Ensembl ID ENSG00000149136 Gene ID 6749 Accession 11327
Gene Symbol SSRP1 Alias FACT;T160;FACT80 Full Name structure specific recognition protein 1
Position 11 : 57325988 - 57335892 Length 9905 bases Strand Minus strand
Status Confidence Main interacting RNAsN.A.RBP type Non-canonical_RBPs
Summary The protein encoded by this gene is a subunit of a heterodimer that, along with SUPT16H, forms chromatin transcriptional elongation factor FACT. FACT interacts specifically with histones H2A/H2B to effect nucleosome disassembly and transcription elongation. FACT and cisplatin-damaged DNA may be crucial to the anticancer mechanism of cisplatin. This encoded protein contains a high mobility group box which most likely constitutes the structure recognition element for cisplatin-modified DNA. This protein also functions as a co-activator of the transcriptional activator p63. An alternatively spliced transcript variant of this gene has been described, but its full-length nature is not known. [provided by RefSeq, Jul 2008]

ENSG00000149136 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000149136 0.44 1.19e-11 HNSC
ENSG00000149136 0.42 1.13e-13 BRCA
ENSG00000149136 0.56 6.32e-15 COAD
ENSG00000149136 0.95 1.85e-44 LUSC
ENSG00000149136 0.56 1.22e-15 LUAD
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000149136 cancer 17954908
ENSG00000149136 cancer 19372586
ENSG00000149136 tumor 21998152
ENSG00000149136 tumor 24870930
ENSG00000149136 tumor 25402820
ENSG00000149136 tumor 26354769
ENSG00000149136 breast cancer 26755331
ENSG00000149136 Cancer 28416484
ENSG00000149136 cancer 28496363
ENSG00000149136 tumor 29048646
ENSG00000149136 colorectal cancer 30616889
ENSG00000149136 colorectal cancer 30762286
ENSG00000149136 GBM 31358880
ENSG00000149136 colorectal cancer 31839745
ENSG00000149136 tumor 31949834
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000149136 MESO 0.00063 high
ENSG00000149136 CHOL 0.026 low
ENSG00000149136 UVM 0.032 low
ENSG00000149136 PAAD 0.00011 high
ENSG00000149136 LGG 0.0077 low
ENSG00000149136 HNSC 0.034 high
ENSG00000149136 KICH 0.016 high
ENSG00000149136 LUAD 0.006 high
ENSG00000149136 THYM 0.012 low
ENSG00000149136 UCS 0.028 low
ENSG00000149136 OV 0.022 low
ENSG00000149136 DLBC 0.0057 low
ENSG00000149136 KIRC 0.024 low
ENSG00000149136 BLCA 0.012 high
ENSG00000149136 LAML 0.0038 high
ENSG00000149136 SKCM 0.043 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000149136 HNSC Amp 0.614470 0.112902 0.398834 0.222222
ENSG00000149136 BRCA Del 1.144655 0.067666 0.432774 0.209259