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PAFAH1B2P1 PAFAH1B2 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 139957, updated on 11-Jun-2021

Summary

Official Symbol
PAFAH1B2P1provided by HGNC
Official Full Name
PAFAH1B2 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:54905
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

See PAFAH1B2P1 in Genome Data Viewer
Location:
Xp21.3
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (25029413..25029976)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (25047530..25048093)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene VISTA enhancer hs145 Neighboring gene aristaless related homeobox polyalanine expansion region Neighboring gene aristaless related homeobox Neighboring gene RNA, 7SL, cytoplasmic 91, pseudogene Neighboring gene METTL1 pseudogene 1

Genomic regions, transcripts, and products

General gene information

Other Names

  • platelet activating factor acetylhydrolase 1b catalytic subunit 2 pseudogene
  • platelet-activating factor acetylhydrolase 1b, catalytic subunit 2 (30kDa) 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.

Genomic

  1. NG_006977.3 

    Range
    101..664
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    GenBank, FASTA, Sequence Viewer (Graphics)

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
    25029413..25029976
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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