Homo sapiens (human): 23186 Help Entry 23186             CDS       T01001                                  Symbol RCOR1, COREST, RCOR Name (RefSeq) REST corepressor 1   KO K11829   REST corepressor 1 Organism hsa  Homo sapiens (human) Pathway hsa05016   Huntington disease Network nt06440  Transcription nt06461  Huntington disease   Element N00980   Mutation-caused aberrant Htt to REST-mediated transcriptional repression Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09164 Neurodegenerative disease    05016 Huntington disease     23186 (RCOR1)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03036 Chromosome and associated proteins [BR:hsa03036]     23186 (RCOR1) Chromosome and associated proteins [BR:hsa03036]  Eukaryotic type   Histone modification proteins    HDAC complexes     BRAF-HDAC complex      23186 (RCOR1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Myb_DNA-binding ELM2 Myb_DNA-bind_7 Myb_DNA-bind_6 Motif Other DBs NCBI-GeneID:  23186 NCBI-ProteinID:  NP_055971 OMIM:  607675 HGNC:  17441 Ensembl:  ENSG00000089902 Pharos:  Q9UKL0(Tbio) UniProt:  Q9UKL0 Structure PDB LinkDB All DBs Position 14:102592649..102730561 Genome browser AA seq 485 aa AA seqDB search MPAMVEKGPEVSGKRRGRNNAAASASAAAASAAASAACASPAATAASGAAASSASAAAAS AAAAPNNGQNKSLAAAAPNGNSSSNSWEEGSSGSSSDEEHGGGGMRVGPQYQAVVPDFDP AKLARRSQERDNLGMLVWSPNQNLSEAKLDEYIAIAKEKHGYNMEQALGMLFWHKHNIEK SLADLPNFTPFPDEWTVEDKVLFEQAFSFHGKTFHRIQQMLPDKSIASLVKFYYSWKKTR TKTSVMDRHARKQKREREESEDELEEANGNNPIDIEVDQNKESKKEVPPTETVPQVKKEK HSTQAKNRAKRKPPKGMFLSQEDVEAVSANATAATTVLRQLDMELVSVKRQIQNIKQTNS ALKEKLDGGIEPYRLPEVIQKCNARWTTEEQLLAVQAIRKYGRDFQAISDVIGNKSVVQV KNFFVNYRRRFNIDEVLQEWEAEHGKEETNGPSNQKPVKSPDNSIKMPEEEDEAPVLDVR YASAS NT seq 1458 nt NT seq  +upstreamnt  +downstreamnt atgccggccatggtggagaagggccccgaggtctcagggaagcggagagggaggaacaac gcggccgcctccgcctccgccgccgccgcctccgccgccgcctcggccgcctgcgcctcg ccagccgccactgccgcctcgggcgccgccgcctcctcagcctcggccgccgccgcctca gccgccgccgcccccaataatggccagaataaaagtttggcggcggcggcgcccaatggc aacagcagcagcaactcctgggaggaaggcagctcgggctcgtccagcgacgaggagcac ggtggcggtggcatgagggtcggaccccagtaccaggcggtggtgcccgacttcgacccc gccaaactggcaagacgcagtcaagaacgggacaatcttggcatgttggtctggtcaccc aatcaaaatctgtcagaagcaaagttggatgaatacattgccattgccaaagaaaagcat gggtacaacatggaacaggctcttgggatgctcttctggcataaacataatatcgaaaag tcattggctgatttgcccaactttacccctttcccagatgagtggactgtggaagataaa gtcttatttgagcaagcctttagttttcatgggaaaacttttcatagaatccaacaaatg cttccagataaatctatagcaagtctggtgaaattttactattcttggaagaagacgagg actaaaactagtgtgatggatcgccatgcccggaaacaaaaacgggagcgggaggagagc gaggatgaactggaagaggcaaatggaaacaatcccattgacattgaggttgatcaaaac aaggaaagcaaaaaggaggttccccctactgagacagttcctcaggtcaaaaaagaaaaa catagcacacaagctaaaaatagagcaaaaaggaaacctccaaaaggaatgtttctttct caagaagatgtggaggctgtttctgccaatgccactgctgctaccacggtgctgagacaa ctagacatggaattggtttcagtcaaacgacagatccagaatattaaacagacaaacagt gctctcaaagaaaaacttgatggtggaatagaaccatatcgacttccagaggtcattcag aaatgtaatgcacgttggactacagaagagcagcttctcgccgtacaagccatcaggaaa tatggccgagattttcaggcaatctcagacgtgattgggaacaaatcagtggtacaagtg aaaaacttttttgtaaattatcgacgccgcttcaacatagatgaagttttacaagaatgg gaggcagaacatggtaaagaagagaccaatgggcccagtaaccagaagcctgtgaagtcc ccagataattccattaagatgcccgaagaggaagacgaggctcctgttctggatgtcaga tatgcatctgcctcctga

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