LOCUS       HM217026                1422 bp    mRNA    linear   HUM 21-JUN-2010
DEFINITION  Homo sapiens cell-line ZZH platelet glycoprotein IV variant (CD36)
            mRNA, complete cds.
ACCESSION   HM217026
VERSION     HM217026.1
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 1422)
  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  JOURNAL   Unpublished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 1422)
  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..1422
                     /db_xref="H-InvDB:HIT000649283"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="7"
                     /map="7q11.2"
                     /cell_line="ZZH"
     gene            1..1422
                     /gene="CD36"
     CDS             89..1390
                     /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="ADI80546.1"
                     /translation="MGCDRNCGLIAGAVIGAVLAVFGGILMPVGDLLIQKTIKKQVVL
                     EEGTIAFKNWVKTGTEVYRQFWIFDVQNPQEVMMNSSNIQVKQRGPYTYRVRFLAKEN
                     VTQDAEDNTVSFLQPNGAIFEPSLSVGTEADNFTVLNLAVAAASHIYQNQFVQMILNS
                     LINKSKSSMFQVRTLRELLWGYRDPFLSLVPYPVTTTVGLFYPYNNTADGVYKVFNGK
                     DNISKVAIIDTYKGKRSIYAVFESDVNLKGIPVYRFVLPSKAFASPVENPDNYCFCTE
                     KIISKNCTSYGVLDISKCKEGRPVYISLPHFLYASPDVSEPIDGLNPNEEEHRTYLDI
                     EPITGFTLQFAKRLQVNLLVKPSEKIQVLKNLKRNYIVPILWLNETGTIGDEKANMFR
                     SQVTGKINLLGLIEMILLSVGVVMFVAFMISYCACRSKTIK"
     variation       790^791
                     /gene="CD36"
                     /note="exon 6 and 7 deletion"
BASE COUNT          456 a          270 c          285 g          411 t
ORIGIN      
        1 accagagctt gtagaaacca ctttaatcat atccaggagt ttgcaagaaa caggtgctta
       61 acactaattc acctcctgaa caagaaaaat gggctgtgac cggaactgtg ggctcatcgc
      121 tggggctgtc attggtgctg tcctggctgt gtttggaggt attctaatgc cagttggaga
      181 cctgcttatc cagaagacaa ttaaaaagca agttgtcctc gaagaaggta caattgcttt
      241 taaaaattgg gttaaaacag gcacagaagt ttacagacag ttttggatct ttgatgtgca
      301 aaatccacag gaagtgatga tgaacagcag caacattcaa gttaagcaaa gaggtcctta
      361 tacgtacaga gttcgttttc tagccaagga aaatgtaacc caggacgctg aggacaacac
      421 agtctctttc ctgcagccca atggtgccat cttcgaacct tcactatcag ttggaacaga
      481 ggctgacaac ttcacagttc tcaatctggc tgtggcagct gcatcccata tctatcaaaa
      541 tcaatttgtt caaatgatcc tcaattcact tattaacaag tcaaaatctt ctatgttcca
      601 agtcagaact ttgagagaac tgttatgggg ctatagggat ccatttttga gtttggttcc
      661 gtaccctgtt actaccacag ttggtctgtt ttatccttac aacaatactg cagatggagt
      721 ttataaagtt ttcaatggaa aagataacat aagtaaagtt gccataatcg acacatataa
      781 aggtaaaagg tcaatctatg ctgtatttga atccgacgtt aatctgaaag gaatccctgt
      841 gtatagattt gttcttccat ccaaggcctt tgcctctcca gttgaaaacc cagacaacta
      901 ttgtttctgc acagaaaaaa ttatctcaaa aaattgtaca tcatatggtg tgctagacat
      961 cagcaaatgc aaagaaggga gacctgtgta catttcactt cctcattttc tgtatgcaag
     1021 tcctgatgtt tcagaaccta ttgatggatt aaacccaaat gaagaagaac ataggacata
     1081 cttggatatt gaacctataa ctggattcac tttacaattt gcaaaacggc tgcaggtcaa
     1141 cctattggtc aagccatcag aaaaaattca agtattaaag aatctgaaga ggaactatat
     1201 tgtgcctatt ctttggctta atgagactgg gaccattggt gatgagaagg caaacatgtt
     1261 cagaagtcaa gtaactggaa aaataaacct ccttggcctg atagaaatga tcttactcag
     1321 tgttggtgtg gtgatgtttg ttgcttttat gatttcatat tgtgcatgca gatcgaaaac
     1381 aataaaataa gtaagtatgt accaaaaaat attgcttcaa tc
//