LOCUS       HUMMEF2X                1919 bp    mRNA    linear   HUM 01-APR-1996
DEFINITION  Human transcription factor (MEF2) mRNA, complete cds.
ACCESSION   L16794
VERSION     L16794.1
KEYWORDS    alternative splicing; transcription factor.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
REFERENCE   1  (bases 1 to 1919)
  AUTHORS   Breitbart,R.E., Liang,C.S., Smoot,L.B., Laheru,D.A., Mahdavi,V. and
            Nadal-Ginard,B.
  TITLE     A fourth human MEF2 transcription factor, hMEF2D, is an early
            marker of the myogenic lineage
  JOURNAL   Development 118 (4), 1095-1106 (1993)
   PUBMED   8269842
COMMENT     Original source text: Homo sapiens (tissue library: lambda ZAP)
            myocardium cDNA to mRNA.
FEATURES             Location/Qualifiers
     source          1..1919
                     /db_xref="H-InvDB:HIT000192291"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /tissue_type="myocardium"
                     /tissue_lib="lambda ZAP"
     gene            1..1919
                     /gene="MEF2"
     5'UTR           1..195
                     /gene="MEF2"
     CDS             196..1761
                     /gene="MEF2"
                     /codon_start=1
                     /product="transcription factor"
                     /protein_id="AAA93194.1"
                     /translation="MGRKKIQIQRITDERNRQVTFTKRKFGLMKKAYELSVLCDCEIA
                     LIIFNHSNKLFQYASTDMDKVLLKYTEYNEPHESRTNADIIETLRKKGFNGCDSPEPD
                     GEDSLEQSPLLEDKYRRASEELDGLFRRYGSTVPAPNFAMPVTVPVSNQSSLQFSNPS
                     GSLVTPSLVTSSLTDPRLLSPQQPALQRNSVSPGLPQRPASAGAMLGGDLNSANGACP
                     SPVGNGYVSARASPGLLPVANGNSLNKVIPAKSPPPPTHSTQLGAPSRKPDLRVITSQ
                     AGKGLMHHLTEDHLDLNNAQRLGVSQSTHSLTTPVVSVATPSLLSQGLPFSSMPTAYN
                     TDYQLTSAELSSLPAFSSPGGLSLGNVTAWQQPQQPQQPQQPQPPQQQPPQPQQPQPQ
                     QPQQPQQPPQQQSHLVPVSLSNLIPGSPLPHVGAALTVTTHPHISIKSEPVSPSRERS
                     PAPPPPAVFPAARPEPGDGLSSPAGGSYETGDRDDGRGDFGPTLGLLRPAPEPEAEGS
                     AVKRMRLDTWTLK"
     misc_feature    749..1033
                     /gene="MEF2"
                     /note="Human Genome Project EST00076"
     3'UTR           1762..1919
                     /gene="MEF2"
BASE COUNT          398 a          685 c          495 g          341 t
ORIGIN      
        1 caggggcgag ggctacccgc tctttgccgt gacaacaccg ttcccccagc cgggctggag
       61 gctgtgcaga aggtatcctg cagaccatga actgagcact gttcccagac cgttcatgag
      121 cacagtgtaa ggtgtgccga gacccaccac ccagcgagcc cctcccctcc gtagcactga
      181 ggacccccgg agaagatggg gaggaaaaag attcagatcc agcgaatcac cgacgagcgg
      241 aaccgacagg tgactttcac caagcggaag tttggcctga tgaagaaggc gtatgagctg
      301 agcgtgctat gtgactgcga gatcgcactc atcatcttca accactccaa caagctgttc
      361 cagtacgcca gcaccgacat ggacaaggtg ctgctcaagt acacggagta caatgagcca
      421 cacgagagcc gcaccaacgc cgacatcatc gagaccctga ggaagaaggg cttcaatggc
      481 tgcgacagcc ccgagcccga cggggaggac tcgctggaac agagccccct gctggaggac
      541 aagtaccgac gcgccagcga ggagctcgac gggctcttcc ggcgctatgg gtcaactgtc
      601 ccggccccca actttgccat gcctgtcacg gtgcccgtgt ccaatcagag ctcactgcag
      661 ttcagcaatc ccagcggctc cctggtcacc ccttccctgg tgacatcatc cctcacggac
      721 ccgcggctcc tgtcccccca gcagccagca ctacagagga acagtgtgtc tcctggcctg
      781 ccccagcggc cagctagtgc gggggccatg ctggggggtg acctgaacag tgctaacgga
      841 gcctgcccca gccctgttgg gaatggctac gtcagtgctc gggcttcccc tggcctcctc
      901 cctgtggcca atggcaacag cctaaacaag gtcatccctg ccaagtctcc gcccccacct
      961 acccacagca cccagcttgg agcccccagc cgcaagcccg acctgcgagt catcacttcc
     1021 caggcaggaa aggggttaat gcatcacttg actgaggacc atttagatct gaacaatgcc
     1081 cagcgccttg gggtctccca gtctactcat tcgctcacca ccccagtggt ttctgtggca
     1141 acgccgagtt tactcagcca gggcctcccc ttctcttcca tgcccactgc ctacaacaca
     1201 gattaccagt tgaccagtgc agagctctcc tccttaccag cctttagttc acctgggggg
     1261 ctgtcgctag gcaatgtcac tgcctggcaa cagccacagc agccccagca gccgcagcag
     1321 ccacagcctc cacagcagca gccaccgcag ccacagcagc cacagccaca gcagcctcag
     1381 cagccgcaac agccacctca gcaacagtcc cacctggtcc ctgtatctct cagcaacctc
     1441 atcccgggca gccccctgcc ccacgtgggt gctgccctca cagtcaccac ccacccccac
     1501 atcagcatca agtcagaacc ggtgtcccca agccgtgagc gcagccctgc gcctccccct
     1561 ccagctgtgt tcccagctgc ccgccctgag cctggcgatg gtctcagcag cccagccggg
     1621 ggatcctatg agacgggaga ccgggatgac ggacgggggg acttcgggcc cacactgggc
     1681 ctgctgcgcc cagccccaga gcctgaggct gagggctcag ctgtgaagag gatgcggctt
     1741 gatacctgga cattaaagtg acgattccca ctcccctcct ctcagcctcc ctgatgaaga
     1801 gttgacaatc tcaccgcccg cccttccctg ccccgggctc ctcccgctcg acccccactt
     1861 cctttcttgt gcttcgtgtc ctgttgacgg ttacatttgt gtataattat tatattatt
//