Format

Send to:

Choose Destination

PRYP1 PTPN13 like Y-linked pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 442863, updated on 23-Nov-2021

Summary

Official Symbol
PRYP1provided by HGNC
Official Full Name
PTPN13 like Y-linked pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:34018
See related
Ensembl:ENSG00000224166
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
PRY4P; PRYP7
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See PRYP1 in Genome Data Viewer
Location:
Yq11.222
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) Y NC_000024.10 (17729799..17744540, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (19841679..19856420, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene chromodomain Y-linked 5 pseudogene Neighboring gene elongin C pseudogene 36 Neighboring gene actin gamma 1 pseudogene 2 Neighboring gene XK related, Y-linked

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_004636.1 

    Range
    213704..228445 complement
    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_000024.10 Reference GRCh38.p13 Primary Assembly

    Range
    17729799..17744540 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_024772.1: Suppressed sequence

    Description
    NG_024772.1: This RefSeq was permanently suppressed because it was redundant with the annotation of GeneID:442863 on NG_004636.1.
Support Center