Homo sapiens (human): 7138 Help Entry 7138              CDS       T01001                                  Symbol TNNT1, ANM, NEM5, STNT, TNT, TNTS Name (RefSeq) troponin T1, slow skeletal type   KO K10372   troponin T, slow skeletal muscle Organism hsa  Homo sapiens (human) Pathway hsa04814   Motor proteins hsa04820   Cytoskeleton in muscle cells Network nt06539  Cytoskeleton in muscle cells   Element N01818   Actin thin filament, muscle contraction Disease H00698   Nemaline myopathy Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09142 Cell motility    04814 Motor proteins     7138 (TNNT1)    04820 Cytoskeleton in muscle cells     7138 (TNNT1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     7138 (TNNT1) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actin-binding proteins     Troponins      7138 (TNNT1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Troponin DUF2828 RlmN_N PAS Motif Other DBs NCBI-GeneID:  7138 NCBI-ProteinID:  NP_003274 OMIM:  191041 HGNC:  11948 Ensembl:  ENSG00000105048 UniProt:  P13805 LinkDB All DBs Position 19:complement(55132698..55149206) Genome browser AA seq 278 aa AA seqDB search MSDTEEQEYEEEQPEEEAAEEEEEAPEEPEPVAEPEEERPKPSRPVVPPLIPPKIPEGER VDFDDIHRKRMEKDLLELQTLIDVHFEQRKKEEEELVALKERIERRRSERAEQQRFRTEK ERERQAKLAEEKMRKEEEEAKKRAEDDAKKKKVLSNMGAHFGGYLVKAEQKRGKRQTGRE MKVRILSERKKPLDIDYMGEEQLRARSAWLPPSQPSCPAREKAQELSDWIHQLESEKFDL MAKLKQQKYEINVLYNRISHAQKFRKGAGKGRVGGRWK NT seq 837 nt NT seq  +upstreamnt  +downstreamnt atgtcggacaccgaggagcaggaatatgaggaggagcagccggaagaggaggctgcggag gaggaggaggaagcccccgaagagccggagccggtggcagagccagaagaggaacgcccc aaaccaagccgccccgtggtgcctcctttgatcccgccaaagatcccagaaggggagcgc gttgacttcgatgacatccaccgcaagcgcatggagaaagacctgctggagctgcagaca ctcatcgatgtacatttcgagcagcggaagaaggaggaagaggagctggttgccttgaag gagcgcattgagcggcgccggtcagagagagccgagcaacagcgcttcagaactgagaag gaacgcgaacgtcaggctaagctggcggaggagaagatgaggaaggaagaggaagaggcc aagaagcgggcagaggatgatgccaagaaaaagaaggtgctgtccaacatgggggcccat tttggcggctacctggtcaaggcagaacagaagcgtggtaagcggcagacggggcgggag atgaaggtgcgcatcctctccgagcgtaagaagcctctggacattgactacatgggggag gaacagctccgggcccggtctgcctggctgcctccatcacagccctcctgccctgccagg gagaaagcccaggagctgtcggactggatccaccagctggagtctgagaagttcgacctg atggcgaagctgaaacagcagaaatatgagatcaacgtgctgtacaaccgcatcagccac gcccagaagttccggaagggggcagggaagggccgcgttggaggccgctggaagtga

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