Homo sapiens (human): 7171 Help Entry 7171              CDS       T01001                                  Symbol TPM4, BDPLT25, HEL-S-108 Name (RefSeq) tropomyosin 4   KO K10375   tropomyosin 4 Organism hsa  Homo sapiens (human) Pathway hsa04260   Cardiac muscle contraction hsa04261   Adrenergic signaling in cardiomyocytes hsa04814   Motor proteins hsa04820   Cytoskeleton in muscle cells hsa05410   Hypertrophic cardiomyopathy hsa05414   Dilated cardiomyopathy Disease H01235   Bleeding disorder platelet-type Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09142 Cell motility    04814 Motor proteins     7171 (TPM4)    04820 Cytoskeleton in muscle cells     7171 (TPM4)  09150 Organismal Systems   09153 Circulatory system    04260 Cardiac muscle contraction     7171 (TPM4)    04261 Adrenergic signaling in cardiomyocytes     7171 (TPM4)  09160 Human Diseases   09166 Cardiovascular disease    05410 Hypertrophic cardiomyopathy     7171 (TPM4)    05414 Dilated cardiomyopathy     7171 (TPM4)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     7171 (TPM4) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actin-binding proteins     Tropomyosins      7171 (TPM4) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Tropomyosin Laminin_II DUF3450 CENP-F_leu_zip FPP Crescentin PUMA_CC TMF_DNA_bd CLZ ADIP CALCOCO1 PspA_IM30 DUF724 ATG16 DUF1664 Nuf2_DHR10-like EzrA DUF745 Fib_alpha XhlA Motif Other DBs NCBI-GeneID:  7171 NCBI-ProteinID:  NP_003281 OMIM:  600317 HGNC:  12013 Ensembl:  ENSG00000167460 UniProt:  P67936 V9HW56 LinkDB All DBs Position 19:16067538..16103002 Genome browser AA seq 248 aa AA seqDB search MAGLNSLEAVKRKIQALQQQADEAEDRAQGLQRELDGERERREKAEGDVAALNRRIQLVE EELDRAQERLATALQKLEEAEKAADESERGMKVIENRAMKDEEKMEIQEMQLKEAKHIAE EADRKYEEVARKLVILEGELERAEERAEVSELKCGDLEEELKNVTNNLKSLEAASEKYSE KEDKYEEEIKLLSDKLKEAETRAEFAERTVAKLEKTIDDLEEKLAQAKEENVGLHQTLDQ TLNELNCI NT seq 747 nt NT seq  +upstreamnt  +downstreamnt atggccggcctcaactccctggaggcggtgaaacgcaagatccaggccctgcagcagcag gcggacgaggcggaagaccgcgcgcagggcctgcagcgggagctggacggcgagcgcgag cggcgcgagaaagctgaaggtgatgtggccgccctcaaccgacgcatccagctcgttgag gaggagttggacagggctcaggaacgactggccacggccctgcagaagctggaggaggca gaaaaagctgcagatgagagtgagagaggaatgaaggtgatagaaaaccgggccatgaag gatgaggagaagatggagattcaggagatgcagctcaaagaggccaagcacattgcggaa gaggctgaccgcaaatacgaggaggtagctcgtaagctggtcatcctggagggtgagctg gagagggcagaggagcgtgcggaggtgtctgaactaaaatgtggtgacctggaagaagaa ctcaagaatgttactaacaatctgaaatctctggaggctgcatctgaaaagtattctgaa aaggaggacaaatatgaagaagaaattaaacttctgtctgacaaactgaaagaggctgag acccgtgctgaatttgcagagagaacggttgcaaaactggaaaagacaattgatgacctg gaagagaaacttgcccaggccaaagaagagaacgtgggcttacatcagacactggatcag acactaaacgaacttaactgtatataa

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