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CDY8P chromodomain Y-linked 8 pseudogene [ Homo sapiens (human) ]

Gene ID: 386732, updated on 17-Sep-2024

Summary

Official Symbol
CDY8Pprovided by HGNC
Official Full Name
chromodomain Y-linked 8 pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:23855
See related
Ensembl:ENSG00000224033 AllianceGenome:HGNC:23855
Gene type
pseudo
RefSeq status
INFERRED
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 CDY8P in Genome Data Viewer
Location:
Yq11.222
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (18022299..18023917)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (18928777..18930392)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (20134179..20135797)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene USP9Y pseudogene 34 Neighboring gene USP9Y pseudogene 32 Neighboring gene chromodomain Y-linked 2A Neighboring gene elongin C pseudogene 12

Genomic regions, transcripts, and products

General gene information

Other Names

  • chromodomain protein, Y-linked 8 pseudogene
  • chromodomain protein, Y-linked, 1 pseudogene

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_083959.1 

    Range
    101..1719
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    18022299..18023917
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    18928777..18930392
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_021112.1: Suppressed sequence

    Description
    NG_021112.1: This RefSeq was permanently suppressed because this pseudogene is annotated on NG_004636.