LOCUS       CR456598                1102 bp    mRNA    linear   HUM 29-JUL-2008
DEFINITION  Homo sapiens TST full length open reading frame (ORF) cDNA clone
            (cDNA clone C22ORF:pGEM.TST).
ACCESSION   CR456598
VERSION     CR456598.1
KEYWORDS    CDNA; chromosome 22; ORF.
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 1102)
  AUTHORS   Collins J.E., Wright C.L., Edwards C.A., Davis M.P., Grinham J.A.,
            Cole C.G., Goward M.E., Aguado B., Mallya M., Mokrab Y.,
            Huckle E.J., Beare D.M., Dunham I.
  TITLE     A genome annotation-driven approach to cloning the human ORFeome
  JOURNAL   Genome Biol. 5(10), R84-R84(2004).
   PUBMED   15461802
REFERENCE   2  (bases 1 to 1102)
  AUTHORS   Collins J.E., Wright C.L., Edwards C.A., Davis M.P., Grinham J.A.,
            Cole C.G., Goward M.E., Aguado B., Mallya M., Mokrab Y.,
            Huckle E.J., Beare D.M., Dunham I.
  JOURNAL   Submitted (23-MAR-2006) to the INSDC. Sanger Institute, Hinxton,
            Cambridgeshire, CB10 1SA, UK. E-mail enquiries: c22g@sanger.ac.uk
COMMENT     Sanger Institute name : pGEM.TST
            Homo sapiens cDNA sequence. This sequence was generated as part of
            The Wellcome Trust Sanger Institute program to isolate cDNA clones
            representing the full length open reading frame of well annotated
            protein coding genes on human chromosome 22.  For more information
            see http://www.sanger.ac.uk/HGP/Chr22/ORFcloning
FEATURES             Location/Qualifiers
     source          1..1102
                     /db_xref="H-InvDB:HIT000267532"
                     /organism="Homo sapiens"
                     /chromosome="22"
                     /lab_host="Mach1"
                     /mol_type="mRNA"
                     /clone="pGEM.TST"
                     /db_xref="taxon:9606"
     CDS             79..972
                     /gene="TST"
                     /db_xref="GOA:Q16762"
                     /db_xref="H-InvDB:HIT000267532.12"
                     /db_xref="HGNC:HGNC:12388"
                     /db_xref="InterPro:IPR001307"
                     /db_xref="InterPro:IPR001763"
                     /db_xref="InterPro:IPR036873"
                     /db_xref="UniProtKB/Swiss-Prot:Q16762"
                     /protein_id="CAG30484.1"
                     /translation="MVHQVLYRALVSTKWLAESIRTGKLGPGLRVLDASWYSPGTREA
                     RKEYLERHVPGASFFDIEECRDTASPYEMMLPSEAGFAEYVGRLGISNHTHVVVYDGE
                     HLGSFYAPRVWWMFRVFGHRTVSVLNGGFRNWLKEGHPVTSEPSRPEPAVFKATLDRS
                     LLKTYEQVLENLESKRFQLVDSRSQGRFLGTEPEPDAVGLDSGHIRGAVNMPFMDFLT
                     EDGFEKGPEELRALFQTKKVDLSQPLIATCRKGVTACHVALAAYLCGKPDVAVYDGSW
                     SEWFRRAPPESRVSQGKSEKA"
BASE COUNT          198 a          340 c          331 g          233 t
ORIGIN      
        1 acacaccgac ttccttcctc acgcctgtct ctctttcctg gttcccaccc gtgccaggtg
       61 acacgcagag ctgaagccat ggttcatcag gtgctctacc gggcgctggt ctccaccaag
      121 tggctggcgg agtccatcag gactggcaag ctggggcccg gcctgcgggt gctggacgcg
      181 tcctggtact caccaggcac ccgagaggcc cgcaaggagt acctcgagcg ccacgtaccc
      241 ggcgcctctt tctttgacat agaagagtgc cgggacacgg cgtcgcccta cgagatgatg
      301 ctgcccagcg aggctggctt cgccgagtat gtgggccgcc tgggcatcag caaccacacg
      361 cacgtggtgg tgtatgatgg tgaacacctg ggcagcttct atgctccccg ggtctggtgg
      421 atgttccgtg tgtttggcca ccgcaccgta tcagtgctca atggtggctt ccggaactgg
      481 ctgaaggagg gccacccggt gacatccgag ccctcacgcc cagaaccggc cgtcttcaaa
      541 gccacactgg accgctccct gctcaagacc tacgagcagg tgctggagaa ccttgaatct
      601 aagaggttcc agctggtgga ttcaaggtct caagggcggt tcctgggcac cgagccggag
      661 ccggatgcag taggactgga ctcgggccat atccgtggtg ccgtcaacat gcctttcatg
      721 gacttcctga ctgaggatgg cttcgagaag ggcccagaag agctccgtgc tctgttccag
      781 accaagaagg tggatctctc gcagcctctc attgccacgt gccgcaaggg agtcaccgcc
      841 tgccacgtgg ccttggctgc ctacctctgc ggcaagcctg atgtggccgt gtacgatggc
      901 tcctggtccg agtggtttcg ccgggccccc ccagagagcc gtgtgtccca gggaaagtct
      961 gagaaggcct gagccgtgac ctcttctgct tactgtaact gcggccggtt tagtgacccc
     1021 atgacttaca gccggttctt acctcttagg tgaaggagat gacatgtttt tagaattgct
     1081 gtgcaaggct caccctctct ct
//