2024-04-18 13:10:35, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_006633 5769 bp mRNA linear PRI 15-JUN-2013 DEFINITION Homo sapiens IQ motif containing GTPase activating protein 2 (IQGAP2), mRNA. ACCESSION NM_006633 VERSION NM_006633.2 GI:116089336 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 5769) AUTHORS Del-Aguila,J.L., Beitelshees,A.L., Cooper-Dehoff,R.M., Chapman,A.B., Gums,J.G., Bailey,K., Gong,Y., Turner,S.T., Johnson,J.A. and Boerwinkle,E. TITLE Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans JOURNAL Pharmacogenomics J. (2013) In press PUBMED 23400010 REMARK Publication Status: Available-Online prior to print REFERENCE 2 (bases 1 to 5769) AUTHORS Xie,Y., Yan,J., Cutz,J.C., Rybak,A.P., He,L., Wei,F., Kapoor,A., Schmidt,V.A., Tao,L. and Tang,D. TITLE IQGAP2, A candidate tumour suppressor of prostate tumorigenesis JOURNAL Biochim. Biophys. Acta 1822 (6), 875-884 (2012) PUBMED 22406297 REMARK GeneRIF: observations strongly indicate that IQGAP2 is a surveillance type of tumour suppressor for prostate cancer REFERENCE 3 (bases 1 to 5769) AUTHORS Flachsbart,F., Franke,A., Kleindorp,R., Caliebe,A., Blanche,H., Schreiber,S. and Nebel,A. TITLE Investigation of genetic susceptibility factors for human longevity - a targeted nonsynonymous SNP study JOURNAL Mutat. Res. 694 (1-2), 13-19 (2010) PUBMED 20800603 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 4 (bases 1 to 5769) AUTHORS Bailey,S.D., Xie,C., Do,R., Montpetit,A., Diaz,R., Mohan,V., Keavney,B., Yusuf,S., Gerstein,H.C., Engert,J.C. and Anand,S. CONSRTM DREAM investigators TITLE Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study JOURNAL Diabetes Care 33 (10), 2250-2253 (2010) PUBMED 20628086 REMARK GeneRIF: Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) REFERENCE 5 (bases 1 to 5769) AUTHORS White,C.D., Khurana,H., Gnatenko,D.V., Li,Z., Odze,R.D., Sacks,D.B. and Schmidt,V.A. TITLE IQGAP1 and IQGAP2 are reciprocally altered in hepatocellular carcinoma JOURNAL BMC Gastroenterol 10, 125 (2010) PUBMED 20977743 REMARK GeneRIF: increased IQGAP1 and/or decreased IQGAP2 contribute to the pathogenesis of human HCC. Publication Status: Online-Only REFERENCE 6 (bases 1 to 5769) AUTHORS Gevaert,K., Goethals,M., Martens,L., Van Damme,J., Staes,A., Thomas,G.R. and Vandekerckhove,J. TITLE Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides JOURNAL Nat. Biotechnol. 21 (5), 566-569 (2003) PUBMED 12665801 REFERENCE 7 (bases 1 to 5769) AUTHORS Schmidt,V.A., Scudder,L., Devoe,C.E., Bernards,A., Cupit,L.D. and Bahou,W.F. TITLE IQGAP2 functions as a GTP-dependent effector protein in thrombin-induced platelet cytoskeletal reorganization JOURNAL Blood 101 (8), 3021-3028 (2003) PUBMED 12515716 REMARK GeneRIF: The gene for the putative rac1/cdc42 effector protein IQGAP2 was found in the PAR gene cluster at 5q13, flanked by PAR1 & encompassing PAR3. It functions as a GTP-dependent effector protein in thrombin-induced platelet cytoskeletal reorganization. REFERENCE 8 (bases 1 to 5769) AUTHORS Wennerberg,K., Ellerbroek,S.M., Liu,R.Y., Karnoub,A.E., Burridge,K. and Der,C.J. TITLE RhoG signals in parallel with Rac1 and Cdc42 JOURNAL J. Biol. Chem. 277 (49), 47810-47817 (2002) PUBMED 12376551 REFERENCE 9 (bases 1 to 5769) AUTHORS McCallum,S.J., Wu,W.J. and Cerione,R.A. TITLE Identification of a putative effector for Cdc42Hs with high sequence similarity to the RasGAP-related protein IQGAP1 and a Cdc42Hs binding partner with similarity to IQGAP2 JOURNAL J. Biol. Chem. 271 (36), 21732-21737 (1996) PUBMED 8702968 REFERENCE 10 (bases 1 to 5769) AUTHORS Brill,S., Li,S., Lyman,C.W., Church,D.M., Wasmuth,J.J., Weissbach,L., Bernards,A. and Snijders,A.J. TITLE The Ras GTPase-activating-protein-related human protein IQGAP2 harbors a potential actin binding domain and interacts with calmodulin and Rho family GTPases JOURNAL Mol. Cell. Biol. 16 (9), 4869-4878 (1996) PUBMED 8756646 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from U51903.1, DB075371.1, AB208856.1 and BI481276.1. On Oct 13, 2006 this sequence version replaced gi:5729886. Summary: This gene encodes a member of the IQGAP family. The protein contains three IQ domains, one calponin homology domain, one Ras-GAP domain and one WW domain. It interacts with components of the cytoskeleton, with cell adhesion molecules, and with several signaling molecules to regulate cell morphology and motility. [provided by RefSeq, Jul 2008]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: U51903.1, AK291066.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025084, ERS025088 [ECO:0000348] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-1802 U51903.1 1-1802 1803-1815 DB075371.1 299-311 1816-2108 U51903.1 1816-2108 2109-2765 AB208856.1 627-1283 2766-5065 U51903.1 2766-5065 5066-5764 AB208856.1 3584-4282 5765-5767 U51903.1 5765-5767 5768-5769 BI481276.1 283-284 FEATURES Location/Qualifiers source 1..5769 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="5" /map="5q13.3" gene 1..5769 /gene="IQGAP2" /note="IQ motif containing GTPase activating protein 2" /db_xref="GeneID:10788" /db_xref="HGNC:6111" /db_xref="MIM:605401" exon 1..268 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 11 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:116588852" variation 14 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:371320955" variation 46 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:1122654" misc_feature 103..105 /gene="IQGAP2" /note="upstream in-frame stop codon" variation 103 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:112531987" variation 204 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:368092917" CDS 223..4950 /gene="IQGAP2" /codon_start=1 /product="ras GTPase-activating-like protein IQGAP2" /protein_id="NP_006624.2" /db_xref="GI:116089337" /db_xref="CCDS:CCDS34188.1" /db_xref="GeneID:10788" /db_xref="HGNC:6111" /db_xref="MIM:605401" /translation="
MPHEELPSLQRPRYGSIVDDERLSAEEMDERRRQNIAYEYLCHLEEAKRWMEVCLVEELPPTTELEEGLRNGVYLAKLAKFFAPKMVSEKKIYDVEQTRYKKSGLHFRHTDNTVQWLRAMESIGLPKIFYPETTDVYDRKNIPRMIYCIHALSLYLFKLGIAPQIQDLLGKVDFTEEEISNMRKELEKYGIQMPSFSKIGGILANELSVDEAALHAAVIAINEAVEKGIAEQTVVTLRNPNAVLTLVDDNLAPEYQKELWDAKKKKEENARLKNSCISEEERDAYEELLTQAEIQGNINKVNRQAAVDHINAVIPEGDPENTLLALKKPEAQLPAVYPFAAAMYQNELFNLQKQNTMNYLAHEELLIAVEMLSAVALLNQALESNDLVSVQNQLRSPAIGLNNLDKAYVERYANTLLSVKLEVLSQGQDNLSWNEIQNCIDMVNAQIQEENDRVVAVGYINEAIDEGNPLRTLETLLLPTANISDVDPAHAQHYQDVLYHAKSQKLGDSESVSKVLWLDEIQQAVDDANVDEDRAKQWVTLVVDVNQCLEGKKSSDILSVLKSSTSNANDIIPECADKYYDALVKAKELKSERVSSDGSWLKLNLHKKYDYYYNTDSKESSWVTPESCLYKESWLTGKEIEDIIEEVTVGYIRENIWSASEELLLRFQATSSGPILREEFEARKSFLHEQEENVVKIQAFWKGYKQRKEYMHRRQTFIDNTDSIVKIQSWFRMATARKSYLSRLQYFRDHNNEIVKIQSLLRANKARDDYKTLVGSENPPLTVIRKFVYLLDQSDLDFQEELEVARLREEVVTKIRANQQLEKDLNLMDIKIGLLVKNRITLEDVISHSKKLNKKKGGEMEILNNTDNQGIKSLSKERRKTLETYQQLFYLLQTNPLYLAKLIFQMPQNKSTKFMDTVIFTLYNYASNQREEYLLLKLFKTALEEEIKSKVDQVQDIVTGNPTVIKMVVSFNRGARGQNTLRQLLAPVVKEIIDDKSLIINTNPVEVYKAWVNQLETQTGEASKLPYDVTTEQALTYPEVKNKLEASIENLRRVTDKVLNSIISSLDLLPYGLRYIAKVLKNSIHEKFPDATEDELLKIVGNLLYYRYMNPAIVAPDGFDIIDMTAGGQINSDQRRNLGSVAKVLQHAASNKLFEGENEHLSSMNNYLSETYQEFRKYFKEACNVPEPEEKFNMDKYTDLVTVSKPVIYISIEEIISTHSLLLEHQDAIAPEKNDLLSELLGSLGEVPTVESFLGEGAVDPNDPNKANTLSQLSKTEISLVLTSKYDIEDGEAIDSRSLMIKTKKLIIDVIRNQPGNTLTEILETPATAQQEVDHATDMVSRAMIDSRTPEEMKHSQSMIEDAQLPLEQKKRKIQRNLRTLEQTGHVSSENKYQDILNEIAKDIRNQRIYRKLRKAELAKLQQTLNALNKKAAFYEEQINYYDTYIKTCLDNLKRKNTRRSIKLDGKGEPKGAKRAKPVKYTAAKLHEKGVLLDIDDLQTNQFKNVTFDIIATEDVGIFDVRSKFLGVEMEKVQLNIQDLLQMQYEGVAVMKMFDKVKVNVNLLIYLLNKKFYGK
" misc_feature 268..270 /gene="IQGAP2" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q13576.4); phosphorylation site" misc_feature 346..690 /gene="IQGAP2" /note="Calponin homology domain; actin-binding domain which may be present as a single copy or in tandem repeats (which increases binding affinity). The CH domain is found in cytoskeletal and signal transduction proteins, including actin-binding proteins like...; Region: CH; cd00014" /db_xref="CDD:28898" misc_feature order(346..351,355..363,370..372,379..381,571..576, 583..585,592..594,598..600,649..654,661..666,670..675, 682..687) /gene="IQGAP2" /note="putative actin binding surface [polypeptide binding]; other site" /db_xref="CDD:28898" misc_feature 2287..2352 /gene="IQGAP2" /note="Calmodulin-binding motif; Region: IQ; smart00015" /db_xref="CDD:197470" misc_feature 2998..4014 /gene="IQGAP2" /note="IQGAP2 is a member of the IQGAP family that contains a calponin-homology (CH) domain which binds F-actin, IQGAP-specific repeat, a single WW domain, four IQ motifs which mediate interactions with calmodulin, and a Ras-GTPase-activating protein (GAP)...; Region: RasGAP_IQGAP2; cd05131" /db_xref="CDD:88571" misc_feature 4318..4725 /gene="IQGAP2" /note="RasGAP C-terminus; Region: RasGAP_C; pfam03836" /db_xref="CDD:146459" variation 223 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:370320521" exon 269..368 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 279 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:372040696" variation 281 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:148247178" variation 315 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:376030929" variation 320 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:369302838" variation 321 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:141290804" variation 324 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:373606679" variation 345 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:139165349" exon 369..525 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 415 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:139440648" variation 431 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:369077131" variation 449 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:373370094" variation 507 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:148174773" variation 517 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:376517879" exon 526..603 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 544 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:192694811" variation 561 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:115631027" variation 578 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:146065067" exon 604..680 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 634 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:200135774" variation 662 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:140724393" variation 673 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:201291442" exon 681..748 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 684 /gene="IQGAP2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1131232" variation 700 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:375045201" variation 709 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:202016097" exon 749..862 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 756 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:143699665" variation 775 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:201127307" variation 842 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:34833676" exon 863..1041 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 864 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:148953280" variation 865 /gene="IQGAP2" /replace="c" /replace="g" /db_xref="dbSNP:201525266" variation 872 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:111655897" variation 892 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:199711600" variation 899 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:374036965" variation 921 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:200319462" variation 922 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:147531108" variation 943 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:201309376" variation 977 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:376703431" variation 1005 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:151083253" exon 1042..1129 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 1090 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:373714955" variation 1095 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:142653944" variation 1108 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:377573714" exon 1130..1293 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 1137 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:141398992" variation 1154 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:371271172" variation 1159 /gene="IQGAP2" /replace="c" /replace="g" /db_xref="dbSNP:137915513" variation 1166 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:141913830" variation 1167 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:371048498" variation 1180 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:150086790" variation 1187 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:375606140" variation 1227 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:368353933" variation 1260 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:369254878" variation 1274 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:373251555" variation 1277 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:181258165" exon 1294..1454 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 1309 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:199507670" variation 1354 /gene="IQGAP2" /replace="c" /replace="g" /db_xref="dbSNP:376410723" variation 1377 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:140342604" variation 1414 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:138552758" variation 1433 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:374157441" variation 1454 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:377512838" exon 1455..1579 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 1475 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:373926073" variation 1489 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:149265572" variation 1502 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:144559978" variation 1504 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:137988082" variation 1546 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:73766943" variation 1553 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:376098110" exon 1580..1743 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 1581 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:370560776" variation 1586 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:7722711" variation 1587 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:139972010" variation 1604 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:201516054" variation 1612 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:368535679" variation 1617 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:11553735" variation 1658 /gene="IQGAP2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:3822530" variation 1668 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:371624599" variation 1686 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:34535949" variation 1692 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:36087650" variation 1700 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:374553088" exon 1744..1834 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 1763 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:139421974" variation 1794 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:2431351" variation 1798 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:145465543" variation 1803 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:2431352" variation 1810 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:368255249" variation 1814 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:143443092" variation 1816 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:2909888" variation 1833 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:376719498" exon 1835..2002 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 1845 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:140885056" variation 1968 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:144805046" exon 2003..2145 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 2008 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:369081736" variation 2013 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:2910819" variation 2049 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:150366195" variation 2067 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:373417790" variation 2106 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:138150085" variation 2109 /gene="IQGAP2" /replace="c" /replace="g" /db_xref="dbSNP:2455230" variation 2113 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:181383719" variation 2115 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:138758867" variation 2142 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:140853165" exon 2146..2316 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 2160 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:145113303" variation 2161 /gene="IQGAP2" /replace="c" /replace="g" /db_xref="dbSNP:35544895" variation 2180 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:375933191" variation 2190 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:368537160" variation 2207 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:111675976" variation 2209 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:373264194" variation 2223 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:76713554" variation 2224 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:200306861" variation 2240 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:371907881" variation 2243 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:376526797" variation 2259 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:147514296" variation 2261 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:148549280" variation 2278 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:368456798" variation 2301 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:201322324" variation 2305 /gene="IQGAP2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:79871053" variation 2307 /gene="IQGAP2" /replace="c" /replace="g" /db_xref="dbSNP:372017854" exon 2317..2400 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 2341 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:375342547" variation 2342 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:151128648" variation 2360 /gene="IQGAP2" /replace="c" /replace="g" /db_xref="dbSNP:139973941" variation 2362 /gene="IQGAP2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:35366349" variation 2369 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:199827196" variation 2392 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:2431363" exon 2401..2472 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 2416 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:373704383" variation 2417 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:112380748" variation 2419 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:199567785" variation 2441 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:377569601" exon 2473..2542 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 2503 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:377698465" variation 2511 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:371448195" exon 2543..2751 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 2586 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:140923952" variation 2589 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:368438960" variation 2636 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:372033178" variation 2730 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:373890004" exon 2752..2901 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 2757 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:144641342" variation 2766 /gene="IQGAP2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:253093" variation 2801 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:200795118" variation 2825 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:201059481" variation 2831 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:201642967" variation 2839 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:200362498" variation 2869 /gene="IQGAP2" /replace="c" /replace="g" /db_xref="dbSNP:34968964" variation 2898 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:148071477" exon 2902..3065 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 2903 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:34950321" variation 2963 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:146422169" variation 2990 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:201385729" variation 2998 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:188847941" variation 3010 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:377130667" variation 3011 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:138998729" exon 3066..3290 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 3099 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:143119515" variation 3147 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:143839039" variation 3149 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:148082215" variation 3185 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:374151074" variation 3202 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:138211969" variation 3204 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:76979655" variation 3213 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:144328533" variation 3240 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:201177978" exon 3291..3431 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 3313 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:376921394" variation 3372 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:200705388" variation 3377 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:2287932" variation 3384 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:200616670" variation 3387 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:143869334" variation 3388 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:145945229" variation 3397 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:375412628" variation 3406 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:139792880" variation 3431 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:200940839" exon 3432..3516 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 3449 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:368432599" variation 3456 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:145178581" variation 3472 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:371564584" variation 3496 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:151182090" exon 3517..3749 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 3543 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:112301923" variation 3598 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:140188703" variation 3614 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:199960498" variation 3617 /gene="IQGAP2" /replace="c" /replace="g" /db_xref="dbSNP:201879277" variation 3663 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:375463609" variation 3697 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:149940408" variation 3701 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:201262213" variation 3740 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:369959488" exon 3750..3882 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 3750 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:202217286" variation 3773 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:10454915" variation 3788 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:142296855" variation 3802 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:373729319" variation 3804 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:368996458" variation 3824 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:146071185" variation 3832 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:201192766" variation 3867 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:457937" exon 3883..3985 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 3920 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:373530105" variation 3951 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:34076951" variation 3970 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:185223948" exon 3986..4127 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 4018 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:141592712" variation 4079 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:143650393" variation 4093 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:376614167" variation 4117 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:147002427" exon 4128..4215 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 4156 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:373730789" variation 4190 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:367797221" variation 4192 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:192621142" STS 4193..4660 /gene="IQGAP2" /standard_name="Iqgap2" /db_xref="UniSTS:256441" variation 4208 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:148122303" exon 4216..4428 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 4220 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:141880135" variation 4226 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:377308848" variation 4283 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:61739347" variation 4293 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:182860123" variation 4301 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:372408098" variation 4357 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:17681908" variation 4362 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:142258030" variation 4374 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:146380825" variation 4415 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:139757749" variation 4416 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:369344159" variation 4421 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:373452467" exon 4429..4589 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 4436 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:189501812" variation 4497 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:374869048" variation 4509 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:143210414" variation 4517 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:181359610" variation 4519 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:144434710" variation 4556 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:369078465" exon 4590..4727 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 4598 /gene="IQGAP2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:34592828" variation 4612 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:142548903" STS 4614..4813 /gene="IQGAP2" /standard_name="MARC_17727-17728:1031758304:1" /db_xref="UniSTS:268387" variation 4626 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:201596632" variation 4641 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:190325896" variation 4647 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:150986204" variation 4649 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:142120814" variation 4686 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:377118954" variation 4700 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:370452996" variation 4701 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:374871150" variation 4713 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:144405948" variation 4714 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:147860676" variation 4724 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:199687430" exon 4728..4836 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 4745 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:141420081" variation 4756 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:368828240" variation 4787 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:371330018" variation 4792 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:368752328" variation 4812 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:150409607" variation 4814 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:201571668" variation 4818 /gene="IQGAP2" /replace="c" /replace="g" /db_xref="dbSNP:145165340" variation 4824 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:375336707" variation 4829 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:201167699" exon 4837..5769 /gene="IQGAP2" /inference="alignment:Splign:1.39.8" variation 4856 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:202207724" variation 4921 /gene="IQGAP2" /replace="c" /replace="g" /db_xref="dbSNP:372834701" STS 4965..5115 /gene="IQGAP2" /standard_name="RH70668" /db_xref="UniSTS:82051" variation 4967 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:377567632" variation 4973 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:370207767" variation 5058..5059 /gene="IQGAP2" /replace="" /replace="t" /db_xref="dbSNP:75247437" variation 5066 /gene="IQGAP2" /replace="a" /replace="t" /db_xref="dbSNP:463188" variation 5070 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:464494" variation 5116 /gene="IQGAP2" /replace="" /replace="t" /db_xref="dbSNP:5868837" variation 5129 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:139058911" variation 5154..5155 /gene="IQGAP2" /replace="" /replace="g" /db_xref="dbSNP:35189434" variation 5235 /gene="IQGAP2" /replace="c" /replace="g" /db_xref="dbSNP:74508809" variation 5285 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:185366183" variation 5294 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:12735" variation 5318 /gene="IQGAP2" /replace="c" /replace="t" /db_xref="dbSNP:371685030" variation 5353 /gene="IQGAP2" /replace="a" /replace="g" /db_xref="dbSNP:190155250" variation 5502 /gene="IQGAP2" /replace="a" /replace="c" /db_xref="dbSNP:182824032" STS 5530..5730 /gene="IQGAP2" /standard_name="D5S2432" /db_xref="UniSTS:78227" variation 5673..5674 /gene="IQGAP2" /replace="" /replace="t" /db_xref="dbSNP:201953417" variation 5679 /gene="IQGAP2" /replace="g" /replace="t" /db_xref="dbSNP:72761042" variation 5753..5755 /gene="IQGAP2" /replace="" /replace="ttac" /db_xref="dbSNP:144991649" variation 5753 /gene="IQGAP2" /replace="" /replace="ttac" /db_xref="dbSNP:34872448" variation 5760 /gene="IQGAP2" /replace="" /replace="ctta" /db_xref="dbSNP:1610959" ORIGIN
gagggaggagagttcacttttacttcagtgtcagcgcgcggcggccgtggctggctctggcgagagagcaccgagggagtgggtcgcagatcttcgggcggctaggggaaatcggcgagaggcgggatccgagcgcgccggcggggcgcagagcccgcgagcctggccagcgagggtagccgcggggggcgcgccccgggcgggcccccggagacgcgcaggatgccacacgaagagctgccgtcgctgcagagaccccgctatggctctattgtggacgatgaaaggctctctgcagaggagatggatgagaggaggcggcagaacattgcttatgaatatctgtgccacttagaggaagccaaaaggtggatggaagtttgcttagttgaagaattgccaccaaccactgaattggaagaagggctccggaatggagtttaccttgcaaagttagccaagttctttgccccgaaaatggtatcagagaaaaagatctatgatgtggaacaaacacgttataagaagtctggccttcattttcgacacacagataataccgtccagtggttaagagcgatggagtctattggtctacccaagatattttatccagaaacaacagatgtctatgatcggaaaaacataccaagaatgatatattgcattcacgcactgagtttgtatctgttcaaactaggaatagcaccccagatccaggatttgttgggcaaagtagacttcacagaggaggaaatcagtaatatgagaaaagaacttgagaaatatggaatacagatgccatctttcagcaaaataggtggtattctggccaatgaactgtccgtggatgaagctgcattacatgctgcagttatagccattaatgaagcagttgaaaaaggaatagcagagcaaaccgttgtaacactaagaaacccaaatgcggttttaactttagtggatgacaaccttgcaccagaatatcagaaagaactctgggatgccaaaaagaaaaaagaggaaaatgcaagactgaagaatagctgtatttcagaagaagaaagagatgcttatgaagaactgctgacacaagcagaaatccaaggcaatattaataaagtcaacaggcaggctgcagtggaccatatcaatgctgtcattccggaaggtgaccccgagaatacgctgcttgcactgaagaaaccagaggcccagctgcctgctgtttatccctttgctgctgccatgtatcagaacgaacttttcaacctccagaaacagaacaccatgaactacttggcccacgaggagcttttgattgctgtggaaatgttgtctgctgttgctttactaaaccaggccttggaaagcaacgatcttgtgtctgtgcagaatcaactcagaagccccgcaataggcttaaacaatctggacaaggcatatgtggaacgttatgcaaacacactactctctgttaaactagaagttttatcccaagggcaagataacttaagctggaatgaaattcagaattgtattgatatggttaatgctcaaattcaagaagaaaatgaccgagttgtagctgtagggtacatcaatgaagctattgatgaagggaatcctttgaggactttagaaactttgctcctacctactgcgaatattagtgatgtggacccagcccatgcccagcactaccaggatgttttataccatgctaaatcacagaaactcggagactctgagagtgtttccaaagtgctttggctggatgagatacagcaagccgtcgatgatgccaacgtggacgaggacagagcaaaacaatgggttactctggtggttgatgttaatcagtgtttggaaggaaaaaaatcaagtgatattttgtctgtattgaagtcttccacttctaatgcaaatgacataatcccggagtgtgctgacaaatactatgatgcccttgtgaaggcaaaagagctcaaatctgaaagagtgtctagtgacggttcatggctcaaactcaacctgcacaaaaaatatgactactattacaacactgattcaaaagagagttcctgggtcacacctgaatcatgcttgtataaagaatcatggctcacaggaaaagaaatcgaggacattattgaggaagtcacagtaggttacattcgtgagaatatatggtctgcttcagaagagttgcttcttcgctttcaagccacaagctcaggacccatccttagggaagagtttgaagctagaaaatcatttttgcatgaacaagaagagaatgtggtcaaaatacaggctttttggaaaggatataaacaacggaaggagtatatgcacaggcggcaaacgttcattgataatactgattctattgtgaagattcagtcctggttccgaatggcaactgcaagaaagagctatctttcaagactacagtatttcagagatcataataatgaaattgtgaaaatacagtcactgttgagagcgaacaaagctagagatgactacaaaacattggttggctctgaaaacccaccattaacagtaattcgcaaatttgtatacctgctggaccaaagtgatttggatttccaggaggaactagaggttgcacgattaagggaagaagtagtgaccaagatcagggccaatcaacagctggaaaaagacctgaacctgatggacatcaagattggactgctggtgaagaacaggatcacactagaggatgtaatttcacacagtaaaaagctgaacaagaaaaaaggaggagaaatggaaatactgaataacaccgacaaccaaggaataaaaagtttgagtaaggagaggagaaaaacactagaaacatatcagcagctgttttaccttttacagaccaaccctttatacttggctaagctgattttccagatgccacagaacaagtccactaaatttatggatactgttattttcacactatataattatgcctctaatcagcgagaagaatatctacttctcaagctttttaaaactgctctggaggaagaaataaaatcaaaagtggaccaggtacaggacatagttactggtaaccctacagtcatcaagatggtcgtcagcttcaatagaggtgcccggggacagaacaccctgcgccaactcctggctccagtggtaaaagagatcatcgacgacaagtcgctgattatcaacacaaaccctgtagaggtgtacaaggcttgggtgaaccaactagaaacacagactggagaggccagcaagttgccttatgatgtgaccacagaacaagctctaacatacccagaagtgaaaaataaactggaggcttccattgagaacctgagaagggtcaccgacaaagtcctgaattctatcatttcttcccttgatctactgccttatggattgaggtatatagccaaagtactgaagaattcgatccatgagaaattccccgatgcaacagaagatgagctattaaagattgttggaaacctcctgtactatcggtacatgaatccagccattgtagctccagatggctttgatatcatcgacatgacagctggaggtcagataaattctgaccaaaggagaaacttaggatcagtggccaaggttcttcagcacgcagcctccaacaagctgtttgaaggagaaaatgagcatctctcatctatgaacaattatttatcagagacgtatcaggaattcaggaaatatttcaaagaagcatgtaatgtccctgagccagaagagaagtttaatatggacaaatacacagacctggtgacagtcagcaaaccagtcatttatatttcaattgaagaaatcatcagcacacactcactcctgttggaacaccaggatgcaattgcccctgagaaaaatgacttactgagtgaattgctggggtcgctgggagaggtgccaaccgtggaatcttttcttggggaaggagcagttgaccccaatgaccctaacaaggcaaatacactaagtcagctttcaaagaccgagatttctcttgtcttgacaagcaaatatgacatagaggacggtgaagctatagatagccgaagcctcatgataaagaccaagaagctgataattgatgtgatccggaaccagccagggaacacattgacagaaatcttagagacaccagcaactgcgcaacaggaggtagaccatgccacggacatggtgagccgtgcaatgatagattccaggactccagaagaaatgaagcatagccaatctatgattgaagatgcacagctgcctcttgagcagaagaagaggaaaatccagaggaatcttcggacgttggaacagactggacacgtgtcatccgaaaataaataccaagacattctcaatgagattgccaaggatattcgaaatcaaagaatctatcgtaagcttcgaaaagctgaattggcaaaacttcagcagaccctgaatgcacttaacaagaaggcagcattttatgaagagcaaatcaattattatgacacctacataaagacttgtttagacaacttaaaaagaaaaaatactcggagatcaattaaactagatggaaaaggagaacccaaaggggcgaagagagcgaagccagtgaagtacactgcagcaaagctgcatgagaaaggtgtcctgctagatatagatgatcttcaaacaaaccagtttaagaatgttacatttgatatcatagctactgaagatgtaggcattttcgatgtaagatcaaaattccttggtgttgagatggaaaaggtgcaactcaatattcaggatttacttcagatgcaatatgaaggagtagctgtaatgaaaatgtttgataaggttaaagtgaatgtaaaccttctcatatacctgctgaacaagaagttctatggaaagtgaagtgcctacagaaatttcttggattctgtatcatctggattaggaaatgaatttgtttaatatttttgtttttaaacatgattgaaatcactgcttataaatgtgtgatttttttaaaacgaccaaaactgttctgaagaatgtacccaggtgcctttttgctaatttgatactataatagaatgagacataaaatgaattaatggaaacatatccacactgtactgtgatataggtactctgatttaaaactttggacatcctgtgatctgttttaaagttggggggtgggaaatttagctgactagggacaaacatgtaaacctattttcctatgaaaaaaattttaaatgtcccacttgaataacgtaattcttcatagtttttttaatctatggataaatggaaacctaattatttgtaatgaattatttagacagttctaagccctgtcttctgggagttatcaattttaaagagaacttttgtgcaattcaaatgaagtttttataagtaattgaaaatgacaacacaataacactttctgtataaaagtatatattttatgtgatttattcctactaaatgaaagtgcactactgcctcatgtaaagactcttgcacgcagagcctttaagtgactaaggaacaacatagatagtgagcatagtccccacctccacccctcacaatttatttgaatacttcaattgtgcctctcaattttttgtaatgctaaaaaatcagtatctagatggtttttaaatgtattctctggaaattgttttatgtaaaataaatgttacttaattccattaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:10788 -> Molecular function: GO:0003779 [actin binding] evidence: TAS GeneID:10788 -> Molecular function: GO:0005095 [GTPase inhibitor activity] evidence: TAS GeneID:10788 -> Molecular function: GO:0005099 [Ras GTPase activator activity] evidence: IEA GeneID:10788 -> Molecular function: GO:0005516 [calmodulin binding] evidence: IEA GeneID:10788 -> Biological process: GO:0007165 [signal transduction] evidence: TAS GeneID:10788 -> Biological process: GO:0007264 [small GTPase mediated signal transduction] evidence: IEA GeneID:10788 -> Cellular component: GO:0005874 [microtubule] evidence: IDA GeneID:10788 -> Cellular component: GO:0005902 [microvillus] evidence: IEA GeneID:10788 -> Cellular component: GO:0015629 [actin cytoskeleton] evidence: TAS
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