2024-03-29 15:34:53, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001037332 6791 bp mRNA linear PRI 15-JUN-2013 DEFINITION Homo sapiens cytoplasmic FMR1 interacting protein 2 (CYFIP2), transcript variant 2, mRNA. ACCESSION NM_001037332 VERSION NM_001037332.2 GI:116805787 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 6791) 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 6791) AUTHORS Hoeffer,C.A., Sanchez,E., Hagerman,R.J., Mu,Y., Nguyen,D.V., Wong,H., Whelan,A.M., Zukin,R.S., Klann,E. and Tassone,F. TITLE Altered mTOR signaling and enhanced CYFIP2 expression levels in subjects with fragile X syndrome JOURNAL Genes Brain Behav. 11 (3), 332-341 (2012) PUBMED 22268788 REMARK GeneRIF: Increased expression of the cytoplasmic FMR1-interacting protein 2 (CYFIP2), a known FMRP interactor, is detected in fragile X syndrome. REFERENCE 3 (bases 1 to 6791) AUTHORS Nachmany,H., Wald,S., Abekasis,M., Bulvik,S. and Weil,M. TITLE Two potential biomarkers identified in mesenchymal stem cells and leukocytes of patients with sporadic amyotrophic lateral sclerosis JOURNAL Dis. Markers 32 (4), 211-220 (2012) PUBMED 22430187 REMARK GeneRIF: blood samples of lateral sclerosis patients were found to have significantly different levels of expression of CyFIP2 and RbBP9 compared to the levels of expression in control subjects. REFERENCE 4 (bases 1 to 6791) AUTHORS Mongroo,P.S., Noubissi,F.K., Cuatrecasas,M., Kalabis,J., King,C.E., Johnstone,C.N., Bowser,M.J., Castells,A., Spiegelman,V.S. and Rustgi,A.K. TITLE IMP-1 displays cross-talk with K-Ras and modulates colon cancer cell survival through the novel proapoptotic protein CYFIP2 JOURNAL Cancer Res. 71 (6), 2172-2182 (2011) PUBMED 21252116 REMARK GeneRIF: Studies identify a novel proapoptotic gene target, CYFIP2, which is downregulated by IMP-1, and mediates the regulation of cell survival and K-Ras expression in colon cancer cells. REFERENCE 5 (bases 1 to 6791) AUTHORS Anitei,M., Stange,C., Parshina,I., Baust,T., Schenck,A., Raposo,G., Kirchhausen,T. and Hoflack,B. TITLE Protein complexes containing CYFIP/Sra/PIR121 coordinate Arf1 and Rac1 signalling during clathrin-AP-1-coated carrier biogenesis at the TGN JOURNAL Nat. Cell Biol. 12 (4), 330-340 (2010) PUBMED 20228810 REMARK GeneRIF: Protein complexes containing CYFIP/Sra/PIR121 coordinate Arf1 and Rac1 signalling during clathrin-AP-1-coated carrier biogenesis at the trans-golgi network. Erratum:[Nat Cell Biol. 2010 May;12(5):520] REFERENCE 6 (bases 1 to 6791) AUTHORS Eden,S., Rohatgi,R., Podtelejnikov,A.V., Mann,M. and Kirschner,M.W. TITLE Mechanism of regulation of WAVE1-induced actin nucleation by Rac1 and Nck JOURNAL Nature 418 (6899), 790-793 (2002) PUBMED 12181570 REFERENCE 7 (bases 1 to 6791) AUTHORS Schenck,A., Bardoni,B., Moro,A., Bagni,C. and Mandel,J.L. TITLE A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P JOURNAL Proc. Natl. Acad. Sci. U.S.A. 98 (15), 8844-8849 (2001) PUBMED 11438699 REFERENCE 8 (bases 1 to 6791) AUTHORS Saller,E., Tom,E., Brunori,M., Otter,M., Estreicher,A., Mack,D.H. and Iggo,R. TITLE Increased apoptosis induction by 121F mutant p53 JOURNAL EMBO J. 18 (16), 4424-4437 (1999) PUBMED 10449408 REFERENCE 9 (bases 1 to 6791) AUTHORS Witke,W., Podtelejnikov,A.V., Di Nardo,A., Sutherland,J.D., Gurniak,C.B., Dotti,C. and Mann,M. TITLE In mouse brain profilin I and profilin II associate with regulators of the endocytic pathway and actin assembly JOURNAL EMBO J. 17 (4), 967-976 (1998) PUBMED 9463375 REFERENCE 10 (bases 1 to 6791) AUTHORS Kitamura,T., Kitamura,Y., Yonezawa,K., Totty,N.F., Gout,I., Hara,K., Waterfield,M.D., Sakaue,M., Ogawa,W. and Kasuga,M. TITLE Molecular cloning of p125Nap1, a protein that associates with an SH3 domain of Nck JOURNAL Biochem. Biophys. Res. Commun. 219 (2), 509-514 (1996) PUBMED 8605018 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AL559919.3, BG257432.1, AL136549.1, BC011762.1 and AC008676.6. On Oct 27, 2006 this sequence version replaced gi:82617635. Transcript Variant: This variant (2) represents the longest transcript. Variants 1, 2, and 3 all encode the same protein. 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## CDS exon combination :: BC021008.1, AF160973.1 [ECO:0000331] RNAseq introns :: single sample supports all introns ERS025082, ERS025084 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-48 AL559919.3 4-51 49-375 BG257432.1 17-343 376-638 AL559919.3 380-642 639-1388 AL136549.1 346-1095 1389-2742 BC011762.1 1223-2576 2743-4417 AL136549.1 2450-4124 4418-6791 AC008676.6 158750-161123 c FEATURES Location/Qualifiers source 1..6791 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="5" /map="5q33.3" gene 1..6791 /gene="CYFIP2" /gene_synonym="PIR121" /note="cytoplasmic FMR1 interacting protein 2" /db_xref="GeneID:26999" /db_xref="HGNC:13760" /db_xref="MIM:606323" exon 1..408 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 114 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:370043679" variation 179 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:11551377" misc_feature 342..344 /gene="CYFIP2" /gene_synonym="PIR121" /note="upstream in-frame stop codon" variation 371 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:11551376" variation 376 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:187458" variation 402 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:114654219" exon 409..548 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" CDS 432..4193 /gene="CYFIP2" /gene_synonym="PIR121" /note="p53 inducible protein; p53-inducible protein 121" /codon_start=1 /product="cytoplasmic FMR1-interacting protein 2" /protein_id="NP_001032409.2" /db_xref="GI:116805788" /db_xref="GeneID:26999" /db_xref="HGNC:13760" /db_xref="MIM:606323" /translation="
MTTHVTLEDALSNVDLLEELPLPDQQPCIEPPPSSIMYQANFDTNFEDRNAFVTGIARYIEQATVHSSMNEMLEEGHEYAVMLYTWRSCSRAIPQVKCNEQPNRVEIYEKTVEVLEPEVTKLMKFMYFQRKAIERFCSEVKRLCHAERRKDFVSEAYLLTLGKFINMFAVLDELKNMKCSVKNDHSAYKRAAQFLRKMADPQSIQESQNLSMFLANHNRITQCLHQQLEVIPGYEELLADIVNICVDYYENKMYLTPSEKHMLLKVMGFGLYLMDGNVSNIYKLDAKKRINLSKIDKFFKQLQVVPLFGDMQIELARYIKTSAHYEENKSKWTCTQSSISPQYNICEQMVQIRDDHIRFISELARYSNSEVVTGSGLDSQKSDEEYRELFDLALRGLQLLSKWSAHVMEVYSWKLVHPTDKFCNKDCPGTAEEYERATRYNYTSEEKFAFVEVIAMIKGLQVLMGRMESVFNQAIRNTIYAALQDFAQVTLREPLRQAVRKKKNVLISVLQAIRKTICDWEGGREPPNDPCLRGEKDPKGGFDIKVPRRAVGPSSTQLYMVRTMLESLIADKSGSKKTLRSSLDGPIVLAIEDFHKQSFFFTHLLNISEALQQCCDLSQLWFREFFLELTMGRRIQFPIEMSMPWILTDHILETKEPSMMEYVLYPLDLYNDSAYYALTKFKKQFLYDEIEAEVNLCFDQFVYKLADQIFAYYKAMAGSVLLDKRFRAECKNYGVIIPYPPSNRYETLLKQRHVQLLGRSIDLNRLITQRISAAMYKSLDQAISRFESEDLTSIVELEWLLEINRLTHRLLCKHMTLDSFDAMFREANHNVSAPYGRITLHVFWELNFDFLPNYCYNGSTNRFVRTAIPFTQEPQRDKPANVQPYYLYGSKPLNIAYSHIYSSYRNFVGPPHFKTICRLLGYQGIAVVMEELLKIVKSLLQGTILQYVKTLIEVMPKICRLPRHEYGSPGILEFFHHQLKDIIEYAELKTDVFQSLREVGNAILFCLLIEQALSQEEVCDLLHAAPFQNILPRVYIKEGERLEVRMKRLEAKYAPLHLVPLIERLGTPQQIAIAREGDLLTKERLCCGLSMFEVILTRIRSYLQDPIWRGPPPTNGVMHVDECVEFHRLWSAMQFVYCIPVGTNEFTAEQCFGDGLNWAGCSIIVLLGQQRRFDLFDFCYHLLKVQRQDGKDEIIKNVPLKKMADRIRKYQILNNEVFAILNKYMKSVETDSSTVEHVRCFQPPIHQSLATTC
" misc_feature 1581..4100 /gene="CYFIP2" /gene_synonym="PIR121" /note="Cytoplasmic Fragile-X interacting family; Region: FragX_IP; pfam05994" /db_xref="CDD:218846" misc_feature 3540..3542 /gene="CYFIP2" /gene_synonym="PIR121" /experiment="experimental evidence, no additional details recorded" /note="N6-acetyllysine; propagated from UniProtKB/Swiss-Prot (Q96F07.2); acetylation site" variation 440 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:371578292" variation 470 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:376687042" variation 512 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:367998009" variation 540 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:371710290" variation 542 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:369640959" exon 549..638 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 593 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:375350435" variation 629 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:369941644" exon 639..713 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 664 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:373074465" variation 671 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:376568198" variation 710..712 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="c" /db_xref="dbSNP:5872508" variation 710 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:200051515" exon 714..818 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 725 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:368093712" variation 728 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:139530784" exon 819..1000 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 830 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:148895189" variation 869 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:375762537" variation 928 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:369872275" variation 965 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:369062847" variation 971 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:373151265" exon 1001..1097 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1028 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:185022541" variation 1052 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:199855067" exon 1098..1226 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" exon 1227..1331 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" exon 1332..1423 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1389 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:3207362" exon 1424..1541 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1424 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:376920120" variation 1429 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:148350606" variation 1472 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:373676501" variation 1484 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:372848474" variation 1514 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:376982797" exon 1542..1661 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1580 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:368645883" variation 1601 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:139943836" exon 1662..1787 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1718 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:17054446" variation 1724 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:369323669" variation 1730 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:372259482" exon 1788..1954 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1793 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:6885590" variation 1838 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:377728487" variation 1911 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:370137201" exon 1955..2102 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1955 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:370084969" variation 1956 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:372630008" variation 1961 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:1823035" variation 2078 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:185026624" exon 2103..2256 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 2176 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:370992962" variation 2186 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:142973944" exon 2257..2413 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 2282 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:367974123" variation 2330 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:372104693" variation 2336 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:375426388" variation 2348 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:369858004" exon 2414..2510 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 2444 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:199725246" variation 2450 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:372517333" variation 2453 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:375703811" variation 2492 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:11551374" exon 2511..2587 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" exon 2588..2696 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 2633 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:374669553" variation 2644 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:367713994" variation 2645 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:141399379" variation 2654 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:147011006" variation 2662 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:376060688" variation 2672 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:116817896" exon 2697..2816 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 2708 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:375270131" variation 2743 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:17850790" variation 2778 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:139353471" variation 2779 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:373467559" variation 2804 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:13354242" exon 2817..3016 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 2831 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:377148423" variation 2832 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:201559066" variation 2852 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:369405267" variation 2854 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:374132627" variation 2875 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:377648376" variation 2879 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:371132555" variation 2905 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:58005665" variation 2925 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:11551375" variation 2927 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:373107748" variation 2928 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:377031549" exon 3017..3104 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 3030 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:371766099" variation 3051 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:375088064" variation 3071 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:7705781" variation 3090 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:373799565" exon 3105..3248 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 3140 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:371615057" variation 3177 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:9313557" variation 3206 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:183570769" variation 3215 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:186955009" exon 3249..3339 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 3308 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:373712469" exon 3340..3470 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 3374 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:372286637" variation 3386 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:377070210" variation 3387 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:377125065" variation 3437 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:150652041" exon 3471..3543 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" STS 3482..3546 /gene="CYFIP2" /gene_synonym="PIR121" /standard_name="STS-M62008" /db_xref="UniSTS:55216" variation 3512 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:372902849" exon 3544..3638 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 3553 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:368529367" variation 3569 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:371277463" variation 3573 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:374707103" variation 3584 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:73307968" variation 3593 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:372007539" variation 3626 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:376770442" exon 3639..3877 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 3656 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:369693364" variation 3757 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:200428535" variation 3760 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:374666951" variation 3767 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:114967929" variation 3782 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:373142413" variation 3794 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:199725841" variation 3813 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:376484231" variation 3819 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:199945789" variation 3822 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:201475685" variation 3825 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:369611074" variation 3843 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="t" /db_xref="dbSNP:148677157" variation 3875 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="t" /db_xref="dbSNP:377656882" exon 3878..4025 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 3890 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:368047583" variation 3959 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:200774279" exon 4026..6791 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 4076 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:375350614" STS 4116..4399 /gene="CYFIP2" /gene_synonym="PIR121" /standard_name="RH18378" /db_xref="UniSTS:21434" variation 4123 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:182717318" variation 4129 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:370184404" variation 4146 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:371399881" variation 4147 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:201882855" variation 4157 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:1803834" STS 4163..4293 /gene="CYFIP2" /gene_synonym="PIR121" /standard_name="RH15890" /db_xref="UniSTS:66388" variation 4184 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:375865980" variation 4217 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:150599988" variation 4239 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:373854212" variation 4245 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:199652534" variation 4252 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:13174378" variation 4342 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:73307980" variation 4377 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:188974329" variation 4401..4402 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="a" /db_xref="dbSNP:33954943" variation 4401 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="a" /replace="aa" /db_xref="dbSNP:3052310" variation 4414..4417 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="aaaa" /db_xref="dbSNP:77677846" variation 4454 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:367860573" variation 4612 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:73309941" variation 4620 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:368328314" variation 4640 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:62387481" variation 4688 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:149305788" variation 4737..4738 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="cc" /db_xref="dbSNP:201743820" variation 4738..4739 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="tggcttcccaaagccccattcta" /db_xref="dbSNP:372558922" variation 4743 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="a" /db_xref="dbSNP:199925015" variation 4763 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:147411422" variation 4785 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:140777310" variation 4786 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="c" /db_xref="dbSNP:375776712" variation 4786 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:144727795" variation 4851 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:192134177" variation 4869 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:147444680" STS 4894..5105 /gene="CYFIP2" /gene_synonym="PIR121" /standard_name="A006W02" /db_xref="UniSTS:11242" variation 5007 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:182865053" variation 5070 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:6555991" variation 5142 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:6555992" variation 5157 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:367959403" variation 5313 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:376881838" variation 5353 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:148519938" variation 5402 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:3734034" variation 5498 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:6862302" variation 5510 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:187411866" variation 5539 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:1058517" variation 5589 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:61736011" variation 5674 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:142969781" variation 5807..5808 /gene="CYFIP2" /gene_synonym="PIR121" /replace="gc" /replace="tt" /db_xref="dbSNP:377513219" variation 5807 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:6880851" variation 5808 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:6882097" variation 5835 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:76594372" variation 5839..5840 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="g" /db_xref="dbSNP:370196582" variation 5870 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:141032109" variation 5929 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:375360183" variation 5953 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:184072551" variation 6083 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:11545337" variation 6133 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:80098745" variation 6188 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:113243312" variation 6274 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:143764472" variation 6315 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:146850512" variation 6334 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:140263633" variation 6365 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="t" /db_xref="dbSNP:111840775" variation 6381 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:3087968" variation 6415 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:10073822" variation 6481 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:115781943" variation 6639 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:375053822" variation 6640 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:186546184" variation 6666 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:145397143" variation 6729 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:371519970" ORIGIN
ggacccgccgcagagccaggtaagcggccctcgcaggcctcgggccgggcacggggactaggatgccgccggggacggggatgaggccgtgaggatgcgcgaagggccgccccctctcccggcccgcggggggcgctcggcgctgtgcccgggctagcccgaggcccggcctcaggccccacgcggcccctttccccctcggacccaccgtgcgtcccgcggcacggaccctctgcccgggaggcgcgggcacatcgcggagctccggcgcggcggcgggggagccgcagcagcaggtgcgcggcctgggccggagccgccagcccgggaggaggcggtgctaatctcagggaccggagacacctgcagcggccgcgagcccggcagcggcgacatcctcgagtccagtgcagaatacagaaactgcagccatgaccacgcacgtcaccctggaagatgccctgtccaacgtggacctgcttgaagagcttcccctccccgaccagcagccatgcatcgagcctccaccttcctccatcatgtaccaggctaactttgacacaaactttgaggacaggaatgcatttgtcacgggcattgcaaggtacattgagcaggctacagtccactccagcatgaatgagatgctggaggaaggacatgagtatgcggtcatgctgtacacctggcgcagctgttcccgggccattccccaggtgaaatgcaacgagcagcccaaccgagtagagatctatgagaagacagtagaggtgctggagccggaggtcaccaagctcatgaagttcatgtattttcagcgcaaggccatcgagcggttctgcagcgaggtgaagcggctgtgccatgccgagcgcaggaaggactttgtctctgaggcctacctcctgacccttggcaagttcatcaacatgtttgctgtcctggatgagctaaagaacatgaagtgcagcgtcaagaatgaccactctgcctacaagagggcagcacagttcctgcggaagatggcagatccccagtctatccaggagtcgcagaacctttccatgttcctggccaaccacaacaggatcacccagtgtctccaccagcaacttgaagtgatcccaggctatgaggagctgctggctgacattgtcaacatctgtgtggattactacgagaacaagatgtacctgactcccagtgagaaacatatgctcctcaaggtgatgggctttggcctctacctaatggatggaaatgtcagtaacatttacaaactggatgccaagaagagaattaatcttagcaaaattgataaattctttaagcagctgcaggtggtgccccttttcggcgacatgcagatagagctggccagatacattaagaccagtgctcactatgaagagaacaagtccaagtggacgtgcacccagagcagcatcagcccccagtacaatatctgcgagcagatggttcagatccgggatgaccacatccgcttcatctccgagctcgctcgctacagcaacagtgaggtggtgacgggctcagggctggacagccagaagtcagacgaggagtatcgcgagctcttcgacctagccctgcggggtctgcagcttctatccaagtggagcgcccacgtcatggaggtgtactcttggaagctggttcatcccacagacaagttctgcaacaaggactgtcctggcaccgcggaggaatatgagagagccacacgctacaattacaccagtgaggaaaaatttgccttcgttgaggtgatcgccatgatcaaaggcctgcaggtgctcatgggcaggatggagagcgtcttcaaccaggccatcaggaacaccatctacgcggcattgcaggacttcgcccaggtgacgctgcgtgagcccctgcggcaggcggtacggaagaagaagaatgtcctcatcagcgtcctacaggcaattcgaaagaccatctgtgactgggagggagggcgagagccccctaatgacccatgcttgagaggggagaaggaccccaaaggtggatttgatatcaaggtgccccggcgtgctgtggggccatccagcacacagctgtacatggtgcggaccatgcttgaatcactcattgcagacaaaagcggctccaagaagaccctgaggagcagcctggatggacccattgtcctcgccatagaggactttcacaaacagtccttcttcttcacacatctgctcaacatcagtgaagccctgcagcagtgttgtgacctctcccagctctggttccgagaattcttcctggagttaaccatgggccgacgaatccagttccccatcgagatgtccatgccctggattctaacggaccatatcctggaaaccaaagaaccttccatgatggagtatgtcctctaccctctggatctgtacaacgacagcgcctactatgctctgaccaagtttaaaaagcagttcctgtacgatgagatagaagctgaggtgaacctgtgttttgatcagtttgtctacaagctggcagaccagatctttgcttactacaaagccatggctggcagtgtcctgttggataaacgttttcgagctgagtgtaagaattatggcgtcatcattccgtatccaccgtccaatcgctatgaaacactgctgaagcagagacacgtccagctgttgggtagatcaattgacttgaacagactcattacccagcgcatctctgccgccatgtataaatccttggaccaagctatcagccgctttgagagtgaggacctgacctccattgtggagctggagtggctgctggagattaaccggctcacgcatcggctgctctgtaagcatatgacgctggacagcttcgatgccatgttccgagaggccaatcacaatgtgtccgccccctatggccgtatcaccctgcatgtcttctgggaactgaactttgactttctccccaactactgctacaatgggtccactaaccgttttgtgcggactgccattcctttcacccaagaaccacaacgagacaaacctgccaacgtccagccttattacctctatggatccaagcctctcaacattgcctacagccacatctacagctcctacaggaatttcgtggggccacctcatttcaagactatctgcagactcctgggttatcagggcatcgctgtggtcatggaggaactgctaaagattgtgaagagcttgctccaaggaaccattctccagtatgtgaaaacactgatagaggtgatgcccaagatatgccgcttgccccgacatgagtatggctccccagggatcctggagttcttccaccaccagctgaaggacatcattgagtacgcagagctcaaaacagacgtgttccagagcctgagggaagtgggcaatgccatcctcttctgcctcctcatagagcaagctctgtctcaggaggaggtctgcgatttgctccatgccgcacccttccaaaacatcttgcctagagtctacatcaaagagggggagcgcctggaggtccggatgaaacgtctggaagccaagtatgccccgctccacctggtccctctgatcgagcggctggggacccctcagcaaatcgccattgctcgcgagggtgacctcctgaccaaggagcggctgtgctgtggcctgtccatgttcgaggtcatcctgacccgcattcggagctacctgcaggaccccatctggcggggcccaccgcccaccaatggcgtcatgcacgtcgatgagtgtgtggagttccaccggctgtggagcgccatgcagttcgtgtactgcatccctgtgggaaccaacgagttcacagctgagcagtgtttcggcgatggcttgaactgggctggttgctccatcattgtcctgctgggccagcagcgtcgctttgacctgttcgacttctgttaccacctgctaaaagtgcagaggcaggacgggaaggatgaaatcattaagaatgtgcccctgaagaagatggccgaccggatcaggaagtatcagatcttgaacaatgaggtttttgccatcctgaacaaatacatgaagtccgtggagacagacagttccactgtggagcatgtgcgctgcttccagccacccatccaccagtccttggccaccacttgctaagcagaagatcctgcagacccttatctggaggaggaagagaagcaggagagagaaagccacagccagcctgccataggatccaactggacaacgtgtgggatggacctggaaacaagcacctccccaaacacatcaccactccctagggcggggcctgtgcatgctctcccatgacatctccatgctggtttctccatagcataaatgaaaaaaaaaaaaaaaaagtaaacagggcagtgtgtgctttttcttttctcccccctcaactatattaagaactcctagtttcaccctttctccatcccatcatcccacctatctgtggttgcttcccaagacctcctcccaagatagacatctcctacccagtgcccttgtgtgaccccaggactcaagtctcagactgtgaacagatgtggccatgcccagagacgccagcctggccagaagggcatgcctcagcttactacttcatctctcctggttccctccctgcagtgccccgggtgtcatcttctcccactctgggtaccagggattctaccacataggcttcccaaagccccattctaactcccctctctcagggaagccctagagagaggtccaaaaagcattcacagctgtatcacactctatgcaggtggggtaggagactgatcaggcctgctgtggggaagcagtatgtatgaacacagccagaaatgtcatagtccaaacaggatgctttcaggccatctcagctgcttgatggtgagatggttcccttattccttcaggaaaggcttagcattgggccacataggggaagcagctttgaacaaatcagtcatagcactgcctatagcattagccagtgaccaaattagggacaacgtcttggcacagaattgcttatcaaggaacatttccacaagaaagaaaatattaaggggttatttccacagaagcccaaaacgtcttggaaacacagaggtgaggaggaggaatagtaattgtcaatgagcttttaataccaagatacaccccctgcccccaaagaagagtcctcttttagggaatcagaaccttcattgtcctagaagctgaaagattcttggaacattttagcttttactctcaacttgctgttctctttacattccttaagttagactttcgggtgtggcttctctcccaggggtaacatttacttccattttctagactgaaccaaaagtcttctgcagaatctcccaccgagtgtggtaagaaggaaggacaaaaggctttaggatataaatttcatgttacagagcatgtcattgtcaaaggaaatctgtggccctgagattttaagaacataaaatgtgacatttgatatttctccagcccagggaagtaagatggttagcaatggttgccttaatcaaatggtcccatttttaaccccaaaggaagtgcccacagcaagaggtttgtgtgatgcacttatgtcctccggtgaggaaagggggccacatatgaaaggccccttaggtcagatcctgagagtagcacatttgagtgcagattcctgggccccacctcaaacctactaattctgaatctctgggaatagggccaggaaatctgccctttctacaaactacccaagttgttctgttgcacatcaatgtttgggaaccactgctgtaagggaatcattctggtcaccttgagctttgagctaccactaagccatgaaagaaaatacatcatacagggaagagagaagggaggaggttccaagtagtaactggcagatcctcctgtctggaggtaccaccttctattctggtttctgacttttccttcttgatgaccatagatgtgttccagaggcaaaagagacacattatcccagatggcagaacatgctttcaaaacatataaaatgtcaaagttccagatccttctacatctttagtcctgtctgaggatggtagctggctctctgtagctgatagatggctagagttccatccaaatccttgaccacgacttcatggagatttgaataatctatttgatgagatttctatttcaataacccacctctctcaccccacattcatatccctaaatttgaccctctgggccgagtcacattaccttcaggagacttgatcccagtagactgaggtcttccctttcagcagaaagatttcatttccctggcttgccagtggcactgatttccgaacacccaatgagtttaatattctttcctccttggcattactgccccagcctctttttattttttttgtgtgtgtctaataaccaggaaaaaaataaagcttaggttttaaaaagttttaaaaataatctgtttcagaaactgtcaaatgtaccatatttgtattaagagttgttgggaatttttgtacaatgaatttacatttatttatggtgacatatttacgcttgtgatcaaataatgatgttaaattcttaaatcatatttgctatgcagctgaagatgatattttgatttgtattttgggggtacctgtgttgagttgataaacatttccatcttcattaaaactgcttccaaactagtaaaaccagcaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:26999 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:26999 -> Biological process: GO:0006915 [apoptotic process] evidence: IDA GeneID:26999 -> Biological process: GO:0016337 [cell-cell adhesion] evidence: IDA GeneID:26999 -> Biological process: GO:0038096 [Fc-gamma receptor signaling pathway involved in phagocytosis] evidence: TAS GeneID:26999 -> Biological process: GO:0045087 [innate immune response] evidence: TAS GeneID:26999 -> Biological process: GO:0045862 [positive regulation of proteolysis] evidence: IDA GeneID:26999 -> Biological process: GO:0097202 [activation of cysteine-type endopeptidase activity] evidence: IDA GeneID:26999 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA GeneID:26999 -> Cellular component: GO:0005829 [cytosol] evidence: TAS GeneID:26999 -> Cellular component: GO:0030054 [cell junction] evidence: IEA GeneID:26999 -> Cellular component: GO:0043005 [neuron projection] evidence: IEA GeneID:26999 -> Cellular component: GO:0045202 [synapse] evidence: IDA GeneID:26999 -> Cellular component: GO:0048471 [perinuclear region of cytoplasm] evidence: IDA
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