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PRORY proline rich Y-linked [ Homo sapiens (human) ]

Gene ID: 100533178, updated on 23-Nov-2021

Summary

Official Symbol
PRORYprovided by HGNC
Official Full Name
proline rich Y-linkedprovided by HGNC
Primary source
HGNC:HGNC:38732
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
CYorf17
Expression
Low expression observed in reference dataset See more
Orthologs
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Genomic context

See PRORY in Genome Data Viewer
Location:
Yq11.223
Exon count:
5
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) Y NC_000024.10 (21381905..21451846, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (23543791..23613732, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107987346 Neighboring gene uncharacterized LOC107987347 Neighboring gene RNA binding motif protein Y-linked family 2 member S, pseudogene Neighboring gene RNA binding motif protein Y-linked family 2 member E, pseudogene Neighboring gene RNA binding motif protein Y-linked family 2 member T, pseudogene Neighboring gene testis specific protein Y-linked 14, pseudogene Neighboring gene RNA binding motif protein Y-linked family 1 member H, pseudogene

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

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_004832.1 

    Range
    72301..75700 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. NR_170372.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC010086

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
    21381905..21451846 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001282471.1: Suppressed sequence

    Description
    NM_001282471.1: This RefSeq was removed because it is now thought that this gene does not encode a protein.
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