EBI Dbfetch

ID   S76088; SV 1; linear; genomic DNA; STD; HUM; 211 BP.
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AC   S76088;
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DT   29-JUL-1995 (Rel. 44, Created)
DT   01-SEP-2004 (Rel. 81, Last updated, Version 4)
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DE   type I serine protease protein C {exon 6} [human, thrombophilia patient
DE   PCClamart, peripheral blood cells, Genomic Mutant, 211 nt].
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KW   .
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OS   Homo sapiens (human)
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
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RN   [1]
RC   GenBank staff at the National Library of Medicine created this entry [NCBI
RC   gibbsq 162002] from the original journal article.
RP   1-211
RX   PUBMED; 7878626.
RA   Long G.L., Tomczak J.A., Rainville I.R., Dreyfus M., Schramm W.,
RA   Schwarz H.P.;
RT   "Homozygous type I protein C deficiency in two unrelated families
RT   exhibiting thrombophilia related to Ala136-->Pro or Arg286-->His
RT   mutations";
RL   Thromb. Haemost. 72(4):526-533(1994).
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DR   GOA; P04070.
DR   HGNC; 9451; PROC.
DR   InterPro; IPR001314; Peptidase_S1A.
DR   PDB; 1AUT; X-ray.
DR   UniProtKB/Swiss-Prot; P04070; PROC_HUMAN.
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FH   Key             Location/Qualifiers
FH
FT   source          1..211
FT                   /organism="Homo sapiens"
FT                   /mol_type="genomic DNA"
FT                   /db_xref="taxon:9606"
FT   gene            1..211
FT                   /gene="type I serine protease protein C"
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SQ   Sequence 211 BP; 36 A; 68 C; 62 G; 36 T; 9 other;
     ngcccnnatn nccgcgccct cccctgcccg cagaggtgag nttcctcaat tgctctctgg        60
     acaacggcgg ctgcacgcat tactgactag aggaggtggg ctggcggcgc tgtagctgtg       120
     cgcctggcta caagctgggg gacgacctcc tgcagtgtca ccccccaggt gagangcccc       180
     caatacatcg nccaggaata ctggacgncg t                                      211
//