LOCUS       AL137431                1905 bp    mRNA    linear   HTC 22-SEP-2004
DEFINITION  Homo sapiens mRNA; cDNA DKFZp761D2324 (from clone DKFZp761D2324).
ACCESSION   AL137431
VERSION     AL137431.1
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 1905)
  AUTHORS   Bloecker H., Boecher M., Brandt P., 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 GBF (National Research Centre for Biotechnology Ltd.,
            Braunschweig/Germany) within the cDNA sequencing consortium of the
            German
            Genome Project.
            This clone (DKFZp761D2324) 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=DKFZp761D2324
            Further information about the clone and the sequencing project is
            available at http://mips.gsf.de/projects/cdna/
FEATURES             Location/Qualifiers
     source          1..1905
                     /db_xref="H-InvDB:HIT000025719"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /dev_stage="adult"
                     /clone_lib="761 (synonym: hamy2). Vector pSport1; host
                     DH10B; sites NotI + SalI"
                     /clone="DKFZp761D2324"
                     /tissue_type="amygdala"
                     /note="Williams Beuren syndrome chromosome region 17,
                     N-terminus truncated"
                     /db_xref="taxon:9606"
     CDS             <3..404
                     /codon_start=1
                     /gene="DKFZp761D2324"
                     /product="hypothetical protein"
                     /db_xref="GOA:Q6IS24"
                     /db_xref="H-InvDB:HIT000025719.20"
                     /db_xref="HGNC:HGNC:16347"
                     /db_xref="InterPro:IPR000772"
                     /db_xref="InterPro:IPR001173"
                     /db_xref="InterPro:IPR029044"
                     /db_xref="InterPro:IPR035992"
                     /db_xref="UniProtKB/Swiss-Prot:Q6IS24"
                     /protein_id="CAB70734.1"
                     /translation="YGELRNNKAKDVCLDQGPLENHTAILYPCHGWGPQLARYTKEGF
                     LHLGALGTTTLLPDTRCLVDNSKSRLPQLLDCDKVKSSLYKRWNFIQNGAIMNKGTGR
                     CLEVENRGLAGIDLILRSCTGQRWTIKNSIK"
BASE COUNT          417 a          572 c          522 g          394 t
ORIGIN      
        1 cttacgggga gcttcgcaac aacaaggcaa aagacgtctg cttggaccag gggccgctgg
       61 agaaccacac agcaatattg tatccgtgcc atggctgggg accacagctt gcccgctaca
      121 ccaaggaagg cttcctgcac ttgggtgccc tggggaccac cacactcctc cctgacaccc
      181 gctgcctggt ggacaactcc aagagtcggc tgccccagct cctggactgc gacaaggtca
      241 agagcagcct gtacaagcgc tggaacttca tccagaatgg agccatcatg aacaagggca
      301 cgggacgctg cctggaggtg gagaaccggg gcctggctgg catcgacctc atcctccgca
      361 gctgcacagg tcagaggtgg accattaaga actccatcaa gtagagggag ggagctgggg
      421 cactggagcc tggcccccag gacatggctc ctccccccaa catctggacc agctgccctg
      481 gcggagagac agcaaggggc cggcaggtgc tcgatgggcc ccccagggct tctccagggc
      541 agcacaggga ccccggatga agactctgtc ccccctcagg cattcagctg cccacaagtt
      601 tcctgcaccc tggaaaagcc ccccaccctt cctctgggaa actgacagct gtcttccaca
      661 gcctctgatg tggacctggt actgaggagc aagactgtcc agttctcctc cacatctccc
      721 atcccagaat caggatctgg gactggcagg gtcccctcct gtgtctcatc tcttgcagca
      781 gcagctgctg aactccagcc atcaacacgg tgggaggcag cgggggcttc agccatgtcc
      841 tagctccccg ccctaaaagg aggcagtgag gaccaggcac tatttcctcc gaggttactt
      901 ctacccagat gacacctgcc tgttcacgcc ccaaggcagc tactgcccct aacccttccc
      961 accagggtag ctttgggcac tgcagctctg gacttttctg gcccctcctg agatgacctg
     1021 atggagctga tgctttctct cctaatccct gggcactagg ctcttatcaa tgtgcttggg
     1081 ccagctctcc tgcctgtgtc tagaggaagc cagagacaga aataggctaa gcctgcagta
     1141 ggatctcagc cacaagggcc ccgcaggatg gagctgggtc aaggaccagg gagccctgac
     1201 tcccagaggc tgccaccggg gagaagcagc ggtcctccat ccagaaccta agggctgaag
     1261 caaaggctgc caggaccctt gaagatgctt ttggctcacc tcatttcacc ccacgctctg
     1321 ctggctggca gaggagaagg cagtcgtttc ctctctgaag agtatttttt tcgattgccc
     1381 tctggttagg gtgcacatat aaatcagagt taatatatga acgcgtgtgc atgcacaagt
     1441 gtgtgtgtgc ctgcgtgctg tgcgtggcag ggtgtgtgtg tgtgtgtctg gctgtgcgtt
     1501 ccggagtgtg tgacgatgct gacctagctg tgtggccttg ggcttgctgc ttcattactc
     1561 acctggatgg ggacgaggga tgagaagggt gtgggtttgg ccccatgtca ctggccggaa
     1621 ggatgtgtct cagccctgcc ctgtggggtg cccccgatgg gaggctgtcc catctcccag
     1681 tccccatctc tttttcccca cactgtccct ggccaagccc tgcccagagc tgaaccctgt
     1741 agctgccccc ttgccctgtg tgggattcgc agtgtctcat ttggtgacgt cttactggtg
     1801 atcatctcct caccccatct cccaccttgt ggaataaata catgttagca cttcccaaaa
     1861 aaaaaaaaaa aaaaaaaaaa aaaaagaaaa aaaaaaaaaa aaaaa
//