LOCUS       AB025256                 887 bp    mRNA    linear   HUM 27-MAR-2002
DEFINITION  Homo sapiens Fc-gamma receptor IIIB mRNA for Fc-gamma receptor
            IIIb (CD 16), complete cds.
ACCESSION   AB025256
VERSION     AB025256.1
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 887)
  AUTHORS   Watanabe,Y.
  TITLE     Direct Submission
  JOURNAL   Submitted (23-MAR-1999) to the DDBJ/EMBL/GenBank databases.
            Contact:Yoshihisa Watanabe
            Japanese Red Cross Central Blood Center, Transfusion Information
            Department; 4-1-31 Hiroo, Shibuya-ku, Tokyo 150-0012, Japan
REFERENCE   2
  AUTHORS   Watanabe,Y., Shimada,E., Fujiwara,K., Niihara,H., Shimano,K.,
            Mitsunaga,S., Tadokoro,K. and Juji,T.
  TITLE     Nucleotide sequence of a new Fc gamma receptor IIIB allele that
            codes for a neutrophil antigen
  JOURNAL   Tissue Antigens 56, 272-275 (2000)
COMMENT     
FEATURES             Location/Qualifiers
     source          1..887
                     /cell_line="primary-peripheral blood granulocytes"
                     /db_xref="H-InvDB:HIT000058829"
                     /db_xref="taxon:9606"
                     /mol_type="mRNA"
                     /organism="Homo sapiens"
     CDS             34..735
                     /codon_start=1
                     /db_xref="IMGT/LIGM:AB025256"
                     /gene="Fc-gamma receptor IIIB"
                     /product="Fc-gamma receptor IIIb (CD 16)"
                     /protein_id="BAA83803.1"
                     /transl_table=1
                     /translation="MWQLLLPTALLLLVSAGMRTEDLPKAVVFLEPQWYSVLEKDSVT
                     LKCQGAYSPKDNSTQWFHNESLISSQASSYFIDAATVNDSGEYRCQTNLSTLSDPVQL
                     EVHIGWLLLQAPRWVFKEEDPIHLRCHSWKNTALHKVTYLQNGKDRKYFHHNSDFHIP
                     KATLKDSGSYFCRGLVGSKNVSSETVNITITQGLAVSTISSFSPPGYQVSFCLVMVLL
                     FAVDTGLYFSVKTNI"
     variation       193
                     /note="Lys is Glu in allele(NA-2), Acc#:X16863"
                     /note="a is g in allele(NA-2), Acc#:X16863"
                     /replace="g"
BASE COUNT          229 a          236 c          205 g          217 t
ORIGIN      
        1 tctttggtga cttgtccact ccagtgtggc atcatgtggc agctgctcct cccaactgct
       61 ctgctacttc tagtttcagc tggcatgcgg actgaagatc tcccaaaggc tgtggtgttc
      121 ctggagcctc aatggtacag cgtgcttgag aaggacagtg tgactctgaa gtgccaggga
      181 gcctactccc ctaaggacaa ttccacacag tggtttcaca atgagagcct catctcaagc
      241 caggcctcga gctacttcat tgacgctgcc acagtcaacg acagtggaga gtacaggtgc
      301 cagacaaacc tctccaccct cagtgacccg gtgcagctag aagtccatat cggctggctg
      361 ttgctccagg cccctcggtg ggtgttcaag gaggaagacc ctattcacct gaggtgtcac
      421 agctggaaga acactgctct gcataaggtc acatatttac agaatggcaa agacaggaag
      481 tattttcatc ataattctga cttccacatt ccaaaagcca cactcaaaga tagcggctcc
      541 tacttctgca gggggcttgt tgggagtaaa aatgtgtctt cagagactgt gaacatcacc
      601 atcactcaag gtttggcagt gtcaaccatc tcatcattct ctccacctgg gtaccaagtc
      661 tctttctgct tggtgatggt actccttttt gcagtggaca caggactata tttctctgtg
      721 aagacaaaca tttgaagctc aacaagagac tggaaggacc ataaacttaa atggagaaag
      781 gaccctcaag acaaatgacc cccatcccat gggagtaata agagcagtgg cagcagcatc
      841 tctgaacatt tctctggatt tgcaacccca tcatcctcag gcctctc
//