Homo sapiens (human): 6756 Help Entry 6756              CDS       T01001                                  Symbol SSX1, CT5.1, SPGFX5, SSRC Name (RefSeq) protein SSX1   KO K15624   protein SSX Organism hsa  Homo sapiens (human) Pathway hsa05202   Transcriptional misregulation in cancer Network nt06240  Transcription (cancer)   Element N00142   SYT-SSX fusion to transcriptional repression Disease H00050   Synovial sarcoma H01282   Spermatogenic failure Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09161 Cancer: overview    05202 Transcriptional misregulation in cancer     6756 (SSX1) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  SSXRD KRAB Motif Other DBs NCBI-GeneID:  6756 NCBI-ProteinID:  NP_001265620 OMIM:  312820 HGNC:  11335 UniProt:  Q16384 Structure PDBPDBj LinkDB All DBs Position X:48255392..48267444 Genome browser AA seq 188 aa AA seqDB search MNGDDTFAKRPRDDAKASEKRSKAFDDIATYFSKKEWKKMKYSEKISYVYMKRNYKAMTK LGFKVTLPPFMCNKQATDFQGNDFDNDHNRRIQVEHPQMTFGRLHRIIPKIMPKKPAEDE NDSKGVSEASGPQNDGKQLHPPGKANISEKINKRSGPKRGKHAWTHRLRERKQLVIYEEI SDPEEDDE NT seq 567 nt NT seq  +upstreamnt  +downstreamnt atgaacggagacgacacctttgcaaagagacccagggatgatgctaaagcatcagagaag agaagcaaggcctttgatgatattgccacatacttctctaagaaagagtggaaaaagatg aaatactcggagaaaatcagctatgtgtatatgaagagaaactataaggccatgactaaa ctaggtttcaaagtcaccctcccacctttcatgtgtaataaacaggccacagacttccag gggaatgattttgataatgaccataaccgcaggattcaggttgaacatcctcagatgact ttcggcaggctccacagaatcatcccgaagatcatgcccaagaagccagcagaggacgaa aatgattcgaagggagtgtcagaagcatctggcccacaaaacgatgggaaacaactgcac cccccaggaaaagcaaatatttctgagaagattaataagagatctggacccaaaaggggg aaacatgcctggacccacagactgcgtgagagaaagcagctggtgatttatgaagagatc agtgaccctgaggaagatgacgagtaa

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