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SSX6P SSX family member 6, pseudogene [ Homo sapiens (human) ]

Gene ID: 280657, updated on 6-Jul-2026
Official Symbol
SSX6Pprovided by HGNC
Official Full Name
SSX family member 6, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:19652
See related
MIM:300541; AllianceGenome:HGNC:19652
Gene type
pseudo
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
SSX6; SSXP2; psiSSX2; dJ54B20.1
Summary
This gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. SSX1, SSX2 and SSX4 genes have been involved in the t(X;18) translocation characteristically found in all synovial sarcomas. This gene is classified as a pseudogene because a splice donor in the 3' UTR has changed compared to other family members, rendering the transcript a candidate for nonsense-mediated mRNA decay (NMD). [provided by RefSeq, Aug 2009]
Expression
Low expression observed in reference dataset See more
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See SSX6P in Genome Data Viewer
Location:
Xp11.23
Exon count:
8
Annotation release Status Assembly Chr Location
RS_2025_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (48107982..48120686)
RS_2025_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (47518129..47530833)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (47967367..47980068)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene ZNF630 antisense RNA 1 Neighboring gene zinc finger protein 630 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:47931149-47931345 Neighboring gene small nucleolar RNA U13 Neighboring gene sperm acrosome associated 5B Neighboring gene ornithine aminotransferase pseudogene Neighboring gene RNA, U6 small nuclear 707, pseudogene

  • Project title: Tissue-specific circular RNA induction during human fetal development
  • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
  • BioProject: PRJNA270632
  • Publication: PMID 26076956
  • Analysis date: Mon Apr 2 22:54:59 2018

Related articles in PubMed

Products Interactant Other Gene Complex Source Pubs Description

Markers

Other Names

  • SSX family pseudogene 2
  • SSX2 pseudogene
  • synovial sarcoma X breakpoint 6 protein
  • synovial sarcoma, X breakpoint 6 (pseudogene)

Clone Names

  • FLJ53113

Gene Ontology Provided by GOA

Process Evidence Code Pubs
involved_in regulation of DNA-templated transcription IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
is_active_in nucleus IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in nucleus IEA
Inferred from Electronic Annotation
more info
 

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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_028366.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AC244636

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2025_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    48107982..48120686
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    47518129..47530833
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_002582.2: Suppressed sequence

    Description
    NG_002582.2: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.
  2. NM_173357.2: Suppressed sequence

    Description
    NM_173357.2: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.