Neogale vison (American mink): 122906919 Help Entry 122906919         CDS       T08764                                  Symbol SGCG Name (RefSeq) gamma-sarcoglycan isoform X1   KO K12564   gamma-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     122906919 (SGCG)  09160 Human Diseases   09166 Cardiovascular disease    05410 Hypertrophic cardiomyopathy     122906919 (SGCG)    05412 Arrhythmogenic right ventricular cardiomyopathy     122906919 (SGCG)    05414 Dilated cardiomyopathy     122906919 (SGCG)    05416 Viral myocarditis     122906919 (SGCG) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Sarcoglycan_1 DUF2345 PRA-CH TRAM Motif Other DBs NCBI-GeneID:  122906919 NCBI-ProteinID:  XP_044105347 LinkDB All DBs Position 5:85854292..85993563 Genome browser AA seq 291 aa AA seqDB search MVREQYTTTTEGTHIQRPENQCVYKIGIYGWRKRCLYLFVLLLLIILLVNFALTIWILKV MWFSPTGMGHLRVTKDGLRLEGESEFLFPLYAKEIHSRVDSSLLLQSTQNVTVNARNSEG EVTGRLKVGPKMVEVQSQQFQINSKDGKTLFTVDEKEVVVGTDKLRVTGPEGALFEHSVE TPLVRADPFQDLRLESPTRSLSMDAPKGVHIKAHAGKIEALSQMDIIFQSSDGMLVLDAE TVCLPKLVQGTQSAAGNSQRLYEICVCPDGKLYLSVAGAGTTCHENSHICL NT seq 876 nt NT seq  +upstreamnt  +downstreamnt atggtccgtgaacaatacactacaaccacagaaggcacccacatacagaggccagagaac cagtgtgtctacaagattggcatttatggctggagaaagcgttgtctgtacttatttgtt cttcttttactcatcatcctcctcgtgaattttgctcttacaatttggattcttaaagtg atgtggttttccccaacaggaatgggtcacttgcgtgttacaaaagatggtcttcgccta gaaggagaatcagaatttttattcccattgtatgccaaggaaatacactccagagtggac tcatctcttcttctgcagtcaactcagaatgtgactgtcaatgcacgcaactctgaagga gaggtcacgggcagattaaaagtgggtcccaaaatggtagaagtccagagtcaacagttt cagatcaactccaaggatggcaagacactatttactgtcgatgaaaaggaagttgtggtt ggtacagataaacttcgagtaactgggcccgagggtgctctttttgaacattcagtggag acccccctcgtaagagccgacccatttcaggacctcagattagaatcccccacacggagt ctaagcatggatgccccaaagggtgttcatattaaagctcatgctgggaaaattgaggct ctttctcaaatggatatcatttttcaaagtagtgatggaatgcttgtgcttgatgctgaa actgtgtgtttacccaagttggttcaggggactcagagtgccgccggcaactcacagaga ctgtatgaaatctgtgtgtgtccggatgggaagctttacctgtctgtggctggcgcaggt accacgtgccatgaaaacagtcacatctgtctctaa

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