Format

Send to:

Choose Destination

PPIAP89 peptidylprolyl isomerase A pseudogene 89 [ Homo sapiens (human) ]

Gene ID: 442460, updated on 23-Nov-2021

Summary

Official Symbol
PPIAP89provided by HGNC
Official Full Name
peptidylprolyl isomerase A pseudogene 89provided by HGNC
Primary source
HGNC:HGNC:53713
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See PPIAP89 in Genome Data Viewer
Location:
Xq22.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (100800092..100800822, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (100055081..100055811, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene sushi repeat containing protein X-linked 2 Neighboring gene synaptotagmin like 4 Neighboring gene Sharpr-MPRA regulatory region 15282 Neighboring gene RAD21 pseudogene 1 Neighboring gene cleavage stimulation factor subunit 2 Neighboring gene NADPH oxidase 1

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_030260.3 

    Range
    101..831
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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
    100800092..100800822 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center