Homo sapiens (human): 10214 Help Entry 10214             CDS       T01001                                  Symbol SSX3, CT5.3 Name (RefSeq) SSX family member 3   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     10214 (SSX3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SSXRD KRAB RepA_N Motif Other DBs NCBI-GeneID:  10214 NCBI-ProteinID:  NP_066294 OMIM:  300325 HGNC:  11337 Ensembl:  ENSG00000165584 UniProt:  Q99909 LinkDB All DBs Position X:complement(48346427..48356703) Genome browser AA seq 188 aa AA seqDB search MNGDDTFARRPTVGAQIPEKIQKAFDDIAKYFSKEEWEKMKVSEKIVYVYMKRKYEAMTK LGFKAILPSFMRNKRVTDFQGNDFDNDPNRGNQVQRPQMTFGRLQGIFPKIMPKKPAEEG NVSKEVPEASGPQNDGKQLCPPGKPTTSEKINMISGPKRGEHAWTHRLRERKQLVIYEEI SDPEEDDE NT seq 567 nt NT seq  +upstreamnt  +downstreamnt atgaacggagatgacacctttgcaaggagacccacggttggtgctcaaataccagagaag atacaaaaggccttcgatgatattgccaaatacttctctaaggaagagtgggaaaagatg aaagtctcggagaaaatcgtctatgtgtatatgaagagaaagtatgaggccatgactaaa ctaggtttcaaggccatcctcccatctttcatgcgtaataaacgggtcacagacttccag gggaatgattttgataatgaccctaaccgtgggaatcaggttcaacgtcctcagatgact ttcggcaggctccagggaatcttcccgaagatcatgcccaagaagccagcagaggaagga aatgtttcgaaggaagtgccagaagcatctggcccacaaaacgatgggaaacagctgtgc cccccgggaaaaccaactacctctgagaagattaacatgatatctggacccaaaaggggg gaacatgcctggacccacagactgcgtgagagaaagcagctggtgatttatgaagagatc agcgatcctgaggaagatgatgagtaa

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