Homo sapiens (human): 6663 Help Entry 6663              CDS       T01001                                  Symbol SOX10, DOM, PCWH, SOX-10, WS2E, WS4, WS4C Name (RefSeq) transcription factor SOX-10   KO K09270   transcription factor SOX7/8/10/18 (SOX group E/F) Organism hsa  Homo sapiens (human) Disease H00759   Waardenburg syndrome H02356   PCWH syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03000 Transcription factors [BR:hsa03000]     6663 (SOX10) Transcription factors [BR:hsa03000]  Eukaryotic type   beta-Scaffold factors with minor groove contacts    HMG SOX     6663 (SOX10) SSDB OrthologParalogGFIT Motif Pfam:  Sox_N HMG_box HMG_box_2 HMG_WDHD1 Motif Other DBs NCBI-GeneID:  6663 NCBI-ProteinID:  NP_008872 OMIM:  602229 HGNC:  11190 Ensembl:  ENSP00000380093.2 UniProt:  P56693 LinkDB All DBs Position 22:complement(37972312..37984555) Genome browser AA seq 466 aa AA seqDB search MAEEQDLSEVELSPVGSEEPRCLSPGSAPSLGPDGGGGGSGLRASPGPGELGKVKKEQQD GEADDDKFPVCIREAVSQVLSGYDWTLVPMPVRVNGASKSKPHVKRPMNAFMVWAQAARR KLADQYPHLHNAELSKTLGKLWRLLNESDKRPFIEEAERLRMQHKKDHPDYKYQPRRRKN GKAAQGEAECPGGEAEQGGTAAIQAHYKSAHLDHRHPGEGSPMSDGNPEHPSGQSHGPPT PPTTPKTELQSGKADPKRDGRSMGEGGKPHIDFGNVDIGEISHEVMSNMETFDVAELDQY LPPNGHPGHVSSYSAAGYGLGSALAVASGHSAWISKPPGVALPTVSPPGVDAKAQVKTET AGPQGPPHYTDQPSTSQIAYTSLSLPHYGSAFPSISRPQFDYSDHQPSGPYYGHSGQASG LYSAFSYMGPSQRPLYTAISDPSPSGPQSHSPTHWEQPVYTTLSRP NT seq 1401 nt NT seq  +upstreamnt  +downstreamnt atggcggaggagcaggacctatcggaggtggagctgagccccgtgggctcggaggagccc cgctgcctgtccccggggagcgcgccctcgctagggcccgacggcggcggcggcggatcg ggcctgcgagccagcccggggccaggcgagctgggcaaggtcaagaaggagcagcaggac ggcgaggcggacgatgacaagttccccgtgtgcatccgcgaggccgtcagccaggtgctc agcggctacgactggacgctggtgcccatgcccgtgcgcgtcaacggcgccagcaaaagc aagccgcacgtcaagcggcccatgaacgccttcatggtgtgggctcaggcagcgcgcagg aagctcgcggaccagtacccgcacctgcacaacgctgagctcagcaagacgctgggcaag ctctggaggctgctgaacgaaagtgacaagcgccccttcatcgaggaggctgagcggctc cgtatgcagcacaagaaagaccacccggactacaagtaccagcccaggcggcggaagaac gggaaggccgcccagggcgaggcggagtgccccggtggggaggccgagcaaggtgggacc gccgccatccaggcccactacaagagcgcccacttggaccaccggcacccaggagagggc tcccccatgtcagatgggaaccccgagcacccctcaggccagagccatggcccacccacc cctccaaccaccccgaagacagagctgcagtcgggcaaggcagacccgaagcgggacggg cgctccatgggggagggcgggaagcctcacatcgacttcggcaacgtggacattggtgag atcagccacgaggtaatgtccaacatggagacctttgatgtggctgagttggaccagtac ctgccgcccaatgggcacccaggccatgtgagcagctactcagcagccggctatgggctg ggcagtgccctggccgtggccagtggacactccgcctggatctccaagccaccaggcgtg gctctgcccacggtctcaccacctggtgtggatgccaaagcccaggtgaagacagagacc gcggggccccaggggcccccacactacaccgaccagccatccacctcacagatcgcctac acctccctcagcctgccccactatggctcagccttcccctccatctcccgcccccagttt gactactctgaccatcagccctcaggaccctattatggccactcgggccaggcctctggc ctctactcggccttctcctatatggggccctcgcagcggcccctctacacggccatctct gaccccagcccctcagggccccagtcccacagccccacacactgggagcagccagtatat acgacactgtcccggccctaa

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