Homo sapiens (human): 56203 Help Entry 56203             CDS       T01001                                  Symbol LMOD3, NEM10 Name (RefSeq) leiomodin 3   KO K22030   leiomodin Organism hsa  Homo sapiens (human) Pathway hsa04820   Cytoskeleton in muscle cells Network nt06539  Cytoskeleton in muscle cells   Element N01819   Actin thin filament, length regulation Disease H00698   Nemaline myopathy Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09142 Cell motility    04820 Cytoskeleton in muscle cells     56203 (LMOD3)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     56203 (LMOD3) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actin-binding proteins     Others      56203 (LMOD3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Tropomodulin LRR_6 Motif Other DBs NCBI-GeneID:  56203 NCBI-ProteinID:  NP_001291347 OMIM:  616112 HGNC:  6649 Ensembl:  ENSG00000163380 UniProt:  Q0VAK6 LinkDB All DBs Position 3:complement(69106065..69122595) Genome browser AA seq 560 aa AA seqDB search MSEHSRNSDQEELLDEEINEDEILANLSAEELKELQSEMEVMAPDPSLPVGMIQKDQTDK PPTGNFNHKSLVDYMYWEKASRRMLEEERVPVTFVKSEEKTQEEHEEIEKRNKNMAQYLK EKLNNEIVANKRESKGSSNIQETDEEDEEEEDDDDDDEGEDDGEESEETNREEEGKAKEQ IRNCENNCQQVTDKAFKEQRDRPEAQEQSEKKISKLDPKKLALDTSFLKVSTRPSGNQTD LDGSLRRVRKNDPDMKELNLNNIENIPKEMLLDFVNAMKKNKHIKTFSLANVGADENVAF ALANMLRENRSITTLNIESNFITGKGIVAIMRCLQFNETLTELRFHNQRHMLGHHAEMEI ARLLKANNTLLKMGYHFELPGPRMVVTNLLTRNQDKQRQKRQEEQKQQQLKEQKKLIAML ENGLGLPPGMWELLGGPKPDSRMQEFFQPPPPRPPNPQNVPFSQRSEMMKKPSQAPKYRT DPDSFRVVKLKRIQRKSRMPEAREPPEKTNLKDVIKTLKPVPRNRPPPLVEITPRDQLLN DIRHSSVAYLKPVQLPKELA NT seq 1683 nt NT seq  +upstreamnt  +downstreamnt atgtcagagcacagcagaaattcagatcaagaagaacttctcgatgaggagattaatgaa gatgaaatcttggccaacttgtctgctgaagaactgaaagaactgcagtcggaaatggaa gtcatggcccctgaccccagccttcccgtgggaatgattcagaaagatcaaactgacaag ccaccgacaggaaacttcaatcataaatctcttgttgattatatgtattgggaaaaggca tccaggcgcatgctggaagaggaacgagttcctgtcacctttgtgaaatccgaggaaaag actcaagaagagcatgaagaaatagaaaaacgtaataaaaatatggcccagtatttaaaa gaaaagctcaataatgaaatagttgcaaataaaagagaatcaaagggcagcagcaatatc caagaaacagatgaagaagatgaagaagaagaagatgatgatgatgacgacgaaggagaa gatgatggtgaagagagtgaagaaacgaacagagaagaggaaggcaaagcaaaggaacaa attagaaattgtgagaacaactgccagcaggtaactgacaaagcattcaaagaacagaga gacagaccagaggcccaagaacaaagtgagaaaaaaatatcgaaattagatcctaagaag ttagctctagacaccagctttttgaaggtaagtacaaggccttcaggaaaccagacagac ctggatgggagcttgaggagagttaggaaaaatgatcctgacatgaaggaactcaacctg aacaacattgaaaacatccccaaagaaatgttactggactttgtcaatgcaatgaagaaa aacaagcacatcaaaacattcagtttagccaatgtgggtgcagatgagaatgtagcattt gccttggctaacatgttgcgtgaaaatagaagcatcaccactctcaacatcgagtccaat ttcatcacaggtaaagggattgtggccatcatgaggtgtctccagtttaatgagacgcta actgagcttcggtttcacaatcagaggcacatgttgggtcaccatgctgaaatggaaata gccaggcttttgaaggcaaacaacactctcctgaagatgggctaccattttgagcttccg ggtcccagaatggtggtcactaatctgctcaccaggaatcaggataaacaaaggcagaaa cgacaggaagagcaaaaacagcagcaactcaaggaacagaagaagctgatagccatgtta gagaatgggttggggctgccccctgggatgtgggagctgttgggaggacccaagccagat tccagaatgcaggaattcttccagccaccgccacctcggcctcccaacccccaaaatgtc ccctttagtcaacgcagtgaaatgatgaaaaagccatcgcaggccccgaagtacaggaca gaccctgactccttccgggtggtgaagctgaagagaatccagcgcaaatctcggatgccg gaagccagagaaccacccgagaaaaccaacctcaaagatgtcatcaaaacgctcaagcca gtgccgagaaacaggccacccccattggtggaaatcactcccagagatcagctgctaaac gacattcgtcacagcagtgtcgcctatcttaaacctgtgcaactgccaaaagaactggcg taa

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