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CDY12P chromodomain Y-linked 12 pseudogene [ Homo sapiens (human) ]

Gene ID: 386734, updated on 23-Nov-2021

Summary

Official Symbol
CDY12Pprovided by HGNC
Official Full Name
chromodomain Y-linked 12 pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:23856
See related
Ensembl:ENSG00000228850
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 CDY12P in Genome Data Viewer
Location:
Yq11.223
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) Y NC_000024.10 (22064597..22065805)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (24210744..24211952)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene USP9Y pseudogene 17 Neighboring gene heat shock transcription factor Y-linked 5, pseudogene Neighboring gene elongin C pseudogene 15 Neighboring gene PTPN13 like Y-linked 2

Genomic regions, transcripts, and products

General gene information

Other Names

  • chromodomain protein, Y-linked 12 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_004755.2 

    Range
    253711..254919
    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_000024.10 Reference GRCh38.p13 Primary Assembly

    Range
    22064597..22065805
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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