2024-03-29 18:39:40, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_020066 6440 bp mRNA linear PRI 29-JUN-2013 DEFINITION Homo sapiens formin 2 (FMN2), mRNA. ACCESSION NM_020066 XM_371352 VERSION NM_020066.4 GI:160707880 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 6440) AUTHORS Sherva,R., Tripodis,Y., Bennett,D.A., Chibnik,L.B., Crane,P.K., de Jager,P.L., Farrer,L.A., Saykin,A.J., Shulman,J.M. and Green,R.C. CONSRTM The GENAROADS Consortium, and The Alzheimer's Disease Neuroimaging Initiative TITLE Genome-wide association study of the rate of cognitive decline in Alzheimer's disease JOURNAL Alzheimers Dement (2013) In press PUBMED 23535033 REMARK Publication Status: Available-Online prior to print REFERENCE 2 (bases 1 to 6440) AUTHORS Yamada,K., Ono,M., Perkins,N.D., Rocha,S. and Lamond,A.I. TITLE Identification and functional characterization of FMN2, a regulator of the cyclin-dependent kinase inhibitor p21 JOURNAL Mol. Cell 49 (5), 922-933 (2013) PUBMED 23375502 REMARK GeneRIF: results identify FMN2 as a crucial component in the regulation of p21 and consequent oncogene/stress-induced cell-cycle arrest in human cells. REFERENCE 3 (bases 1 to 6440) 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 4 (bases 1 to 6440) AUTHORS Paternoster,L., Lorentzon,M., Lehtimaki,T., Eriksson,J., Kahonen,M., Raitakari,O., Laaksonen,M., Sievanen,H., Viikari,J., Lyytikainen,L.P., Mellstrom,D., Karlsson,M., Ljunggren,O., Grundberg,E., Kemp,J.P., Sayers,A., Nethander,M., Evans,D.M., Vandenput,L., Tobias,J.H. and Ohlsson,C. TITLE Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure JOURNAL PLoS Genet. 9 (2), E1003247 (2013) PUBMED 23437003 REFERENCE 5 (bases 1 to 6440) AUTHORS Zeth,K., Pechlivanis,M., Samol,A., Pleiser,S., Vonrhein,C. and Kerkhoff,E. TITLE Molecular basis of actin nucleation factor cooperativity: crystal structure of the Spir-1 kinase non-catalytic C-lobe domain (KIND)*formin-2 formin SPIR interaction motif (FSI) complex JOURNAL J. Biol. Chem. 286 (35), 30732-30739 (2011) PUBMED 21705804 REMARK GeneRIF: analysis of the molecular basis of the Spir1/formin-2 interaction REFERENCE 6 (bases 1 to 6440) CONSRTM Wellcome Trust Case Control Consortium TITLE Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls JOURNAL Nature 447 (7145), 661-678 (2007) PUBMED 17554300 REFERENCE 7 (bases 1 to 6440) AUTHORS Ryley,D.A., Wu,H.H., Leader,B., Zimon,A., Reindollar,R.H. and Gray,M.R. TITLE Characterization and mutation analysis of the human formin-2 (FMN2) gene in women with unexplained infertility JOURNAL Fertil. Steril. 83 (5), 1363-1371 (2005) PUBMED 15866570 REMARK GeneRIF: It is likely that FMN2 has the same function as Fmn2 in the mouse, i.e., maintenance of the meiotic spindle. Identification of patients with meiosis I arrest is necessary to determine whether FMN2 mutations are a cause of unexplained infertility. REFERENCE 8 (bases 1 to 6440) AUTHORS Katoh,M. and Katoh,M. TITLE Characterization of FMN2 gene at human chromosome 1q43 JOURNAL Int. J. Mol. Med. 14 (3), 469-474 (2004) PUBMED 15289902 REMARK GeneRIF: FMN2 was characterized at human chromosome 1q43. REFERENCE 9 (bases 1 to 6440) AUTHORS Leader,B., Lim,H., Carabatsos,M.J., Harrington,A., Ecsedy,J., Pellman,D., Maas,R. and Leder,P. TITLE Formin-2, polyploidy, hypofertility and positioning of the meiotic spindle in mouse oocytes JOURNAL Nat. Cell Biol. 4 (12), 921-928 (2002) PUBMED 12447394 REFERENCE 10 (bases 1 to 6440) AUTHORS Leader,B. and Leder,P. TITLE Formin-2, a novel formin homology protein of the cappuccino subfamily, is highly expressed in the developing and adult central nervous system JOURNAL Mech. Dev. 93 (1-2), 221-231 (2000) PUBMED 10781961 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from DB476003.1, AL359918.43, AF218941.1, DN990332.1, AF218942.1 and AF225426.1. On Nov 20, 2007 this sequence version replaced gi:74136553. Summary: Formin homology (FH) domain proteins (see FMN1; MIM 136535) play a role in cytoskeletal organization and/or establishment of cell polarity.[supplied by OMIM, Apr 2010]. 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## RNAseq introns :: single sample supports all introns ERS025084, ERS025098 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-489 DB476003.1 1-489 490-1410 AL359918.43 74553-75473 1411-1637 AF218941.1 1-227 1638-1638 AL359918.43 75701-75701 1639-2405 AF218941.1 229-995 2406-4003 AL359918.43 189172-190769 4004-4506 DN990332.1 8-510 4507-6417 AF218942.1 7-1917 6418-6440 AF225426.1 1941-1963 FEATURES Location/Qualifiers source 1..6440 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="1" /map="1q43" gene 1..6440 /gene="FMN2" /note="formin 2" /db_xref="GeneID:56776" /db_xref="HGNC:14074" /db_xref="MIM:606373" exon 1..1840 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 19 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:12727981" variation 77 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:6675871" variation 193 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:371374779" CDS 226..5394 /gene="FMN2" /codon_start=1 /product="formin-2" /protein_id="NP_064450.3" /db_xref="GI:160707881" /db_xref="CCDS:CCDS31069.2" /db_xref="GeneID:56776" /db_xref="HGNC:14074" /db_xref="MIM:606373" /translation="
MGNQDGKLKRSAGDALHEGGGGAEDALGPRDVEATKKGSGGKKALGKHGKGGGGGGGGGESGKKKSKSDSRASVFSNLRIRKNLSKGKGAGGSREDVLDSQALQTGELDSAHSLLTKTPDLSLSADEAGLSDTECADPFEVTGPGGPGPAEARVGGRPIAEDVETAAGAQDGQRTSSGSDTDIYSFHSATEQEDLLSDIQQAIRLQQQQQQQLQLQLQQQQQQQQLQGAEEPAAPPTAVSPQPGAFLGLDRFLLGPSGGAGEAPGSPDTEQALSALSDLPESLAAEPREPQQPPSPGGLPVSEAPSLPAAQPAAKDSPSSTAFPFPEAGPGEEAAGAPVRGAGDTDEEGEEDAFEDAPRGSPGEEWAPEVGEDAPQRLGEEPEEEAQGPDAPAAASLPGSPAPSQRCFKPYPLITPCYIKTTTRQLSSPNHSPSQSPNQSPRIKRRPEPSLSRGSRTALASVAAPAKKHRADGGLAAGLSRSADWTEELGARTPRVGGSAHLLERGVASDSGGGVSPALAAKASGAPAAADGFQNVFTGRTLLEKLFSQQENGPPEEAEKFCSRIIAMGLLLPFSDCFREPCNQNAQTNAASFDQDQLYTWAAVSQPTHSLDYSEGQFPRRVPSMGPPSKPPDEEHRLEDAETESQSAVSETPQKRSDAVQKEVVDMKSEGQATVIQQLEQTIEDLRTKIAELERQYPALDTEVASGHQGLENGVTASGDVCLEALRLEEKEVRHHRILEAKSIQTSPTEEGGVLTLPPVDGLPGRPPCPPGAESGPQTKFCSEISLIVSPRRISVQLDSHQPTQSISQPPPPPSLLWSAGQGQPGSQPPHSISTEFQTSHEHSVSSAFKNSCNIPSPPPLPCTESSSSMPGLGMVPPPPPPLPGMTVPTLPSTAIPQPPPLQGTEMLPPPPPPLPGAGIPPPPPLPGAGILPLPPLPGAGIPPPPPLPGAAIPPPPPLPGAGIPLPPPLPGAGIPPPPPLPGAGIPPPPPLPGAGIPPPPPLPGAGIPPPPPLPGAGIPPPPPLPGAGIPPPPPLPGAGIPPPPPLPGAGIPPPPPLPGAGIPPPPPLPGAGIPPPPPLPGAGIPPPPPLPGAGIPPPPPLPGVGIPPPPPLPGAGIPPPPPLPGAGIPPPPPLPGAGIPPPPPLPRVGIPPPPPLPGAGIPPPPPLPGAGIPPPPPLPGVGIPPPPPLPGVGIPPPPPLPGAGIPPPPPLPGMGIPPAPAPPLPPPGTGIPPPPLLPVSGPPLLPQVGSSTLPTPQVCGFLPPPLPSGLFGLGMNQDKGSRKQPIEPCRPMKPLYWTRIQLHSKRDSSTSLIWEKIEEPSIDCHEFEELFSKTAVKERKKPISDTISKTKAKQVVKLLSNKRSQAVGILMSSLHLDMKDIQHAVVNLDNSVVDLETLQALYENRAQSDELEKIEKHGRSSKDKENAKSLDKPEQFLYELSLIPNFSERVFCILFQSTFSESICSIRRKLELLQKLCETLKNGPGVMQVLGLVLAFGNYMNGGNKTRGQADGFGLDILPKLKDVKSSDNSRSLLSYIVSYYLRNFDEDAGKEQCLFPLPEPQDLFQASQMKFEDFQKDLRKLKKDLKACEVEAGKVYQVSSKEHMQPFKENMEQFIIQAKIDQEAEENSLTETHKCFLETTAYFFMKPKLGEKEVSPNAFFSIWHEFSSDFKDFWKKENKLLLQERVKEAEEVCRQKKGKSLYKIKPRHDSGIKAKISMKT
" misc_feature 4072..5244 /gene="FMN2" /note="Formin Homology 2 Domain; Region: FH2; pfam02181" /db_xref="CDD:202141" misc_feature 4075..5358 /gene="FMN2" /note="Formin Homology 2 Domain; Region: FH2; smart00498" /db_xref="CDD:197762" variation 256 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:200734668" variation 358..359 /gene="FMN2" /replace="" /replace="cgg" /db_xref="dbSNP:10613472" variation 383..384 /gene="FMN2" /replace="" /replace="ggc" /db_xref="dbSNP:140531536" variation 385..386 /gene="FMN2" /replace="" /replace="cgg" /db_xref="dbSNP:71929261" variation 385 /gene="FMN2" /replace="" /replace="ggc" /db_xref="dbSNP:35817759" variation 389..391 /gene="FMN2" /replace="" /replace="gcg" /db_xref="dbSNP:72215772" variation 401 /gene="FMN2" /replace="" /replace="cgg" /db_xref="dbSNP:71168893" variation 405 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:199572295" variation 451 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:201857219" variation 477 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:200561900" variation 501 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:145799385" variation 546 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:376733678" variation 563 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:372489487" variation 588 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:112904598" variation 609 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:200157875" variation 624 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:375101837" variation 651 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:143096048" variation 662 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:138394305" variation 693 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:370945971" variation 739 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:142782397" variation 756 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:148480631" variation 800 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:150505248" variation 843 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:200364388" variation 921 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:11583501" variation 928 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:149103365" variation 987 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:142232913" variation 1003 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:147858483" variation 1026 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:369650259" variation 1108 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:201538863" variation 1395 /gene="FMN2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:202231609" variation 1407 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:372473032" variation 1454 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:201437013" variation 1469 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:200347646" variation 1484 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:146681532" variation 1488 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:374512507" variation 1509 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:150033699" variation 1514 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:201430864" variation 1519 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:368925775" variation 1575 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:377516551" variation 1577 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:145379416" variation 1583 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:147961923" variation 1591 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:141492081" variation 1597 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:142335257" variation 1602 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:138052423" variation 1634 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:201558855" variation 1638 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:10926124" variation 1653 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:374209120" variation 1670 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:377670694" variation 1748 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:376836605" variation 1761..1762 /gene="FMN2" /replace="" /replace="gggggg" /db_xref="dbSNP:139188401" exon 1841..2007 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 1848 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:367849953" variation 1857 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:372095380" variation 1876 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:370593818" variation 1878 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:149514160" variation 1882 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:201654893" variation 1895 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:113562797" variation 1914 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:141488751" variation 1915 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:147501995" variation 1938 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:368340532" variation 1941 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:372544106" variation 1944 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:200336233" variation 1972 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:146195271" exon 2008..2155 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 2028 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:375865107" variation 2055 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:3765588" variation 2056 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:200182734" variation 2094 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:147945249" variation 2109 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:369120788" variation 2121 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:141897898" exon 2156..2211 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 2163 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:74784382" variation 2183 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:141043862" variation 2187 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:144870942" variation 2191 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:199730080" variation 2192 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:371725737" exon 2212..4145 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 2221 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:141879002" variation 2248 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:370558399" variation 2325 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:145252718" variation 2337 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:137903301" variation 2348 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:375178797" variation 2355 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:149459435" variation 2368 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:76382773" variation 2376 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:201885010" variation 2392 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:201575501" variation 2399 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:142397272" variation 2416 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:147518212" variation 2425 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:145706266" variation 2426 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:140911005" variation 2427 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:148757660" variation 2431 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:148963860" variation 2448 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:144753167" variation 2454 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:368104157" variation 2456 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:200185606" variation 2467 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:200439578" variation 2471 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:371967368" variation 2481 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:140392779" variation 2482 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:367554600" variation 2529 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:371254127" variation 2534 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:368527329" variation 2551 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:148060493" variation 2554 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:201800161" variation 2582 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:201048870" variation 2589 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:372839255" variation 2616 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:200499808" variation 2617 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:370148847" variation 2671 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:150519570" variation 2672 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:149284185" variation 2696 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:140042858" variation 2729 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:147318481" variation 2742 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:10926166" variation 2758 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:146579158" variation 2797 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:140315493" variation 2800 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:145077825" variation 2815 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:114291166" variation 2820 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:143847498" variation 2849 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:202173304" variation 2881 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:146945154" variation 2882 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:146874723" variation 2952..2953 /gene="FMN2" /replace="" /replace="ccccct" /db_xref="dbSNP:200863572" variation 2959 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:186784023" variation 2961 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:72475042" variation 2962..2964 /gene="FMN2" /replace="" /replace="cct" /db_xref="dbSNP:201217362" variation 2988 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:200259735" variation 2993 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:149443295" variation 2997 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:148496994" variation 3007 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:150996647" variation 3026 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:140879072" variation 3043 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:371697625" variation 3045 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:145628188" variation 3046 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:141094573" variation 3047 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:4997328" variation 3048 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:188083977" variation 3053 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:199628038" variation 3054 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:4997329" variation 3059 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:193049501" variation 3064 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:150891575" variation 3065 /gene="FMN2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:201741828" variation 3069 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:142725738" variation 3078 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:146070457" variation 3079 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:367627381" variation 3080..3113 /gene="FMN2" /replace="" /replace="gaatacctcctccgccccctctacccggagcgg" /db_xref="dbSNP:71170718" variation 3080 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:200503778" variation 3081 /gene="FMN2" /replace="" /replace="a" /db_xref="dbSNP:72444563" variation 3081 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:200886762" variation 3084 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:144739133" variation 3085 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:372401580" variation 3087 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:142178619" variation 3098..3130 /gene="FMN2" /replace="" /replace="ctctacccggagcggcaataccccctccgcccc" /db_xref="dbSNP:6143701" variation 3098 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:111896385" variation 3102 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:201221641" variation 3106 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:145005157" variation 3108 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:201866430" variation 3111 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:199866405" variation 3122 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:200975594" variation 3132 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:202054320" variation 3141 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:150923193" variation 3142 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:138468405" variation 3144 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:140720010" variation 3147 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:150102515" variation 3153 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:200418654" variation 3155 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:150843940" variation 3156 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:376697094" variation 3159 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:201199944" variation 3160 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:199853440" variation 3162 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:149715160" variation 3168 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:369734693" variation 3178 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:139764401" variation 3179 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:141912031" variation 3180 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:373490785" variation 3188 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:71646825" variation 3198 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:71646826" variation 3209 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:375298881" variation 3210 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:71646827" variation 3212 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:202207586" variation 3213 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:71646887" variation 3219 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:11586155" variation 3225 /gene="FMN2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:71646889" variation 3231 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:71646890" variation 3234 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:71646891" variation 3254..3255 /gene="FMN2" /replace="" /replace="tcctcccccacttcccggagcgggcatacctcctccaccccctctacc cggagcgggcataccccc" /db_xref="dbSNP:71170719" variation 3258 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:71535326" variation 3261 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:201918371" variation 3264 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:71646892" variation 3284 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:373388302" variation 3285 /gene="FMN2" /replace="ccctcctcccccactt" /replace="tcctccaccccctcta" /db_xref="dbSNP:71297736" variation 3291 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:200618987" variation 3300 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:71646893" variation 3303 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:201810089" variation 3308 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:111629917" variation 3309 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:201173147" variation 3318..3336 /gene="FMN2" /replace="ccctccgcccccacttcct" /replace="tcctccaccccctctaccc" /db_xref="dbSNP:71297737" variation 3323 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:200366868" variation 3324 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:201587786" variation 3330 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:199897169" variation 3334 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:148115484" variation 3351 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:201302496" variation 3356 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:202165125" variation 3357 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:200328010" variation 3386 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:201048681" variation 3390 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:200857897" variation 3396 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:201761863" variation 3399 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:200287374" variation 3407 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:201685864" variation 3417 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:71646894" variation 3423 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:201229245" variation 3440 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:200276415" variation 3441 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:71646895" variation 3456 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:200416403" variation 3462 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:141917612" variation 3468 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:201681961" variation 3486 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:199766654" variation 3501 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:372592302" variation 3506 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:201701711" variation 3521 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:370099468" variation 3522 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:373533409" variation 3526 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:377496280" variation 3527 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:199799762" variation 3531 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:201253596" variation 3539 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:200640213" variation 3554 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:370745797" variation 3555 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:191253930" variation 3572 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:201396397" variation 3573 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:367816204" variation 3575 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:199702261" variation 3580 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:112021213" variation 3582 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:199920451" variation 3584 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:200800873" variation 3585 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:181634878" variation 3588 /gene="FMN2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:200682272" variation 3597 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:202006855" variation 3600 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:200022577" variation 3615 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:200984130" variation 3617 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:201911169" variation 3618 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:372049087" variation 3621 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:201646328" variation 3627 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:75765330" variation 3630 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:369474345" variation 3638 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:199570117" variation 3639 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:200036152" variation 3642 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:75688931" variation 3654 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:202161866" variation 3667 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:12732924" variation 3671 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:12737015" variation 3687 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:12750401" variation 3721 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:201329780" variation 3732 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:374929692" variation 3737 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:190820789" variation 3752 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:142072223" variation 3753 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:183336748" variation 3758 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:76758921" variation 3781 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:369075397" variation 3785 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:372947608" variation 3786 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:376983479" variation 3813 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:140228578" variation 3819 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:200759129" variation 3825 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:138448278" variation 3844 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:145138533" variation 3865 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:368876164" variation 3931 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:200053623" variation 3934 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:111521184" variation 4011 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:202169567" variation 4019 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:147210965" variation 4028 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:377271075" variation 4038 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:200892944" variation 4049 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:371426944" variation 4064 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:373721402" variation 4113 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:149661682" exon 4146..4290 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 4154 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:201716974" variation 4165 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:373007799" variation 4186 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:199721402" variation 4192 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:145474534" variation 4200 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:369796046" variation 4206 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:144021481" exon 4291..4378 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 4293 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:141335669" variation 4348 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:146873580" exon 4379..4440 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 4398 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:113021213" variation 4428 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:200267919" exon 4441..4532 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 4443 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:150401752" variation 4461 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:374165127" variation 4479 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:6677726" exon 4533..4662 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 4536 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:143591952" variation 4542 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:374500757" variation 4593 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:368774315" variation 4628 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:3795677" variation 4636 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:12031760" exon 4663..4809 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 4675 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:375018806" variation 4705 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:374743076" exon 4810..4869 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 4815 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:368399693" variation 4844 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:150801382" variation 4845 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:369715134" exon 4870..4990 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 4902 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:146444036" variation 4932 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:139884638" exon 4991..5083 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 5040 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:370415981" variation 5072 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:373287219" exon 5084..5135 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 5098 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:200959613" variation 5099 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:112553360" exon 5136..5285 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 5151 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:368475818" variation 5190 /gene="FMN2" /replace="c" /replace="g" /db_xref="dbSNP:201067071" variation 5235 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:149004492" variation 5237 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:199995902" exon 5286..5367 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 5297 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:183078344" variation 5342 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:150138448" variation 5361 /gene="FMN2" /replace="g" /replace="t" /db_xref="dbSNP:143796494" exon 5368..6429 /gene="FMN2" /inference="alignment:Splign:1.39.8" variation 5402 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:371497648" variation 5426 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:201324843" variation 5430 /gene="FMN2" /replace="a" /replace="c" /db_xref="dbSNP:376076479" variation 5439 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:76724708" variation 5460..5461 /gene="FMN2" /replace="" /replace="gt" /db_xref="dbSNP:371083983" variation 5476 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:369556407" variation 5511 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:882869" variation 5707 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:35166026" variation 5713 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:74149141" variation 5717 /gene="FMN2" /replace="" /replace="a" /db_xref="dbSNP:111431164" STS 5724..6030 /gene="FMN2" /standard_name="SHGC-148105" /db_xref="UniSTS:176196" variation 5765 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:180839468" variation 5788 /gene="FMN2" /replace="c" /replace="t" /db_xref="dbSNP:72769840" variation 5955..5956 /gene="FMN2" /replace="" /replace="t" /db_xref="dbSNP:139197792" variation 5964..5965 /gene="FMN2" /replace="" /replace="t" /db_xref="dbSNP:71650012" variation 5978 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:190173841" variation 5995 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:181319897" variation 6036 /gene="FMN2" /replace="a" /replace="t" /db_xref="dbSNP:146057851" variation 6178 /gene="FMN2" /replace="a" /replace="g" /db_xref="dbSNP:113776485" variation 6226 /gene="FMN2" /replace="" /replace="t" /db_xref="dbSNP:142674996" variation 6275..6276 /gene="FMN2" /replace="" /replace="tgt" /db_xref="dbSNP:368769176" ORIGIN
agccgcagccgcagcgacggcagccacgggagccgccgcgcattatgcaaagcggcggcagatgcgagcggggccagccgggcgcgcgtcggcctcccctcccagcggctccccccgccgccgcctgactctcccgggagactccctaggcccggacctggggccgaggagggccgggatggcctgagtgcccgcggcgcggcggcgcagcagcgggattgcaccatggggaaccaggatgggaagctgaagaggagcgcaggtgatgctttgcacgaaggcggcggtggcgccgaggatgcgctggggcccagggatgtggaagccacaaagaaggggagcgggggcaagaaggcgctaggcaagcacggcaaggggggagggggcggcggcggcggcggggagtcgggcaagaagaagagcaagtccgactccagagcctcggtgttttccaacctgcggatcaggaagaatctgtccaaggggaaaggcgccggcggctcccgcgaagatgtactggattcccaggccctgcagaccggggagctggacagcgctcactccctgctcaccaagactccagacctcagcctctcggcggacgaggccggcctgtcggataccgagtgtgcggacccttttgaggtgaccggtccagggggtcctgggcctgccgaggctagggtcgggggccggccgatcgccgaggatgtggaaactgcagcaggggcgcaggatggacaaaggaccagctcgggctcggacacggacatctatagcttccattcggctacggagcaagaggatttgctttcagacatccagcaggcgatccgcctgcagcagcagcagcagcagcagctccagctccagctccagcaacagcagcagcagcagcagctccagggcgccgaggagcctgcagcgccccccactgccgtctcccctcagcccggggccttcctgggcctggaccggttcctgctggggccgagcggcggggctggggaggccccgggcagtccggacaccgagcaggcgctgtccgcgctctccgacctgcccgagagcctggccgccgagccccgggagccccagcaaccgccgtcccccggcggcctcccggtctccgaggcgcccagtctcccggcagcgcaacccgcggccaaagactcgccctcctccacggctttcccatttcccgaggccgggccgggggaggaagcggccggagcccccgtgcgaggggctggggacacggatgaggagggtgaggaggatgcttttgaggatgcgccccggggctctccgggggaggagtgggccccggaggtgggagaggacgccccgcagaggctgggggaagagccggaggaggaggcgcaaggacctgacgcccccgcggccgcttccctgcccggcagccccgcgcctagccagcgctgtttcaagccctacccgctcatcaccccctgctacatcaagaccaccacccggcagctcagctcgcccaatcactccccgtctcagtcccctaatcagagccccaggatcaagaggcggccggaaccctccctgagccgagggtccagaactgccctggcctccgtagccgccccggccaagaagcaccgggccgacggcggccttgcggccggcctgagccgctcggctgactggacggaggagctaggcgcccgcacgccccgggtgggaggctccgcgcacctgctggagcgcggggtggcgagtgacagcggcggtggggtgtccccagcactggccgccaaggcgtctggggcccccgcggctgcggatggcttccagaacgtgttcacagggcgaacgctgttggagaagctgttcagccagcaggagaacgggcctccagaagaagcagagaagttttgctcccggatcattgccatgggtcttctccttccttttagtgattgcttcagggaaccgtgtaatcagaatgcccagacgaatgcagcttcgtttgatcaagatcaactttatacctgggctgcagttagtcaacccacacactcattggactattcagaagggcagtttcctaggcgagttccatccatggggccaccatccaaacctcccgatgaggaacacaggctcgaggatgctgaaacagaatctcaatctgctgtttcagaaactccccaaaaacgctcagatgctgtccagaaggaagttgttgacatgaagtctgagggacaggccactgtaattcagcagctggaacagactattgaggatctgagaaccaaaatagctgaactagagaggcagtatcctgccctggacacagaggtggccagtggtcatcaagggcttgagaatggagtgacagcctcaggcgatgtctgtctcgaagctctcaggttagaagaaaaggaagtacggcatcataggattttagaggcgaaatcgatacagacttcccccacggaagagggcggggtgctgacactgcctcctgtggatgggctgccagggcgtcctccatgcccccctggggctgaaagtggacctcagacaaagttctgttcagagatttctttgattgtgtctccaaggcgaatatcagtccagctcgacagccatcagcccacacagagcatctcacagcctccaccacctccatcccttctgtggtctgctgggcaaggacagcctgggtcacagccgccccattctatttctaccgagtttcaaaccagccacgaacactctgtttcctctgcctttaaaaacagctgtaacatcccatctccaccacctctgccttgcacagagtcctccagctccatgcctggcctgggcatggtgcctcccccacctccccctctccctggcatgacagtgcctactctgcccagtacagccattccccaacctcctcctctgcagggtacagaaatgctgccaccccctccccctcctcttcccggagcgggcatacctcctccgccgcctctacccggagcaggcatactccctctgccccctctacccggagcgggaatacctcctccgccccctctacccggagcggcaataccccctccgccccctcttcccggggcaggcataccccttcctccccctcttcccggagcaggaatacctcctccaccccctctacccggagcgggcataccccctcctcccccacttcccggagcgggcataccccctccgcccccacttcccggagcgggcataccccctcctccccctcttcccggagcgggcatacctcctccaccccctctacccggagcgggcataccccctccgcccccacttcccggagcgggcataccccctccgcccccacttcccggagcgggcataccccctcctccccctcttcccggagcgggcatacctcctccaccccctctacccggagcgggcataccccctccgcccccacttcccggagcgggcatacccccacctccccctctacccggagcgggcataccccctccgccccctctacccggagtgggcatacctcctccgccccctctacccggagcgggcataccccctcctccccctctacccggagcgggcataccccctcctccccctcttcccggagcgggcatacctcctccaccccctctacccagagtgggcataccccctccgcccccacttcccggagcgggcatacccccacctccccctctacccggagcgggcataccccctccgccccctctacctggagtgggaatacctcctccgccccctctacctggagtgggaatacctcctccgccccctctacctggtgctgggattcccccacctcctcccttgccaggtatggggattccacctgctccagctcccccactccctccacctgggacaggaatcccaccgccccctctgcttcctgtatcaggccctccactcctcccacaagttgggagtagcactttaccaaccccacaggtgtgtggatttcttcctcctccattgccaagtggcttgtttggattagggatgaatcaggacaaagggagtaggaagcagcccatagagccttgtcgaccaatgaagcctctttactggaccaggattcaactacatagtaaaagagactccagtacttcacttatttgggaaaaaattgaagagccatccatagattgtcatgaatttgaggaattattttctaaaactgctgtaaaggagagaaagaaacctatctctgatactatctcaaagacgaaggctaaacaagttgtcaagttattaagcaacaaaagatcacaagcagttggaatactaatgtctagccttcatttagatatgaaagacatacaacatgctgttgtgaacttggataattctgtggttgacctggagacccttcaagctctctatgagaatagagcacagtcagacgaactcgaaaaaatagaaaagcatggccgatcttccaaagacaaggaaaatgccaagtctctggacaaacctgaacagttcctttatgaactgtcactaatccccaacttttcagagcgagtcttttgcatcctgttccagtccacattttcagaaagcatttgctcaattcgtcgcaaactggaattactacagaaattgtgtgagacattaaaaaatggcccaggggttatgcaggttctaggtttggttcttgcctttggcaactacatgaatggaggaaataagactcgaggacaggcagatggctttggattagacattcttccaaaactgaaagatgtcaagagcagtgacaatagcagaagccttttgtcatatattgtttcgtattatctccgaaattttgatgaggatgctggaaaagaacagtgcctctttccactgccagaaccccaggacctttttcaggcctcacagatgaagtttgaagattttcaaaaagatctcagaaaactgaagaaagacttgaaagcctgtgaagttgaagcagggaaagtataccaggtctcctcaaaagagcatatgcagcctttcaaggaaaacatggaacaatttattattcaagccaaaattgaccaagaggcagaggaaaattcactgacagagactcataaatgctttttggagaccacggcatatttcttcatgaaaccaaaacttggagagaaggaggtgtccccaaatgctttcttcagtatctggcatgaattcagctctgactttaaagacttctggaagaaagagaacaaacttcttctacaagagagagtaaaagaagccgaagaggtgtgtagacagaagaaaggaaaatcactttataaaataaaaccaagacatgactctggaattaaagcaaagataagcatgaaaacttgaacaatgaaaagcagaatgaaaatgagtcattgcaacgactttcacaaaattcagctgacctgagagtgggagggaaactaccgtcattctgctcatgtttcttcttgacctcttgcataatctttttgttttctagacagttcactaattgttgaattttactgtatattcatataaaaatgcaaacgtactagaccagtggagaatttgacaccttttctttttgtaaaagtttatggtattataccgatagaccaaaacagcatgtgtaagaggcagtatctgcactaattctcaacatgctaaacattaactacaattcactgttgtgagaatattcctcgtcacagcaaaaacactttcctttctactgacaaccagtcctccacatcacagcatttagacatatgggtaaaatgttatttctagtgaattgtttgtatcagtttcatgtctaagtataaattttctattttaaaatttaagaaccgtttataatcagtgctttcccaactcttgggttgctctccataactatgtatttgtgaaagaaaatggtcattttttttactgaagtcatataatgacttgggtcagctcgtaatgcattgtgatggttttgtatgagctgggtgtttttttccattacttttaatgatcttcgttgcaagttatagttgtggataaaggggagaatttattgctcttgcaaaccaattatggaaagcaacttaagaaaaccaatgttctaaatcataattgtttgtatttatgtaaagtatggtctcttactttttagtttgtagtttaagtgcaaagaaacagtagtggttttttttctattgttttgtagtcttcctgtccccttcagtccctccagtgtgtatattaccattctccaatgaaataatagggcatttaacaaagatcgctatgtgcaatactgtatttagtgtttctatttcaatttttctaggatgttaatttatatgaaaataaaatgaataataaaagaataaagatacttgcaaaagaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:56776 -> Molecular function: GO:0003674 [molecular_function] evidence: ND GeneID:56776 -> Molecular function: GO:0003779 [actin binding] evidence: IDA GeneID:56776 -> Biological process: GO:0006915 [apoptotic process] evidence: IMP GeneID:56776 -> Biological process: GO:0006974 [response to DNA damage stimulus] evidence: IMP GeneID:56776 -> Biological process: GO:0007275 [multicellular organismal development] evidence: IEA GeneID:56776 -> Biological process: GO:0015031 [protein transport] evidence: IEA GeneID:56776 -> Biological process: GO:0016192 [vesicle-mediated transport] evidence: ISS GeneID:56776 -> Biological process: GO:0035556 [intracellular signal transduction] evidence: IEA GeneID:56776 -> Biological process: GO:0040038 [polar body extrusion after meiotic divisions] evidence: ISS GeneID:56776 -> Biological process: GO:0042177 [negative regulation of protein catabolic process] evidence: IMP GeneID:56776 -> Biological process: GO:0045010 [actin nucleation] evidence: IEA GeneID:56776 -> Biological process: GO:0046907 [intracellular transport] evidence: ISS GeneID:56776 -> Biological process: GO:0048477 [oogenesis] evidence: ISS GeneID:56776 -> Biological process: GO:0051295 [establishment of meiotic spindle localization] evidence: ISS GeneID:56776 -> Biological process: GO:0051758 [homologous chromosome movement towards spindle pole involved in homologous chromosome segregation] evidence: ISS GeneID:56776 -> Biological process: GO:0070649 [formin-nucleated actin cable assembly] evidence: ISS GeneID:56776 -> Biological process: GO:0071456 [cellular response to hypoxia] evidence: IMP GeneID:56776 -> Cellular component: GO:0005575 [cellular_component] evidence: ND GeneID:56776 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA GeneID:56776 -> Cellular component: GO:0005829 [cytosol] evidence: IDA GeneID:56776 -> Cellular component: GO:0005884 [actin filament] evidence: IEA GeneID:56776 -> Cellular component: GO:0005886 [plasma membrane] evidence: IEA GeneID:56776 -> Cellular component: GO:0005938 [cell cortex] evidence: ISS GeneID:56776 -> Cellular component: GO:0015629 [actin cytoskeleton] evidence: IDA GeneID:56776 -> Cellular component: GO:0030659 [cytoplasmic vesicle membrane] evidence: ISS GeneID:56776 -> Cellular component: GO:0048471 [perinuclear region of cytoplasm] evidence: IEA
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