LOCUS       CR456590                 767 bp    mRNA    linear   HUM 16-OCT-2008
DEFINITION  Homo sapiens SYNGR1 full length open reading frame (ORF) cDNA clone
            (cDNA clone C22ORF:pGEM.SYNGR1).
ACCESSION   CR456590
VERSION     CR456590.1
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 767)
  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 767)
  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.SYNGR1
            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..767
                     /db_xref="H-InvDB:HIT000267524"
                     /organism="Homo sapiens"
                     /chromosome="22"
                     /lab_host="Mach1"
                     /mol_type="mRNA"
                     /clone="pGEM.SYNGR1"
                     /db_xref="taxon:9606"
     CDS             11..715
                     /gene="SYNGR1"
                     /db_xref="GOA:O43759"
                     /db_xref="H-InvDB:HIT000267524.12"
                     /db_xref="HGNC:HGNC:11498"
                     /db_xref="InterPro:IPR008253"
                     /db_xref="InterPro:IPR016579"
                     /db_xref="UniProtKB/Swiss-Prot:O43759"
                     /protein_id="CAG30476.1"
                     /translation="MEGGAYGAGKAGGAFDPYTLVRQPHTILRVVSWLFSIVVFGSIV
                     NEGYLNSASEGEEFCIYNRNPNACSYGVAVGVLAFLTCLLYLALDVYFPQISSVKDRK
                     KAVLSDIGVSAFWAFLWFVGFCYLANQWQVSKPKDNPLNEGTDAARAAIAFSFFSIFT
                     WAGQAVLAFQRYQIGADSALFSQDYMDPSQDSSMPYAPYVEPNTGPDPAGMGGTYQQP
                     ANTFDTEPQGYQSQGY"
BASE COUNT          128 a          285 c          214 g          140 t
ORIGIN      
        1 tgcagccacg atggaagggg gtgcgtacgg agcgggcaaa gccgggggcg ccttcgaccc
       61 ctacaccctg gtccggcagc cgcacaccat cctgcgcgtc gtgtcttggc tgttctccat
      121 agtggtgttc ggctccatcg tgaacgaggg ctacctcaac agcgcctccg agggggagga
      181 gttctgcatc tacaaccgca accccaacgc ctgcagctat ggcgtggccg tgggcgtgct
      241 cgccttcctc acctgcctgc tgtacctggc cctggacgtg tacttcccgc agatcagcag
      301 cgtcaaggac cgcaagaaag ccgtcctgtc cgacatcggt gtctcggcct tctgggcttt
      361 cctctggttc gtgggattct gctacctggc caaccagtgg caggtctcca agcccaagga
      421 caacccactg aacgaaggga cggacgcagc ccgggccgcc atcgccttct cctttttctc
      481 catcttcacc tgggcgggcc aggctgtgct ggccttccag cggtaccaga ttggcgccga
      541 ctcggccctc ttctcccagg actacatgga ccccagccag gactccagca tgccttacgc
      601 gccctacgtg gagcccaaca ctgggccgga tcccgccggt atgggcggca cctaccagca
      661 gccggccaac accttcgaca ccgagcccca gggctaccag tcgcagggct actgagccac
      721 agtgaccgcc tgcccccgcc cctccccatc tgtcccctct ctccaca
//