Homo sapiens (human): 59 Help Entry 59                CDS       T01001                                  Symbol ACTA2, ACTSA, SMDYS Name (RefSeq) actin alpha 2, smooth muscle   KO K12313   actin, aortic smooth muscle Organism hsa  Homo sapiens (human) Pathway hsa04270   Vascular smooth muscle contraction hsa04371   Apelin signaling pathway hsa04814   Motor proteins hsa04926   Relaxin signaling pathway Disease H00801   Familial thoracic aortic aneurysm and dissection H01396   Moyamoya disease Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04371 Apelin signaling pathway     59 (ACTA2)  09140 Cellular Processes   09142 Cell motility    04814 Motor proteins     59 (ACTA2)  09150 Organismal Systems   09152 Endocrine system    04926 Relaxin signaling pathway     59 (ACTA2)   09153 Circulatory system    04270 Vascular smooth muscle contraction     59 (ACTA2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     59 (ACTA2)    04147 Exosome [BR:hsa04147]     59 (ACTA2) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actins     Actins      59 (ACTA2) Exosome [BR:hsa04147]  Exosomal proteins   Exosomal proteins of colorectal cancer cells    59 (ACTA2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Actin Motif Other DBs NCBI-GeneID:  59 NCBI-ProteinID:  NP_001135417 OMIM:  102620 HGNC:  130 Ensembl:  ENSG00000107796 UniProt:  P62736 D2JYH4 LinkDB All DBs Position 10:complement(88935074..88991337) Genome browser AA seq 377 aa AA seqDB search MCEEEDSTALVCDNGSGLCKAGFAGDDAPRAVFPSIVGRPRHQGVMVGMGQKDSYVGDEA QSKRGILTLKYPIEHGIITNWDDMEKIWHHSFYNELRVAPEEHPTLLTEAPLNPKANREK MTQIMFETFNVPAMYVAIQAVLSLYASGRTTGIVLDSGDGVTHNVPIYEGYALPHAIMRL DLAGRDLTDYLMKILTERGYSFVTTAEREIVRDIKEKLCYVALDFENEMATAASSSSLEK SYELPDGQVITIGNERFRCPETLFQPSFIGMESAGIHETTYNSIMKCDIDIRKDLYANNV LSGGTTMYPGIADRMQKEITALAPSTMKIKIIAPPERKYSVWIGGSILASLSTFQQMWIS KQEYDEAGPSIVHRKCF NT seq 1134 nt NT seq  +upstreamnt  +downstreamnt atgtgtgaagaagaggacagcactgccttggtgtgtgacaatggctctgggctctgtaag gccggctttgctggggacgatgctcccagggctgttttcccatccattgtgggacgtccc agacatcagggggtgatggtgggaatgggacaaaaagacagctacgtgggtgacgaagca cagagcaaaagaggaatcctgaccctgaagtacccgatagaacatggcatcatcaccaac tgggacgacatggaaaagatctggcaccactctttctacaatgagcttcgtgttgcccct gaagagcatcccaccctgctcacggaggcacccctgaaccccaaggccaaccgggagaaa atgactcaaattatgtttgagactttcaatgtcccagccatgtatgtggctatccaggcg gtgctgtctctctatgcctctggacgcacaactggcatcgtgctggactctggagatggt gtcacccacaatgtccccatctatgagggctatgccttgccccatgccatcatgcgtctg gatctggctggccgagatctcactgactacctcatgaagatcctgactgagcgtggctat tccttcgttactactgctgagcgtgagattgtccgggacatcaaggagaaactgtgttat gtagctctggactttgaaaatgagatggccactgccgcatcctcatcctcccttgagaag agttacgagttgcctgatgggcaagtgatcaccatcggaaatgaacgtttccgctgccca gagaccctgttccagccatccttcatcgggatggagtctgctggcatccatgaaaccacc tacaacagcatcatgaagtgtgatattgacatcaggaaggacctctatgctaacaatgtc ctatcagggggcaccactatgtaccctggcattgccgaccgaatgcagaaggagatcacg gccctagcacccagcaccatgaagatcaagatcattgcccctccggagcgcaaatactct gtctggatcggtggctccatcctggcctctctgtccaccttccagcagatgtggatcagc aaacaggaatacgatgaagccgggccttccattgtccaccgcaaatgcttctaa

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