LOCUS       AB237911                1363 bp    mRNA    linear   HUM 03-JUN-2021
DEFINITION  Homo sapiens CD177 mRNA for CD177, complete cds.
ACCESSION   AB237911
VERSION     AB237911.1
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 1363)
  AUTHORS   Odagiri,M., Watanabe,Y. and Kamata,H.N.
  TITLE     Direct Submission
  JOURNAL   Submitted (12-OCT-2005) to the DDBJ/EMBL/GenBank databases.
            Contact:Yoshihisa Watanabe
            Japanese Red Cross Central Blood Institute, Research and
            Development Department; 3-30-1 Nakarokugo, Ota-ku, Tokyo 144-0055,
            Japan
REFERENCE   2
  AUTHORS   Odagiri,M., Watanabe,Y., Kamata,H.N., Mazda,T., Okazaki,H.,
            Ohshima,H. and Juji,T.
  TITLE     Loss of HNA-2a(NB1,CD177) expression on the neutrophil surface
            caused by a nonsense mutation in the carboxyl-terminal signal for
            GPI modification.
  JOURNAL   Unpublished (2006)
COMMENT     
FEATURES             Location/Qualifiers
     source          1..1363
                     /cell_type="granulocyte"
                     /chromosome="19"
                     /country="Japan"
                     /db_xref="H-InvDB:HIT000330040"
                     /db_xref="taxon:9606"
                     /map="19q13,31"
                     /mol_type="mRNA"
                     /organism="Homo sapiens"
     CDS             9..1262
                     /codon_start=1
                     /gene="CD177"
                     /product="CD177"
                     /protein_id="BAE93254.1"
                     /transl_table=1
                     /translation="MSAVLLLALLGFILPLPGVQALLCQFGTVQHVWKVSDLPRQWTP
                     KNTSCDSGLGCQDTLMLIESGPQVSLVLSKGCTEAKDQEPRVTEHRMGPGLSLISYTF
                     VCRQEDFCNNLVNSLPLWAPQPPADPGSLRCPVCLSMEGCLEGTTEEICPKGTTHCYD
                     GLLRLRGGGIFSNLRVQGCMPQPGCNLLNGTQEIGPVGMTENCNRKDFLTCHRGTTIM
                     THGNLAQEPTDWTTSNTEMCEVGQVCQEMLLLIDVGLTSTLVGTKGCSTVGAQNSQKT
                     TIHSAPPGVLVASYTHFCSSDLCNSASSSSVLLNSLPPQAAPVPGDRQCPTCVQPLGT
                     CSSGSPRMTCPRGATHCYDGYIHLSGGGLSTKMSIQGCVAQPSSFLLNHTRQIGIFSA
                     REKRDVQPPASQHEGGGAEGLESLT"
     exon            9..60
                     /gene="CD177"
     exon            61..201
                     /gene="CD177"
     exon            202..387
                     /gene="CD177"
     exon            388..510
                     /gene="CD177"
     exon            511..627
                     /gene="CD177"
     exon            628..768
                     /gene="CD177"
     variation       748
                     /inference="similar to sequence:INSD:AF146747.1"
                     /note="This substitution causes an amino acid
                     substitution from Thr to Met."
                     /replace="c"
     exon            769..954
                     /gene="CD177"
     exon            955..1089
                     /gene="CD177"
     exon            1090..1262
                     /gene="CD177"
     variation       1262
                     /inference="similar to sequence:INSD:AF146747.1"
                     /note="This substitution causes substitution from Trp to
                     stop codon."
                     /replace="g"
BASE COUNT          274 a          418 c          389 g          282 t
ORIGIN      
        1 gacgggtcat gagcgcggta ttactgctgg ccctcctggg gttcatcctc ccactgccag
       61 gagtgcaggc gctgctctgc cagtttggga cagttcagca tgtgtggaag gtgtccgacc
      121 tgccccggca atggacccct aagaacacca gctgcgacag cggcttgggg tgccaggaca
      181 cgttgatgct cattgagagc ggaccccaag tgagcctggt gctctccaag ggctgcacgg
      241 aggccaagga ccaggagccc cgcgtcactg agcaccggat gggccccggc ctctccctga
      301 tctcctacac cttcgtgtgc cgccaggagg acttctgcaa caacctcgtt aactccctcc
      361 cgctttgggc cccacagccc ccagcagacc caggatcctt gaggtgccca gtctgcttgt
      421 ctatggaagg ctgtctggag gggacaacag aagagatctg ccccaagggg accacacact
      481 gttatgatgg cctcctcagg ctcaggggag gaggcatctt ctccaatctg agagtccagg
      541 gatgcatgcc ccagccaggt tgcaacctgc tcaatgggac acaggaaatt gggcccgtgg
      601 gtatgactga gaactgcaat aggaaagatt ttctgacctg tcatcggggg accaccatta
      661 tgacacacgg aaacttggct caagaaccca ctgattggac cacatcgaat accgagatgt
      721 gcgaggtggg gcaggtgtgt caggagatgc tgctgctcat agatgtagga ctcacatcaa
      781 ccctggtggg gacaaaaggc tgcagcactg ttggggctca aaattcccag aagaccacca
      841 tccactcagc ccctcctggg gtgcttgtgg cctcctatac ccacttctgc tcctcggacc
      901 tgtgcaatag tgccagcagc agcagcgttc tgctgaactc cctccctcct caagctgccc
      961 ctgtcccagg agaccggcag tgtcctacct gtgtgcagcc ccttggaacc tgttcaagtg
     1021 gctccccccg aatgacctgc cccaggggcg ccactcattg ttatgatggg tacattcatc
     1081 tctcaggagg tgggctgtcc accaaaatga gcattcaggg ctgcgtggcc caaccttcca
     1141 gcttcttgtt gaaccacacc agacaaatcg ggatcttctc tgcgcgtgag aagcgtgatg
     1201 tgcagcctcc tgcctctcag catgagggag gtggggctga gggcctggag tctctcactt
     1261 gaggggtggg gctggcactg gccccagcgc tgtggtgggg agtggtttgc ccttcctgct
     1321 aactctatta cccccacgat tcttcaccgc tgctgaccac cca
//