LOCUS       HM217025                1359 bp    mRNA    linear   HUM 21-JUN-2010
DEFINITION  Homo sapiens cell-line WGM platelet glycoprotein IV variant (CD36)
            mRNA, complete cds.
ACCESSION   HM217025
VERSION     HM217025.1
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 1359)
  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  JOURNAL   Unpublished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 1359)
  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..1359
                     /db_xref="H-InvDB:HIT000649282"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="7"
                     /map="7q11.2"
                     /cell_line="WGM"
     gene            1..1359
                     /gene="CD36"
     CDS             98..964
                     /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="ADI80545.1"
                     /translation="MGCDRNCGLIAGAVIGAVLAVFGGILMPVGDLLIQKTIKKQVVL
                     EEGTIAFKNWVKTGTEVYRQFWIFDVQNPQEVMMNSSNIQVKQRGPYTYRVRFLAKEN
                     VTQDAEDNTVSFLQPNGAIFEPSLSVGTEADNFTVLNLAVAAASHIYQNQFVQMILNS
                     LINKSKSSMFQVRTLRELLWGYRDPFLSLVPYPVTTTVGLFYPYNNTADGVYKVFNGK
                     DNISKVAIIDTYKGKRNLSYWESHCDMINGTDAASFPPFVEKSQVLQFFSSDICRETC
                     VHFTSSFSVCKS"
     variation       913^914
                     /gene="CD36"
                     /note="exon 8 deletion"
BASE COUNT          429 a          253 c          280 g          397 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 gtggcagctg catcccatat
      541 ctatcaaaat caatttgttc aaatgatcct caattcactt attaacaagt caaaatcttc
      601 tatgttccaa gtcagaactt tgagagaact gttatggggc tatagggatc catttttgag
      661 tttggttccg taccctgtta ctaccacagt tggtctgttt tatccttaca acaatactgc
      721 agatggagtt tataaagttt tcaatggaaa agataacata agtaaagttg ccataatcga
      781 cacatataaa ggtaaaagga atctgtccta ttgggaaagt cactgcgaca tgattaatgg
      841 tacagatgca gcctcatttc caccttttgt tgagaaaagc caggtattgc agttcttttc
      901 ttctgatatt tgcagggaga cctgtgtaca tttcacttcc tcattttctg tatgcaagtc
      961 ctgatgtttc agaacctatt gatggattaa acccaaatga agaagaacat aggacatact
     1021 tggatattga acctataact ggattcactt tacaatttgc aaaacggctg caggtcaacc
     1081 tattggtcaa gccatcagaa aaaattcaag tattaaagaa tctgaagagg aactatattg
     1141 tgcctattct ttggcttaat gagactggga ccattggtga tgagaaggca aacatgttca
     1201 gaagtcaagt aactggaaaa ataaacctcc ttggcctgat agaaatgatc ttactcagtg
     1261 ttggtgtggt gatgtttgtt gcttttatga tttcatattg tgcatgcaga tcgaaaacaa
     1321 taaaataagt aagtatgtac caaaaaatat tgcttcaat
//