Homo sapiens (human): 401138 Help Entry 401138            CDS       T01001                                  Symbol AMTN, AI3B, UNQ689 Name (RefSeq) amelotin isoform 1 precursor   KO K25225   amelotin 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     401138 (AMTN) SSDB OrthologParalogGFIT Motif Pfam:  Amelotin Motif Other DBs NCBI-GeneID:  401138 NCBI-ProteinID:  NP_997722 OMIM:  610912 HGNC:  33188 Ensembl:  ENSP00000341013.4 UniProt:  Q6UX39 F1T0L8 LinkDB All DBs Position 4:70518569..70532743 Genome browser AA seq 209 aa AA seqDB search MRSTILLFCLLGSTRSLPQLKPALGLPPTKLAPDQGTLPNQQQSNQVFPSLSLIPLTQML TLGPDLHLLNPAAGMTPGTQTHPLTLGGLNVQQQLHPHVLPIFVTQLGAQGTILSSEELP QIFTSLIIHSLFPGGILPTSQAGANPDVQDGSLPAGGAGVNPATQGTPAGRLPTPSGTDD DFAVTTPAGIQRSTHAIEEATTESANGIQ NT seq 630 nt NT seq  +upstreamnt  +downstreamnt atgaggagtacgattctactgttttgtcttctaggatcaactcggtcattaccacagctc aaacctgctttgggactccctcccacaaaactggctccggatcagggaacactaccaaac caacagcagtcaaatcaggtctttccttctttaagtctgataccattaacacagatgctc acactggggccagatctgcatctgttaaatcctgctgcaggaatgacacctggtacccag acccacccattgaccctgggagggttgaatgtacaacagcaactgcacccacatgtgtta ccaatttttgtcacacaacttggagcccagggcactatcctaagctcagaggaattgcca caaatcttcacgagcctcatcatccattccttgttcccgggaggcatcctgcccaccagt caggcaggggctaatccagatgtccaggatggaagccttccagcaggaggagcaggtgta aatcctgccacccagggaaccccagcaggccgcctcccaactcccagtggcacagatgac gactttgcagtgaccacccctgcaggcatccaaaggagcacacatgccatcgaggaagcc accacagaatcagcaaatggaattcagtaa

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