Homo sapiens (human): 2010 Help Entry 2010              CDS       T01001                                  Symbol EMD, EDMD, LEMD5, STA Name (RefSeq) emerin   KO K12569   emerin Organism hsa  Homo sapiens (human) Pathway hsa04820   Cytoskeleton in muscle cells hsa05410   Hypertrophic cardiomyopathy hsa05412   Arrhythmogenic right ventricular cardiomyopathy hsa05414   Dilated cardiomyopathy Network nt06539  Cytoskeleton in muscle cells   Element N01822   Linker of nucleoskeleton and cytoskeleton (LINC) complex Disease H00563   Emery-Dreifuss muscular dystrophy Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09142 Cell motility    04820 Cytoskeleton in muscle cells     2010 (EMD)  09160 Human Diseases   09166 Cardiovascular disease    05410 Hypertrophic cardiomyopathy     2010 (EMD)    05412 Arrhythmogenic right ventricular cardiomyopathy     2010 (EMD)    05414 Dilated cardiomyopathy     2010 (EMD) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  LEM DotU MGC-24 Motif Other DBs NCBI-GeneID:  2010 NCBI-ProteinID:  NP_000108 OMIM:  300384 HGNC:  3331 Ensembl:  ENSG00000102119 UniProt:  P50402 Structure PDB LinkDB All DBs Position X:154379295..154381523 Genome browser AA seq 254 aa AA seqDB search MDNYADLSDTELTTLLRRYNIPHGPVVGSTRRLYEKKIFEYETQRRRLSPPSSSAASSYS FSDLNSTRGDADMYDLPKKEDALLYQSKGYNDDYYEESYFTTRTYGEPESAGPSRAVRQS VTSFPDADAFHHQVHDDDLLSSSEEECKDRERPMYGRDSAYQSITHYRPVSASRSSLDLS YYPTSSSTSFMSSSSSSSSWLTRRAIRPENRAPGAGLGQDRQVPLWGQLLLFLVFVIVLF FIYHFMQAEEGNPF NT seq 765 nt NT seq  +upstreamnt  +downstreamnt atggacaactacgcagatctttcggataccgagctgaccaccttgctgcgccggtacaac atcccgcacgggcctgtagtaggatcaactcgtaggctttacgagaagaagatcttcgag tacgagacccagaggcggcggctctcgccccccagctcgtccgccgcctcctcttatagc ttctctgacttgaattcgactagaggggatgcagatatgtatgatcttcccaagaaagag gacgctttactctaccagagcaagggctacaatgacgactactatgaagagagctacttc accaccaggacttatggggagcccgagtctgccggcccgtccagggctgtccgccagtca gtgacttcattcccagatgctgacgctttccatcaccaggtgcatgatgacgatcttttg tcttcttctgaagaggagtgcaaggatagggaacgccccatgtacggccgggacagtgcc taccagagcatcacgcactaccgccctgtttcagcctccaggagctccctggacctgtcc tattatcctacttcctcctccacctcttttatgtcctcctcatcatcttcctcttcatgg ctcacccgccgtgccatccggcctgaaaaccgtgctcctggggctgggctgggccaggat cgccaggtcccgctctggggccagctgctgcttttcctggtctttgtgatcgtcctcttc ttcatttaccacttcatgcaggctgaagaaggcaaccccttctag

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