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2024-04-19 11:01:02, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_000132               9048 bp    mRNA    linear   PRI 07-JUL-2013
DEFINITION  Homo sapiens coagulation factor VIII, procoagulant component (F8),
            transcript variant 1, mRNA.
ACCESSION   NM_000132
VERSION     NM_000132.3  GI:192448441
KEYWORDS    RefSeq.
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 9048)
  AUTHORS   Chen Z, Tang H, Qayyum R, Schick UM, Nalls MA, Handsaker R, Li J,
            Lu Y, Yanek LR, Keating B, Meng Y, van Rooij FJ, Okada Y, Kubo M,
            Rasmussen-Torvik L, Keller MF, Lange L, Evans M, Bottinger EP,
            Linderman MD, Ruderfer DM, Hakonarson H, Papanicolaou G, Zonderman
            AB, Gottesman O, Thomson C, Ziv E, Singleton AB, Loos RJ, Sleiman
            PM, Ganesh S, McCarroll S, Becker DM, Wilson JG, Lettre G and
            Reiner AP.
  CONSRTM   BioBank Japan Project; CHARGE Consortium
  TITLE     Genome-wide association analysis of red blood cell traits in
            African Americans: the COGENT Network
  JOURNAL   Hum. Mol. Genet. 22 (12), 2529-2538 (2013)
   PUBMED   23446634
REFERENCE   2  (bases 1 to 9048)
  AUTHORS   Walter,J.D., Werther,R.A., Polozova,M.S., Pohlman,J., Healey,J.F.,
            Meeks,S.L., Lollar,P. and Spiegel,P.C. Jr.
  TITLE     Characterization and solution structure of the factor VIII C2
            domain in a ternary complex with classical and non-classical
            inhibitor antibodies
  JOURNAL   J. Biol. Chem. 288 (14), 9905-9914 (2013)
   PUBMED   23417672
  REMARK    GeneRIF: Characterization and solution structure of the factor VIII
            C2 domain in a ternary complex with classical and non-classical
            inhibitor antibodies
REFERENCE   3  (bases 1 to 9048)
  AUTHORS   Markovitz,R.C., Healey,J.F., Parker,E.T., Meeks,S.L. and Lollar,P.
  TITLE     The diversity of the immune response to the A2 domain of human
            factor VIII
  JOURNAL   Blood 121 (14), 2785-2795 (2013)
   PUBMED   23349389
  REMARK    GeneRIF: We characterized 29 anti-human A2 monoclonal Abs (mAbs)
            produced in a murine hemophilia A model.
REFERENCE   4  (bases 1 to 9048)
  AUTHORS   Takeyama,M., Wintermute,J.M., Manithody,C., Rezaie,A.R. and
            Fay,P.J.
  TITLE     Variable contributions of basic residues forming an APC exosite in
            the binding and inactivation of factor VIIIa
  JOURNAL   Biochemistry 52 (13), 2228-2235 (2013)
   PUBMED   23480827
  REMARK    GeneRIF: These results show a variable contribution of basic
            residues comprising the activated protein C exosite, with
            significant contributions from Lys39, Arg67, and Arg74 to forming a
            FVIIIa-interactive site.
REFERENCE   5  (bases 1 to 9048)
  AUTHORS   Eikenboom J, Federici AB, Dirven RJ, Castaman G, Rodeghiero F,
            Budde U, Schneppenheim R, Batlle J, Canciani MT, Goudemand J, Peake
            I and Goodeve A.
  CONSRTM   MCMDM-1VWD Study Group
  TITLE     VWF propeptide and ratios between VWF, VWF propeptide, and FVIII in
            the characterization of type 1 von Willebrand disease
  JOURNAL   Blood 121 (12), 2336-2339 (2013)
   PUBMED   23349392
  REMARK    GeneRIF: The ratios of VWFpp/VWF:Ag and FVIII:C/VWF:Ag indicate
            that the pathophysiological mechanisms of type 1 VWD include
            reduced production and accelerated clearance of VWF, but that often
            a combination of both mechanisms is implicated.
REFERENCE   6  (bases 1 to 9048)
  AUTHORS   Gitschier,J. and Wood,W.I.
  TITLE     Sequence of the exon-containing regions of the human factor VIII
            gene
  JOURNAL   Hum. Mol. Genet. 1 (3), 199-200 (1992)
   PUBMED   1303178
REFERENCE   7  (bases 1 to 9048)
  AUTHORS   Jonsdottir,S., Diamond,C., Levinson,B., Magnusson,S., Jensson,O.
            and Gitschier,J.
  TITLE     Missense mutations causing mild hemophilia A in Iceland detected by
            denaturing gradient gel electrophoresis
  JOURNAL   Hum. Mutat. 1 (6), 506-508 (1992)
   PUBMED   1301960
REFERENCE   8  (bases 1 to 9048)
  AUTHORS   Diamond,C., Kogan,S., Levinson,B. and Gitschier,J.
  TITLE     Amino acid substitutions in conserved domains of factor VIII and
            related proteins: study of patients with mild and moderately severe
            hemophilia A
  JOURNAL   Hum. Mutat. 1 (3), 248-257 (1992)
   PUBMED   1301932
REFERENCE   9  (bases 1 to 9048)
  AUTHORS   Nafa,K., Baudis,M., Deburgrave,N., Bardin,J.M., Sultan,Y.,
            Kaplan,J.C. and Delpech,M.
  TITLE     A novel mutation (Arg-->Leu in exon 18) in factor VIII gene
            responsible for moderate hemophilia A
  JOURNAL   Hum. Mutat. 1 (1), 77-78 (1992)
   PUBMED   1301194
REFERENCE   10 (bases 1 to 9048)
  AUTHORS   Zucker,M.B., Broekman,M.J. and Kaplan,K.L.
  TITLE     Factor VIII-related antigen in human blood platelets: localization
            and release by thrombin and collagen
  JOURNAL   J. Lab. Clin. Med. 94 (5), 675-682 (1979)
   PUBMED   501196
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from M14113.1 and BC022513.1.
            This sequence is a reference standard in the RefSeqGene project.
            On Jun 24, 2008 this sequence version replaced gi:10518504.
            
            Summary: This gene encodes coagulation factor VIII, which
            participates in the intrinsic pathway of blood coagulation; factor
            VIII is a cofactor for factor IXa which, in the presence of Ca+2
            and phospholipids, converts factor X to the activated form Xa.
            This gene produces two alternatively spliced transcripts.
            Transcript variant 1 encodes a large glycoprotein, isoform a, which
            circulates in plasma and associates with von Willebrand factor in a
            noncovalent complex. This protein undergoes multiple cleavage
            events. Transcript variant 2 encodes a putative small protein,
            isoform b, which consists primarily of the phospholipid binding
            domain of factor VIIIc. This binding domain is essential for
            coagulant activity. Defects in this gene results in hemophilia A, a
            common recessive X-linked coagulation disorder. [provided by
            RefSeq, Jul 2008].
            
            Transcript Variant: This variant (1) consists of 26 exons and
            encodes the full-length isoform (a).
            
            Publication Note:  This RefSeq record includes a subset of the
            publications that are available for this gene. Please see the Gene
            record to access additional publications.
            
            ##Evidence-Data-START##
            Transcript exon combination :: M14113.1, K01740.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025098 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-9029              M14113.1           1-9029
            9030-9048           BC022513.1         2518-2536
FEATURES             Location/Qualifiers
     source          1..9048
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="X"
                     /map="Xq28"
     gene            1..9048
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="coagulation factor VIII, procoagulant component"
                     /db_xref="GeneID:2157"
                     /db_xref="HGNC:3546"
                     /db_xref="HPRD:02384"
                     /db_xref="MIM:300841"
     exon            1..314
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     STS             1..170
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="GDB:452843"
                     /db_xref="UniSTS:99489"
     misc_feature    166..168
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="upstream in-frame stop codon"
     CDS             172..7227
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="isoform a precursor is encoded by transcript
                     variant 1; factor VIII F8B; coagulation factor VIIIc;
                     antihemophilic factor"
                     /codon_start=1
                     /product="coagulation factor VIII isoform a precursor"
                     /protein_id="NP_000123.1"
                     /db_xref="GI:4503647"
                     /db_xref="CCDS:CCDS35457.1"
                     /db_xref="GeneID:2157"
                     /db_xref="HGNC:3546"
                     /db_xref="HPRD:02384"
                     /db_xref="MIM:300841"
                     /translation="
MQIELSTCFFLCLLRFCFSATRRYYLGAVELSWDYMQSDLGELPVDARFPPRVPKSFPFNTSVVYKKTLFVEFTDHLFNIAKPRPPWMGLLGPTIQAEVYDTVVITLKNMASHPVSLHAVGVSYWKASEGAEYDDQTSQREKEDDKVFPGGSHTYVWQVLKENGPMASDPLCLTYSYLSHVDLVKDLNSGLIGALLVCREGSLAKEKTQTLHKFILLFAVFDEGKSWHSETKNSLMQDRDAASARAWPKMHTVNGYVNRSLPGLIGCHRKSVYWHVIGMGTTPEVHSIFLEGHTFLVRNHRQASLEISPITFLTAQTLLMDLGQFLLFCHISSHQHDGMEAYVKVDSCPEEPQLRMKNNEEAEDYDDDLTDSEMDVVRFDDDNSPSFIQIRSVAKKHPKTWVHYIAAEEEDWDYAPLVLAPDDRSYKSQYLNNGPQRIGRKYKKVRFMAYTDETFKTREAIQHESGILGPLLYGEVGDTLLIIFKNQASRPYNIYPHGITDVRPLYSRRLPKGVKHLKDFPILPGEIFKYKWTVTVEDGPTKSDPRCLTRYYSSFVNMERDLASGLIGPLLICYKESVDQRGNQIMSDKRNVILFSVFDENRSWYLTENIQRFLPNPAGVQLEDPEFQASNIMHSINGYVFDSLQLSVCLHEVAYWYILSIGAQTDFLSVFFSGYTFKHKMVYEDTLTLFPFSGETVFMSMENPGLWILGCHNSDFRNRGMTALLKVSSCDKNTGDYYEDSYEDISAYLLSKNNAIEPRSFSQNSRHPSTRQKQFNATTIPENDIEKTDPWFAHRTPMPKIQNVSSSDLLMLLRQSPTPHGLSLSDLQEAKYETFSDDPSPGAIDSNNSLSEMTHFRPQLHHSGDMVFTPESGLQLRLNEKLGTTAATELKKLDFKVSSTSNNLISTIPSDNLAAGTDNTSSLGPPSMPVHYDSQLDTTLFGKKSSPLTESGGPLSLSEENNDSKLLESGLMNSQESSWGKNVSSTESGRLFKGKRAHGPALLTKDNALFKVSISLLKTNKTSNNSATNRKTHIDGPSLLIENSPSVWQNILESDTEFKKVTPLIHDRMLMDKNATALRLNHMSNKTTSSKNMEMVQQKKEGPIPPDAQNPDMSFFKMLFLPESARWIQRTHGKNSLNSGQGPSPKQLVSLGPEKSVEGQNFLSEKNKVVVGKGEFTKDVGLKEMVFPSSRNLFLTNLDNLHENNTHNQEKKIQEEIEKKETLIQENVVLPQIHTVTGTKNFMKNLFLLSTRQNVEGSYDGAYAPVLQDFRSLNDSTNRTKKHTAHFSKKGEEENLEGLGNQTKQIVEKYACTTRISPNTSQQNFVTQRSKRALKQFRLPLEETELEKRIIVDDTSTQWSKNMKHLTPSTLTQIDYNEKEKGAITQSPLSDCLTRSHSIPQANRSPLPIAKVSSFPSIRPIYLTRVLFQDNSSHLPAASYRKKDSGVQESSHFLQGAKKNNLSLAILTLEMTGDQREVGSLGTSATNSVTYKKVENTVLPKPDLPKTSGKVELLPKVHIYQKDLFPTETSNGSPGHLDLVEGSLLQGTEGAIKWNEANRPGKVPFLRVATESSAKTPSKLLDPLAWDNHYGTQIPKEEWKSQEKSPEKTAFKKKDTILSLNACESNHAIAAINEGQNKPEIEVTWAKQGRTERLCSQNPPVLKRHQREITRTTLQSDQEEIDYDDTISVEMKKEDFDIYDEDENQSPRSFQKKTRHYFIAAVERLWDYGMSSSPHVLRNRAQSGSVPQFKKVVFQEFTDGSFTQPLYRGELNEHLGLLGPYIRAEVEDNIMVTFRNQASRPYSFYSSLISYEEDQRQGAEPRKNFVKPNETKTYFWKVQHHMAPTKDEFDCKAWAYFSDVDLEKDVHSGLIGPLLVCHTNTLNPAHGRQVTVQEFALFFTIFDETKSWYFTENMERNCRAPCNIQMEDPTFKENYRFHAINGYIMDTLPGLVMAQDQRIRWYLLSMGSNENIHSIHFSGHVFTVRKKEEYKMALYNLYPGVFETVEMLPSKAGIWRVECLIGEHLHAGMSTLFLVYSNKCQTPLGMASGHIRDFQITASGQYGQWAPKLARLHYSGSINAWSTKEPFSWIKVDLLAPMIIHGIKTQGARQKFSSLYISQFIIMYSLDGKKWQTYRGNSTGTLMVFFGNVDSSGIKHNIFNPPIIARYIRLHPTHYSIRSTLRMELMGCDLNSCSMPLGMESKAISDAQITASSYFTNMFATWSPSKARLHLQGRSNAWRPQVNNPKEWLQVDFQKTMKVTGVTTQGVKSLLTSMYVKEFLISSSQDGHQWTLFFQNGKVKVFQGNQDSFTPVVNSLDPPLLTRYLRIHPQSWVHQIALRMEVLGCEAQDLY
"
     sig_peptide     172..228
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="COORDINATES: ab initio prediction:SignalP:4.0"
     mat_peptide     229..7224
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /product="coagulation factor VIIIc, isoform a"
     mat_peptide     229..4167
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /product="activated factor VIIIc heavy chain (200 kda)"
     mat_peptide     229..2448
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /product="activated factor VIIIc heavy chain (92 kda)"
     misc_feature    439..762
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="Cytochrome C oxidase subunit II, periplasmic
                     domain; Region: COX2; cl11412"
                     /db_xref="CDD:209309"
     misc_feature    823..1218
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="Multicopper oxidase; Region: Cu-oxidase; pfam00394"
                     /db_xref="CDD:201203"
     misc_feature    1264..1266
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Sulfotyrosine; propagated from UniProtKB/Swiss-Prot
                     (P00451.1); sulfatation site"
     misc_feature    1342..1347
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="by thrombin; cleavage site"
     misc_feature    1342..1344
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="proteolytic cleavage site; modified site"
                     /db_xref="HPRD:01488"
     misc_feature    1570..1887
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="Cytochrome C oxidase subunit II, periplasmic
                     domain; Region: COX2; cl11412"
                     /db_xref="CDD:209309"
     misc_feature    2380..2382
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Sulfotyrosine; propagated from UniProtKB/Swiss-Prot
                     (P00451.1); sulfatation site"
     misc_feature    2383..2385
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Sulfotyrosine; propagated from UniProtKB/Swiss-Prot
                     (P00451.1); sulfatation site"
     misc_feature    2395..2397
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Sulfotyrosine; propagated from UniProtKB/Swiss-Prot
                     (P00451.1); sulfatation site"
     misc_feature    2446..2451
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="by thrombin; cleavage site"
     misc_feature    2446..2448
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="proteolytic cleavage site; modified site"
                     /db_xref="HPRD:01488"
     misc_feature    2449..5172
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P00451.1);
                     Region: B"
     misc_feature    4165..4170
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Cleavage (activation); propagated from
                     UniProtKB/Swiss-Prot (P00451.1); cleavage site"
     misc_feature    5170..5175
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Cleavage (activation); propagated from
                     UniProtKB/Swiss-Prot (P00451.1); cleavage site"
     mat_peptide     5173..7224
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /product="activated factor VIIIc light chain (80 kda)"
     misc_feature    5218..5220
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Sulfotyrosine; propagated from UniProtKB/Swiss-Prot
                     (P00451.1); sulfatation site"
     misc_feature    5266..5268
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Sulfotyrosine; propagated from UniProtKB/Swiss-Prot
                     (P00451.1); sulfatation site"
     misc_feature    5293..5298
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="by thrombin; active site"
     misc_feature    5293..5295
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="proteolytic cleavage site; modified site"
                     /db_xref="HPRD:01488"
     misc_feature    5914..6279
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="Cytochrome C oxidase subunit II, periplasmic
                     domain; Region: COX2; cl11412"
                     /db_xref="CDD:209309"
     misc_feature    6286..6735
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="Coagulation factor 5/8 C-terminal domain, discoidin
                     domain; Region: FA58C; smart00231"
                     /db_xref="CDD:197589"
     misc_feature    6295..6732
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="Coagulation factor 5/8 C-terminal domain, discoidin
                     domain; Cell surface-attached carbohydrate-binding domain,
                     present in eukaryotes and assumed to have horizontally
                     transferred to eubacterial genomes; Region: FA58C;
                     cd00057"
                     /db_xref="CDD:28939"
     misc_feature    order(6415..6417,6493..6495,6514..6516)
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="sugar binding site [chemical binding]; other site"
                     /db_xref="CDD:28939"
     misc_feature    6745..7224
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="Region: phospholipid binding domain"
     misc_feature    6745..7206
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="Coagulation factor 5/8 C-terminal domain, discoidin
                     domain; Region: FA58C; smart00231"
                     /db_xref="CDD:197589"
     misc_feature    6754..7203
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="Coagulation factor 5/8 C-terminal domain, discoidin
                     domain; Cell surface-attached carbohydrate-binding domain,
                     present in eukaryotes and assumed to have horizontally
                     transferred to eubacterial genomes; Region: FA58C;
                     cd00057"
                     /db_xref="CDD:28939"
     misc_feature    order(6886..6888,6970..6972,6991..6993)
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /note="sugar binding site [chemical binding]; other site"
                     /db_xref="CDD:28939"
     variation       273
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1800283"
     exon            315..436
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     variation       395
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1800288"
     exon            437..559
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            560..772
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            773..841
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            842..958
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            959..1180
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            1181..1442
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     variation       1257
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1800289"
     exon            1443..1614
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            1615..1708
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     variation       1679
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35383156"
     exon            1709..1923
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            1924..2074
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     variation       2037
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1800290"
     exon            2075..2284
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            2285..5390
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     STS             2306..2548
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN91080"
                     /db_xref="UniSTS:415878"
     STS             2541..2786
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN91079"
                     /db_xref="UniSTS:415877"
     STS             2595..3749
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="stSG604349"
                     /db_xref="UniSTS:447656"
     STS             2780..3038
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN91078"
                     /db_xref="UniSTS:415876"
     STS             2809..3645
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="ECD02249"
                     /db_xref="UniSTS:283349"
     STS             3004..3253
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN91077"
                     /db_xref="UniSTS:415875"
     variation       3118
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35295375"
     STS             3227..3468
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN91076"
                     /db_xref="UniSTS:415874"
     STS             3443..3709
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN91075"
                     /db_xref="UniSTS:415873"
     STS             3690..3929
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN91074"
                     /db_xref="UniSTS:415872"
     STS             3723..4519
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="ECD03412"
                     /db_xref="UniSTS:284494"
     STS             3730..5162
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="stSG604348"
                     /db_xref="UniSTS:447655"
     variation       3792
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:28370212"
     STS             3918..4171
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN91073"
                     /db_xref="UniSTS:415871"
     variation       4092
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1800293"
     STS             4151..4408
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN91072"
                     /db_xref="UniSTS:415870"
     variation       4164
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35702375"
     STS             4331..4610
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="GDB:450201"
                     /db_xref="UniSTS:99279"
     STS             4394..4640
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN91071"
                     /db_xref="UniSTS:415869"
     variation       4613
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1800294"
     STS             4622..4873
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN91070"
                     /db_xref="UniSTS:415868"
     variation       4638
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:35207609"
     variation       4671
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:33921347"
     variation       4692
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1800295"
     STS             4837..5080
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN91069"
                     /db_xref="UniSTS:415867"
     STS             5074..5318
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN91068"
                     /db_xref="UniSTS:415866"
     STS             5179..5380
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="GDB:177816"
                     /db_xref="UniSTS:154970"
     exon            5391..5544
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            5545..5757
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            5758..5986
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            5987..6169
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            6170..6286
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     STS             6233..6326
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="GDB:177561"
                     /db_xref="UniSTS:154929"
     exon            6287..6358
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            6359..6444
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            6445..6600
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            6601..6745
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     STS             6609..6737
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="GDB:177706"
                     /db_xref="UniSTS:154951"
     exon            6746..6894
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     variation       6813
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1800296"
     exon            6895..7071
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     exon            7072..9036
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /inference="alignment:Splign:1.39.8"
     STS             7124..7384
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN90902"
                     /db_xref="UniSTS:415700"
     STS             7328..7966
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="ECD09058"
                     /db_xref="UniSTS:290104"
     STS             7365..7631
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN90901"
                     /db_xref="UniSTS:415699"
     STS             7492..8591
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="stSG604326"
                     /db_xref="UniSTS:447636"
     STS             7609..7847
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN90900"
                     /db_xref="UniSTS:415698"
     STS             7836..8084
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN90899"
                     /db_xref="UniSTS:415697"
     STS             8083..8355
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN90898"
                     /db_xref="UniSTS:415696"
     STS             8100..8766
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="ECD08011"
                     /db_xref="UniSTS:289059"
     STS             8327..8552
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN90897"
                     /db_xref="UniSTS:415695"
     variation       8374
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace=""
                     /replace="tccagtctgccatatcac"
                     /db_xref="dbSNP:28370231"
     variation       8391..8392
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace=""
                     /replace="tccagtctgccatatcac"
                     /db_xref="dbSNP:199597237"
     variation       8441
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:34700571"
     variation       8519
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1396947"
     STS             8528..8752
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN90896"
                     /db_xref="UniSTS:415694"
     variation       8606
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:36101366"
     variation       8702
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:34683807"
     STS             8721..8878
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="STS-M14113"
                     /db_xref="UniSTS:50477"
     STS             8751..9005
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /standard_name="REN90895"
                     /db_xref="UniSTS:415693"
     variation       8755
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1803603"
     polyA_signal    9010..9015
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
     polyA_site      9036
                     /gene="F8"
                     /gene_synonym="AHF; DXS1253E; F8B; F8C; FVIII; HEMA"
ORIGIN      
gcttagtgctgagcacatccagtgggtaaagttccttaaaatgctctgcaaagaaattgggacttttcattaaatcagaaattttacttttttcccctcctgggagctaaagatattttagagaagaattaaccttttgcttctccagttgaacatttgtagcaataagtcatgcaaatagagctctccacctgcttctttctgtgccttttgcgattctgctttagtgccaccagaagatactacctgggtgcagtggaactgtcatgggactatatgcaaagtgatctcggtgagctgcctgtggacgcaagatttcctcctagagtgccaaaatcttttccattcaacacctcagtcgtgtacaaaaagactctgtttgtagaattcacggatcaccttttcaacatcgctaagccaaggccaccctggatgggtctgctaggtcctaccatccaggctgaggtttatgatacagtggtcattacacttaagaacatggcttcccatcctgtcagtcttcatgctgttggtgtatcctactggaaagcttctgagggagctgaatatgatgatcagaccagtcaaagggagaaagaagatgataaagtcttccctggtggaagccatacatatgtctggcaggtcctgaaagagaatggtccaatggcctctgacccactgtgccttacctactcatatctttctcatgtggacctggtaaaagacttgaattcaggcctcattggagccctactagtatgtagagaagggagtctggccaaggaaaagacacagaccttgcacaaatttatactactttttgctgtatttgatgaagggaaaagttggcactcagaaacaaagaactccttgatgcaggatagggatgctgcatctgctcgggcctggcctaaaatgcacacagtcaatggttatgtaaacaggtctctgccaggtctgattggatgccacaggaaatcagtctattggcatgtgattggaatgggcaccactcctgaagtgcactcaatattcctcgaaggtcacacatttcttgtgaggaaccatcgccaggcgtccttggaaatctcgccaataactttccttactgctcaaacactcttgatggaccttggacagtttctactgttttgtcatatctcttcccaccaacatgatggcatggaagcttatgtcaaagtagacagctgtccagaggaaccccaactacgaatgaaaaataatgaagaagcggaagactatgatgatgatcttactgattctgaaatggatgtggtcaggtttgatgatgacaactctccttcctttatccaaattcgctcagttgccaagaagcatcctaaaacttgggtacattacattgctgctgaagaggaggactgggactatgctcccttagtcctcgcccccgatgacagaagttataaaagtcaatatttgaacaatggccctcagcggattggtaggaagtacaaaaaagtccgatttatggcatacacagatgaaacctttaagactcgtgaagctattcagcatgaatcaggaatcttgggacctttactttatggggaagttggagacacactgttgattatatttaagaatcaagcaagcagaccatataacatctaccctcacggaatcactgatgtccgtcctttgtattcaaggagattaccaaaaggtgtaaaacatttgaaggattttccaattctgccaggagaaatattcaaatataaatggacagtgactgtagaagatgggccaactaaatcagatcctcggtgcctgacccgctattactctagtttcgttaatatggagagagatctagcttcaggactcattggccctctcctcatctgctacaaagaatctgtagatcaaagaggaaaccagataatgtcagacaagaggaatgtcatcctgttttctgtatttgatgagaaccgaagctggtacctcacagagaatatacaacgctttctccccaatccagctggagtgcagcttgaggatccagagttccaagcctccaacatcatgcacagcatcaatggctatgtttttgatagtttgcagttgtcagtttgtttgcatgaggtggcatactggtacattctaagcattggagcacagactgacttcctttctgtcttcttctctggatataccttcaaacacaaaatggtctatgaagacacactcaccctattcccattctcaggagaaactgtcttcatgtcgatggaaaacccaggtctatggattctggggtgccacaactcagactttcggaacagaggcatgaccgccttactgaaggtttctagttgtgacaagaacactggtgattattacgaggacagttatgaagatatttcagcatacttgctgagtaaaaacaatgccattgaaccaagaagcttctcccagaattcaagacaccctagcactaggcaaaagcaatttaatgccaccacaattccagaaaatgacatagagaagactgacccttggtttgcacacagaacacctatgcctaaaatacaaaatgtctcctctagtgatttgttgatgctcttgcgacagagtcctactccacatgggctatccttatctgatctccaagaagccaaatatgagactttttctgatgatccatcacctggagcaatagacagtaataacagcctgtctgaaatgacacacttcaggccacagctccatcacagtggggacatggtatttacccctgagtcaggcctccaattaagattaaatgagaaactggggacaactgcagcaacagagttgaagaaacttgatttcaaagtttctagtacatcaaataatctgatttcaacaattccatcagacaatttggcagcaggtactgataatacaagttccttaggacccccaagtatgccagttcattatgatagtcaattagataccactctatttggcaaaaagtcatctccccttactgagtctggtggacctctgagcttgagtgaagaaaataatgattcaaagttgttagaatcaggtttaatgaatagccaagaaagttcatggggaaaaaatgtatcgtcaacagagagtggtaggttatttaaagggaaaagagctcatggacctgctttgttgactaaagataatgccttattcaaagttagcatctctttgttaaagacaaacaaaacttccaataattcagcaactaatagaaagactcacattgatggcccatcattattaattgagaatagtccatcagtctggcaaaatatattagaaagtgacactgagtttaaaaaagtgacacctttgattcatgacagaatgcttatggacaaaaatgctacagctttgaggctaaatcatatgtcaaataaaactacttcatcaaaaaacatggaaatggtccaacagaaaaaagagggccccattccaccagatgcacaaaatccagatatgtcgttctttaagatgctattcttgccagaatcagcaaggtggatacaaaggactcatggaaagaactctctgaactctgggcaaggccccagtccaaagcaattagtatccttaggaccagaaaaatctgtggaaggtcagaatttcttgtctgagaaaaacaaagtggtagtaggaaagggtgaatttacaaaggacgtaggactcaaagagatggtttttccaagcagcagaaacctatttcttactaacttggataatttacatgaaaataatacacacaatcaagaaaaaaaaattcaggaagaaatagaaaagaaggaaacattaatccaagagaatgtagttttgcctcagatacatacagtgactggcactaagaatttcatgaagaaccttttcttactgagcactaggcaaaatgtagaaggttcatatgacggggcatatgctccagtacttcaagattttaggtcattaaatgattcaacaaatagaacaaagaaacacacagctcatttctcaaaaaaaggggaggaagaaaacttggaaggcttgggaaatcaaaccaagcaaattgtagagaaatatgcatgcaccacaaggatatctcctaatacaagccagcagaattttgtcacgcaacgtagtaagagagctttgaaacaattcagactcccactagaagaaacagaacttgaaaaaaggataattgtggatgacacctcaacccagtggtccaaaaacatgaaacatttgaccccgagcaccctcacacagatagactacaatgagaaggagaaaggggccattactcagtctcccttatcagattgccttacgaggagtcatagcatccctcaagcaaatagatctccattacccattgcaaaggtatcatcatttccatctattagacctatatatctgaccagggtcctattccaagacaactcttctcatcttccagcagcatcttatagaaagaaagattctggggtccaagaaagcagtcatttcttacaaggagccaaaaaaaataacctttctttagccattctaaccttggagatgactggtgatcaaagagaggttggctccctggggacaagtgccacaaattcagtcacatacaagaaagttgagaacactgttctcccgaaaccagacttgcccaaaacatctggcaaagttgaattgcttccaaaagttcacatttatcagaaggacctattccctacggaaactagcaatgggtctcctggccatctggatctcgtggaagggagccttcttcagggaacagagggagcgattaagtggaatgaagcaaacagacctggaaaagttccctttctgagagtagcaacagaaagctctgcaaagactccctccaagctattggatcctcttgcttgggataaccactatggtactcagataccaaaagaagagtggaaatcccaagagaagtcaccagaaaaaacagcttttaagaaaaaggataccattttgtccctgaacgcttgtgaaagcaatcatgcaatagcagcaataaatgagggacaaaataagcccgaaatagaagtcacctgggcaaagcaaggtaggactgaaaggctgtgctctcaaaacccaccagtcttgaaacgccatcaacgggaaataactcgtactactcttcagtcagatcaagaggaaattgactatgatgataccatatcagttgaaatgaagaaggaagattttgacatttatgatgaggatgaaaatcagagcccccgcagctttcaaaagaaaacacgacactattttattgctgcagtggagaggctctgggattatgggatgagtagctccccacatgttctaagaaacagggctcagagtggcagtgtccctcagttcaagaaagttgttttccaggaatttactgatggctcctttactcagcccttataccgtggagaactaaatgaacatttgggactcctggggccatatataagagcagaagttgaagataatatcatggtaactttcagaaatcaggcctctcgtccctattccttctattctagccttatttcttatgaggaagatcagaggcaaggagcagaacctagaaaaaactttgtcaagcctaatgaaaccaaaacttacttttggaaagtgcaacatcatatggcacccactaaagatgagtttgactgcaaagcctgggcttatttctctgatgttgacctggaaaaagatgtgcactcaggcctgattggaccccttctggtctgccacactaacacactgaaccctgctcatgggagacaagtgacagtacaggaatttgctctgtttttcaccatctttgatgagaccaaaagctggtacttcactgaaaatatggaaagaaactgcagggctccctgcaatatccagatggaagatcccacttttaaagagaattatcgcttccatgcaatcaatggctacataatggatacactacctggcttagtaatggctcaggatcaaaggattcgatggtatctgctcagcatgggcagcaatgaaaacatccattctattcatttcagtggacatgtgttcactgtacgaaaaaaagaggagtataaaatggcactgtacaatctctatccaggtgtttttgagacagtggaaatgttaccatccaaagctggaatttggcgggtggaatgccttattggcgagcatctacatgctgggatgagcacactttttctggtgtacagcaataagtgtcagactcccctgggaatggcttctggacacattagagattttcagattacagcttcaggacaatatggacagtgggccccaaagctggccagacttcattattccggatcaatcaatgcctggagcaccaaggagcccttttcttggatcaaggtggatctgttggcaccaatgattattcacggcatcaagacccagggtgcccgtcagaagttctccagcctctacatctctcagtttatcatcatgtatagtcttgatgggaagaagtggcagacttatcgaggaaattccactggaaccttaatggtcttctttggcaatgtggattcatctgggataaaacacaatatttttaaccctccaattattgctcgatacatccgtttgcacccaactcattatagcattcgcagcactcttcgcatggagttgatgggctgtgatttaaatagttgcagcatgccattgggaatggagagtaaagcaatatcagatgcacagattactgcttcatcctactttaccaatatgtttgccacctggtctccttcaaaagctcgacttcacctccaagggaggagtaatgcctggagacctcaggtgaataatccaaaagagtggctgcaagtggacttccagaagacaatgaaagtcacaggagtaactactcagggagtaaaatctctgcttaccagcatgtatgtgaaggagttcctcatctccagcagtcaagatggccatcagtggactctcttttttcagaatggcaaagtaaaggtttttcagggaaatcaagactccttcacacctgtggtgaactctctagacccaccgttactgactcgctaccttcgaattcacccccagagttgggtgcaccagattgccctgaggatggaggttctgggctgcgaggcacaggacctctactgagggtggccactgcagcacctgccactgccgtcacctctccctcctcagctccagggcagtgtccctccctggcttgccttctacctttgtgctaaatcctagcagacactgccttgaagcctcctgaattaactatcatcagtcctgcatttctttggtggggggccaggagggtgcatccaatttaacttaactcttacctattttctgcagctgctcccagattactccttccttccaatataactaggcaaaaagaagtgaggagaaacctgcatgaaagcattcttccctgaaaagttaggcctctcagagtcaccacttcctctgttgtagaaaaactatgtgatgaaactttgaaaaagatatttatgatgttaacatttcaggttaagcctcatacgtttaaaataaaactctcagttgtttattatcctgatcaagcatggaacaaagcatgtttcaggatcagatcaatacaatcttggagtcaaaaggcaaatcatttggacaatctgcaaaatggagagaatacaataactactacagtaaagtctgtttctgcttccttacacatagatataattatgttatttagtcattatgaggggcacattcttatctccaaaactagcattcttaaactgagaattatagatggggttcaagaatccctaagtcccctgaaattatataaggcattctgtataaatgcaaatgtgcatttttctgacgagtgtccatagatataaagccatttggtcttaattctgaccaataaaaaaataagtcaggaggatgcaattgttgaaagctttgaaataaaataacaatgtcttcttgaaatttgtgatggccaagaaagaaaatgatgatgacattaggcttctaaaggacatacatttaatatttctgtggaaatatgaggaaaatccatggttatctgagataggagatacaaactttgtaattctaataatgcactcagtttactctctccctctactaatttcctgctgaaaataacacaacaaaaatgtaacaggggaaattatataccgtgactgaaaactagagtcctacttacatagttgaaatatcaaggaggtcagaagaaaattggactggtgaaaacagaaaaaacactccagtctgccatatcaccacacaataggatcccccttcttgccctccacccccataagattgtgaagggtttactgctccttccatctgcctgaccccttcactatgactacacagaatctcctgatagtaaagggggctggaggcaaggataagttatagagcagttggaggaagcatccaaagattgcaacccagggcaaatggaaaacaggagatcctaatatgaaagaaaaatggatcccaatctgagaaaaggcaaaagaatggctacttttttctatgctggagtattttctaataatcctgcttgacccttatctgacctctttggaaactataacatagctgtcacagtatagtcacaatccacaaatgatgcaggtgcaaatggtttatagccctgtgaagttcttaaagtttagaggctaacttacagaaatgaataagttgttttgttttatagcccggtagaggagttaaccccaaaggtgatatggttttatttcctgttatgtttaacttgataatcttattttggcattcttttcccattgactatatacatctctatttctcaaatgttcatggaactagctcttttattttcctgctggtttcttcagtaatgagttaaataaaacattgacacatacaaacaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:2157 -> Molecular function: GO:0005507 [copper ion binding] evidence: IEA
            GeneID:2157 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:2157 -> Molecular function: GO:0016491 [oxidoreductase activity] evidence: IEA
            GeneID:2157 -> Biological process: GO:0002576 [platelet degranulation] evidence: TAS
            GeneID:2157 -> Biological process: GO:0006953 [acute-phase response] evidence: IEA
            GeneID:2157 -> Biological process: GO:0007155 [cell adhesion] evidence: IEA
            GeneID:2157 -> Biological process: GO:0007596 [blood coagulation] evidence: TAS
            GeneID:2157 -> Biological process: GO:0007597 [blood coagulation, intrinsic pathway] evidence: TAS
            GeneID:2157 -> Biological process: GO:0030168 [platelet activation] evidence: TAS
            GeneID:2157 -> Cellular component: GO:0005576 [extracellular region] evidence: NAS
            GeneID:2157 -> Cellular component: GO:0005576 [extracellular region] evidence: TAS
            GeneID:2157 -> Cellular component: GO:0005615 [extracellular space] evidence: IEA
            GeneID:2157 -> Cellular component: GO:0005886 [plasma membrane] evidence: TAS
            GeneID:2157 -> Cellular component: GO:0031093 [platelet alpha granule lumen] evidence: TAS

by @meso_cacase at DBCLS
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