SSX2 SSX family member 2

Information
Symbol
SSX2
Type
protein-coding
Description
SSX family member 2
Entrez Gene ID
6757
Genome
hg19
Position
chrX:52,725,946-52,736,211
Genome
hg38
Position
chrX:52,696,896-52,707,161
MIM
300192 OMIM
HGNC
HGNC:11336 HGNC
Ensembl
ENSG00000241476 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
Ranking
ClinVar
0
0
0
0
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CT5.2
SYNONYM CT5.2A
SYNONYM HD21
SYNONYM HOM-MEL-40
SYNONYM SSX
MIM 300192 OMIM
HGNC HGNC:11336 HGNC
Ensembl ENSG00000241476 Ensembl
AllianceGenome HGNC:11336
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000336777.9 hg38 chrX 52,696,896 52,707,161 10,266
ENST00000337502.6 hg38 chrX 52,696,896 52,707,178 10,283
ENST00000336777.9 hg19 chrX 52,725,946 52,736,211 10,266
ENST00000337502.6 hg19 chrX 52,725,946 52,736,228 10,283
KeyValue
strand+
UniProtOG
start52,725,945
Gene SymbolSSX2
Entrez GeneId6,757
Chr BandXp11.23-p11.22
end52,790,616
chrchrX
Namesynovial sarcoma, X breakpoint 2
Genome browser