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UBBP4 ubiquitin B pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 23666, updated on 10-Oct-2023

Summary

Official Symbol
UBBP4provided by HGNC
Official Full Name
ubiquitin B pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:12467
See related
Ensembl:ENSG00000290919 AllianceGenome:HGNC:12467
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See UBBP4 in Genome Data Viewer
Location:
17p11.2
Exon count:
5
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (22090750..22205151)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (22756789..22866794)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (21729601..21731762)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:21561832-21562394 Neighboring gene abhydrolase domain containing 15 pseudogene Neighboring gene MPRA-validated peak2767 silencer Neighboring gene ReSE screen-validated silencer GRCh37_chr17:21532008-21532206 Neighboring gene NCOR1 pseudogene 2 Neighboring gene ferritin light chain pseudogene 13 Neighboring gene long intergenic non-protein coding RNA 2002

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

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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_144546.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC138761
    Related
    ENST00000584755.2
  2. NR_176224.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    ABBA01006765, AC138761
    Related
    ENST00000648259.1

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    22090750..22205151
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    22756789..22866794
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)