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PPIAP30 peptidylprolyl isomerase A pseudogene 30 [ Homo sapiens (human) ]

Gene ID: 100192204, updated on 13-May-2022

Summary

Official Symbol
PPIAP30provided by HGNC
Official Full Name
peptidylprolyl isomerase A pseudogene 30provided by HGNC
Primary source
HGNC:HGNC:44878
See related
Ensembl:ENSG00000206448 AllianceGenome:HGNC:44878
Gene type
pseudo
RefSeq status
PROVISIONAL
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 PPIAP30 in Genome Data Viewer
Location:
10p13
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (15154722..15155347, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (15169216..15169841, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (15196721..15197346, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105376431 Neighboring gene N-myristoyltransferase 2 Neighboring gene uncharacterized LOC107984210 Neighboring gene cytochrome c oxidase subunit NDUFA4-like Neighboring gene uncharacterized LOC105376434

Genomic regions, transcripts, and products

Phenotypes

EBI GWAS Catalog

Description
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles.
EBI GWAS Catalog

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_036506.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    BC157831
    Related
    ENST00000415473.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    15154722..15155347 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    15169216..15169841 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_008791.2: Suppressed sequence

    Description
    NG_008791.2: This RefSeq was permanently suppressed because it is now thought that this gene is a transcribed pseudogene.