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TSPY26P testis specific protein Y-linked 26, pseudogene [ Homo sapiens (human) ]

Gene ID: 128854, updated on 13-May-2022

Summary

Official Symbol
TSPY26Pprovided by HGNC
Official Full Name
testis specific protein Y-linked 26, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:16256
See related
Ensembl:ENSG00000235217 AllianceGenome:HGNC:16256
Gene type
pseudo
RefSeq status
PROVISIONAL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
TSPYL3; bA392M18.1
Summary
Predicted to enable chromatin binding activity and histone binding activity. Predicted to be involved in nucleosome assembly. Predicted to be active in chromatin and nucleus. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

See TSPY26P in Genome Data Viewer
Location:
20q11.21
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 20 NC_000020.11 (32189146..32190360, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 20 NC_060944.1 (33913069..33914283, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (30776949..30778163, complement)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 8915 Neighboring gene ribosomal L24 domain containing 1 pseudogene 6 Neighboring gene PLAG1 like zinc finger 2 Neighboring gene protein O-fucosyltransferase 1 Neighboring gene uncharacterized LOC124904884

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • TSPY-like 3 (pseudogene)

Clone Names

  • MGC126605, MGC126607

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables chromatin binding IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
enables histone binding IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Process Evidence Code Pubs
involved_in nucleosome assembly IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
is_active_in chromatin IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
is_active_in nucleus IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 

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_002781.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    BC101558
    Related
    ENST00000476365.2

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_000020.11 Reference GRCh38.p14 Primary Assembly

    Range
    32189146..32190360 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060944.1 Alternate T2T-CHM13v2.0

    Range
    33913069..33914283 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_178465.1: Suppressed sequence

    Description
    NM_178465.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.