Human (GRCh37.p13)
Description

synovial sarcoma, X breakpoint 2 [Source:HGNC Symbol;Acc:11336]

Gene Synonyms

CT5.2, CT5.2A, CT5.2a, CT5.2b, HD21, HOM-MEL-40, MGC119055, MGC15364, MGC3884, SSX, SSX2A

Location

Chromosome X: 52,725,946-52,736,239 reverse strand.

GRCh37:CM000685.1

View alleles of this gene on alternative sequences

About this gene

This gene has 3 transcripts (splice variants), 1 gene allele, 7 paralogues and is associated with 18 phenotypes.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000336777.5SSX2-0011410223aa
 
Protein coding
CCDS14345Q16385 Q9NZK4 NM_003147.5Ensembl CanonicalGENCODE Basic
ENST00000337502.5SSX2-0021292188aa
 
Protein coding
CCDS14344Q16385 NM_175698.2GENCODE Basic
ENST00000476392.1SSX2-003677No protein
 
Processed transcript
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Name

SSX2 (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: Q16385

CCDS

This gene is a member of the Human CCDS set: CCDS14344.1, CCDS14345.1

Ensembl version

ENSG00000241476.3

Other assemblies

This gene maps to 52,696,896-52,707,189 in GRCh38 coordinates.

Gene type

Protein coding

Annotation method

Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.

Alternative genes

This gene corresponds to the following database identifiers:

Havana gene:
OTTHUMG00000022697 (version 1)

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