceGenome:HGNC:37439
Gene type
pseudo
RefSeq status
PROVISIONAL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
UBE2QP1
Expression
Ubiquitous expression in ovary (RPKM 3.7), testis (RPKM 2.5) and 25 other tissues See more
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Genomic context

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See UBE2Q2P1 in Genome Data Viewer
Location:
15q25.2
Exon count:
6
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 15 NC_000015.10 (84527196..84570795, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (85070427..85114026, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene golgin A6 family like 5, pseudogene Neighboring gene dynamin 1 pseudogene 40 Neighboring gene long intergenic non-protein coding RNA 933 Neighboring gene uncharacterized LOC105370947 Neighboring gene zinc finger and SCAN domain containing 2 Neighboring gene SCAN domain containing 2 pseudogene Neighboring gene egl-9 family hypoxia inducible factor 1 pseudogene 1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • 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

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Related articles in PubMed

  1. RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families. Domarkienė I, et al. Balkan J Med Genet, 2013 Dec. PMID 24778558, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

EBI GWAS Catalog

Description
RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families.
EBI GWAS Catalog

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

General gene information

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Markers

Other Names

  • ubiquitin conjugating enzyme E2 Q2 pseudogene 1
  • ubiquitin conjugating enzyme E2Q family member 2 pseudogene 1
  • ubiquitin-conjugating enzyme E2Q family pseudogene 1

Clone Names

  • FLJ43276

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_003661.2 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC048382
    Related
    ENST00000339094.5

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_000015.10 Reference GRCh38.p13 Primary Assembly

    Range
    84527196..84570795 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_207382.1: Suppressed sequence

    Description
    NM_207382.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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