Homo sapiens (human): 118 Help Entry 118               CDS       T01001                                  Symbol ADD1, ADDA Name (RefSeq) adducin 1   KO K18622   adducin Organism hsa  Homo sapiens (human) Network nt06541  Cytoskeleton in neurons   Element N01848   Membrane-associated periodic skeleton (MPS) Disease H01633   High blood pressure Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     118 (ADD1) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actin-binding proteins     Others      118 (ADD1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Aldolase_II Motif Other DBs NCBI-GeneID:  118 NCBI-ProteinID:  NP_001110 OMIM:  102680 HGNC:  243 Ensembl:  ENSG00000087274 UniProt:  P35611 LinkDB All DBs Position 4:2843844..2930062 Genome browser AA seq 737 aa AA seqDB search MNGDSRAAVVTSPPPTTAPHKERYFDRVDENNPEYLRERNMAPDLRQDFNMMEQKKRVSM ILQSPAFCEELESMIQEQFKKGKNPTGLLALQQIADFMTTNVPNVYPAAPQGGMAALNMS LGMVTPVNDLRGSDSIAYDKGEKLLRCKLAAFYRLADLFGWSQLIYNHITTRVNSEQEHF LIVPFGLLYSEVTASSLVKINLQGDIVDRGSTNLGVNQAGFTLHSAIYAARPDVKCVVHI HTPAGAAVSAMKCGLLPISPEALSLGEVAYHDYHGILVDEEEKVLIQKNLGPKSKVLILR NHGLVSVGESVEEAFYYIHNLVVACEIQVRTLASAGGPDNLVLLNPEKYKAKSRSPGSPV GEGTGSPPKWQIGEQEFEALMRMLDNLGYRTGYPYRYPALREKSKKYSDVEVPASVTGYS FASDGDSGTCSPLRHSFQKQQREKTRWLNSGRGDEASEEGQNGSSPKSKTKWTKEDGHRT STSAVPNLFVPLNTNPKEVQEMRNKIREQNLQDIKTAGPQSQVLCGVVMDRSLVQGELVT ASKAIIEKEYQPHVIVSTTGPNPFTTLTDRELEEYRREVERKQKGSEENLDEAREQKEKS PPDQPAVPHPPPSTPIKLEEDLVPEPTTGDDSDAATFKPTLPDLSPDEPSEALGFPMLEK EEEAHRPPSPTEAPTEASPEPAPDPAPVAEEAAPSAVEEGAAADPGSDGSPGKSPSKKKK KFRTPSFLKKSKKKSDS NT seq 2214 nt NT seq  +upstreamnt  +downstreamnt atgaatggtgattctcgtgctgcggtggtgacctcaccacccccgaccacagcccctcac aaggagaggtacttcgaccgagtagatgagaacaacccagagtacttgagggagaggaac atggcaccagaccttcgccaggacttcaacatgatggagcaaaagaagagggtgtccatg attctgcaaagccctgctttctgtgaagaattggaatcaatgatacaggagcaatttaag aaggggaagaaccccacaggcctattggcattacagcagattgcagattttatgaccacg aatgtaccaaatgtctacccagcagctccgcaaggagggatggctgccttaaacatgagt cttggtatggtgactcctgtgaacgatcttagaggatctgattctattgcgtatgacaaa ggagagaagttattacggtgtaaattggcagcgttttatagactagcagatctctttggg tggtctcagcttatctacaatcatatcacaaccagagtgaactccgagcaggaacacttc ctcattgtcccttttgggcttctttacagtgaagtgactgcatccagtttggttaagatc aatctacaaggagatatagtagatcgtggaagcactaatctgggagtgaatcaggccggc ttcaccttacactctgcaatttatgctgcacgcccggacgtgaagtgcgtcgtgcacatt cacaccccagcaggggctgcggtctctgcaatgaaatgtggcctcttgccaatctccccg gaggcgctttcccttggagaagtggcttatcatgactaccatggcattctggttgatgaa gaggaaaaagttttgattcagaaaaatctggggcctaaaagcaaggttcttattctccgg aaccatgggctcgtgtcagttggagagagcgttgaggaggccttctattacatccataac cttgtggttgcctgtgagatccaggttcgaactctggccagtgcaggaggaccagacaac ttagtcctgctgaatcctgagaagtacaaagccaagtcccgttccccagggtctccggta ggggaaggcactggatcgcctcccaagtggcagattggtgagcaggaatttgaagccctc atgcggatgctcgataatctgggctacagaactggctacccttatcgataccctgctctg agagagaagtctaaaaaatacagcgatgtggaggttcctgctagtgtcacaggttactcc tttgctagtgacggtgattcgggcacttgctccccactcagacacagttttcagaagcag cagcgggagaagacaagatggctgaactctggccggggcgacgaagcttccgaggaaggg cagaatggaagcagtcccaagtcgaagactaagtggactaaagaggatggacatagaact tccacctctgctgtccctaacctgtttgttccattgaacactaacccaaaagaggtccag gagatgaggaacaagatccgagagcagaatttacaggacattaagacggctggccctcag tcccaggttttgtgtggtgtagtgatggacaggagcctcgtccagggagagctggtgacg gcctccaaggccatcattgaaaaggagtaccagccccacgtcattgtgagcaccacgggc cccaaccccttcaccacactcacagaccgtgagctggaggagtaccgcagggaggtggag aggaagcagaagggctctgaagagaatctggacgaggctagagaacagaaagaaaagagt cctccagaccagcctgcggtcccccacccgcctcccagcactcccatcaagctggaggaa gaccttgtgccggagccgactactggagatgacagtgatgctgccacctttaagccaact ctccccgatctgtcccctgatgaaccttcagaagcactcggcttcccaatgttagagaag gaggaggaagcccatagacccccaagccccactgaggcccctactgaggccagccccgag ccagccccagacccagccccggtggctgaagaggctgccccctcagctgtcgaggagggg gccgccgcggaccctggcagcgatgggtctccaggcaagtccccgtccaaaaagaagaag aagttccgtaccccgtcctttctgaagaagagcaagaagaagagtgactcctga

Homo sapiens (human): 119 Help Entry 119               CDS       T01001                                  Symbol ADD2, ADDB Name (RefSeq) adducin 2   KO K18622   adducin Organism hsa  Homo sapiens (human) Network nt06541  Cytoskeleton in neurons   Element N01848   Membrane-associated periodic skeleton (MPS) Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     119 (ADD2) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actin-binding proteins     Others      119 (ADD2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Aldolase_II Mac Motif Other DBs NCBI-GeneID:  119 NCBI-ProteinID:  NP_001171983 OMIM:  102681 HGNC:  244 Ensembl:  ENSG00000075340 UniProt:  P35612 Q05DK5 LinkDB All DBs Position 2:complement(70656784..70768200) Genome browser AA seq 726 aa AA seqDB search MSEETVPEAASPPPPQGQPYFDRFSEDDPEYMRLRNRAADLRQDFNLMEQKKRVTMILQS PSFREELEGLIQEQMKKGNNSSNIWALRQIADFMASTSHAVFPTSSMNVSMMTPINDLHT ADSLNLAKGERLMRCKISSVYRLLDLYGWAQLSDTYVTLRVSKEQDHFLISPKGVSCSEV TASSLIKVNILGEVVEKGSSCFPVDTTGFCLHSAIYAARPDVRCIIHLHTPATAAVSAMK WGLLPVSHNALLVGDMAYYDFNGEMEQEADRINLQKCLGPTCKILVLRNHGVVALGDTVE EAFYKIFHLQAACEIQVSALSSAGGVENLILLEQEKHRPHEVGSVQWAGSTFGPMQKSRL GEHEFEALMRMLDNLGYRTGYTYRHPFVQEKTKHKSEVEIPATVTAFVFEEDGAPVPALR QHAQKQQKEKTRWLNTPNTYLRVNVADEVQRSMGSPRPKTTWMKADEVEKSSSGMPIRIE NPNQFVPLYTDPQEVLEMRNKIREQNRQDVKSAGPQSQLLASVIAEKSRSPSTESQLMSK GDEDTKDDSEETVPNPFSQLTDQELEEYKKEVERKKLELDGEKETAPEEPGSPAKSAPAS PVQSPAKEAETKSPLVSPSKSLEEGTKKTETSKAATTEPETTQPEGVVVNGREEEQTAEE ILSKGLSQMTTSADTDVDTSKDKTESVTSGPMSPEGSPSKSPSKKKKKFRTPSFLKKSKK KEKVES NT seq 2181 nt NT seq  +upstreamnt  +downstreamnt atgagcgaagagacggtccccgaggctgcctcgccgccgcccccgcaggggcagccttac tttgaccgcttctcagaggacgaccccgagtacatgcgccttcgcaaccgggcggcggac ctgcggcaggacttcaacctgatggagcagaagaagcgcgtcaccatgatcctgcagagt ccctctttcagggaggagctggaaggcctcatccaggagcagatgaagaaggggaacaac tcctccaacatctgggccctgcgacagatcgcggacttcatggccagcacctcccacgca gtcttcccgacatcttccatgaatgtctccatgatgacgcctatcaatgacctccacaca gctgactccctgaacctggccaaaggggagcggctcatgcggtgcaagatcagcagtgtc taccgactcctggacctctatggctgggcccagctgagtgacacctatgtcacgttgaga gtcagcaaggagcaggaccacttcctgatcagccctaagggagtttcttgcagtgaagtc acagcgtccagcctgatcaaggtgaacattctgggagaggtggtggagaagggcagcagc tgcttcccagtggacaccacaggcttctgtctgcactcggccatctatgcagcgaggccc gacgtgcgctgcatcatccacctgcacacaccggccacagcagcggtgtcggccatgaag tggggcctcctgcctgtctcccacaatgccctgctggtgggggacatggcctattatgac ttcaatggggaaatggagcaggaagccgatcggatcaacctgcagaagtgccttggaccc acctgcaagatcctggtgctaagaaaccatggagtggttgctctgggtgacacggtagag gaggcattttacaagatcttccacctgcaggctgcatgtgagatacaggtgtcggctctg tccagtgccgggggagtggagaacctcatcctcctggagcaggagaagcaccggccccat gaggtgggctccgtgcagtgggccgggagcacctttgggcctatgcagaagagtcggctg ggggagcatgagtttgaggccctcatgaggatgctggacaacctgggctacagaacaggt tacacgtatcgccacccctttgttcaagagaaaaccaaacacaaaagtgaggtggagatt ccagccacggtcacagccttcgtgtttgaggaggacggtgccccggtgcccgccctgcga cagcatgcccagaagcagcagaaggagaagacccgctggctcaatacgcccaacacctac ctgcgggtcaatgtggccgatgaggtccagaggagcatgggcagcccccgacccaagacc acgtggatgaaggctgacgaggtggagaaatccagcagtggcatgccgattcgcatcgaa aacccaaaccaatttgtgcctctctatactgacccccaggaagtactggagatgaggaac aagattcgagaacaaaaccgacaagatgtgaagtcagcggggcctcagtcccagctcctg gcgagcgtcattgccgagaagagccgaagcccgtctacagagagccagctgatgtccaag ggagacgaggataccaaagacgattcagaggagacggtgcccaaccccttcagccaactc actgaccaggagttggaggagtacaagaaagaggtggagaggaagaaactagaacttgat ggagagaaagaaactgccccagaagagcctggctcacctgcaaagtctgcacctgcttct ccagtgcagagcccagcgaaggaggcagagacaaagagccctttagtctctccttccaag tctttagaggaaggtactaagaagacagaaacaagcaaagccgccaccacagagcccgaa acaacccagccggaaggggtggtggtcaacgggagggaggaggagcagacggcagaggaa atcctcagcaaaggcctgagccagatgaccaccagtgctgacacggatgttgatacctct aaggacaaaaccgagtcggtcaccagcggccccatgtccccagagggctcaccttccaag tctccctcaaagaagaaaaagaaattccgaaccccctccttcctgaaaaagagcaaaaag aaggagaaagtggagtcctga

Homo sapiens (human): 120 Help Entry 120               CDS       T01001                                  Symbol ADD3, ADDL, CPSQ3 Name (RefSeq) adducin 3   KO K18622   adducin Organism hsa  Homo sapiens (human) Network nt06541  Cytoskeleton in neurons   Element N01848   Membrane-associated periodic skeleton (MPS) Disease H01097   Spastic quadriplegic cerebral palsy Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     120 (ADD3) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actin-binding proteins     Others      120 (ADD3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Aldolase_II Motif Other DBs NCBI-GeneID:  120 NCBI-ProteinID:  NP_001307520 OMIM:  601568 HGNC:  245 Ensembl:  ENSG00000148700 UniProt:  Q9UEY8 Q5VU08 Q53FL4 LinkDB All DBs Position 10:109996373..110135565 Genome browser AA seq 706 aa AA seqDB search MSSDASQGVITTPPPPSMPHKERYFDRINENDPEYIRERNMSPDLRQDFNMMEQRKRVTQ ILQSPAFREDLECLIQEQMKKGHNPTGLLALQQIADYIMANSFSGFSSPPLSLGMVTPIN DLPGADTSSYVKGEKLTRCKLASLYRLVDLFGWAHLANTYISVRISKEQDHIIIIPRGLS FSEATASNLVKVNIIGEVVDQGSTNLKIDHTGFSPHAAIYSTRPDVKCVIHIHTLATAAV SSMKCGILPISQESLLLGDVAYYDYQGSLEEQEERIQLQKVLGPSCKVLVLRNHGVVALG ETLEEAFHYIFNVQLACEIQVQALAGAGGVDNLHVLDFQKYKAFTYTVAASGGGGVNMGS HQKWKVGEIEFEGLMRTLDNLGYRTGYAYRHPLIREKPRHKSDVEIPATVTAFSFEDDTV PLSPLKYMAQRQQREKTRWLNSPNTYMKVNVPEESRNGETSPRTKITWMKAEDSSKVSGG TPIKIEDPNQFVPLNTNPNEVLEKRNKIREQNRYDLKTAGPQSQLLAGIVVDKPPSTMQF EDDDHGPPAPPNPFSHLTEGELEEYKRTIERKQQGLEDAEQELLSDDASSVSQIQSQTQS PQNVPEKLEENHELFSKSFISMEVPVMVVNGKDDMHDVEDELAKRVSRLSTSTTIENIEI TIKSPEKIEEVLSPEGSPSKSPSKKKKKFRTPSFLKKNKKKEKVEA NT seq 2121 nt NT seq  +upstreamnt  +downstreamnt atgagctcagatgccagccaaggcgtgattaccactcctcctcctcccagcatgcctcac aaagagagatattttgaccgcatcaatgaaaatgacccagaatacattagggagaggaac atgtctcctgatctacgacaagacttcaacatgatggagcagaggaaacgagttactcag atcctgcaaagtcctgcctttcgggaagacttggaatgccttattcaagaacagatgaag aaaggccacaacccaactggattactagcattacagcagattgcagattacatcatggcc aattctttctcgggtttttcttcacctcctctcagtcttggcatggtcacacctatcaat gaccttcctggtgcagatacatcctcatatgtgaagggagaaaaacttactcgctgtaaa cttgccagcctgtacagacttgtagacttgtttggatgggcacacctggcaaatacctat atctcagtaagaataagtaaggagcaagaccacattataataattcccagaggcctatct ttttctgaagctacagcctccaatttggtgaaagtcaatataataggagaagtggttgac cagggaagtaccaatttgaaaattgaccatacaggattcagtccccatgctgcaatctat tcaacacgtcctgatgttaagtgtgtgatacacatccatacccttgcaacagcagctgta tcctccatgaaatgtgggatccttccaatttctcaagagtctcttcttctgggagatgtt gcctattatgactaccaagggtcacttgaagaacaggaggagagaattcaactgcagaag gttctgggaccaagttgtaaggtgctggtactcaggaatcatggtgtggttgcacttgga gaaacattagaggaggcttttcattatatttttaatgtgcaactagcctgtgagattcag gtgcaggccctagcaggtgcaggtggagtagacaatctccatgtactggactttcagaag tataaagctttcacttacactgtagcagcgtctggtggaggaggtgtgaatatgggttcc catcaaaaatggaaggttggcgaaattgagtttgaagggcttatgaggactctggacaac ttggggtatagaacaggctatgcttacaggcatcctctcattcgagagaagcctaggcac aagagtgatgtggaaatcccagcaactgtgactgctttttcctttgaagacgatacagtg ccactctctcctctcaaatacatggcacagaggcaacagcgtgaaaaaacaagatggctg aactcaccaaatacttacatgaaagtgaatgtgcctgaggagtctcggaacggagaaacc agtccccgaaccaaaatcacgtggatgaaagcagaagactcatctaaagttagtggtgga acacctatcaaaattgaagatccaaatcagtttgttcctttaaacacaaacccgaatgag gtactagaaaagagaaataagattcgggaacaaaatcgatatgacttgaaaacagcagga ccacaatctcagttgcttgctggaattgttgtggataagccaccttctactatgcaattt gaagatgatgatcatggcccaccagctcctcctaacccatttagtcatctcacagaagga gaacttgaagagtataagaggacaatcgaacgtaaacaacaaggcctagaagatgctgag caggaattactctcagatgacgcttcatctgtttcacaaattcagtctcaaactcagtca ccgcaaaatgtccctgaaaaattagaagaaaaccatgagctgttttccaagagcttcatc tccatggaagtgcctgtcatggtagtaaatggcaaggatgatatgcatgatgttgaagat gagcttgctaagcgagtgagtaggttaagcacaagtacaaccatagaaaacatcgagatt actattaagtctccagagaaaatcgaagaagtcctgtcacctgaaggctccccttcaaaa tcgccatccaagaaaaagaagaaattccgcactccttcttttctgaaaaagaacaaaaaa aaggagaaagttgaggcctaa

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 nt06541  Cytoskeleton in neurons   Element N01819   Actin thin filament, length regulation N01848   Membrane-associated periodic skeleton (MPS) 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 PDBPDBj 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 nt06541  Cytoskeleton in neurons   Element N01819   Actin thin filament, length regulation N01848   Membrane-associated periodic skeleton (MPS) 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 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 nt06541  Cytoskeleton in neurons   Element N01819   Actin thin filament, length regulation N01848   Membrane-associated periodic skeleton (MPS) 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 CTD1 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

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