LOCUS       CR749675                1732 bp    mRNA    linear   HTC 22-SEP-2004
DEFINITION  Homo sapiens mRNA; cDNA DKFZp434I2216 (from clone DKFZp434I2216).
ACCESSION   CR749675
VERSION     CR749675.1
KEYWORDS    HTC.
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 1732)
  AUTHORS   Koehrer K., Beyer A., Mewes H.W., Weil B., Amid C., Osanger A.,
            Fobo G., Han M., Wiemann S.
  CONSRTM   The German cDNA Consortium
  JOURNAL   Submitted (22-SEP-2004) to the INSDC. MIPS, Ingolstaedter
            Landstr.1, D-85764 Neuherberg, GERMANY
COMMENT     Clone from S. Wiemann, Molecular Genome Analysis, German Cancer
            Research
            Center (DKFZ); Email s.wiemann@dkfz-heidelberg.de;
            sequenced by BMFZ (Biomedical Research Center at the
            Heinrich-Heine-University, Duesseldorf/Germany) within the cDNA
            sequencing consortium of the German Genome Project.
            This clone (DKFZp434I2216) is available at the RZPD Deutsches
            Ressourcenzentrum fuer Genomforschung GmbH in Berlin, Germany.
            Please contact RZPD for ordering:
            http://www.rzpd.de/cgi-bin/products/cl.cgi?CloneID=DKFZp434I2216
            Further information about the clone and the sequencing project is
            available at http://mips.gsf.de/projects/cdna/
FEATURES             Location/Qualifiers
     source          1..1732
                     /db_xref="H-InvDB:HIT000306671"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /dev_stage="adult"
                     /clone_lib="434 (synonym: htes3). Vector pSport1; host
                     DH10B; sites NotI + SalI"
                     /clone="DKFZp434I2216"
                     /tissue_type="testis"
                     /note="Williams Beuren syndrome chromosome region 17,
                     N-terminus truncated"
                     /db_xref="taxon:9606"
     CDS             <3..164
                     /codon_start=1
                     /gene="DKFZp434I2216"
                     /product="hypothetical protein"
                     /db_xref="H-InvDB:HIT000306671.12"
                     /db_xref="InterPro:IPR000772"
                     /db_xref="InterPro:IPR035992"
                     /db_xref="UniProtKB/TrEMBL:Q68CW8"
                     /protein_id="CAH18466.1"
                     /translation="SSLYKRWNFIQNGAIMNKGTGRCLEVENRGLAGIDLILRSCTGQ
                     RWTIKNSIK"
BASE COUNT          431 a          490 c          457 g          354 t
ORIGIN      
        1 agagcagcct gtacaagcgc tggaacttca tccagaatgg agccatcatg aacaagggca
       61 cgggacgctg cctggaggtg gagaaccggg gcctggctgg catcgacctc atcctccgca
      121 gctgcacagg tcagaggtgg accattaaga actccatcaa gtagagggag ggagctgggg
      181 cactggagcc tggcccccag gacatggctg ctccccccaa catctggacc agctgccctg
      241 gcggagagac agcaaggggc cggcaggtgc tcgatgggcc ccccagggct tctccagggc
      301 agcacaggga ccccggatga agactctgtc ccccctcagg cattcagctg cccacaagtt
      361 tcctgcaccc tggaaaagcc ccccaccctt cctctgggaa actgacagct gtcttccaca
      421 gcctctgatg tggacctggt actgaggagc aagactgtcc agttctcctc cacatctccc
      481 atcccagaat caggatctgg gactggcagg gtcccctcct gtgtctcatc tcttgcagca
      541 gcagctgctg aactccagcc atcaacacgg tgggaggcag cgggggcttc agccatgtcc
      601 tagctccccg ccctaaaagg aggcagtgag gaccaggcac tatttcctcc gaggttactt
      661 ctacccagat gacacctgcc tgttcacgcc ccaaggcagc tactgcccct aacccttccc
      721 accagggtag ctttgggcac tgcagctctg gacttttctg gcccctcctg agatgacctg
      781 atggagctga tgctttctct cctaatccct gggcactagg ctcttatcag tgtgcttggg
      841 ccagctctcc tgcctgtgtc tagaggaagc cagagacaga aataggctaa gcctgcagta
      901 ggatctcagc cacaagggcc ccgcaggatg gagctgggtc aaggaccagg gagccctgac
      961 tcccagaggc tgccaccggg gagaagcagc ggtcctccat ccagaaccta agggctgaag
     1021 caaaggctgc caggaccctt gaagatgctt ttggctcacc tcatttcacc ccacgctctg
     1081 ctggctggca gaggagaagg cagtcgtttc ctctctgaag agtatttttt tcgattgccc
     1141 tctggttagg gtgcacatat aaatcagagt taatatatga acgcgtgtgc atgcacaagt
     1201 gtgtgtgtgc ctgcgtgctg tgcgtggcag ggtgtgtgtg tgtgtgtctg gctgtgcgtt
     1261 ccggagtgtg tgacgatgct gacctagctg tgtggccttg ggcttgctgc ttcattactc
     1321 acctggatgg ggacgaggga tgagaagggt gtgggtttgg ccccatgtca ctggccggaa
     1381 ggatgtgtct cagccctgcc ctgtggggtg cccccgatgg gaggctgtcc catctcccag
     1441 tccccatctc tttttcccca cactgtccct ggccaagccc tgcccagagc tgaaccctgt
     1501 agctgccccc ttgccctgtg tgggattcgc agtgtctcat ttggtgacgt cttactggtg
     1561 atcatctcct caccccatct cccaccttgt ggaataaata catgttagca cttccaaaaa
     1621 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa
     1681 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aa
//