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COP1P1 COP1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 729391, updated on 23-Nov-2021

Summary

Official Symbol
COP1P1provided by HGNC
Official Full Name
COP1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:31900
See related
Ensembl:ENSG00000266613
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RFWD2P; RFWD2P1
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Genomic context

See COP1P1 in Genome Data Viewer
Location:
18p11.23
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 18 NC_000018.10 (8411985..8414631)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (8411983..8414629)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene protein tyrosine phosphatase receptor type M Neighboring gene uncharacterized LOC107985119 Neighboring gene uncharacterized LOC100192426 Neighboring gene RNA, 7SL, cytoplasmic 50, pseudogene Neighboring gene thymocyte selection associated family member 3, pseudogene

Genomic regions, transcripts, and products

General gene information

Other Names

  • ring finger and WD repeat domain 2 pseudogene 1
  • ring finger and WD repeat domain 2, E3 ubiquitin protein ligase pseudogene 1

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.

Genomic

  1. NG_016737.2 

    Range
    101..2747
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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_000018.10 Reference GRCh38.p13 Primary Assembly

    Range
    8411985..8414631
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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