Neogale vison (American mink): 122893575 Help Entry 122893575         CDS       T08764                                  Symbol SGCD Name (RefSeq) delta-sarcoglycan isoform X1   KO K12563   delta-sarcoglycan Organism nvs  Neogale vison (American mink) Pathway nvs04820   Cytoskeleton in muscle cells nvs05410   Hypertrophic cardiomyopathy nvs05412   Arrhythmogenic right ventricular cardiomyopathy nvs05414   Dilated cardiomyopathy nvs05416   Viral myocarditis Brite KEGG Orthology (KO) [BR:nvs00001]  09140 Cellular Processes   09142 Cell motility    04820 Cytoskeleton in muscle cells     122893575 (SGCD)  09160 Human Diseases   09166 Cardiovascular disease    05410 Hypertrophic cardiomyopathy     122893575 (SGCD)    05412 Arrhythmogenic right ventricular cardiomyopathy     122893575 (SGCD)    05414 Dilated cardiomyopathy     122893575 (SGCD)    05416 Viral myocarditis     122893575 (SGCD) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Sarcoglycan_1 DUF2345 Motif Other DBs NCBI-GeneID:  122893575 NCBI-ProteinID:  XP_044086622 LinkDB All DBs Position 1:complement(269309132..270321297) Genome browser AA seq 289 aa AA seqDB search MPQEQYTHHRSTMPSSEGPQVYKVGIYGWRKRCLYFFVLLLMILILVNLAMTIWILKVMN FTIDGMGNLRITDKGLKLEGDSEFLQPLYAKEIQSRPGNALYFKSARNVTVNILNDQTKV LTQLITGPKAVEAYGKKFEVKTVSGKLLFSADNNEVVVGAERLRVLGAEGTVFPKSIETP NVRADPFKELRLESPTRSLVMEAPKGVEINAEAGNMEATCRTELRLESKDGEIKLDAAKI QLPRLPHGSYTPTGTRQKVFEICVCANGRLFLSQAGAGSTCQINTSVCL NT seq 870 nt NT seq  +upstreamnt  +downstreamnt atgcctcaggaacagtacacacaccaccggagcaccatgcccagctccgaggggccacag gtctacaaggtgggcatttatggctggcggaaaagatgcctgtatttcttcgtcctgctc ctgatgattttaatactggtgaacttggccatgaccatctggattctcaaagtcatgaac ttcacaattgatggaatggggaatttgagaatcacagacaaaggtctaaaactagaagga gactcagaattcttgcaacctctctacgccaaagaaatccagtcccgaccaggtaatgcc ctgtacttcaaatcagccagaaatgttacagtgaacattctcaatgaccagactaaagtg ctaactcagctcatcacaggtccaaaagccgtagaagcttatggcaaaaagtttgaagta aagacagtttctggaaaattgctcttctctgcagataacaacgaagtggtggtaggagct gaaagattaagagttttaggagccgagggcacagtgttccctaaatctatagagacacct aatgtcagggcagaccccttcaaggaactaaggttggagtccccgacccggtctctggtg atggaggcccccaaaggagtggaaattaatgcagaagccggcaatatggaagccacctgc agaaccgagctgaggttggagtccaaagacggagagattaagttagatgctgcgaaaatc caactacctagactgcctcacggatcctacacacccacaggaacgaggcagaaggtcttc gagatctgcgtctgcgccaatgggagattattcctgtcccaggcaggagctggttccact tgtcagataaacacaagtgtctgcctttga

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