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ZNF663P zinc finger protein 663, pseudogene [ Homo sapiens (human) ]

Gene ID: 100130934, updated on 13-May-2022

Summary

Official Symbol
ZNF663Pprovided by HGNC
Official Full Name
zinc finger protein 663, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:25342
See related
AllianceGenome:HGNC:25342
Gene type
pseudo
RefSeq status
PROVISIONAL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ZNF663
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Genomic context

See ZNF663P in Genome Data Viewer
Location:
20q13.12
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 20 NC_000020.11 (46456493..46457643, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 20 NC_060944.1 (48192597..48193751, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (45085132..45086282, complement)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124904917 Neighboring gene engulfment and cell motility 2 Neighboring gene uncharacterized LOC105372633 Neighboring gene zinc finger protein 334 Neighboring gene makorin ring finger protein 7, pseudogene Neighboring gene zinc finger protein 840, pseudogene

Genomic regions, transcripts, and products

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_045983.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    BC100777

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000020.11 Reference GRCh38.p14 Primary Assembly

    Range
    46456493..46457643 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060944.1 Alternate T2T-CHM13v2.0

    Range
    48192597..48193751 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_173643.1: Suppressed sequence

    Description
    NM_173643.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.