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PPIAP86 peptidylprolyl isomerase A pseudogene 86 [ Homo sapiens (human) ]

Gene ID: 111082970, updated on 17-Sep-2024

Summary

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Official Symbol
PPIAP86provided by HGNC
Official Full Name
peptidylprolyl isomerase A pseudogene 86provided by HGNC
Primary source
HGNC:HGNC:53710
See related
Ensembl:ENSG00000213873 AllianceGenome:HGNC:53710
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 PPIAP86 in Genome Data Viewer
Location:
8q13.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (65377592..65378111)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (65803331..65803850)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (66289827..66290346)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene NANOG hESC enhancer GRCh37_chr8:66082861-66083386 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:66084099-66085298 Neighboring gene long intergenic non-protein coding RNA 251 Neighboring gene NANOG hESC enhancer GRCh37_chr8:66097743-66098336 Neighboring gene uncharacterized LOC105375881 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:66187065-66187864 Neighboring gene NANOG hESC enhancer GRCh37_chr8:66199936-66200450 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:66367245-66367474 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr8:66419280-66420479 Neighboring gene long intergenic non-protein coding RNA 1299 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:66472804-66473503 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:66528344-66529126 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr8:66546245-66546867 Neighboring gene armadillo repeat containing 1

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_065982.1 

    Range
    101..620
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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
    65377592..65378111
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    65803331..65803850
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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