Homo sapiens (human): 7111 Help Entry 7111              CDS       T01001                                  Symbol TMOD1, D9S57E, ETMOD, TMOD Name (RefSeq) tropomodulin 1   KO K10370   tropomodulin Organism hsa  Homo sapiens (human) Pathway hsa04820   Cytoskeleton in muscle cells Network nt06539  Cytoskeleton in muscle cells   Element N01819   Actin thin filament, length regulation Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09142 Cell motility    04820 Cytoskeleton in muscle cells     7111 (TMOD1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     7111 (TMOD1) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actin-binding proteins     Capping proteins      7111 (TMOD1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Tropomodulin Motif Other DBs NCBI-GeneID:  7111 NCBI-ProteinID:  NP_001159588 OMIM:  190930 HGNC:  11871 Ensembl:  ENSG00000136842 UniProt:  P28289 Structure PDB LinkDB All DBs Position 9:97501180..97601743 Genome browser AA seq 359 aa AA seqDB search MSYRRELEKYRDLDEDEILGALTEEELRTLENELDELDPDNALLPAGLRQKDQTTKAPTG PFKREELLDHLEKQAKEFKDREDLVPYTGEKRGKVWVPKQKPLDPVLESVTLEPELEEAL ANASDAELCDIAAILGMHTLMSNQQYYQALSSSSIMNKEGLNSVIKPTQYKPVPDEEPNS TDVEETLERIKNNDPKLEEVNLNNIRNIPIPTLKAYAEALKENSYVKKFSIVGTRSNDPV AYALAEMLKENKVLKTLNVESNFISGAGILRLVEALPYNTSLVEMKIDNQSQPLGNKVEM EIVSMLEKNATLLKFGYHFTQQGPRLRASNAMMNNNDLVRKRRLADLTGPIIPKCRSGV NT seq 1080 nt NT seq  +upstreamnt  +downstreamnt atgtcgtacagacgagaactagagaaataccgtgacctggatgaagatgaaatccttgga gccctaacagaggaagagctgaggaccctggaaaatgagctggatgagctggaccctgat aatgcactgctgcctgcaggcctgaggcagaaggatcagaccaccaaggcgcccacgggc ccctttaaaagagaggagctcttggatcacttggaaaagcaagcaaaggagtttaaggac cgagaagatctggtcccctacacaggggaaaaacgaggaaaggtctgggttcctaagcag aagccactggatcctgtgctggaaagtgtgacgctggaaccggagctggaggaagccttg gcaaatgcttcagatgcagaactctgtgacattgcagcgatcctgggcatgcacacgctc atgagtaaccagcagtactaccaggccctgagcagcagctccatcatgaacaaggagggg ctcaacagcgtgattaaacccacacaatacaagcctgtgcccgacgaagaaccaaattca acagacgtagaggaaacgctggaacggataaagaacaacgacccaaaacttgaagaagtt aacctcaataatatccggaatatccccatccccaccctcaaggcatatgcagaagccctg aaagaaaactcatatgtgaagaagttcagcatcgtggggacacggagtaatgaccccgtg gcgtatgcccttgctgagatgctcaaggagaacaaggtgttgaagacactgaatgtggaa tccaacttcatttctggagctgggattctgcgcctggtagaagccctcccatacaacact tctctggtggaaatgaaaattgacaaccagagccagcccctgggcaacaaagtggaaatg gagattgtgagcatgttggaaaaaaacgcaacacttctcaaattcggctaccactttacc cagcaaggaccccggcttcgggcatccaacgcaatgatgaacaacaatgaccttgtgagg aagaggaggcttgcggacctgactgggcccatcattcccaagtgccggagtggtgtctag

Homo sapiens (human): 29767 Help Entry 29767             CDS       T01001                                  Symbol TMOD2, N-TMOD, NTMOD Name (RefSeq) tropomodulin 2   KO K10370   tropomodulin Organism hsa  Homo sapiens (human) Pathway hsa04820   Cytoskeleton in muscle cells Network nt06539  Cytoskeleton in muscle cells   Element N01819   Actin thin filament, length regulation Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09142 Cell motility    04820 Cytoskeleton in muscle cells     29767 (TMOD2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     29767 (TMOD2) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actin-binding proteins     Capping proteins      29767 (TMOD2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Tropomodulin LRR_6 Ribosomal_S13 Motif Other DBs NCBI-GeneID:  29767 NCBI-ProteinID:  NP_055363 OMIM:  602928 HGNC:  11872 Ensembl:  ENSG00000128872 UniProt:  Q9NZR1 LinkDB All DBs Position 15:51751597..51816363 Genome browser AA seq 351 aa AA seqDB search MALPFQKELEKYKNIDEDELLGKLSEEELKQLENVLDDLDPESAMLPAGFRQKDQTQKAA TGPFDREHLLMYLEKEALEQKDREDFVPFTGEKKGRVFIPKEKPIETRKEEKVTLDPELE EALASASDTELYDLAAVLGVHNLLNNPKFDEETANNKGGKGPVRNVVKGEKVKPVFEEPP NPTNVEISLQQMKANDPSLQEVNLNNIKNIPIPTLREFAKALETNTHVKKFSLAATRSND PVAIAFADMLKVNKTLTSLNIESNFITGTGILALVEALKENDTLTEIKIDNQRQQLGTAV EMEIAQMLEENSRILKFGYQFTKQGPRTRVAAAITKNNDLVRKKRVEADRR NT seq 1056 nt NT seq  +upstreamnt  +downstreamnt atggcactcccctttcaaaaagagctggagaaatacaagaacattgatgaagatgagctt cttggcaaactctcagaagaggaactgaaacagttggaaaatgttctagatgacctagat cctgagagtgccatgctgccagctggatttcgacagaaagaccagacacagaaggcagcc accggcccctttgaccgcgagcacctcctcatgtacctggagaaggaggctttggaacag aaagacagagaggactttgtgcccttcactggagaaaagaaagggagagtctttatccct aaagaaaagcctatagaaactcgtaaagaagaaaaagtgacccttgacccagaactggaa gaagctttggccagtgcctctgacaccgaactctatgatcttgcagctgtccttggagta cacaatttgctcaacaatccaaagttcgatgaagaaacagccaacaataaaggtggcaaa ggacctgtcagaaatgttgtcaaaggtgaaaaagtaaagccagtatttgaggaaccacca aatcccacaaatgtggaaataagcctgcagcagatgaaagccaatgatcctagcttgcaa gaagtcaacctcaacaacattaagaacattccaattccaaccctgagggaatttgcaaag gctctggagaccaacactcacgtgaagaagttcagcctggccgcaactcgcagcaatgac cctgtggccattgcttttgcagacatgctgaaagtaaacaagaccttgacaagtctaaac atagaatccaattttatcactggaactgggatcctggccctggtagaggcactgaaagaa aatgacaccttgacagaaatcaagattgacaaccagaggcagcagttgggaacagctgta gagatggaaattgcccagatgctggaggagaattcaaggatcctcaagtttggataccag tttaccaagcaagggccacgaacaagggtggcagctgccatcacaaagaataatgacctg gttcgtaagaagagagttgaagcagaccgaaggtaa

Homo sapiens (human): 29766 Help Entry 29766             CDS       T01001                                  Symbol TMOD3, UTMOD Name (RefSeq) tropomodulin 3   KO K10370   tropomodulin Organism hsa  Homo sapiens (human) Pathway hsa04820   Cytoskeleton in muscle cells Network nt06539  Cytoskeleton in muscle cells   Element N01819   Actin thin filament, length regulation Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09142 Cell motility    04820 Cytoskeleton in muscle cells     29766 (TMOD3)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     29766 (TMOD3) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actin-binding proteins     Capping proteins      29766 (TMOD3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Tropomodulin LRR_6 Usher Motif Other DBs NCBI-GeneID:  29766 NCBI-ProteinID:  NP_055362 OMIM:  605112 HGNC:  11873 Ensembl:  ENSG00000138594 UniProt:  Q9NYL9 LinkDB All DBs Position 15:51829653..51915725 Genome browser AA seq 352 aa AA seqDB search MALPFRKDLEKYKDLDEDELLGNLSETELKQLETVLDDLDPENALLPAGFRQKNQTSKST TGPFDREHLLSYLEKEALEHKDREDYVPYTGEKKGKIFIPKQKPVQTFTEEKVSLDPELE EALTSASDTELCDLAAILGMHNLITNTKFCNIMGSSNGVDQEHFSNVVKGEKILPVFDEP PNPTNVEESLKRTKENDAHLVEVNLNNIKNIPIPTLKDFAKALETNTHVKCFSLAATRSN DPVATAFAEMLKVNKTLKSLNVESNFITGVGILALIDALRDNETLAELKIDNQRQQLGTA VELEMAKMLEENTNILKFGYQFTQQGPRTRAANAITKNNDLVRKRRVEGDHQ NT seq 1059 nt NT seq  +upstreamnt  +downstreamnt atggcactgccattccgtaaggacttagaaaagtacaaagaccttgatgaagatgagctc cttgggaatctgtcagaaacagaactgaaacaactggaaactgttttggatgatcttgac cccgagaatgcccttctgcctgcagggttccggcagaagaaccagacatcaaagtccacc acagggccatttgatagagagcatctcctttcatatctggagaaagaagcattggagcat aaagacagggaagactatgtgccctacactggagaaaaaaaagggaaaatatttatcccc aaacagaaacctgtacagacttttacagaagaaaaagtgtctcttgatccagaattagaa gaagctttgacaagtgcttctgatacagaattgtgtgacctcgcagcaattcttgggatg cacaatttgataacgaatacaaagttctgtaatataatgggaagtagtaatggtgttgac caagaacatttttcaaatgtggtcaaaggtgaaaagattcttccggtatttgatgagcca ccaaatccaaccaatgtagaagagagtttgaagagaactaaagaaaacgatgctcatctt gttgaagttaatttgaataatataaagaatatcccaattccaaccctaaaagattttgca aaggctttggaaaccaacacacatgtgaaatgtttcagtcttgcagccacccggagcaat gaccctgttgctactgcttttgcagaaatgctgaaagtgaacaaaactttgaagagctta aatgtggagtccaactttatcacgggagttgggattctggcactgattgatgcgttaaga gataatgaaaccctggcagagctcaagattgacaatcagaggcagcagttggggacagct gtagaattggaaatggccaagatgcttgaggaaaatacaaatatccttaaatttggatat cagtttacacagcagggaccacgaaccagagcagctaatgctataacaaaaaacaatgac ttagtgcgtaagagacgagttgaaggagatcaccagtaa

Homo sapiens (human): 29765 Help Entry 29765             CDS       T01001                                  Symbol TMOD4, SK-TMOD Name (RefSeq) tropomodulin 4   KO K10370   tropomodulin Organism hsa  Homo sapiens (human) Pathway hsa04820   Cytoskeleton in muscle cells Network nt06539  Cytoskeleton in muscle cells   Element N01819   Actin thin filament, length regulation Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09142 Cell motility    04820 Cytoskeleton in muscle cells     29765 (TMOD4)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     29765 (TMOD4) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actin-binding proteins     Capping proteins      29765 (TMOD4) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Tropomodulin LRR_6 Motif Other DBs NCBI-GeneID:  29765 NCBI-ProteinID:  NP_037485 OMIM:  605834 HGNC:  11874 Ensembl:  ENSG00000163157 UniProt:  Q9NZQ9 LinkDB All DBs Position 1:complement(151169987..151175981) Genome browser AA seq 345 aa AA seqDB search MSSYQKELEKYRDIDEDEILRTLSPEELEQLDCELQEMDPENMLLPAGLRQRDQTKKSPT GPLDREALLQYLEQQALEVKERDDLVPFTGEKKGKPYIQPKREIPAEEQITLEPELEEAL AHATDAEMCDIAAILDMYTLMSNKQYYDALCSGEICNTEGISSVVQPDKYKPVPDEPPNP TNIEEILKRVRSNDKELEEVNLNNIQDIPIPMLSELCEAMKANTYVRSFSLVATRSGDPI ANAVADMLRENRSLQSLNIESNFISSTGLMAVLKAVRENATLTELRVDNQRQWPGDAVEM EMATVLEQCPSIVRFGYHFTQQGPRARAAQAMTRNNELRRQQKKR NT seq 1038 nt NT seq  +upstreamnt  +downstreamnt atgtcatcatatcagaaggaactggagaaatacagagacatagatgaagatgagatccta aggaccttgagccccgaggagctagagcagctggactgcgaactacaggagatggatcct gagaacatgctcctgccagctggactaagacaacgtgaccagacaaagaagagcccaacg gggccactggaccgagaggcccttttgcagtacttggagcaacaggcactagaagtcaaa gagcgtgatgacttggtgcccttcacaggcgagaagaaggggaaaccctatattcagccc aagagggaaatcccagcagaggagcagatcaccctggagcctgagctggaggaggcactg gcacatgccacagatgctgaaatgtgtgacattgcagcaattctggacatgtacacactg atgagtaacaagcaatactatgatgccctctgcagtggagaaatctgcaacactgaaggc attagcagtgtggtacagcctgacaagtataagccagtgccggatgaacccccaaatccc acaaacattgaggagatactaaagagggtccgaagcaatgacaaggagctggaggaggtg aacttgaataatatacaggacatcccaatacccatgctaagtgagctgtgtgaggcaatg aaggcaaatacctatgtgcggagcttcagtctggtagccacgaggagtggtgaccccatt gccaatgcagtggctgacatgttgcgtgagaatcgtagcctccagagcctaaacatcgaa tccaacttcattagcagcacaggactcatggctgtgctgaaggcagttcgggaaaatgcc acactcactgagctccgtgtagacaatcagcgccagtggcctggtgatgcagtggagatg gagatggccaccgtgctagagcagtgtccctctattgtccgctttggctaccactttaca cagcaggggccacgagctcgggcagcccaggccatgacccgaaacaatgaactacgtcgc cagcaaaagaagagataa

Homo sapiens (human): 25802 Help Entry 25802             CDS       T01001                                  Symbol LMOD1, 1D, 64kD, D1, MMIHS3, SM-LMOD, SMLMOD Name (RefSeq) leiomodin 1   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 H01869   Megacystis microcolon intestinal hypoperistalsis syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09142 Cell motility    04820 Cytoskeleton in muscle cells     25802 (LMOD1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     25802 (LMOD1) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actin-binding proteins     Others      25802 (LMOD1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Tropomodulin WH2 LRR_6 Motif Other DBs NCBI-GeneID:  25802 NCBI-ProteinID:  NP_036266 OMIM:  602715 HGNC:  6647 Ensembl:  ENSG00000163431 UniProt:  P29536 Structure PDB LinkDB All DBs Position 1:complement(201896456..201946548) Genome browser AA seq 600 aa AA seqDB search MSRVAKYRRQVSEDPDIDSLLETLSPEEMEELEKELDVVDPDGSVPVGLRQRNQTEKQST GVYNREAMLNFCEKETKKLMQREMSMDESKQVETKTDAKNGEERGRDASKKALGPRRDSD LGKEPKRGGLKKSFSRDRDEAGGKSGEKPKEEKIIRGIDKGRVRAAVDKKEAGKDGRGEE RAVATKKEEEKKGSDRNTGLSRDKDKKREEMKEVAKKEDDEKVKGERRNTDTRKEGEKMK RAGGNTDMKKEDEKVKRGTGNTDTKKDDEKVKKNEPLHEKEAKDDSKTKTPEKQTPSGPT KPSEGPAKVEEEAAPSIFDEPLERVKNNDPEMTEVNVNNSDCITNEILVRFTEALEFNTV VKLFALANTRADDHVAFAIAIMLKANKTITSLNLDSNHITGKGILAIFRALLQNNTLTEL RFHNQRHICGGKTEMEIAKLLKENTTLLKLGYHFELAGPRMTVTNLLSRNMDKQRQKRLQ EQRQAQEAKGEKKDLLEVPKAGAVAKGSPKPSPQPSPKPSPKNSPKKGGAPAAPPPPPPP LAPPLIMENLKNSLSPATQRKMGDKVLPAQEKNSRDQLLAAIRSSNLKQLKKVEVPKLLQ NT seq 1803 nt NT seq  +upstreamnt  +downstreamnt atgtctagagtagccaaatatcgccggcaggtgagtgaagaccccgacatcgacagcctg ctggagaccctgtctcccgaggagatggaggagctggagaaggagctggacgtggtggac ccagacgggagtgttcccgtggggctgcggcagagaaaccagacggagaaacagtccacg ggtgtgtacaaccgggaggccatgctcaacttctgtgaaaaggagaccaagaaacttatg cagagggagatgtccatggatgaaagcaagcaagtggagaccaagacagatgccaagaat ggagaggaaaggggcagagatgccagcaaaaaagccctgggccccagacgggactcagat ctggggaaggagccaaagaggggtggtttaaagaaaagcttctctagagacagagatgaa gctggtggcaagagtggcgagaagcccaaggaggagaagatcatccggggcattgacaag ggccgggtcagggctgcagtggataagaaggaggcagggaaggatgggagaggagaggag agggcagtggccaccaagaaggaagaggagaagaaagggagtgacaggaacacaggcttg agcagggacaaggataaaaagagagaggagatgaaggaggtggccaagaaagaggatgat gagaaggtaaaaggggagcgtaggaacacagacaccagaaaagagggtgagaagatgaaa agagcaggtgggaacacagacatgaaaaaggaggatgagaaggtaaaaagaggaactggg aacacagacaccaaaaaggacgatgaaaaagtcaagaagaatgaacccttacatgaaaag gaagccaaggatgacagcaagaccaaaacacccgagaaacagacgcccagtggccccacc aagccctctgaaggaccggccaaggtggaggaggaggcagctcccagcatatttgatgag cctctggagagagtgaagaacaatgaccccgagatgactgaggtgaacgtcaacaactca gactgcatcacaaatgagatcttggtccggtttactgaggctctggagttcaacactgtg gttaagctgttcgccttggccaacacgcgagccgatgaccacgtggcctttgccattgcc atcatgctcaaggccaacaagaccatcaccagcctcaacctggactccaaccacatcaca ggcaaaggcatcctggccatcttccgggccctcctccagaacaacacgctgaccgagctc cgcttccacaaccagcgacacatctgtggaggcaagacggagatggagatcgccaagctg ctgaaggagaatactaccctgctcaagctgggctaccattttgagctggccgggccccga atgactgtcaccaatctgctcagccgcaacatggacaagcagagacaaaagcggctgcag gagcaaaggcaggcacaggaagccaagggagagaagaaggatctgctggaggtacccaag gccggggccgtggctaagggctccccaaaaccttcacctcaaccatctccaaagccctct ccaaagaactcacccaaaaaagggggtgctccagctgccccaccaccccctccccctccc ttggctccaccccttatcatggagaacctgaagaattcactctcaccagctacccagagg aagatgggagacaaagtcctccctgcccaggagaagaactcccgtgaccagctattggct gccatccgctccagcaacctcaagcagctcaagaaggtggaagtgcccaaactgcttcag tag

Homo sapiens (human): 442721 Help Entry 442721            CDS       T01001                                  Symbol LMOD2, C-LMOD, CLMOD, CMD2G Name (RefSeq) leiomodin 2   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 H00294   Dilated cardiomyopathy Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09142 Cell motility    04820 Cytoskeleton in muscle cells     442721 (LMOD2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     442721 (LMOD2) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actin-binding proteins     Others      442721 (LMOD2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Tropomodulin WH2 Motif Other DBs NCBI-GeneID:  442721 NCBI-ProteinID:  NP_997046 OMIM:  608006 HGNC:  6648 Ensembl:  ENSG00000170807 UniProt:  Q6P5Q4 Structure PDB LinkDB All DBs Position 7:123655866..123664290 Genome browser AA seq 547 aa AA seqDB search MSTFGYRRGLSKYESIDEDELLASLSAEELKELERELEDIEPDRNLPVGLRQKSLTEKTP TGTFSREALMAYWEKESQKLLEKERLGECGKVAEDKEESEEELIFTESNSEVSEEVYTEE EEEESQEEEEEEDSDEEERTIETAKGINGTVNYDSVNSDNSKPKIFKSQIENINLTNGSN GRNTESPAAIHPCGNPTVIEDALDKIKSNDPDTTEVNLNNIENITTQTLTRFAEALKDNT VVKTFSLANTHADDSAAMAIAEMLKVNEHITNVNVESNFITGKGILAIMRALQHNTVLTE LRFHNQRHIMGSQVEMEIVKLLKENTTLLRLGYHFELPGPRMSMTSILTRNMDKQRQKRL QEQKQQEGYDGGPNLRTKVWQRGTPSSSPYVSPRHSPWSSPKLPKKVQTVRSRPLSPVAT PPPPPPPPPPPPPSSQRLPPPPPPPPPPLPEKKLITRNIAEVIKQQESAQRALQNGQKKK KGKKVKKQPNSILKEIKNSLRSVQEKKMEDSSRPSTPQRSAHENLMEAIRGSSIKQLKRV EVPEALR NT seq 1644 nt NT seq  +upstreamnt  +downstreamnt atgtctacctttggctaccgaagaggactcagtaaatacgaatccatcgacgaggatgaa ctcctcgcctccctgtcagccgaggagctgaaggagctagagagagagttggaagacatt gaacctgaccgcaaccttcccgtggggctaaggcaaaagagcctgacagagaaaaccccc acagggacattcagcagagaggcactgatggcctattgggaaaaggagtcccaaaaactc ttggagaaggagaggctgggggaatgtggaaaggttgcagaagacaaagaggaaagtgaa gaagagcttatctttactgaaagtaacagtgaggtttctgaggaagtgtatacagaggag gaggaggaggagtcccaggaggaagaggaggaagaagacagtgacgaagaggaaagaaca attgaaactgcaaaagggattaatggaactgtaaattatgatagtgtcaattctgacaac tctaagccaaagatatttaaaagtcaaatagagaacataaatttgaccaatggcagcaat gggaggaacacagagtccccagctgccattcacccttgtggaaatcctacagtgattgag gacgctttggacaagattaaaagcaatgaccctgacaccacagaagtcaatttgaacaac attgagaacatcacaacacagacccttacccgctttgctgaagccctcaaggacaacact gtggtgaagacgttcagtctggccaacacgcatgccgacgacagtgcagccatggccatt gcagagatgctcaaagtcaatgagcacatcaccaacgtaaacgtcgagtccaacttcata acgggaaaggggatcctggccatcatgagagctctccagcacaacacggtgctcacggag ctgcgtttccataaccagaggcacatcatgggcagccaggtggaaatggagattgtcaag ctgctgaaggagaacacgacgctgctgaggctgggataccattttgaactcccaggacca agaatgagcatgacgagcattttgacaagaaatatggataaacagaggcaaaaacgtttg caggagcaaaaacagcaggagggatacgatggaggacccaatcttaggaccaaagtctgg caaagaggaacacctagctcttcaccttatgtatctcccaggcactcaccctggtcatcc ccaaaactccccaaaaaagtccagactgtgaggagccgtcctctgtctcctgtggccaca cctcctcctcctccccctcctcctcctcctccccctccttcttcccaaaggctgccacca cctcctcctcctccccctcctccactcccagagaaaaagctcattaccagaaacattgca gaagtcatcaaacaacaggagagtgcccaacgggcattacaaaatggacaaaaaaagaaa aaagggaaaaaggtcaagaaacagccaaacagtattctaaaggaaataaaaaattctctg aggtcagtgcaagagaagaaaatggaagacagttcccgaccttctaccccacagagatca gctcatgagaatctcatggaagcaattcggggaagcagcataaaacagctaaagcgggtg gaagttccagaagccctgcgataa

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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