Home |
Help |
Advanced search
2024-04-23 23:25:24, 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 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
This page is licensed under a Creative Commons Attribution 2.1 Japan License.