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 JOURNAL Unpublished (2006) COMMENT FEATURES Location/Qualifiers source 1..1363 /cell_type="granulocyte" /chromosome="19" /country="Japan" /db_xref="H-InvDB:HIT000330040"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 //