Homo sapiens (human): 258 Help Entry 258               CDS       T01001                                  Symbol AMBN, AI1F Name (RefSeq) ameloblastin   KO K23442   ameloblastin Organism hsa  Homo sapiens (human) Disease H00615   Amelogenesis imperfecta Brite KEGG Orthology (KO) [BR:hsa00001]  09190 Not Included in Pathway or Brite   09193 Unclassified: signaling and cellular processes    99992 Structural proteins     258 (AMBN) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Amelin Motif Other DBs NCBI-GeneID:  258 NCBI-ProteinID:  NP_057603 OMIM:  601259 HGNC:  452 Ensembl:  ENSG00000178522 UniProt:  Q9NP70 Q546D7 LinkDB All DBs Position 4:70592256..70607288 Genome browser AA seq 447 aa AA seqDB search MSASKIPLFKMKDLILILCLLEMSFAVPFFPQQSGTPGMASLSLETMRQLGSLQRLNTLS QYSRYGFGKSFNSLWMHGLLPPHSSLPWMRPREHETQQYEYSLPVHPPPLPSQPSLKPQQ PGLKPFLQSAAATTNQATALKEALQPPIHLGHLPLQEGELPLVQQQVAPSDKPPKPELPG VDFADPQGPSLPGMDFPDPQGPSLPGLDFADPQGSTIFQIARLISHGPMPQNKQSPLYPG MLYVPFGANQLNAPARLGIMSSEEVAGGREDPMAYGAMFPGFGGMRPGFEGMPHNPAMGG DFTLEFDSPVAATKGPENEEGGAQGSPMPEANPDNLENPAFLTELEPAPHAGLLALPKDD IPGLPRSPSGKMKGLPSVTPAAADPLMTPELADVYRTYDADMTTSVDFQEEATMDTTMAP NSLQTSMPGNKAQEPEMMHDAWHFQEP NT seq 1344 nt NT seq  +upstreamnt  +downstreamnt atgtcagcatctaagattccacttttcaaaatgaaggacctgatactgatcctatgcctc ctggaaatgagttttgcagtgccgttctttcctcagcaatctggaacaccgggtatggct agtttgagccttgagacaatgagacagttgggaagtctgcagagattaaacacactttct cagtattctagatacggctttggaaaatcatttaattctttgtggatgcacggtctcctc ccaccacattcctctcttccatggatgaggccaagagaacatgaaactcaacagtatgaa tattctttgcctgtgcatcccccacctctcccatcacagccatccttgaagcctcaacag ccaggactgaaaccttttctccagtctgctgctgcaaccaccaaccaggccacagcactg aaagaagcacttcagcctccaattcacctgggacatctgcccttgcaggaaggagaactg cctctggttcagcagcaggtggcaccatcagataagccaccaaagcctgagctcccagga gtagattttgctgatccacaaggtccatcactcccaggaatggattttcctgatccacaa ggtccatcactcccaggattggattttgctgatccacaaggttcaacaattttccaaata gcccgtttgatttctcacggaccaatgccacaaaataaacaatctccactttatccagga atgttgtacgtgccttttggagcaaatcaattgaatgcccctgccagacttggcatcatg agttcagaagaagtggcaggcgggagagaagacccaatggcctatggagccatgtttcca ggatttggaggcatgaggcccggctttgagggaatgccccacaacccagctatgggcggt gacttcactctggaatttgactccccagtggctgccaccaaaggccctgagaacgaagaa ggaggtgcacaaggctcccctatgccggaggccaacccagacaatctagaaaacccagct ttccttacagagctagaacctgctccccacgcagggctccttgctctccctaaggatgac attcccggcctgccaaggagcccttcagggaagatgaagggactccccagcgtcacccca gcagctgctgacccactgatgacccctgaattagctgatgtttataggacctacgatgct gacatgaccacatccgtggatttccaggaagaagcaaccatggataccacgatggcccca aactctctgcaaacatccatgccaggaaacaaagcccaggagcccgagatgatgcatgac gcatggcatttccaagagccctga

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