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PIN1P1 peptidylprolyl cis/trans isomerase, NIMA-interacting 1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 5301, updated on 13-May-2022

Summary

Official Symbol
PIN1P1provided by HGNC
Official Full Name
peptidylprolyl cis/trans isomerase, NIMA-interacting 1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:8989
See related
Ensembl:ENSG00000229359 MIM:602051; AllianceGenome:HGNC:8989
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
PIN1L
Summary
Predicted to enable peptidyl-prolyl cis-trans isomerase activity. Predicted to be involved in protein peptidyl-prolyl isomerization. Predicted to be active in cytosol and nucleus. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

See PIN1P1 in Genome Data Viewer
Location:
1p31.1
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (69919322..69920317)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (69797484..69798479)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (70385005..70386000)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene leucine rich repeat containing 7 Neighboring gene uncharacterized LOC124904199 Neighboring gene RNA, 7SL, cytoplasmic 538, pseudogene Neighboring gene LRRC7 antisense RNA 1 Neighboring gene Sharpr-MPRA regulatory region 9273

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • peptidylprolyl cis/trans isomerase, NIMA-interacting 1-like (pseudogene)
  • protein (peptidylprolyl cis/trans isomerase) NIMA-interacting 1-like (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.

RNA

  1. NR_023916.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    U82382
    Related
    ENST00000412108.1

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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    69919322..69920317
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    69797484..69798479
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_006222.1: Suppressed sequence

    Description
    NM_006222.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.