ID   O43705_HUMAN            Unreviewed;        59 AA.
AC   O43705;
DT   01-JUN-1998, integrated into UniProtKB/TrEMBL.
DT   01-JUN-1998, sequence version 1.
DT   22-FEB-2023, entry version 75.
DE   SubName: Full=Platelet glycoprotein IX {ECO:0000313|EMBL:BAA24428.1};
DE   Flags: Fragment;
OS   Homo sapiens (Human).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
OX   NCBI_TaxID=9606 {ECO:0000313|EMBL:BAA24428.1};
RN   [1] {ECO:0000313|EMBL:BAA24428.1}
RP   NUCLEOTIDE SEQUENCE.
RX   PubMed=9432024; DOI=10.1046/j.1365-2141.1997.4753275.x;
RA   Suzuki K., Hayashi T., Yahagi A., Akiba J., Tajima K., Satoh S., Sasaki H.;
RT   "Novel point mutation in the leucine-rich motif of the platelet
RT   glycoprotein IX associated with Bernard-Soulier syndrome.";
RL   Br. J. Haematol. 99:794-800(1997).
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DR   EMBL; D89621; BAA24428.1; -; Genomic_DNA.
DR   AlphaFoldDB; O43705; -.
DR   PeptideAtlas; O43705; -.
DR   Gene3D; 3.80.10.10; Ribonuclease Inhibitor; 1.
DR   InterPro; IPR001611; Leu-rich_rpt.
DR   InterPro; IPR032675; LRR_dom_sf.
DR   PANTHER; PTHR22650; GLYCOPROTEIN IB BETA; 1.
DR   PANTHER; PTHR22650:SF6; PLATELET GLYCOPROTEIN IX; 1.
DR   Pfam; PF13855; LRR_8; 1.
DR   SUPFAM; SSF52058; L domain-like; 1.
PE   4: Predicted;
FT   REGION          36..59
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   NON_TER         1
FT                   /evidence="ECO:0000313|EMBL:BAA24428.1"
FT   NON_TER         59
FT                   /evidence="ECO:0000313|EMBL:BAA24428.1"
SQ   SEQUENCE   59 AA;  6434 MW;  6C138A00835F3FF5 CRC64;
     MGLWVDCRGH GLTALPALPA RTRHLLLANN SLQSVPPGAS DHLPQLQTLD VTQNPWHCD
//