Entrez Gene ID | 6749 |
---|---|
Official Gene Symbol | SSRP1 (GeneCards) |
Full name | structure specific recognition protein 1 |
Location | 11q12.1 |
Other ids | Vega : OTTHUMG00000167024 MIM : 604328 HGNC : HGNC:11327 Ensembl : ENSG00000149136 |
Other names | FACT, T160, FACT80 |
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] |
Found 4 variants in this database.
Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
---|---|---|---|---|---|---|---|
1544 | 6749 | SSRP1 | 11 | 57102018 | 57102018 | Autism Spectrum Disorders | NextSeq500 v2 |
29170 | 6749 | SSRP1 | 11 | 57099680 | 57099680 | Autism Spectrum Disorders | NextSeq500 v2 PASM |
29614 | 6749 | SSRP1 | 11 | 57099680 | 57099680 | Autism Spectrum Disorders | NextSeq500 v2 PASM MiSeq |
29845 | 6749 | SSRP1 | 11 | 57102018 | 57102018 | Autism Spectrum Disorders | NextSeq500 v2 PASM MiSeq NextSeq500 |