Homo sapiens (human): 4091 Help Entry 4091              CDS       T01001                                  Symbol SMAD6, AOVD2, HsT17432, MADH6, MADH7 Name (RefSeq) SMAD family member 6   KO K04677   mothers against decapentaplegic homolog 6 Organism hsa  Homo sapiens (human) Pathway hsa04350   TGF-beta signaling pathway Disease H00554   Aortic valve disease H02160   Craniosynostoses Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04350 TGF-beta signaling pathway     4091 (SMAD6) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  MH2 MH1 Motif Other DBs NCBI-GeneID:  4091 NCBI-ProteinID:  NP_005576 OMIM:  602931 HGNC:  6772 Ensembl:  ENSG00000137834 UniProt:  O43541 LinkDB All DBs Position 15:66702236..66782849 Genome browser AA seq 496 aa AA seqDB search MFRSKRSGLVRRLWRSRVVPDREEGGSGGGGGGDEDGSLGSRAEPAPRAREGGGCGRSEV RPVAPRRPRDAVGQRGAQGAGRRRRAGGPPRPMSEPGAGAGSSLLDVAEPGGPGWLPESD CETVTCCLFSERDAAGAPRDASDPLAGAALEPAGGGRSREARSRLLLLEQELKTVTYSLL KRLKERSLDTLLEAVESRGGVPGGCVLVPRADLRLGGQPAPPQLLLGRLFRWPDLQHAVE LKPLCGCHSFAAAADGPTVCCNPYHFSRLCGPESPPPPYSRLSPRDEYKPLDLSDSTLSY TETEATNSLITAPGEFSDASMSPDATKPSHWCSVAYWEHRTRVGRLYAVYDQAVSIFYDL PQGSGFCLGQLNLEQRSESVRRTRSKIGFGILLSKEPDGVWAYNRGEHPIFVNSPTLDAP GGRALVVRKVPPGYSIKVFDFERSGLQHAPEPDAADGPYDPNSVRISFAKGWGPCYSRQF ITSCPCWLEILLNNPR NT seq 1491 nt NT seq  +upstreamnt  +downstreamnt atgttcaggtccaaacgctcggggctggtgcggcgactttggcgaagtcgtgtggtcccc gaccgggaggaaggcggcagcggcggcggcggtggcggcgacgaggatgggagcttgggc agccgagctgagccggccccgcgggcaagagagggcggaggctgcggccgctccgaagtc cgcccggtagccccgcggcggccccgggacgcagtgggacagcgaggcgcccagggcgcg gggaggcgccggcgcgcagggggccccccgaggcccatgtcggagccaggggccggcgct gggagctccctgctggacgtggcggagccgggaggcccgggctggctgcccgagagtgac tgcgagacggtgacctgctgtctcttttcggagcgggacgccgccggcgcgccccgggac gccagcgaccccctggccggggcggccctggagccggcgggcggcgggcggagtcgcgaa gcgcgctcgcggctgctgctgctggagcaggaactcaaaaccgtcacgtactcgctgctg aagcggctcaaggagcgctcgctggacacgctgctggaggcggtggagtcccgcggcggc gtgccgggcggctgcgtgctggtgccgcgcgccgacctccgcctgggcggccagcccgcg ccgccgcagctgctgctcggccgcctctttcgctggcccgacctgcagcacgccgtggag ctgaagcccctgtgcggctgccacagcttcgccgccgccgccgacggccctaccgtgtgc tgcaacccctaccacttcagccggctctgcgggcccgaatctccgccacctccctactct cggctgtctcctcgcgacgagtacaagccactggatctgtccgattccacattgtcttac actgaaacggaggctaccaactccctcatcactgctccgggtgaattctcagacgccagc atgtctccggacgccaccaagccgagccactggtgcagcgtggcgtactgggagcaccgg acgcgcgtgggccgcctctatgcggtgtacgaccaggccgtcagcatcttctacgaccta cctcagggcagcggcttctgcctgggccagctcaacctggagcagcgcagcgagtcggtg cggcgaacgcgcagcaagatcggcttcggcatcctgctcagcaaggagcccgacggcgtg tgggcctacaaccgcggcgagcaccccatcttcgtcaactccccgacgctggacgcgccc ggcggccgcgccctggtcgtgcgcaaggtgccccccggctactccatcaaggtgttcgac ttcgagcgctcgggcctgcagcacgcgcccgagcccgacgccgccgacggcccctacgac cccaacagcgtccgcatcagcttcgccaagggctgggggccctgctactcccggcagttc atcacctcctgcccctgctggctggagatcctcctcaacaaccccagatag

Homo sapiens (human): 4092 Help Entry 4092              CDS       T01001                                  Symbol SMAD7, CRCS3, MADH7, MADH8 Name (RefSeq) SMAD family member 7   KO K19631   mothers against decapentaplegic homolog 7 Organism hsa  Homo sapiens (human) Pathway hsa04350   TGF-beta signaling pathway hsa04390   Hippo signaling pathway Disease H00020   Colorectal cancer Drug target Mongersen (DG02694):  D10955 D10956 Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04350 TGF-beta signaling pathway     4092 (SMAD7)    04390 Hippo signaling pathway     4092 (SMAD7) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  MH2 MH1 Motif Other DBs NCBI-GeneID:  4092 NCBI-ProteinID:  NP_005895 OMIM:  602932 HGNC:  6773 Ensembl:  ENSG00000101665 UniProt:  O15105 Structure PDB LinkDB All DBs Position 18:complement(48919853..48950965) Genome browser AA seq 426 aa AA seqDB search MFRTKRSALVRRLWRSRAPGGEDEEEGAGGGGGGGELRGEGATDSRAHGAGGGGPGRAGC CLGKAVRGAKGHHHPHPPAAGAGAAGGAEADLKALTHSVLKKLKERQLELLLQAVESRGG TRTACLLLPGRLDCRLGPGAPAGAQPAQPPSSYSLPLLLCKVFRWPDLRHSSEVKRLCCC ESYGKINPELVCCNPHHLSRLCELESPPPPYSRYPMDFLKPTADCPDAVPSSAETGGTNY LAPGGLSDSQLLLEPGDRSHWCVVAYWEEKTRVGRLYCVQEPSLDIFYDLPQGNGFCLGQ LNSDNKSQLVQKVRSKIGCGIQLTREVDGVWVYNRSSYPIFIKSATLDNPDSRTLLVHKV FPGFSIKAFDYEKAYSLQRPNDHEFMQQPWTGFTVQISFVKGWGQCYTRQFISSCPCWLE VIFNSR NT seq 1281 nt NT seq  +upstreamnt  +downstreamnt atgttcaggaccaaacgatctgcgctcgtccggcgtctctggaggagccgtgcgcccggc ggcgaggacgaggaggagggcgcagggggaggtggaggaggaggcgagctgcggggagaa ggggcgacggacagccgagcgcatggggccggtggcggcggcccgggcagggctggatgc tgcctgggcaaggcggtgcgaggtgccaaaggtcaccaccatccccacccgccagccgcg ggcgccggcgcggccgggggcgccgaggcggatctgaaggcgctcacgcactcggtgctc aagaaactgaaggagcggcagctggagctgctgctccaggccgtggagtcccgcggcggg acgcgcaccgcgtgcctcctgctgcccggccgcctggactgcaggctgggcccgggggcg cccgccggcgcgcagcctgcgcagccgccctcgtcctactcgctccccctcctgctgtgc aaagtgttcaggtggccggatctcaggcattcctcggaagtcaagaggctgtgttgctgt gaatcttacgggaagatcaaccccgagctggtgtgctgcaacccccatcaccttagccga ctctgcgaactagagtctcccccccctccttactccagatacccgatggattttctcaaa ccaactgcagactgtccagatgctgtgccttcctccgctgaaacagggggaacgaattat ctggcccctggggggctttcagattcccaacttcttctggagcctggggatcggtcacac tggtgcgtggtggcatactgggaggagaagacgagagtggggaggctctactgtgtccag gagccctctctggatatcttctatgatctacctcaggggaatggcttttgcctcggacag ctcaattcggacaacaagagtcagctggtgcagaaggtgcggagcaaaatcggctgcggc atccagctgacgcgggaggtggatggtgtgtgggtgtacaaccgcagcagttaccccatc ttcatcaagtccgccacactggacaacccggactccaggacgctgttggtacacaaggtg ttccccggtttctccatcaaggctttcgactacgagaaggcgtacagcctgcagcggccc aatgaccacgagtttatgcagcagccgtggacgggctttaccgtgcagatcagctttgtg aagggctggggccagtgctacacccgccagttcatcagcagctgcccgtgctggctagag gtcatcttcaacagccggtag

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