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ZYXP1 zyxin pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 106480342, updated on 10-Oct-2023

Summary

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Official Symbol
ZYXP1provided by HGNC
Official Full Name
zyxin pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:51695
See related
Ensembl:ENSG00000274572 AllianceGenome:HGNC:51695
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

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See ZYXP1 in Genome Data Viewer
Location:
8q24.23
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (137424904..137425021, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (138542354..138542471, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (138437147..138437264, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107986905 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:138293314-138294513 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr8:138298975-138300174 Neighboring gene uncharacterized LOC101927915 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr8:138427125-138427755 Neighboring gene NANOG hESC enhancer GRCh37_chr8:138648708-138649265 Neighboring gene nucleolar and coiled-body phosphoprotein 1 pseudogene Neighboring gene NANOG hESC enhancer GRCh37_chr8:138749730-138750231 Neighboring gene uncharacterized LOC105375776

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

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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_044600.1 

    Range
    101..218
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    137424904..137425021 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    138542354..138542471 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Molecular Biology Databases
Research Materials