LOCUS       HM217023                1370 bp    mRNA    linear   HUM 21-JUN-2010
DEFINITION  Homo sapiens cell-line CWS platelet glycoprotein IV variant (CD36)
            mRNA, complete cds.
ACCESSION   HM217023
VERSION     HM217023.1
KEYWORDS    .
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 1370)
  AUTHORS   Wu,G.-G., Curtis,B.R., He,B.-R., Zhou,Z.-L., Zhou,Y., Yang,Y.-L.,
            Li,H.-Y., Shen,W.-D., Liu,J.-L. and Zhao,T.-M.
  TITLE     Frequency of CD36 deficiency and identification of novel CD36 gene
            mutations in the Chinese population
  JOURNAL   Unpublished
REFERENCE   2  (bases 1 to 1370)
  AUTHORS   Wu,G.-G., Curtis,B.R., He,B.-R., Zhou,Z.-L., Zhou,Y., Yang,Y.-L.,
            Li,H.-Y., Shen,W.-D., Liu,J.-L. and Zhao,T.-M.
  TITLE     Direct Submission
  JOURNAL   Submitted (11-MAY-2010) Cytokine Biology Section, NIAID, National
            Institutes of Health, 50 South Drive, Bethesda, MD 20892, USA
FEATURES             Location/Qualifiers
     source          1..1370
                     /db_xref="H-InvDB:HIT000649280"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="7"
                     /map="7q11.2"
                     /cell_line="CWS"
     gene            1..1370
                     /gene="CD36"
     CDS             98..1336
                     /gene="CD36"
                     /note="thrombospondin receptor; fourth major glycoprotein
                     of the platelet surface; receptor for thrombospondin in
                     platelets and various cell lines"
                     /codon_start=1
                     /product="platelet glycoprotein IV variant"
                     /protein_id="ADI80543.1"
                     /translation="MGCDRNCGLIAGAVIGAVLAVFGGILMPVGDLLIQKTIKKQVVL
                     EEGTIAFKNWVKTGTEVYRQFWIFDVQNPQEVMMNSSNIQVKQRGPYTYRVRFLAKEN
                     VTQDAEDNTVSFLQPNGAIFEPSLSVGTEADNFTVLNLAVAYNNTADGVYKVFNGKDN
                     ISKVAIIDTYKGKRNLSYWESHCDMINGTDAASFPPFVEKSQVLQFFSSDICRSIYAV
                     FESDVNLKGIPVYRFVLPSKAFASPVENPDNYCFCTEKIISKNCTSYGVLDISKCKEG
                     RPVYISLPHFLYASPDVSEPIDGLNPNEEEHRTYLDIEPITGFTLQFAKRLQVNLLVK
                     PSEKIQVLKNLKRNYIVPILWLNETGTIGDEKANMFRSQVTGKINLLGLIEMILLSVG
                     VVMFVAFMISYCACRSKTIK"
     variation       526^527
                     /gene="CD36"
                     /note="exon 4 deletion"
BASE COUNT          444 a          254 c          283 g          389 t
ORIGIN      
        1 tgaataagaa ccagagcttg tagaaaccac tttaatcata tccaggagtt tgcaagaaac
       61 aggtgcttaa cactaattca cctcctgaac aagaaaaatg ggctgtgacc ggaactgtgg
      121 gctcatcgct ggggctgtca ttggtgctgt cctggctgtg tttggaggta ttctaatgcc
      181 agttggagac ctgcttatcc agaagacaat taaaaagcaa gttgtcctcg aagaaggtac
      241 aattgctttt aaaaattggg ttaaaacagg cacagaagtt tacagacagt tttggatctt
      301 tgatgtgcaa aatccacagg aagtgatgat gaacagcagc aacattcaag ttaagcaaag
      361 aggtccttat acgtacagag ttcgttttct agccaaggaa aatgtaaccc aggacgctga
      421 ggacaacaca gtctctttcc tgcagcccaa tggtgccatc ttcgaacctt cactatcagt
      481 tggaacagag gctgacaact tcacagttct caatctggct gtggcataca acaatactgc
      541 agatggagtt tataaagttt tcaatggaaa agataacata agtaaagttg ccataatcga
      601 cacatataaa ggtaaaagga atctgtccta ttgggaaagt cactgcgaca tgattaatgg
      661 tacagatgca gcctcatttc caccttttgt tgagaaaagc caggtattgc agttcttttc
      721 ttctgatatt tgcaggtcaa tctatgctgt atttgaatcc gacgttaatc tgaaaggaat
      781 ccctgtgtat agatttgttc ttccatccaa ggcctttgcc tctccagttg aaaacccaga
      841 caactattgt ttctgcacag aaaaaattat ctcaaaaaat tgtacatcat atggtgtgct
      901 agacatcagc aaatgcaaag aagggagacc tgtgtacatt tcacttcctc attttctgta
      961 tgcaagtcct gatgtttcag aacctattga tggattaaac ccaaatgaag aagaacatag
     1021 gacatacttg gatattgaac ctataactgg attcacttta caatttgcaa aacggctgca
     1081 ggtcaaccta ttggtcaagc catcagaaaa aattcaagta ttaaagaatc tgaagaggaa
     1141 ctatattgtg cctattcttt ggcttaatga gactgggacc attggtgatg agaaggcaaa
     1201 catgttcaga agtcaagtaa ctggaaaaat aaacctcctt ggcctgatag aaatgatctt
     1261 actcagtgtt ggtgtggtga tgtttgttgc ttttatgatt tcatattgtg catgcagatc
     1321 gaaaacaata aaataagtaa gtatgtacca aaaaatattg cttcaataat
//