LOCUS       NM_001278063            4109 bp    mRNA    linear   PRI 17-APR-2022
DEFINITION  Homo sapiens SKI family transcriptional corepressor 2 (SKOR2),
            transcript variant 1, mRNA.
ACCESSION   NM_001278063 XM_001715219 XM_003403698 XM_003960751 XM_006722525
VERSION     NM_001278063.4
KEYWORDS    RefSeq; MANE Select.
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 4109)
  AUTHORS   Yin Y, Morgunova E, Jolma A, Kaasinen E, Sahu B, Khund-Sayeed S,
            Das PK, Kivioja T, Dave K, Zhong F, Nitta KR, Taipale M, Popov A,
            Ginno PA, Domcke S, Yan J, Schubeler D, Vinson C and Taipale J.
  TITLE     Impact of cytosine methylation on DNA binding specificities of
            human transcription factors
  JOURNAL   Science 356 (6337) (2017)
   PUBMED   28473536
REFERENCE   2  (bases 1 to 4109)
  AUTHORS   Perry JR, Day F, Elks CE, Sulem P, Thompson DJ, Ferreira T, He C,
            Chasman DI, Esko T, Thorleifsson G, Albrecht E, Ang WQ, Corre T,
            Cousminer DL, Feenstra B, Franceschini N, Ganna A, Johnson AD,
            Kjellqvist S, Lunetta KL, McMahon G, Nolte IM, Paternoster L, Porcu
            E, Smith AV, Stolk L, Teumer A, Tsernikova N, Tikkanen E, Ulivi S,
            Wagner EK, Amin N, Bierut LJ, Byrne EM, Hottenga JJ, Koller DL,
            Mangino M, Pers TH, Yerges-Armstrong LM, Zhao JH, Andrulis IL,
            Anton-Culver H, Atsma F, Bandinelli S, Beckmann MW, Benitez J,
            Blomqvist C, Bojesen SE, Bolla MK, Bonanni B, Brauch H, Brenner H,
            Buring JE, Chang-Claude J, Chanock S, Chen J, Chenevix-Trench G,
            Collee JM, Couch FJ, Couper D, Coveillo AD, Cox A, Czene K, D'adamo
            AP, Smith GD, De Vivo I, Demerath EW, Dennis J, Devilee P,
            Dieffenbach AK, Dunning AM, Eiriksdottir G, Eriksson JG, Fasching
            PA, Ferrucci L, Flesch-Janys D, Flyger H, Foroud T, Franke L,
            Garcia ME, Garcia-Closas M, Geller F, de Geus EE, Giles GG,
            Gudbjartsson DF, Gudnason V, Guenel P, Guo S, Hall P, Hamann U,
            Haring R, Hartman CA, Heath AC, Hofman A, Hooning MJ, Hopper JL, Hu
            FB, Hunter DJ, Karasik D, Kiel DP, Knight JA, Kosma VM, Kutalik Z,
            Lai S, Lambrechts D, Lindblom A, Magi R, Magnusson PK, Mannermaa A,
            Martin NG, Masson G, McArdle PF, McArdle WL, Melbye M, Michailidou
            K, Mihailov E, Milani L, Milne RL, Nevanlinna H, Neven P, Nohr EA,
            Oldehinkel AJ, Oostra BA, Palotie A, Peacock M, Pedersen NL,
            Peterlongo P, Peto J, Pharoah PD, Postma DS, Pouta A, Pylkas K,
            Radice P, Ring S, Rivadeneira F, Robino A, Rose LM, Rudolph A,
            Salomaa V, Sanna S, Schlessinger D, Schmidt MK, Southey MC, Sovio
            U, Stampfer MJ, Stockl D, Storniolo AM, Timpson NJ, Tyrer J, Visser
            JA, Vollenweider P, Volzke H, Waeber G, Waldenberger M,
            Wallaschofski H, Wang Q, Willemsen G, Winqvist R, Wolffenbuttel BH,
            Wright MJ, Boomsma DI, Econs MJ, Khaw KT, Loos RJ, McCarthy MI,
            Montgomery GW, Rice JP, Streeten EA, Thorsteinsdottir U, van Duijn
            CM, Alizadeh BZ, Bergmann S, Boerwinkle E, Boyd HA, Crisponi L,
            Gasparini P, Gieger C, Harris TB, Ingelsson E, Jarvelin MR, Kraft
            P, Lawlor D, Metspalu A, Pennell CE, Ridker PM, Snieder H, Sorensen
            TI, Spector TD, Strachan DP, Uitterlinden AG, Wareham NJ, Widen E,
            Zygmunt M, Murray A, Easton DF, Stefansson K, Murabito JM and Ong
            KK.
  CONSRTM   Australian Ovarian Cancer Study; GENICA Network; kConFab; LifeLines
            Cohort Study; InterAct Consortium; Early Growth Genetics (EGG)
            Consortium
  TITLE     Parent-of-origin-specific allelic associations among 106 genomic
            loci for age at menarche
  JOURNAL   Nature 514 (7520), 92-97 (2014)
   PUBMED   25231870
REFERENCE   3  (bases 1 to 4109)
  AUTHORS   Rietveld CA, Esko T, Davies G, Pers TH, Turley P, Benyamin B,
            Chabris CF, Emilsson V, Johnson AD, Lee JJ, de Leeuw C, Marioni RE,
            Medland SE, Miller MB, Rostapshova O, van der Lee SJ, Vinkhuyzen
            AA, Amin N, Conley D, Derringer J, van Duijn CM, Fehrmann R, Franke
            L, Glaeser EL, Hansell NK, Hayward C, Iacono WG, Ibrahim-Verbaas C,
            Jaddoe V, Karjalainen J, Laibson D, Lichtenstein P, Liewald DC,
            Magnusson PK, Martin NG, McGue M, McMahon G, Pedersen NL, Pinker S,
            Porteous DJ, Posthuma D, Rivadeneira F, Smith BH, Starr JM,
            Tiemeier H, Timpson NJ, Trzaskowski M, Uitterlinden AG, Verhulst
            FC, Ward ME, Wright MJ, Davey Smith G, Deary IJ, Johannesson M,
            Plomin R, Visscher PM, Benjamin DJ, Cesarini D and Koellinger PD.
  TITLE     Common genetic variants associated with cognitive performance
            identified using the proxy-phenotype method
  JOURNAL   Proc Natl Acad Sci U S A 111 (38), 13790-13794 (2014)
   PUBMED   25201988
  REMARK    Erratum:[Proc Natl Acad Sci U S A. 2015 Jan 27;112(4):E380. PMID:
            25572966]
REFERENCE   4  (bases 1 to 4109)
  AUTHORS   Elks CE, Perry JR, Sulem P, Chasman DI, Franceschini N, He C,
            Lunetta KL, Visser JA, Byrne EM, Cousminer DL, Gudbjartsson DF,
            Esko T, Feenstra B, Hottenga JJ, Koller DL, Kutalik Z, Lin P,
            Mangino M, Marongiu M, McArdle PF, Smith AV, Stolk L, van Wingerden
            SH, Zhao JH, Albrecht E, Corre T, Ingelsson E, Hayward C, Magnusson
            PK, Smith EN, Ulivi S, Warrington NM, Zgaga L, Alavere H, Amin N,
            Aspelund T, Bandinelli S, Barroso I, Berenson GS, Bergmann S,
            Blackburn H, Boerwinkle E, Buring JE, Busonero F, Campbell H,
            Chanock SJ, Chen W, Cornelis MC, Couper D, Coviello AD, d'Adamo P,
            de Faire U, de Geus EJ, Deloukas P, Doring A, Smith GD, Easton DF,
            Eiriksdottir G, Emilsson V, Eriksson J, Ferrucci L, Folsom AR,
            Foroud T, Garcia M, Gasparini P, Geller F, Gieger C, Gudnason V,
            Hall P, Hankinson SE, Ferreli L, Heath AC, Hernandez DG, Hofman A,
            Hu FB, Illig T, Jarvelin MR, Johnson AD, Karasik D, Khaw KT, Kiel
            DP, Kilpelainen TO, Kolcic I, Kraft P, Launer LJ, Laven JS, Li S,
            Liu J, Levy D, Martin NG, McArdle WL, Melbye M, Mooser V, Murray
            JC, Murray SS, Nalls MA, Navarro P, Nelis M, Ness AR, Northstone K,
            Oostra BA, Peacock M, Palmer LJ, Palotie A, Pare G, Parker AN,
            Pedersen NL, Peltonen L, Pennell CE, Pharoah P, Polasek O, Plump
            AS, Pouta A, Porcu E, Rafnar T, Rice JP, Ring SM, Rivadeneira F,
            Rudan I, Sala C, Salomaa V, Sanna S, Schlessinger D, Schork NJ,
            Scuteri A, Segre AV, Shuldiner AR, Soranzo N, Sovio U, Srinivasan
            SR, Strachan DP, Tammesoo ML, Tikkanen E, Toniolo D, Tsui K,
            Tryggvadottir L, Tyrer J, Uda M, van Dam RM, van Meurs JB,
            Vollenweider P, Waeber G, Wareham NJ, Waterworth DM, Weedon MN,
            Wichmann HE, Willemsen G, Wilson JF, Wright AF, Young L, Zhai G,
            Zhuang WV, Bierut LJ, Boomsma DI, Boyd HA, Crisponi L, Demerath EW,
            van Duijn CM, Econs MJ, Harris TB, Hunter DJ, Loos RJ, Metspalu A,
            Montgomery GW, Ridker PM, Spector TD, Streeten EA, Stefansson K,
            Thorsteinsdottir U, Uitterlinden AG, Widen E, Murabito JM, Ong KK
            and Murray A.
  CONSRTM   GIANT Consortium
  TITLE     Thirty new loci for age at menarche identified by a meta-analysis
            of genome-wide association studies
  JOURNAL   Nat Genet 42 (12), 1077-1085 (2010)
   PUBMED   21102462
REFERENCE   5  (bases 1 to 4109)
  AUTHORS   Bennett KL, Lee W, Lamarre E, Zhang X, Seth R, Scharpf J, Hunt J
            and Eng C.
  TITLE     HPV status-independent association of alcohol and tobacco exposure
            or prior radiation therapy with promoter methylation of FUSSEL18,
            EBF3, IRX1, and SEPT9, but not SLC5A8, in head and neck squamous
            cell carcinomas
  JOURNAL   Genes Chromosomes Cancer 49 (4), 319-326 (2010)
   PUBMED   20029986
  REMARK    GeneRIF: Results verify IRX1, EBF3, SLC5A8, SEPT9, and FUSSEL18 as
            valid methylation markers in two separate sets of HNSCC specimens;
            also preliminarily show a trend between HPV16 positivity and target
            gene hypermethylation of IRX1, EBF3, SLC5A8, and SEPT9.
REFERENCE   6  (bases 1 to 4109)
  AUTHORS   Vaquerizas JM, Kummerfeld SK, Teichmann SA and Luscombe NM.
  TITLE     A census of human transcription factors: function, expression and
            evolution
  JOURNAL   Nat Rev Genet 10 (4), 252-263 (2009)
   PUBMED   19274049
  REMARK    Review article
REFERENCE   7  (bases 1 to 4109)
  AUTHORS   Minaki Y, Nakatani T, Mizuhara E, Inoue T and Ono Y.
  TITLE     Identification of a novel transcriptional corepressor, Corl2, as a
            cerebellar Purkinje cell-selective marker
  JOURNAL   Gene Expr Patterns 8 (6), 418-423 (2008)
   PUBMED   18522874
  REMARK    GeneRIF: Experiments performed using mice, but the observations
            maybe relevant to other organisms as well.
REFERENCE   8  (bases 1 to 4109)
  AUTHORS   Arndt S, Poser I, Schubert T, Moser M and Bosserhoff AK.
  TITLE     Cloning and functional characterization of a new Ski homolog,
            Fussel-18, specifically expressed in neuronal tissues
  JOURNAL   Lab Invest 85 (11), 1330-1341 (2005)
   PUBMED   16200078
REFERENCE   9  (bases 1 to 4109)
  AUTHORS   Castelo R, Reymond A, Wyss C, Camara F, Parra G, Antonarakis SE,
            Guigo R and Eyras E.
  TITLE     Comparative gene finding in chicken indicates that we are closing
            in on the set of multi-exonic widely expressed human genes
  JOURNAL   Nucleic Acids Res 33 (6), 1935-1939 (2005)
   PUBMED   15809229
  REMARK    Publication Status: Online-Only
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AC051635.7 and DW009659.1.
            
            On Jul 3, 2019 this sequence version replaced NM_001278063.3.
            
            Transcript Variant: This variant (1) represents the longer
            transcript, and encodes the longer isoform (1).
            
            Sequence Note: This RefSeq record was created from transcript and
            genomic sequence data to make the sequence consistent with the
            reference genome assembly. The genomic coordinates used for the
            transcript record were based on transcript alignments.
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000425639.3/ ENSP00000414750.3
            RefSeq Select criteria :: based on conservation, longest protein
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-287               AC051635.7         29059-29345
            288-2947            AC051635.7         31489-34148
            2948-3152           DW009659.1         98-302
            3153-3251           AC051635.7         50162-50260
            3252-3319           AC051635.7         60709-60776
            3320-3385           AC051635.7         68568-68633
            3386-4109           AC051635.7         73827-74550
FEATURES             Location/Qualifiers
     source          1..4109
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="18"
                     /map="18q21.1"
     gene            1..4109
                     /gene="SKOR2"
                     /gene_synonym="CH18515; CORL2; FUSSEL18"
                     /note="SKI family transcriptional corepressor 2"
                     /db_xref="GeneID:652991"
                     /db_xref="HGNC:HGNC:32695"
                     /db_xref="MIM:617138"
     exon            1..287
                     /gene="SKOR2"
                     /gene_synonym="CH18515; CORL2; FUSSEL18"
                     /inference="alignment:Splign:2.1.0"
     exon            288..2947
                     /gene="SKOR2"
                     /gene_synonym="CH18515; CORL2; FUSSEL18"
                     /inference="alignment:Splign:2.1.0"
     CDS             335..3382
                     /gene="SKOR2"
                     /gene_synonym="CH18515; CORL2; FUSSEL18"
                     /note="isoform 1 is encoded by transcript variant 1;
                     functional smad suppressing element 18; ladybird homeobox
                     corepressor 1-like protein; fussel-18; LBX1 corepressor
                     1-like protein; functional Smad-suppressing element on
                     chromosome 18"
                     /codon_start=1
                     /product="SKI family transcriptional corepressor 2 isoform
                     1"
                     /protein_id="NP_001264992.1"
                     /db_xref="CCDS:CCDS74222.1"
                     /db_xref="GeneID:652991"
                     /db_xref="HGNC:HGNC:32695"
                     /db_xref="MIM:617138"
                     /translation="MASSPLPGPNDILLASPSSAFQPDTLSQPRPGHANLKPNQVGQV
                     ILYGIPIVSLVIDGQERLCLAQISNTLLKNFSYNEIHNRRVALGITCVQCTPVQLEIL
                     RRAGAMPISSRRCGMITKREAERLCKSFLGENRPPKLPDNFAFDVSHECAWGCRGSFI
                     PARYNSSRAKCIKCSYCNMYFSPNKFIFHSHRTPDAKYTQPDAANFNSWRRHLKLTDK
                     SPQDELVFAWEDVKAMFNGGSRKRALPQPGAHPACHPLSSVKAAAVAAAAAVAGGGGL
                     LGPHLLGAPPPPPPPPPPLAELAGAPHAHHKRPRFDDDDDSLQEAAVVAAASLSAAAA
                     SLSVAAASGGAGTGGGGAGGGCVAGVGVGAGAGAGAGAGAKGPRSYPVIPVPSKGSFG
                     GVLQKFPGCGGLFPHPYTFPAAAAAFSLCHKKEDAGAAAEALGGAGAGGAGAAPKAGL
                     SGLFWPAGRKDAFYPPFCMFWPPRTPGGLPVPTYLQPPPQPPSALGCALGESPALLRQ
                     AFLDLAEPGGAAGSAEAAPPPGQPPQVVANGPGSGPPPPAGGAGSRDALFESPPGGSG
                     GDCSAGSTPPADSVAAAGAGAAAAGSGPAGSRVPAPHHPHLLEGRKAGGGSYHHSSAF
                     RPVGGKDDAESLAKLHGASAGAPHSAQTHPHHHHHPHHHHHHHHPPQPPSPLLLLPPQ
                     PDEPGSERHHPAPPPPPPPPPPPPLAQHPHHRGLLSPGGTSCCYPSEDSSEDEDDEEE
                     EQEVDVEGHKPPEGEEEEEGRDPDDDEEEDEETEVLLGDPLVGGGRFLQGRGPSEKGS
                     SRDRAPAVAGAFPLGLNSSRLLQEDGKLGDPGSDLPPPPPPPLAPQKASGGGSSSPGS
                     PVHHPSLEEQPSYKDSQKTKENNQVIVSTKDDNSFSDKNKEHSFFITDSDASGGDFWR
                     ERSGEHTQETNSPHSLKKDVENMGKEELQKVLFEQIDLRRRLEQEFQVLKGNTSFPVF
                     NNFQDQMKRELAYREEMVQQLQIIPYAASLIRKEKLGAHLSKS"
     exon            2948..3011
                     /gene="SKOR2"
                     /gene_synonym="CH18515; CORL2; FUSSEL18"
                     /inference="alignment:Splign:2.1.0"
     exon            3012..3086
                     /gene="SKOR2"
                     /gene_synonym="CH18515; CORL2; FUSSEL18"
                     /inference="alignment:Splign:2.1.0"
     exon            3087..3152
                     /gene="SKOR2"
                     /gene_synonym="CH18515; CORL2; FUSSEL18"
                     /inference="alignment:Splign:2.1.0"
     exon            3153..3251
                     /gene="SKOR2"
                     /gene_synonym="CH18515; CORL2; FUSSEL18"
                     /inference="alignment:Splign:2.1.0"
     exon            3252..3319
                     /gene="SKOR2"
                     /gene_synonym="CH18515; CORL2; FUSSEL18"
                     /inference="alignment:Splign:2.1.0"
     exon            3320..3385
                     /gene="SKOR2"
                     /gene_synonym="CH18515; CORL2; FUSSEL18"
                     /inference="alignment:Splign:2.1.0"
     exon            3386..4109
                     /gene="SKOR2"
                     /gene_synonym="CH18515; CORL2; FUSSEL18"
                     /inference="alignment:Splign:2.1.0"
     regulatory      4089..4094
                     /regulatory_class="polyA_signal_sequence"
                     /gene="SKOR2"
                     /gene_synonym="CH18515; CORL2; FUSSEL18"
                     /note="hexamer: AATAAA"
     polyA_site      4109
                     /gene="SKOR2"
                     /gene_synonym="CH18515; CORL2; FUSSEL18"
                     /note="major polyA site"
ORIGIN      
        1 agagacagac gctgtcagac tgcgctccac ttggggctct cctgccgcgg gtttctgcgt
       61 acccacactt tctgcggtgg aggggacgcc ccgccgcaat tcaggccgtc attctcccca
      121 ggccggggtt tgagcgccat tcgctcgggc cagagcccgg atcttcgcgc ggagcccgcc
      181 agagtcccgc ccgctggata cgaggacccg cttggatgct tcgcctccga gcgccctcgg
      241 aagatgggcc ggcagccaca cgcctaaaga cacccagagg ttaccagtgt ccaaggcaga
      301 cctgtagggc tcggcccggg gttctgcggc ggagatggct tccagtccgc tgccagggcc
      361 caacgacatc ctgctggcgt cgccgtcgag cgccttccag cccgacacgc tgagccagcc
      421 gcggccaggg cacgccaacc tcaaacccaa ccaggtgggc caggtgatcc tctacggcat
      481 tcccatcgtg tcgttggtga tcgacgggca agagcgcctg tgcctggcgc agatctccaa
      541 cactctgctc aagaacttca gctacaacga gatccacaac cgtcgcgtgg cactgggcat
      601 cacgtgtgtg cagtgcacgc cggtgcaact ggagatcctg cggcgtgccg gggccatgcc
      661 catctcatcg cgccgctgcg gcatgatcac caaacgcgag gccgagcgtc tgtgcaagtc
      721 gttcctgggc gaaaacaggc cgcccaagct gccagacaat ttcgccttcg acgtgtcaca
      781 cgagtgcgcc tggggctgcc gcggcagctt cattcccgcg cgctacaaca gctcgcgcgc
      841 caagtgcatc aaatgcagct actgcaacat gtacttctcg cccaacaagt tcattttcca
      901 ctcccaccgc acgcccgacg ccaagtacac tcagccagac gcagccaact tcaactcgtg
      961 gcgccgtcat ctcaagctca ccgacaagag tccccaggac gagctggtct tcgcctggga
     1021 ggacgtcaag gccatgttca acggcggcag ccgcaagcgc gcactgcccc agccgggcgc
     1081 gcaccccgcc tgccacccgc tcagctctgt gaaggcggcc gccgtggccg ccgcggccgc
     1141 ggtggccgga ggcgggggtc tgctgggccc ccacctgctg ggtgcgcccc cgccgccgcc
     1201 gccgccaccg ccgcccttgg cagagctggc tggtgccccg cacgcccatc acaagcggcc
     1261 gcgcttcgac gacgacgacg actccttgca ggaggccgcc gtagtggccg ccgccagcct
     1321 ctcggccgca gccgccagcc tctctgtggc tgctgcttcg ggcggcgcgg ggactggtgg
     1381 gggcggcgct gggggtggct gtgtggccgg cgtgggcgtg ggcgcgggcg cgggggcggg
     1441 tgccggggca ggggccaaag gcccgcgcag ctacccagtc atcccggtgc ccagcaaggg
     1501 ctcgttcggg ggcgtcctgc agaagttccc gggctgcggc gggctcttcc cgcaccccta
     1561 caccttccct gccgcggccg ccgccttcag cttgtgccat aagaaagagg atgcgggtgc
     1621 cgccgctgag gccctggggg gcgcgggcgc aggcggcgcg ggcgcggcgc ccaaggccgg
     1681 cttgtccggc ctcttctggc ccgcgggccg caaggacgcc ttctatccgc ccttctgcat
     1741 gttctggccg ccgcggaccc ctggcgggct cccggtgccc acctacctgc agcccccgcc
     1801 tcagccgccc tcggcgctag gctgcgcgct aggcgaaagc ccggccctgc tgcgccaggc
     1861 cttcctggac ctggctgagc caggcggtgc tgctgggagc gccgaggccg cgcccccgcc
     1921 ggggcagccc ccgcaggtag tggccaacgg cccgggctcc ggcccacctc ctcctgccgg
     1981 gggcgccggc tctcgcgacg cgctcttcga gtcgcccccg ggcggcagcg gcggggactg
     2041 cagcgcgggc tccacgccgc ccgcggactc tgtggcagct gccggggcag gggccgcggc
     2101 cgccgggtct ggccccgcgg gctcccgggt tccggcgccc caccatccgc accttctgga
     2161 ggggcgcaaa gcgggcggtg gcagctacca ccattccagc gccttccggc cagtgggcgg
     2221 caaggacgac gcggagagcc tggccaagct gcacggggcg tcggcgggcg cgccccactc
     2281 ggcccagacg catccccacc accatcacca ccctcaccac caccaccacc accaccaccc
     2341 cccgcagccg ccgtcgccgc ttctgctgct gcccccgcag cccgacgagc cgggttccga
     2401 gcgccaccac ccggccccgc cgccgccgcc gccgccgccc ccgccgcccc ctctggccca
     2461 gcacccgcac caccgaggcc ttctgtctcc cgggggaacc agctgctgct accccagcga
     2521 ggacagctcc gaggacgagg acgacgagga agaagagcag gaggtggacg tggagggcca
     2581 caagcccccc gagggcgagg aagaggagga aggtcgagac cctgacgacg acgaggaaga
     2641 ggacgaggag acggaggtcc tactcggcga ccccttagtc gggggcggcc ggttcctcca
     2701 gggccgaggg ccgtcggaga aggggagcag ccgggaccgc gcgccggccg tcgcgggcgc
     2761 gttcccgctc ggcctgaact cctccaggct gctgcaggaa gacgggaaac tcggggaccc
     2821 cggctcggac ctgcccccgc ccccgccgcc gcccctggcc ccccagaagg cgagtggcgg
     2881 cggcagcagc agcccgggca gcccagttca ccatccatca ctggaggagc agccctccta
     2941 caaagatagt cagaaaacta aggaaaataa ccaagtaatt gtatctacaa aggatgacaa
     3001 cagcttttca gataagaaca aggagcatag ctttttcatc acagactctg atgcttctgg
     3061 aggagatttt tggagagaaa gatcaggtga acatacacaa gaaaccaact cacctcattc
     3121 actgaaaaag gatgtagaaa atatggggaa agaagaactt cagaaggttt tatttgaaca
     3181 aatagattta cggagacgac tggaacaaga attccaggtg ttaaaaggaa acacatcttt
     3241 cccagtattc aataattttc aggatcagat gaaaagggag ctagcctacc gagaagaaat
     3301 ggtgcaacag ttacaaatta tcccctatgc agcaagtttg atcaggaaag aaaagcttgg
     3361 cgcccatctc agcaaaagct aaaaggtgca cagaactact tactcttgtt ctcttgtaag
     3421 atacagcctg ccatggagca cttctgaccc gtgttaaaga ctgcagatcg aaagggcttg
     3481 ggaattaaat acaaaatcag gttcaggaga acctaaggac aagtgacctc aaaacagcat
     3541 ggacaaccat gtaaaataga ctgtagcagc cattcattag tggggggagg ggggagccaa
     3601 ccagagcagt caatgcttgt tgcatctttt ggtggaacca aagttcgagt ctttgtgttt
     3661 ttaaaggata gctgaaccca gagcatggga agtgctgtta gccagttggg atgggaaatc
     3721 agcggatggt cccaggcagt ctcagtcctg cacacatgga gaaagcaact ctacaaaact
     3781 gtcttctctt tttgaagaag tgattcttgg tggaagaaaa cacaagaccc atcctaggag
     3841 tggggatagc gtttcaatgg atgggaaggc accagccgta caaacctgct tttcatagca
     3901 aactggacag acttacatgt ggccccttcc tctctgtact ttgcctgctg tatgaatgag
     3961 gattgtattc ctttggaaat attttacagt ttaatattga gtgtaattaa gaatataatc
     4021 atgttatcaa aaatggcatt taactctgtt gtagtttctt taacattcat gtggataaaa
     4081 aagtctataa taaaaaaact atgaagtaa
//
