Homo sapiens (human): 265 Help Entry 265               CDS       T01001                                  Symbol AMELX, AI1E, AIH1, ALGN, AMG, AMGL, AMGX Name (RefSeq) amelogenin X-linked   KO K23443   amelogenin 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     265 (AMELX) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Amelogenin Motif Other DBs NCBI-GeneID:  265 NCBI-ProteinID:  NP_001133 OMIM:  300391 HGNC:  461 Ensembl:  ENSG00000125363 UniProt:  Q99217 LinkDB All DBs Position X:11293413..11309588 Genome browser AA seq 191 aa AA seqDB search MGTWILFACLLGAAFAMPLPPHPGHPGYINFSYEVLTPLKWYQSIRPPYPSYGYEPMGGW LHHQIIPVLSQQHPPTHTLQPHHHIPVVPAQQPVIPQQPMMPVPGQHSMTPIQHHQPNLP PPAQQPYQPQPVQPQPHQPMQPQPPVHPMQPLPPQPPLPPMFPMQPLPPMLPDLTLEAWP STDKTKREEVD NT seq 576 nt NT seq  +upstreamnt  +downstreamnt atggggacctggattttatttgcctgcctcctgggagcagcttttgccatgcctctacca cctcatcctgggcaccctggttatatcaacttcagctatgaggtgcttacccctttgaag tggtaccagagcataaggccaccgtacccttcctatggttacgagcccatgggtggatgg ctgcaccaccaaatcatccccgtgctgtcccaacagcaccccccgactcacaccctgcag cctcatcaccacatcccagtggtgccagctcagcagcccgtgatcccccagcaaccaatg atgcccgttcctggccaacactccatgactccaatccaacaccaccagccaaacctccct ccgcccgcccagcagccctaccagccccagcctgttcagccacagcctcaccagcccatg cagccccagccacctgtgcaccccatgcagcccctgccgccacagccacctctgcctccg atgttccccatgcagcccctgcctcccatgcttcctgatctgactctggaagcttggcca tcaacagacaagaccaagcgggaggaagtggattaa

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