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VENTXP1 VENT homeobox pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 139538, updated on 11-Jun-2021

Summary

Official Symbol
VENTXP1provided by HGNC
Official Full Name
VENT homeobox pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:30900
See related
Ensembl:ENSG00000259849
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
CT18; NA88A; VENTX2P1
Summary
Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the Vent homeobox gene family. [provided by RefSeq, Jul 2008]
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Genomic context

See VENTXP1 in Genome Data Viewer
Location:
Xp21.3
Exon count:
1
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (26558337..26561052)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (26576454..26579169)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene phenazine biosynthesis like protein domain containing pseudogene Neighboring gene FMN2 pseudogene 1 Neighboring gene VENTX pseudogene 8 Neighboring gene ribosomal protein L7 pseudogene 58 Neighboring gene high mobility group AT-hook 1 pseudogene 1

Genomic regions, transcripts, and products

Phenotypes

Associated conditions

Description Tests
Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.
GeneReviews: Not available

General gene information

Other Names

  • VENT-like homeobox 2 pseudogene 1
  • cancer/testis antigen 18
  • tumor antigen NA88A

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_001559.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC079178
    Related
    ENST00000569334.2

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    26558337..26561052
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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