Homo sapiens (human): 280658 Help Entry 280658            CDS       T01001                                  Symbol SSX7 Name (RefSeq) SSX family member 7   KO K15624   protein SSX Organism hsa  Homo sapiens (human) Pathway hsa05202   Transcriptional misregulation in cancer Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09161 Cancer: overview    05202 Transcriptional misregulation in cancer     280658 (SSX7) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SSXRD KRAB Motif Other DBs NCBI-GeneID:  280658 NCBI-ProteinID:  NP_775494 OMIM:  300542 HGNC:  19653 Ensembl:  ENSG00000187754 UniProt:  Q7RTT5 LinkDB All DBs Position X:complement(52644061..52654900) Genome browser AA seq 188 aa AA seqDB search MNGDDAFARRPRAGAQIPEKIQKSFDDIAKYFSKKEWEKMKSLEKISYVYMKRKYEAMTK LGFKATLPPFMHNTGATDLQGNDFDNDRNQGNQVERPQMTFCRLQRIFPKIMPKKPAEEG NDSKGVPEASGSQNDGKHLCPPGKPSTSEKINKTSGPKRGKHAWTHRLRERKQLVIYEEI SDPEEDDE NT seq 567 nt NT seq  +upstreamnt  +downstreamnt atgaacggagacgacgcctttgcaaggagacctagggctggtgctcaaataccagagaag atccaaaagtccttcgatgatattgccaaatacttctctaagaaagagtgggaaaagatg aaatccttggagaaaatcagctatgtgtatatgaagagaaagtatgaggccatgactaaa ctaggcttcaaggccaccctcccacctttcatgcataatacaggggccacagacctccag gggaatgattttgataatgaccgtaaccaagggaatcaggttgaacgtcctcagatgact ttttgcaggctccagagaatcttcccgaagatcatgcccaagaagccagcagaggaagga aatgattcgaagggagtgccagaagcatctggctcacagaacgatgggaaacacctgtgc cctccaggaaaaccaagtacctctgagaagattaacaagacatccggacccaaaaggggg aaacatgcctggacccacagactgcgtgagagaaagcagctggtgatttatgaagagatc agcgaccctgaagaagacgacgagtaa

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