Path: utzoo!utgpu!watserv1!watmath!uunet!mcsun!unido!fauern!ira.uka.de!sol.ctr.columbia.edu!emory!samsung!zaphod.mps.ohio-state.edu!mips!pacbell.com!decwrl!stanford.edu!agate!bionet!root From: GenBank-Updates@genbank.bio.net Newsgroups: bionet.molbio.genbank.updates Subject: Human Duchenne muscular dystrophy protein (DMD) mRNA, 3' end. Message-ID: Date: 14 Mar 91 13:06:54 GMT Sender: root@genbank.bio.net Distribution: bionet Lines: 37 Approved: lear@genbank.bio.net Checksum: 23671 2 LOCUS HUMDMDC 362 bp ss-mRNA PRI 14-MAR-1991 DEFINITION Human Duchenne muscular dystrophy protein (DMD) mRNA, 3' end. ACCESSION M63072 KEYWORDS Duchenne muscular dystrophy protein. SOURCE Human muscle cell, cDNA to mRNA. ORGANISM Homo sapiens Eukaryota; Animalia; Metazoa; Chordata; Vertebrata; Mammalia; Theria; Eutheria; Primates; Haplorhini; Catarrhini; Hominidae. REFERENCE 1 (bases 1 to 362) AUTHORS Chelly,J., Gilgenkrantz,H., Lambert,M., Hamard,G., Chafey,P., Recan,D., Katz,P., de la Chapelle,A., Koenig,M., Ginjaar,I.B., Fardeau,M., Tome,F., Kahn,A. and Kaplan,J.-C. TITLE Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies JOURNAL Cell 63, 1239-1248 (1990) STANDARD full staff_review FEATURES Location/Qualifiers CDS 1..93 /note="deletion of exon 5 causes frame shift and a premature stop codon" /product="Duchenne muscular dystrophy protein" /gene="DMD" /codon_start=1 /partial misc_recomb 66^67 /note="exon 49 DNA end/exon 51 DNA start" /gene="DMD" BASE COUNT 105 a 82 c 89 g 86 t ORIGIN 1 gtggaagaga ttttgtctaa agggcagcat ttgtacaagg aaaaaccagc cactcagcca 61 gtgaagctcc tactcagact gttactctgg tgacacaacc tgtggttact aaggaaactg 121 ccatctccaa actagaaatg ccatcttcct tgatgttgga ggtacctgct ctggcagatt 181 tcaaccgggc ttggacagaa cttaccgact ggctttctct gcttgatcaa gttataaaat 241 cacagagggt gatggtgggt gaccttgagg atatcaacga gatgatcatc aagcagaagg 301 caacaatgca ggatttggaa cagaggcgtc cccagttgga agaactcatt accgctgccc 361 aa //