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DEFA9P defensin alpha 9, pseudogene [ Homo sapiens (human) ]

Gene ID: 449492, updated on 8-Nov-2023

Summary

Official Symbol
DEFA9Pprovided by HGNC
Official Full Name
defensin alpha 9, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:31800
See related
Ensembl:ENSG00000233238 AllianceGenome:HGNC:31800
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
DEFAP2
Expression
Low expression observed in reference dataset See more
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Genomic context

Location:
8p23.1
Exon count:
2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (6959289..6960161, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (6713955..6714827, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (6816811..6817683, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18889 Neighboring gene defensin alpha 4 Neighboring gene defensin alpha 8, pseudogene Neighboring gene defensin alpha 10, pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:6828716-6829216 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:6829217-6829717 Neighboring gene uncharacterized LOC124901873 Neighboring gene defensin alpha 1

Genomic regions, transcripts, and products

Expression

  • 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

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_073408.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AY746434
    Related
    ENST00000433042.1

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
    6959289..6960161 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_018654717.1 Reference GRCh38.p14 PATCHES

    Range
    354399..355271 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    6713955..6714827 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_008304.2: Suppressed sequence

    Description
    NG_008304.2: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.