2024-03-29 08:58:38, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001037333 6498 bp mRNA linear PRI 15-JUN-2013 DEFINITION Homo sapiens cytoplasmic FMR1 interacting protein 2 (CYFIP2), transcript variant 1, mRNA. ACCESSION NM_001037333 VERSION NM_001037333.1 GI:82617633 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 6498) 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 6498) 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 6498) 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 6498) 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 6498) 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 6498) 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 6498) 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 6498) 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 6498) 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 6498) 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 AL136549.1, BC011762.1 and AC008676.6. Transcript Variant: This variant (1) uses a different splice site in the 5' UTR, compared to variant 2. 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## Transcript exon combination :: AL136549.1, AF160973.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025082, ERS025083 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-1095 AL136549.1 1-1095 1096-2449 BC011762.1 1223-2576 2450-4124 AL136549.1 2450-4124 4125-6498 AC008676.6 158750-161123 c FEATURES Location/Qualifiers source 1..6498 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="5" /map="5q33.3" gene 1..6498 /gene="CYFIP2" /gene_synonym="PIR121" /note="cytoplasmic FMR1 interacting protein 2" /db_xref="GeneID:26999" /db_xref="HGNC:13760" /db_xref="HPRD:07556" /db_xref="MIM:606323" exon 1..115 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 18 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:62383002" exon 116..255 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" CDS 139..3900 /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_001032410.1" /db_xref="GI:82617634" /db_xref="GeneID:26999" /db_xref="HGNC:13760" /db_xref="HPRD:07556" /db_xref="MIM:606323" /translation="
MTTHVTLEDALSNVDLLEELPLPDQQPCIEPPPSSIMYQANFDTNFEDRNAFVTGIARYIEQATVHSSMNEMLEEGHEYAVMLYTWRSCSRAIPQVKCNEQPNRVEIYEKTVEVLEPEVTKLMKFMYFQRKAIERFCSEVKRLCHAERRKDFVSEAYLLTLGKFINMFAVLDELKNMKCSVKNDHSAYKRAAQFLRKMADPQSIQESQNLSMFLANHNRITQCLHQQLEVIPGYEELLADIVNICVDYYENKMYLTPSEKHMLLKVMGFGLYLMDGNVSNIYKLDAKKRINLSKIDKFFKQLQVVPLFGDMQIELARYIKTSAHYEENKSKWTCTQSSISPQYNICEQMVQIRDDHIRFISELARYSNSEVVTGSGLDSQKSDEEYRELFDLALRGLQLLSKWSAHVMEVYSWKLVHPTDKFCNKDCPGTAEEYERATRYNYTSEEKFAFVEVIAMIKGLQVLMGRMESVFNQAIRNTIYAALQDFAQVTLREPLRQAVRKKKNVLISVLQAIRKTICDWEGGREPPNDPCLRGEKDPKGGFDIKVPRRAVGPSSTQLYMVRTMLESLIADKSGSKKTLRSSLDGPIVLAIEDFHKQSFFFTHLLNISEALQQCCDLSQLWFREFFLELTMGRRIQFPIEMSMPWILTDHILETKEPSMMEYVLYPLDLYNDSAYYALTKFKKQFLYDEIEAEVNLCFDQFVYKLADQIFAYYKAMAGSVLLDKRFRAECKNYGVIIPYPPSNRYETLLKQRHVQLLGRSIDLNRLITQRISAAMYKSLDQAISRFESEDLTSIVELEWLLEINRLTHRLLCKHMTLDSFDAMFREANHNVSAPYGRITLHVFWELNFDFLPNYCYNGSTNRFVRTAIPFTQEPQRDKPANVQPYYLYGSKPLNIAYSHIYSSYRNFVGPPHFKTICRLLGYQGIAVVMEELLKIVKSLLQGTILQYVKTLIEVMPKICRLPRHEYGSPGILEFFHHQLKDIIEYAELKTDVFQSLREVGNAILFCLLIEQALSQEEVCDLLHAAPFQNILPRVYIKEGERLEVRMKRLEAKYAPLHLVPLIERLGTPQQIAIAREGDLLTKERLCCGLSMFEVILTRIRSYLQDPIWRGPPPTNGVMHVDECVEFHRLWSAMQFVYCIPVGTNEFTAEQCFGDGLNWAGCSIIVLLGQQRRFDLFDFCYHLLKVQRQDGKDEIIKNVPLKKMADRIRKYQILNNEVFAILNKYMKSVETDSSTVEHVRCFQPPIHQSLATTC
" misc_feature 1288..3807 /gene="CYFIP2" /gene_synonym="PIR121" /note="Cytoplasmic Fragile-X interacting family; Region: FragX_IP; pfam05994" /db_xref="CDD:218846" misc_feature 3247..3249 /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 147 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:371578292" variation 177 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:376687042" variation 219 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:367998009" variation 247 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:371710290" variation 249 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:369640959" exon 256..345 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 300 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:375350435" variation 336 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:369941644" exon 346..420 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 371 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:373074465" variation 378 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:376568198" variation 417..419 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="c" /db_xref="dbSNP:5872508" variation 417 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:200051515" exon 421..525 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 432 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:368093712" variation 435 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:139530784" exon 526..707 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 537 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:148895189" variation 576 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:375762537" variation 635 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:369872275" variation 672 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:369062847" variation 678 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:373151265" exon 708..804 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 735 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:185022541" variation 759 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:199855067" exon 805..933 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" exon 934..1038 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" exon 1039..1130 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1096 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:3207362" exon 1131..1248 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1131 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:376920120" variation 1136 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:148350606" variation 1179 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:373676501" variation 1191 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:372848474" variation 1221 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:376982797" exon 1249..1368 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1287 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:368645883" variation 1308 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:139943836" exon 1369..1494 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1425 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:17054446" variation 1431 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:369323669" variation 1437 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:372259482" exon 1495..1661 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1500 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:6885590" variation 1545 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:377728487" variation 1618 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:370137201" exon 1662..1809 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1662 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:370084969" variation 1663 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:372630008" variation 1668 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:1823035" variation 1785 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:185026624" exon 1810..1963 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1883 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:370992962" variation 1893 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:142973944" exon 1964..2120 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 1989 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:367974123" variation 2037 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:372104693" variation 2043 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:375426388" variation 2055 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:369858004" exon 2121..2217 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 2151 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:199725246" variation 2157 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:372517333" variation 2160 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:375703811" variation 2199 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:11551374" exon 2218..2294 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" exon 2295..2403 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 2340 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:374669553" variation 2351 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:367713994" variation 2352 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:141399379" variation 2361 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:147011006" variation 2369 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:376060688" variation 2379 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:116817896" exon 2404..2523 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 2415 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:375270131" variation 2450 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:17850790" variation 2485 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:139353471" variation 2486 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:373467559" variation 2511 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:13354242" exon 2524..2723 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 2538 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:377148423" variation 2539 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:201559066" variation 2559 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:369405267" variation 2561 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:374132627" variation 2582 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:377648376" variation 2586 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:371132555" variation 2612 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:58005665" variation 2632 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:11551375" variation 2634 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:373107748" variation 2635 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:377031549" exon 2724..2811 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 2737 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:371766099" variation 2758 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:375088064" variation 2778 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:7705781" variation 2797 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:373799565" exon 2812..2955 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 2847 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:371615057" variation 2884 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:9313557" variation 2913 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:183570769" variation 2922 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:186955009" exon 2956..3046 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 3015 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:373712469" exon 3047..3177 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 3081 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:372286637" variation 3093 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:377070210" variation 3094 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:377125065" variation 3144 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:150652041" exon 3178..3250 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" STS 3189..3253 /gene="CYFIP2" /gene_synonym="PIR121" /standard_name="STS-M62008" /db_xref="UniSTS:55216" variation 3219 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:372902849" exon 3251..3345 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 3260 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:368529367" variation 3276 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:371277463" variation 3280 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:374707103" variation 3291 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:73307968" variation 3300 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:372007539" variation 3333 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:376770442" exon 3346..3584 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 3363 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:369693364" variation 3464 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:200428535" variation 3467 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:374666951" variation 3474 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:114967929" variation 3489 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:373142413" variation 3501 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:199725841" variation 3520 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:376484231" variation 3526 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:199945789" variation 3529 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:201475685" variation 3532 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:369611074" variation 3550 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="t" /db_xref="dbSNP:148677157" variation 3582 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="t" /db_xref="dbSNP:377656882" exon 3585..3732 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 3597 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:368047583" variation 3666 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:200774279" exon 3733..6498 /gene="CYFIP2" /gene_synonym="PIR121" /inference="alignment:Splign:1.39.8" variation 3783 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:375350614" STS 3823..4106 /gene="CYFIP2" /gene_synonym="PIR121" /standard_name="RH18378" /db_xref="UniSTS:21434" variation 3830 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:182717318" variation 3836 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:370184404" variation 3853 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:371399881" variation 3854 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:201882855" variation 3864 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:1803834" STS 3870..4000 /gene="CYFIP2" /gene_synonym="PIR121" /standard_name="RH15890" /db_xref="UniSTS:66388" variation 3891 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:375865980" variation 3924 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:150599988" variation 3946 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:373854212" variation 3952 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:199652534" variation 3959 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:13174378" variation 4049 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:73307980" variation 4084 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:188974329" variation 4108..4109 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="a" /db_xref="dbSNP:33954943" variation 4108 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="a" /replace="aa" /db_xref="dbSNP:3052310" variation 4121..4124 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="aaaa" /db_xref="dbSNP:77677846" variation 4161 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:367860573" variation 4319 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:73309941" variation 4327 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:368328314" variation 4347 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:62387481" variation 4395 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:149305788" variation 4444..4445 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="cc" /db_xref="dbSNP:201743820" variation 4445..4446 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="tggcttcccaaagccccattcta" /db_xref="dbSNP:372558922" variation 4450 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="a" /db_xref="dbSNP:199925015" variation 4470 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:147411422" variation 4492 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:140777310" variation 4493 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="c" /db_xref="dbSNP:375776712" variation 4493 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:144727795" variation 4558 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:192134177" variation 4576 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:147444680" STS 4601..4812 /gene="CYFIP2" /gene_synonym="PIR121" /standard_name="A006W02" /db_xref="UniSTS:11242" variation 4714 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:182865053" variation 4777 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:6555991" variation 4849 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:6555992" variation 4864 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:367959403" variation 5020 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:376881838" variation 5060 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:148519938" variation 5109 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:3734034" variation 5205 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:6862302" variation 5217 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:187411866" variation 5246 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:1058517" variation 5296 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:61736011" variation 5381 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:142969781" variation 5514..5515 /gene="CYFIP2" /gene_synonym="PIR121" /replace="gc" /replace="tt" /db_xref="dbSNP:377513219" variation 5514 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:6880851" variation 5515 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:6882097" variation 5542 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:76594372" variation 5546..5547 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="g" /db_xref="dbSNP:370196582" variation 5577 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:141032109" variation 5636 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:375360183" variation 5660 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:184072551" variation 5790 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:11545337" variation 5840 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="c" /db_xref="dbSNP:80098745" variation 5895 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:113243312" variation 5981 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:143764472" variation 6022 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:146850512" variation 6041 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:140263633" variation 6072 /gene="CYFIP2" /gene_synonym="PIR121" /replace="" /replace="t" /db_xref="dbSNP:111840775" variation 6088 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:3087968" variation 6122 /gene="CYFIP2" /gene_synonym="PIR121" /replace="a" /replace="g" /db_xref="dbSNP:10073822" variation 6188 /gene="CYFIP2" /gene_synonym="PIR121" /replace="g" /replace="t" /db_xref="dbSNP:115781943" variation 6346 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:375053822" variation 6347 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:186546184" variation 6373 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="t" /db_xref="dbSNP:145397143" variation 6436 /gene="CYFIP2" /gene_synonym="PIR121" /replace="c" /replace="g" /db_xref="dbSNP:371519970" ORIGIN
cggggccggggcggggccgagcgcggcgcagcggagcggggcagagcatcctgcgccccggcgcggggccctgcggtagcctcaggcccctcccctggacccgccgcagagccagtgcagaatacagaaactgcagccatgaccacgcacgtcaccctggaagatgccctgtccaacgtggacctgcttgaagagcttcccctccccgaccagcagccatgcatcgagcctccaccttcctccatcatgtaccaggctaactttgacacaaactttgaggacaggaatgcatttgtcacgggcattgcaaggtacattgagcaggctacagtccactccagcatgaatgagatgctggaggaaggacatgagtatgcggtcatgctgtacacctggcgcagctgttcccgggccattccccaggtgaaatgcaacgagcagcccaaccgagtagagatctatgagaagacagtagaggtgctggagccggaggtcaccaagctcatgaagttcatgtattttcagcgcaaggccatcgagcggttctgcagcgaggtgaagcggctgtgccatgccgagcgcaggaaggactttgtctctgaggcctacctcctgacccttggcaagttcatcaacatgtttgctgtcctggatgagctaaagaacatgaagtgcagcgtcaagaatgaccactctgcctacaagagggcagcacagttcctgcggaagatggcagatccccagtctatccaggagtcgcagaacctttccatgttcctggccaaccacaacaggatcacccagtgtctccaccagcaacttgaagtgatcccaggctatgaggagctgctggctgacattgtcaacatctgtgtggattactacgagaacaagatgtacctgactcccagtgagaaacatatgctcctcaaggtgatgggctttggcctctacctaatggatggaaatgtcagtaacatttacaaactggatgccaagaagagaattaatcttagcaaaattgataaattctttaagcagctgcaggtggtgccccttttcggcgacatgcagatagagctggccagatacattaagaccagtgctcactatgaagagaacaagtccaagtggacgtgcacccagagcagcatcagcccccagtacaatatctgcgagcagatggttcagatccgggatgaccacatccgcttcatctccgagctcgctcgctacagcaacagtgaggtggtgacgggctcagggctggacagccagaagtcagacgaggagtatcgcgagctcttcgacctagccctgcggggtctgcagcttctatccaagtggagcgcccacgtcatggaggtgtactcttggaagctggttcatcccacagacaagttctgcaacaaggactgtcctggcaccgcggaggaatatgagagagccacacgctacaattacaccagtgaggaaaaatttgccttcgttgaggtgatcgccatgatcaaaggcctgcaggtgctcatgggcaggatggagagcgtcttcaaccaggccatcaggaacaccatctacgcggcattgcaggacttcgcccaggtgacgctgcgtgagcccctgcggcaggcggtacggaagaagaagaatgtcctcatcagcgtcctacaggcaattcgaaagaccatctgtgactgggagggagggcgagagccccctaatgacccatgcttgagaggggagaaggaccccaaaggtggatttgatatcaaggtgccccggcgtgctgtggggccatccagcacacagctgtacatggtgcggaccatgcttgaatcactcattgcagacaaaagcggctccaagaagaccctgaggagcagcctggatggacccattgtcctcgccatagaggactttcacaaacagtccttcttcttcacacatctgctcaacatcagtgaagccctgcagcagtgttgtgacctctcccagctctggttccgagaattcttcctggagttaaccatgggccgacgaatccagttccccatcgagatgtccatgccctggattctaacggaccatatcctggaaaccaaagaaccttccatgatggagtatgtcctctaccctctggatctgtacaacgacagcgcctactatgctctgaccaagtttaaaaagcagttcctgtacgatgagatagaagctgaggtgaacctgtgttttgatcagtttgtctacaagctggcagaccagatctttgcttactacaaagccatggctggcagtgtcctgttggataaacgttttcgagctgagtgtaagaattatggcgtcatcattccgtatccaccgtccaatcgctatgaaacactgctgaagcagagacacgtccagctgttgggtagatcaattgacttgaacagactcattacccagcgcatctctgccgccatgtataaatccttggaccaagctatcagccgctttgagagtgaggacctgacctccattgtggagctggagtggctgctggagattaaccggctcacgcatcggctgctctgtaagcatatgacgctggacagcttcgatgccatgttccgagaggccaatcacaatgtgtccgccccctatggccgtatcaccctgcatgtcttctgggaactgaactttgactttctccccaactactgctacaatgggtccactaaccgttttgtgcggactgccattcctttcacccaagaaccacaacgagacaaacctgccaacgtccagccttattacctctatggatccaagcctctcaacattgcctacagccacatctacagctcctacaggaatttcgtggggccacctcatttcaagactatctgcagactcctgggttatcagggcatcgctgtggtcatggaggaactgctaaagattgtgaagagcttgctccaaggaaccattctccagtatgtgaaaacactgatagaggtgatgcccaagatatgccgcttgccccgacatgagtatggctccccagggatcctggagttcttccaccaccagctgaaggacatcattgagtacgcagagctcaaaacagacgtgttccagagcctgagggaagtgggcaatgccatcctcttctgcctcctcatagagcaagctctgtctcaggaggaggtctgcgatttgctccatgccgcacccttccaaaacatcttgcctagagtctacatcaaagagggggagcgcctggaggtccggatgaaacgtctggaagccaagtatgccccgctccacctggtccctctgatcgagcggctggggacccctcagcaaatcgccattgctcgcgagggtgacctcctgaccaaggagcggctgtgctgtggcctgtccatgttcgaggtcatcctgacccgcattcggagctacctgcaggaccccatctggcggggcccaccgcccaccaatggcgtcatgcacgtcgatgagtgtgtggagttccaccggctgtggagcgccatgcagttcgtgtactgcatccctgtgggaaccaacgagttcacagctgagcagtgtttcggcgatggcttgaactgggctggttgctccatcattgtcctgctgggccagcagcgtcgctttgacctgttcgacttctgttaccacctgctaaaagtgcagaggcaggacgggaaggatgaaatcattaagaatgtgcccctgaagaagatggccgaccggatcaggaagtatcagatcttgaacaatgaggtttttgccatcctgaacaaatacatgaagtccgtggagacagacagttccactgtggagcatgtgcgctgcttccagccacccatccaccagtccttggccaccacttgctaagcagaagatcctgcagacccttatctggaggaggaagagaagcaggagagagaaagccacagccagcctgccataggatccaactggacaacgtgtgggatggacctggaaacaagcacctccccaaacacatcaccactccctagggcggggcctgtgcatgctctcccatgacatctccatgctggtttctccatagcataaatgaaaaaaaaaaaaaaaaagtaaacagggcagtgtgtgctttttcttttctcccccctcaactatattaagaactcctagtttcaccctttctccatcccatcatcccacctatctgtggttgcttcccaagacctcctcccaagatagacatctcctacccagtgcccttgtgtgaccccaggactcaagtctcagactgtgaacagatgtggccatgcccagagacgccagcctggccagaagggcatgcctcagcttactacttcatctctcctggttccctccctgcagtgccccgggtgtcatcttctcccactctgggtaccagggattctaccacataggcttcccaaagccccattctaactcccctctctcagggaagccctagagagaggtccaaaaagcattcacagctgtatcacactctatgcaggtggggtaggagactgatcaggcctgctgtggggaagcagtatgtatgaacacagccagaaatgtcatagtccaaacaggatgctttcaggccatctcagctgcttgatggtgagatggttcccttattccttcaggaaaggcttagcattgggccacataggggaagcagctttgaacaaatcagtcatagcactgcctatagcattagccagtgaccaaattagggacaacgtcttggcacagaattgcttatcaaggaacatttccacaagaaagaaaatattaaggggttatttccacagaagcccaaaacgtcttggaaacacagaggtgaggaggaggaatagtaattgtcaatgagcttttaataccaagatacaccccctgcccccaaagaagagtcctcttttagggaatcagaaccttcattgtcctagaagctgaaagattcttggaacattttagcttttactctcaacttgctgttctctttacattccttaagttagactttcgggtgtggcttctctcccaggggtaacatttacttccattttctagactgaaccaaaagtcttctgcagaatctcccaccgagtgtggtaagaaggaaggacaaaaggctttaggatataaatttcatgttacagagcatgtcattgtcaaaggaaatctgtggccctgagattttaagaacataaaatgtgacatttgatatttctccagcccagggaagtaagatggttagcaatggttgccttaatcaaatggtcccatttttaaccccaaaggaagtgcccacagcaagaggtttgtgtgatgcacttatgtcctccggtgaggaaagggggccacatatgaaaggccccttaggtcagatcctgagagtagcacatttgagtgcagattcctgggccccacctcaaacctactaattctgaatctctgggaatagggccaggaaatctgccctttctacaaactacccaagttgttctgttgcacatcaatgtttgggaaccactgctgtaagggaatcattctggtcaccttgagctttgagctaccactaagccatgaaagaaaatacatcatacagggaagagagaagggaggaggttccaagtagtaactggcagatcctcctgtctggaggtaccaccttctattctggtttctgacttttccttcttgatgaccatagatgtgttccagaggcaaaagagacacattatcccagatggcagaacatgctttcaaaacatataaaatgtcaaagttccagatccttctacatctttagtcctgtctgaggatggtagctggctctctgtagctgatagatggctagagttccatccaaatccttgaccacgacttcatggagatttgaataatctatttgatgagatttctatttcaataacccacctctctcaccccacattcatatccctaaatttgaccctctgggccgagtcacattaccttcaggagacttgatcccagtagactgaggtcttccctttcagcagaaagatttcatttccctggcttgccagtggcactgatttccgaacacccaatgagtttaatattctttcctccttggcattactgccccagcctctttttattttttttgtgtgtgtctaataaccaggaaaaaaataaagcttaggttttaaaaagttttaaaaataatctgtttcagaaactgtcaaatgtaccatatttgtattaagagttgttgggaatttttgtacaatgaatttacatttatttatggtgacatatttacgcttgtgatcaaataatgatgttaaattcttaaatcatatttgctatgcagctgaagatgatattttgatttgtattttgggggtacctgtgttgagttgataaacatttccatcttcattaaaactgcttccaaactagtaaaaccagcaa
//
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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