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ZNF204P zinc finger protein 204, pseudogene [ Homo sapiens (human) ]

Gene ID: 7754, updated on 23-Nov-2021


Official Symbol
ZNF204Pprovided by HGNC
Official Full Name
zinc finger protein 204, pseudogeneprovided by HGNC
Primary source
See related
Gene type
RefSeq status
Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ZNF204; ZNF315P; b24o18.1; ZNF184-Lp
This locus represents a transcribed pseudogene, possibly of ZNF79 (GeneID 7633). The protein encoded by this locus would have significant N-terminal truncation, and would lack the KRAB domain and the C2H2 type zinc finger domain, compared to ZNF79. [provided by RefSeq, Jun 2011]
Broad expression in thyroid (RPKM 7.5), brain (RPKM 5.5) and 23 other tissues See more
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Genomic context

See ZNF204P in Genome Data Viewer
Exon count:
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 6 NC_000006.12 (27357823..27375374, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (27325602..27343153, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene tRNA-iMet (anticodon CAT) 1-5 Neighboring gene tRNA-Lys (anticodon TTT) 6-1 Neighboring gene zinc finger protein 391 Neighboring gene zinc finger protein 184 Neighboring gene multiple coagulation factor deficiency 2 pseudogene 1 Neighboring gene uncharacterized LOC105375001 Neighboring gene tRNA-Ser (anticodon AGA) 2-2

Genomic regions, transcripts, and products


  • 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

General gene information


Other Names

  • zinc finger protein 315 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.


  1. NR_002722.2 RNA Sequence

    Status: VALIDATED

    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    AL833520, BC067282, BU173489, CD511209, DB063011
  2. NR_024553.1 RNA Sequence

    Status: VALIDATED

    Transcript Variant: This variant (2) lacks an alternate segment resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    AL833520, BC067282, DA147897, DB031764

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


  1. NC_000006.12 Reference GRCh38.p13 Primary Assembly

    27357823..27375374 complement
    GenBank, FASTA, Sequence Viewer (Graphics)
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