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2019-03-23 03:35:10, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_015026              10379 bp    mRNA    linear   PRI 15-JUN-2013
DEFINITION  Homo sapiens MON2 homolog (S. cerevisiae) (MON2), transcript
            variant 1, mRNA.
ACCESSION   NM_015026 XM_051091
VERSION     NM_015026.2  GI:114326551
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 10379)
  AUTHORS   Lauc,G., Huffman,J.E., Pucic,M., Zgaga,L., Adamczyk,B., Muzinic,A.,
            Novokmet,M., Polasek,O., Gornik,O., Kristic,J., Keser,T.,
            Vitart,V., Scheijen,B., Uh,H.W., Molokhia,M., Patrick,A.L.,
            McKeigue,P., Kolcic,I., Lukic,I.K., Swann,O., van Leeuwen,F.N.,
            Ruhaak,L.R., Houwing-Duistermaat,J.J., Slagboom,P.E., Beekman,M.,
            de Craen,A.J., Deelder,A.M., Zeng,Q., Wang,W., Hastie,N.D.,
            Gyllensten,U., Wilson,J.F., Wuhrer,M., Wright,A.F., Rudd,P.M.,
            Hayward,C., Aulchenko,Y., Campbell,H. and Rudan,I.
  TITLE     Loci associated with N-glycosylation of human immunoglobulin G show
            pleiotropy with autoimmune diseases and haematological cancers
  JOURNAL   PLoS Genet. 9 (1), E1003225 (2013)
   PUBMED   23382691
REFERENCE   2  (bases 1 to 10379)
  AUTHORS   Tomita,Y., Noda,T., Fujii,K., Watanabe,T., Morikawa,Y. and
            Kawaoka,Y.
  TITLE     The cellular factors Vps18 and Mon2 are required for efficient
            production of infectious HIV-1 particles
  JOURNAL   J. Virol. 85 (11), 5618-5627 (2011)
   PUBMED   21450827
  REMARK    GeneRIF: Depletion of hVps18 or hMon2 reduced the efficient
            production of infectious HIV-1 virions in human cells.
REFERENCE   3  (bases 1 to 10379)
  AUTHORS   Singer-Kruger,B., Lasic,M., Burger,A.M., Hausser,A., Pipkorn,R. and
            Wang,Y.
  TITLE     Yeast and human Ysl2p/hMon2 interact with Gga adaptors and mediate
            their subcellular distribution
  JOURNAL   EMBO J. 27 (10), 1423-1435 (2008)
   PUBMED   18418388
  REMARK    GeneRIF: Ysl2p represents an essential, evolutionarily conserved
            member of a network controlling direct binding and membrane docking
            of Ggas.
REFERENCE   4  (bases 1 to 10379)
  AUTHORS   Gillingham,A.K., Whyte,J.R., Panic,B. and Munro,S.
  TITLE     Mon2, a relative of large Arf exchange factors, recruits Dop1 to
            the Golgi apparatus
  JOURNAL   J. Biol. Chem. 281 (4), 2273-2280 (2006)
   PUBMED   16301316
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            DA125763.1, AB017814.1, AL834320.1 and AC026115.27.
            On Sep 14, 2006 this sequence version replaced gi:55741668.
            
            Transcript Variant: This variant (1) encodes the longest isoform
            (1).
            
            ##Evidence-Data-START##
            Transcript exon combination :: BX537415.1, AB017814.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025083, ERS025084 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-277               DA125763.1         1-277
            278-1971            AB017814.1         3-1696
            1972-8406           AL834320.1         930-7364
            8407-10379          AC026115.27        93005-94977
FEATURES             Location/Qualifiers
     source          1..10379
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="12"
                     /map="12q14.1"
     gene            1..10379
                     /gene="MON2"
                     /note="MON2 homolog (S. cerevisiae)"
                     /db_xref="GeneID:23041"
                     /db_xref="HGNC:29177"
     exon            1..502
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       42
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:367726960"
     variation       117
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192909077"
     variation       121
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78282415"
     variation       198
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12829785"
     variation       200..201
                     /gene="MON2"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:34690918"
     variation       220
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:184094253"
     variation       318
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:143636182"
     misc_feature    335..337
                     /gene="MON2"
                     /note="upstream in-frame stop codon"
     variation       373
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373365293"
     CDS             392..5545
                     /gene="MON2"
                     /note="isoform 1 is encoded by transcript variant 1;
                     protein MON2 homolog"
                     /codon_start=1
                     /product="protein MON2 homolog isoform 1"
                     /protein_id="NP_055841.2"
                     /db_xref="GI:114326552"
                     /db_xref="CCDS:CCDS31849.1"
                     /db_xref="GeneID:23041"
                     /db_xref="HGNC:29177"
                     /translation="
MSGTSSPEAVKKLLENMQSDLRALSLECKKKFPPVKEAAESGIIKVKTIAARNTEILAALKENSSEVVQPFLMGCGTKEPKITQLCLAAIQRLMSHEVVSETAAGNIINMLWQLMENSLEELKLLQTVLVLLTTNTVVHDEALSKAIVLCFRLHFTKDNITNNTAAATVRQVVTVVFERMVAEDERHRDIIEQPVLVQGNSNRRSVSTLKPCAKDAYMLFQDLCQLVNADAPYWLVGMTEMTRTFGLELLESVLNDFPQVFLQHQEFSFLLKERVCPLVIKLFSPNIKFRQGSSTSSSPAPVEKPYFPICMRLLRVVSVLIKQFYSLLVTECEIFLSLLVKFLDADKPQWLRAVAVESIHRFCVQPQLLRSFCQSYDMKQHSTKVFRDIVNALGSFIQSLFLVPPTGNPATSNQAGNNNLGGSVSAPANSGMVGIGGGVTLLPAFEYRGTWIPILTITVQGSAKATYLEMLDKVEPPTIPEGYAMSVAFHCLLDLVRGITSMIEGELGELETECQTTTEEGSSPTQSTEQQDLQSTSDQMDKEIVSRAVWEEMVNACWCGLLAALSLLLDASTDEAATENILKAELTMAALCGRLGLVTSRDAFITAICKGSLPPHYALTVLNTTTAATLSNKSYSVQGQSVMMISPSSESHQQVVAVGQPLAVQPQGTVMLTSKNIQCMRTLLNLAHCHGAVLGTSWQLVLATLQHLVWILGLKPSSGGALKPGRAVEGPSTVLTTAVMTDLPVISNILSRLFESSQYLDDVSLHHLINALCSLSLEAMDMAYGNNKEPSLFAVAKLLETGLVNMHRIEILWRPLTGHLLEVCQHPNSRMREWGAEALTSLIKAGLTFNHDPPLSQNQRLQLLLLNPLKEMSNINHPDIRLKQLECVLQILQSQGDSLGPGWPLVLGVMGAIRNDQGESLIRTAFQCLQLVVTDFLPTMPCTCLQIVVDVAGSFGLHNQELNISLTSIGLLWNISDYFFQRGETIEKELNKEEAAQQKQAEEKGVVLNRPFHPAPPFDCLWLCLYAKLGELCVDPRPAVRKSAGQTLFSTIGAHGTLLQHSTWHTVIWKVLFHLLDRVRESSTTADKEKIESGGGNILIHHSRDTAEKQWAETWVLTLAGVARIFNTRRYLLQPLGDFSRAWDVLLDHIQSAALSKNNEVSLAALKSFQEILQIVSPVRDSDKPETPPVVNVPVPVLIGPISGMSRPFVRTDSIGEKLGRYSSSEPPIVTDELEDLNLWWAAWNTWYRIGSESTKPPITFDKLTFIPSQPFLTALIQIFPALYQHIKTGFNMDDLQKLGVILHSAISVPISSDASPFILPSYTEAVLTSLQEAVLTALDVLQKAICVGPENMQIMYPAIFDQLLAFVEFSCKPPQYGQLETKHIANAKYNQIQLFAPAEWVALNYVPFAERSLEVVVDLYQKTACHKAVVNEKVLQNIIKTLRVPLSLKYSCPSESTWKLAVSSLLRVLSIGLPVARQHASSGKFDSMWPELANTFEDFLFTKSIPPDNLSIQEFQRNENIDVEVVQLISNEILPYANFIPKEFVGQIMTMLNKGSIHSQSSSFTEAEIDIRLREEFSKMCFETLLQFSFSNKVTTPQEGYISRMALSVLLKRSQDVLHRYIEDERLSGKCPLPRQQVTEIIFVLKAVSTLIDSLKKTQPENVDGNTWAQVIALYPTLVECITCSSSEVCSALKEALVPFKDFMQPPASRVQNGES
"
     misc_feature    1004..1006
                     /gene="MON2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q7Z3U7.2); phosphorylation site"
     misc_feature    1016..1549
                     /gene="MON2"
                     /note="Guanine nucleotide exchange factor in Golgi
                     transport N-terminal; Region: Sec7_N; pfam12783"
                     /db_xref="CDD:205070"
     misc_feature    <3005..3187
                     /gene="MON2"
                     /note="Domain of unknown function (DUF1981); Region:
                     DUF1981; pfam09324"
                     /db_xref="CDD:204198"
     variation       418
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141050692"
     variation       428
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377369516"
     variation       445
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370175705"
     variation       447
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78504538"
     variation       487
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199872329"
     exon            503..566
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       518
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373833745"
     variation       527
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:192228504"
     variation       542
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:184783078"
     variation       546
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201342842"
     variation       552
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199985838"
     exon            567..694
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       589
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:150263185"
     variation       598
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367768584"
     variation       659
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371169990"
     variation       666
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202179158"
     variation       677
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375291950"
     variation       685
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:138944932"
     exon            695..826
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       788
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:75261573"
     variation       822
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1795717"
     exon            827..956
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       850
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149446479"
     variation       869
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145936574"
     variation       945..946
                     /gene="MON2"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:35447314"
     exon            957..1054
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       977
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:202015814"
     variation       1029
                     /gene="MON2"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:201958152"
     variation       1030
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:17120341"
     exon            1055..1180
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       1074
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:370658932"
     variation       1116
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200959175"
     variation       1123
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199633652"
     variation       1124
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:202041870"
     variation       1180
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200323905"
     exon            1181..1375
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       1279
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374317455"
     variation       1280
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:376188370"
     variation       1282
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:183705841"
     variation       1306
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369425233"
     variation       1342
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373491785"
     exon            1376..1500
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       1409
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377426342"
     variation       1432
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148446628"
     variation       1442
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:142628881"
     exon            1501..1637
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       1531
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150576914"
     variation       1565
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192635468"
     variation       1572
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:139628241"
     variation       1602
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144560708"
     exon            1638..1791
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       1644
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142746051"
     variation       1709
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141578066"
     variation       1710
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145410390"
     variation       1743
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368333470"
     variation       1747
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201932585"
     exon            1792..2024
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       1810..1812
                     /gene="MON2"
                     /replace="ag"
                     /replace="gt"
                     /db_xref="dbSNP:71453870"
     variation       1860
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368807713"
     variation       1912
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202106381"
     variation       1972
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7957417"
     variation       1975
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:149178566"
     variation       1983
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143346269"
     variation       1998
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147998476"
     exon            2025..2106
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       2033
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10219555"
     variation       2062
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374699348"
     variation       2086
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145910619"
     variation       2103
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138520786"
     exon            2107..2291
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       2153
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141548503"
     variation       2166
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:75976037"
     variation       2183
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371674915"
     variation       2184
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:192823209"
     variation       2204
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369551379"
     variation       2208
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201233366"
     variation       2251
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146204905"
     variation       2253
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199641023"
     variation       2267
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:137984661"
     variation       2276
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375994478"
     variation       2282
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201313378"
     variation       2291
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142893848"
     exon            2292..2404
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       2299
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77761138"
     variation       2300
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372685910"
     variation       2319
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113956829"
     variation       2330
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:370180495"
     variation       2350
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144030277"
     variation       2364
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201951697"
     variation       2387
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373777338"
     exon            2405..2509
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       2419
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200884151"
     variation       2440
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199939127"
     variation       2454
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370920946"
     variation       2464
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:79202632"
     variation       2494
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138597890"
     exon            2510..2590
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       2547
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371457996"
     variation       2548..2549
                     /gene="MON2"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:376918430"
     variation       2564
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147434526"
     exon            2591..2664
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       2620
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138097256"
     variation       2643
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:199890435"
     variation       2650
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181083326"
     exon            2665..2755
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       2750
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:199853497"
     exon            2756..2857
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       2792
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145370457"
     variation       2814
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201799263"
     exon            2858..2968
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       2865
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151054514"
     variation       2909
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139761408"
     variation       2928
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:140799300"
     variation       2933
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:368286304"
     exon            2969..3144
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       2971
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145811980"
     variation       2989
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:76979587"
     variation       2994
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370714902"
     variation       2995
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140685723"
     variation       3052
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145857077"
     variation       3053
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201327821"
     variation       3055
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146636697"
     variation       3087
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376355817"
     variation       3097
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201479557"
     exon            3145..3307
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       3206
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:71465159"
     variation       3209
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370276486"
     variation       3218
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199611893"
     variation       3273
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:56260916"
     exon            3308..3601
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       3343
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:200753362"
     variation       3386
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:147472788"
     variation       3394
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200756958"
     variation       3395
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148114740"
     variation       3406
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:147989888"
     variation       3407
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372150008"
     variation       3497
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373887162"
     variation       3517
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112464579"
     variation       3545..3546
                     /gene="MON2"
                     /replace=""
                     /replace="cc"
                     /db_xref="dbSNP:71775142"
     variation       3552
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150125859"
     exon            3602..3800
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       3630
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138816741"
     variation       3662
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142808679"
     variation       3663
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138210046"
     variation       3681
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185149041"
     variation       3682
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:141496035"
     variation       3709
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76996863"
     variation       3732
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371751043"
     variation       3733
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375812777"
     exon            3801..4423
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       3820
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:143767639"
     variation       3831..3832
                     /gene="MON2"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:71774028"
     variation       3919
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374782840"
     variation       3987
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200738634"
     variation       3992
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368625495"
     variation       4012
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184173771"
     variation       4023
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372807434"
     variation       4035
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144223000"
     variation       4108
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148729903"
     variation       4120
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375777277"
     variation       4166
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202036287"
     variation       4173
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369166192"
     variation       4188
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371284233"
     variation       4199
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113897435"
     variation       4201
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:61748729"
     variation       4202
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376277172"
     variation       4236
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147032618"
     variation       4313
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369230152"
     variation       4320
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200683652"
     variation       4332
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:375193969"
     variation       4345
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61752537"
     variation       4363
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151276772"
     variation       4364
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199973736"
     variation       4391
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369441708"
     exon            4424..4567
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       4475
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:139653688"
     variation       4517
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201309945"
     variation       4531
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370541225"
     variation       4544
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11174549"
     exon            4568..4585
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       4585
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146625340"
     exon            4586..4714
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       4588
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141408825"
     variation       4609
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372875511"
     variation       4615
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150277877"
     variation       4632
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375554863"
     variation       4666
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144890374"
     variation       4712
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200302237"
     exon            4715..4905
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       4724
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:149042861"
     variation       4772
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:376842498"
     variation       4787
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201728670"
     variation       4799
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373162493"
     variation       4819
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377424436"
     variation       4824
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200943148"
     variation       4835
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200313038"
     variation       4850
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2133305"
     exon            4906..4966
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       4963
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143056389"
     exon            4967..5090
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       4975
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138748859"
     exon            5091..5298
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       5106
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368920235"
     variation       5108..5109
                     /gene="MON2"
                     /replace=""
                     /replace="at"
                     /db_xref="dbSNP:71677212"
     variation       5110
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369895677"
     variation       5174
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142788333"
     variation       5233
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11174557"
     variation       5241
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371055664"
     variation       5252
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375029048"
     variation       5259
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201522160"
     variation       5269
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:61753654"
     exon            5299..5381
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       5330
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370471896"
     variation       5332
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200438950"
     exon            5382..10379
                     /gene="MON2"
                     /inference="alignment:Splign:1.39.8"
     variation       5464
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368019236"
     variation       5512
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372535871"
     variation       5516
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:185959477"
     variation       5547
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139671233"
     variation       5548
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375501733"
     variation       5563
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200770164"
     variation       5636
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12357"
     variation       5718
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:12510"
     variation       5777
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:74095830"
     variation       5997
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191663015"
     variation       6014
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:117990646"
     variation       6150
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:183064205"
     variation       6305
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:117752865"
     variation       6358
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371096108"
     variation       6370
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:143317696"
     variation       6502
                     /gene="MON2"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:113422385"
     variation       6521
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375656986"
     variation       6535
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146695704"
     variation       6629
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12582679"
     variation       6709
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:12825969"
     variation       6782
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188010179"
     variation       6920
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112459344"
     variation       7012
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368088274"
     variation       7101
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191577817"
     variation       7148..7149
                     /gene="MON2"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:34571562"
     variation       7304
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10161549"
     variation       7441
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1056340"
     variation       7509
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367615489"
     variation       7553
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:77895978"
     variation       7794
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372803692"
     variation       7942
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:73124331"
     variation       7944
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:185948125"
     variation       7954
                     /gene="MON2"
                     /replace=""
                     /replace="tc"
                     /db_xref="dbSNP:78738838"
     STS             8008..8175
                     /gene="MON2"
                     /standard_name="G35510"
                     /db_xref="UniSTS:44150"
     variation       8035
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:182200752"
     variation       8058
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1692032"
     variation       8126
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:10877884"
     variation       8144
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:186760613"
     variation       8157
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:112062794"
     STS             8167..8237
                     /gene="MON2"
                     /standard_name="D5S2354"
                     /db_xref="UniSTS:473392"
     variation       8233
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372003134"
     variation       8284
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115640042"
     variation       8374
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:138070398"
     variation       8458
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:117772925"
     variation       8525
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11610858"
     variation       8698
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:149121779"
     variation       8800
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143652389"
     variation       8801
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113871644"
     variation       8938
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138344140"
     variation       8985
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:79851656"
     variation       9185
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:112835316"
     variation       9295
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7294575"
     variation       9406
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143838487"
     variation       9419
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7960329"
     variation       9431
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:7975337"
     variation       9652
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:192441347"
     variation       9694
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376984102"
     variation       9716
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184767948"
     variation       9756
                     /gene="MON2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:188550904"
     variation       9823
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147261541"
     variation       9887
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:7963657"
     variation       9962
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192910438"
     variation       10061
                     /gene="MON2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:79217268"
     variation       10062
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:74095831"
     STS             10117..10284
                     /gene="MON2"
                     /standard_name="97460"
     STS             10117..10284
                     /gene="MON2"
                     /standard_name="RH103126"
                     /db_xref="UniSTS:97460"
     variation       10148
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139158364"
     variation       10203
                     /gene="MON2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:184721348"
     variation       10264
                     /gene="MON2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189537374"
     variation       10316
                     /gene="MON2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:12581582"
     variation       10362
                     /gene="MON2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:181505200"
ORIGIN      
attgtgggcgactcggctaatggcgtcggcgagtcttaggggcctggggagctggcgctgaagcttcttgccaggttggctggtgacacccggtgtggctgggccccgcggcagcggagggacctgcccgccttgtgggtttctcggccagagtcggcggagcctagcgggacggtgcgactgcggggggcgcctccgagaaaagccagaggtgttgcggggaagctgctgggggacgctcgagcaggctccgggttcgcagcccagggcccaagaagcgggctgctgaaggaccagagacaccgggagggagctgcctgtggccctaaggagctgaccgtgccagagcttgtttgtacctctcggaaattggctgggaccttggaggatcatgtccggcaccagcagccccgaggcggtgaagaagctgctggagaatatgcagagcgacttgcgcgccttgtcactggagtgcaagaagaaattcccacctgtcaaagaggctgctgaatcaggaataataaaagttaaaacaattgctgcacgaaacactgaaattttggcagcactgaaagagaacagctcagaggttgtacagccttttttaatgggttgtggaaccaaggaaccgaagatcactcagctatgtttggctgctattcagagactcatgtcacatgaagtcgtgtctgagactgcagctggaaatataattaacatgctttggcagctaatggagaatagtcttgaagaacttaagctacttcaaacagttcttgttcttttaacaaccaatacagtagttcatgatgaggcactttctaaggcaatcgttctttgttttcgactacacttcacaaaagataatattacaaataatacagctgctgctacagtgcgacaagttgttactgttgtttttgagaggatggttgctgaagatgaacgacacagagatattatagaacaaccagtactggtacaaggaaatagtaacagaagatctgtcagtaccctcaaaccttgtgctaaagatgcatatatgcttttccaggatctttgtcagttggttaatgctgatgctccttattggctagtgggcatgacagaaatgactcggacgtttggcctcgaattacttgagtcagtcctcaatgattttccgcaggtctttttacaacaccaagaatttagtttcctcctcaaagaaagggtatgtcctcttgtgataaagctcttttctccaaatataaagttcagacaaggttccagcacctcatcttctccagcaccagttgaaaaaccatattttcctatctgcatgcgtttgctgagagtagtatctgttctgattaagcagttttacagtcttttggtaactgaatgtgagatatttctgtcacttctggtgaaatttctggatgcagataaaccacagtggctacgagctgttgcggtggaatcaatacacagattctgtgtgcagcctcaactattaaggtcattttgtcagtcctatgatatgaaacagcattctaccaaggtttttcgtgatattgtaaatgcactgggatcttttatacagtccttgtttcttgtcccccctactggaaatcctgcaacaagcaaccaagctggaaacaataatttaggtggctcagtctcagcaccagctaactcaggaatggtggggattggtggaggtgttactttgctaccagcatttgaatataggggaacctggatacctattctgacaatcacagttcaaggcagtgctaaagccacctacttagaaatgttggacaaagttgagcctccaactatacctgaaggttacgccatgtctgtggcattccattgtttgctagaccttgttcgtggaatcacaagtatgattgaaggagagctaggagagcttgaaacagaatgtcaaaccaccactgaagaaggttcttcaccaacacagtcgacagaacagcaggatttacagtcaacatcagaccaaatggataaggaaattgttagtagggctgtttgggaagaaatggtgaatgcctgctggtgtggtcttcttgctgcactctcactccttcttgatgccagcacagatgaagctgccactgagaatattttaaaagctgaactgactatggctgctctttgtggaagactgggccttgtaacttcaagagatgcctttataactgcaatatgcaaaggttccctgcctccccattatgctcttactgtattgaataccaccactgcagctacactttccaacaaatcatattccgttcagggccaaagtgttatgatgataagtccatcaagtgaatctcaccaacaagttgtggcagtgggtcaacctttagcagtccagcctcaagggacagtaatgctgacttccaaaaatatccagtgtatgaggactttacttaacttggcgcattgccatggggctgttcttggaacatcatggcaacttgtcttggcaactcttcagcatcttgtgtggattctgggattaaagcctagtagtggcggtgccttgaaacctgggagagctgtagaaggacccagtacagttctaacaacagcagtgatgacagatttaccagtgatttccaatatactttcaagattgtttgaaagctcacagtatcttgatgatgtatcactgcatcatttaataaatgcactttgctccttgtctctagaagcaatggatatggcctatggaaataataaggaaccatctctttttgctgttgccaaattgttagaaactggtttagttaatatgcaccgaatagaaattctgtggagacctctgactggccatctacttgaggtctgccagcatccaaactctcgaatgagagaatggggagcagaagctttaacttctcttattaaagcaggattaacatttaaccatgatcctccactctcacaaaaccagaggctgcagttgcttttattgaacccgttaaaggagatgtccaatattaatcatccagatattcgactcaagcagttagaatgcgtgttgcagattctgcagagtcagggagacagtcttgggcctggatggccattagtgcttggagtcatgggagcaatcagaaatgatcaaggagaatccttgatacgaactgcattccagtgtcttcagttggttgtgacagattttctaccaacaatgccttgtacttgcctgcaaatagttgtagatgttgcaggtagctttggcctccataaccaagaactcaatattagtttaacttcaataggtttattgtggaatatttcagattattttttccaaagaggggaaactattgaaaaagaactaaataaggaagaggcagcacagcaaaagcaggcagaagagaaaggagttgttttaaatcggccattccaccctgcaccgccatttgattgcttgtggttatgtctttatgcaaaattgggtgaactatgtgtggatccccgtcctgctgtcaggaagagtgcagggcaaactctgttttctacaattggtgcgcatggaactttattacagcattcaacctggcacactgttatctggaaggtactctttcatctactggacagagttcgagagtcctctaccactgcagacaaagaaaagattgagtctggaggtggcaatattctcattcatcattcaagggacaccgccgagaagcaatgggctgagacgtgggtattaacattggctggagtagcaaggatcttcaacactagaagatatttgctgcagcctttaggagatttttcaagagcttgggatgttcttcttgaccatatacagtcagcagcactcagcaaaaacaatgaagtatctctggctgctctgaaaagcttccaggaaattttacagattgtgtcccctgtcagagactcagataagcctgagacaccacctgtagttaatgtacctgtgcctgttcttatagggcccatatcaggcatgagcaggccatttgtaagaacagattccattggagaaaaactaggaagatatagtagctctgagccacccattgttactgatgagcttgaagatttgaatctatggtgggctgcgtggaatacctggtatagaattggatctgaaagtactaagcctcctattacttttgataaactaacttttattcctagccagccttttcttacagctttaattcagatatttccagctctctaccaacacataaaaactggtttcaatatggatgacttgcaaaagttgggagtcatattgcacagtgctatttcagtcccaataagttcagatgcatccccttttattcttccatcttataccgaagcagttttgacaagtttacaggaagctgtacttacagctttagatgttctccaaaaggccatttgtgtaggaccagaaaacatgcagataatgtatccagctatatttgaccagttgttggcatttgtagaattttcctgtaaacctccacagtatggacagctggaaacaaagcacattgcaaatgcaaaatataatcagatccaactatttgcaccggcggaatgggtagccttgaattatgtgccgtttgctgaaaggtctttagaagtagttgtggatttataccaaaaaacagcgtgtcacaaagcagtggtgaatgagaaagtgctccagaatattattaagactcttagggttcctctcagtttgaagtattcctgcccttctgaaagcacatggaaactagcagtatcctctctcctcagagttctttctattgggctacctgttgcccggcagcatgcttcttctggaaaatttgacagtatgtggccagaactagccaatacttttgaagattttctctttactaaaagcatacctccagataatctctctattcaagagtttcaaagaaatgaaaatattgatgtcgaggtagttcaacttatcagcaatgagatactaccttatgccaattttattcctaaggaatttgttggtcaaataatgacaatgcttaacaagggctcaatacattctcagtcatcttcatttacagaagcagagattgatattcgtttgagagaggaattttctaaaatgtgttttgaaacattactccagttttccttcagtaataaagtcacaacacctcaagaaggctacatctcacgaatggcactctcagtgcttttaaagaggtcccaagatgtactacatcgctatatagaggatgaaagattaagtggtaaatgccctcttccaaggcaacaagtaacagaaattatatttgttttaaaagcagtcagtactcttattgattcacttaagaaaactcagcctgagaatgttgatggaaatacctgggcacaagtaattgccttatacccaactttagtagaatgcatcacctgttcttcttcagaagtctgttctgcacttaaagaggcactagttccttttaaggatttcatgcagccaccagcatccagagttcaaaatggagaatcttgaccggctacaatatatttgaaagcaggaagatagtctaaaaaatgtttgctcctaattgagtcttctgtgagaaggacatttcttactgcagataattcttggcagctgttgttggcctcctttaaattctacttacctgagttcagtaattcatattacaggcttgcacatcaacaaaggctcctgaatgaacagcagtgtaaggctttaataaattaaactgatgggagggataattaacactacagtatacatgctaccatatctccagttggtgatttaaagtgagcttatgtacagtttgtggtgtatgtgttaatgatgtactttttaaaaagaaagaagagatatttcaattcagtcagatttattagtctggtgtttttgcaccctttttcaagtacaaaatcgtactagaattttatgcaagatggtactgtaacattccatattatctataaccagcctttgttaacaaagggaactgatatacttgtgtgtataataaatggtacagttctgtataaaatagtgcatttatttaaattttaaaagtattgataatgttaaatgcttaaagctctatttattattaatacaaaattgtttgcttacatttttacttataatttgccttcatatgtggcggataagctcaccatatgatcatgcagttagcttcatgcttattttaaatgtattattagtgaccattaaacatctgaccagtaaggtcatgtgaacacagcagcaaatagtttatgatttgctgattttggagctttgaaatataggttcttaatacattgatacatattgtagcactatgacttcatcatacctcatttctttaaacagctctccaagctttcactgaagtctgtctgttttttatattggctgtctggattttaaagacttttcatattttatatttctactgattttgtttcccctaacaacatttgtcactgtctttgaattatgacccaggcaagatgatttcagattttctaaaatcttgcctgtgaggttttgttcatatcagtgcttcattttgtaatgtcttctcaagaaaaatacctatgttaactcacaagtataaaatatgtgtgtattataaaacaatgaaaagtgtatttttggagatagtcaagcatttagaagtgcagtgaacttgctgtcacggagtaaaatgctaattatgtttcactttcctagcctagtgaaaaagaaaagtgctcttgagtacaataccttaattatttcttaaaatactgactttgacctagctcactgtattttttatttaatggattatggattacagtatttttcttctgagttaaattttcataatttatgtgaagacacaaagatgtttaaaacaatgattattcataagaaatcatgatggtctcagtattattttagtgtattggaaggtctttgatcttaatagaatttataaatttcagcttctccagaataatcataaaactgcaaaaagatattataattgagtcatgattgagatacagttttgaggctattataattgtataattatttaatttgcattatctgtaaaatgtagtaaggtctttgaggggatattttttatttacatgaattactgaatttctattttattatttcacctaaaattaaggtaaaatatggcatttcataagttctgctttcagcattttccttaaagttgtaaaaaatcaagctatgtacttattttctatatttgggtgtgttaaattgaggattagaaaaatccacataatcactgataaagcattgaaacagaataacccaagggtagtgtaccgattcagtaacatgttaaaaatattgctatgcatttattcaaaggaaaatggtctgttcttgagaaataaaagatcagttgcaattaggataattaaatagttaaatatgagtcaagtgtatgcaatatacatttatatgaaccaaagcttgctttatcaggaccatgccctacagttcaaaacataaacatagtgaatgtgttaatatcatataataaggtaataaatgccagtcttagtgtgaagcaagtgggtggcccccttggtagtataattggacaggattttcctccagaatatttcctgtcaccctccaagagtcactacagtaattgattgctggcatggaacacattgcccttgtcttgttagtatgaattgggttctccagtgactagaagaactggggtgtgtgaaagtattcgatgccaggagattcaaaaaggaagctctcaaagataagatcattttatggcacaattgagtctataaccagccctttaagcagtagtaaaaatgtcctttgtcatacttactagaaatactatgagttttttttttttttttcatttgagacggagtctcgctctgtcacccaggctggaatgcagtggcacgatcttggctcactgcaacctctgcttcccgggttcaagcagtttcctgcttcagacttccaagtagctgggattacagacatgccaccatgccaggctaatttttttaatatttttagtagagatggggtttcaccattttggccattctagtcttgaactcctgacctcaggtgatctgcccgccttggcctcccaaagtgctgacattacaggcctgagccactgcgcccagccaataccatgagttttaagcctcacatcgtcacttgctgtcactgccagtgcctgttttattcatattgctggacaacagacatatgccaccaattgtatgattaataaagtctttttctggccattttgtccattataaaggaaataaactaattgttaacttgcatagattacttcttagtttcctatgctaccaccactgccaagggagaaaaaaatacatcattttgtaatgtctttagtatttctttataactagtgttaaggttttgttaattttattgtatacatttgtaacatttattaggagccttttaggttccaaaacaaacaaaaggcataaaaaagtctagcttagaaccacttttcacttgctttcatttttaattttattcacttaacagctaacatctttcttgtttcttgttttttccattatatggttatcgattcaactcttgctatattccttaaatttgtatgtatcatcagaagaaagagatgaacaatttagtgtagatattttattctggagaataatattcaattaaattatttctacagcaggccagtaacaactagattatttgtcctttctcagtataattttaaagagcattttgttttattgtcacaatttggtaccactagtcccaggtaaccattgggccaaaggatcagttgagaaacagttaaggatgaattagcataagttatggaacagtgttagaaaacaactcaaaagtatattctttattaatgaggtggtcattattacatttgtgtcaatgaagggcagtgtagttattttaaaatgactaatattttctccccaaatacagaataattcagatgggcaaccaagttttcaagagactgctgtaggtgaagtctgtctagccaaggcagaacacttacaggagtccctaactgtgccacccttggaatgggttagtgtacaggctcagaatattgtggattacagtttttcagagaaaactaccacagatgtagacaaaaatgatctctgaaagcattgccagcagccaggtatgttccttagatttccacttaggtttggcattttggcagataagctaatcttgtataaagcatcacattttactatgcttagtgttcctgggttgtatttatctacattattagagggaatttttattttaaaaaaattgtcattcatgagaagaatgggagttcatgccacatagtattttaccaatttatataaagtgggaaaagtctttaatacttcatgatcacttgaattaaagtttttgtatctctggaaagtagaatagtgctttcatttgaatgaaaagtgtttatagattcagaaagagagatgatatctttgtatcttgatttatatacagaccatttcagaggaagttaaatgtcttacaaatccaatactttctaatgctctaacagtgttggctatttaaaagaacatgtggcaagttctatatgaatattcttggtcatctcgactaattctgaggcaatgatggacagagatgctacttcttatttaactctaggcatgttgacttttcaaagcggtttccttatttctaaacagagatgatgatcaatgagttactaattctttagaggaaaaaatgcataatttgagtgtggagttgattttaatgacagggtaattcaagttgtttgataaatttattactatattgtaagagagatctttgaccatttttcttcctttttcttggacatcactttcttccctccccttctctcttttatgtttttatccttgttaaattttatgtttacgttaccatctttcttatactttcccctgatttttctcttttaattcctctttcattctctgcctcttctctttcagctctttctctaattgtgcctattccttgttcataagaagtggagctgttagtggtagaaccactgctcatggttctaccactacaaagtggaaagtagaaatactttgcactttggccactgttgcgtttttgccaaggtaaagttcccctgccattttgaaatagctgaacaagttaaagtaatatgttccaaaaactggaagtgccataaaaaactaaaaataaaaaaaaattgtgacta
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:23041 -> Molecular function: GO:0005086 [ARF guanyl-nucleotide exchange factor activity] evidence: IBA
            GeneID:23041 -> Biological process: GO:0006895 [Golgi to endosome transport] evidence: ISS
            GeneID:23041 -> Biological process: GO:0015031 [protein transport] evidence: IEA
            GeneID:23041 -> Biological process: GO:0016192 [vesicle-mediated transport] evidence: IBA
            GeneID:23041 -> Biological process: GO:0030036 [actin cytoskeleton organization] evidence: IBA
            GeneID:23041 -> Cellular component: GO:0005802 [trans-Golgi network] evidence: IBA

by @meso_cacase at DBCLS
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