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HERC2P9 HERC2 pseudogene 9 [ Homo sapiens (human) ]

Gene ID: 440248, updated on 23-Nov-2021

Summary

Official Symbol
HERC2P9provided by HGNC
Official Full Name
HERC2 pseudogene 9provided by HGNC
Primary source
HGNC:HGNC:30495
See related
Ensembl:ENSG00000206149
Gene type
pseudo
RefSeq status
PROVISIONAL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Ubiquitous expression in urinary bladder (RPKM 20.7), brain (RPKM 19.3) and 25 other tissues See more
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Genomic context

See HERC2P9 in Genome Data Viewer
Location:
15q13.1
Exon count:
14
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 15 NC_000015.10 (28654442..28685264)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (28899588..28930410)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene pectinesterase inhibitor 10-like Neighboring gene HERC2 pseudogene 11 Neighboring gene HECT and RLD domain containing E3 ubiquitin protein ligase 2 pseudogene Neighboring gene uncharacterized LOC107984746 Neighboring gene golgin A8 family member M Neighboring gene RNA, 7SL, cytoplasmic 719, pseudogene Neighboring gene WHAMM pseudogene 2

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

General gene information

Markers

Other Names

  • hect domain and RLD 2 pseudogene 9

Clone Names

  • FLJ59185

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_036443.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    BC047911
    Related
    ENST00000528584.5

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
    28654442..28685264
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 PATCHES

Genomic

  1. NW_011332701.1 Reference GRCh38.p13 PATCHES

    Range
    816447..847268
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 ALT_REF_LOCI_2

Genomic

  1. NT_187660.1 Reference GRCh38.p13 ALT_REF_LOCI_2

    Range
    930233..961054
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_006524.1: Suppressed sequence

    Description
    NG_006524.1: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.
  2. NG_025368.1: Suppressed sequence

    Description
    NG_025368.1: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.
  3. NM_199045.1: Suppressed sequence

    Description
    NM_199045.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.
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