LOCUS       NM_024669               2471 bp    mRNA    linear   PRI 03-OCT-2024
DEFINITION  Homo sapiens ankyrin repeat domain 55 (ANKRD55), mRNA.
ACCESSION   NM_024669
VERSION     NM_024669.3
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 2471)
  AUTHORS   Yazdanpanah,M., Jalilian,N., Abdollah Zadeh,R., Sahraian,M.A. and
            Noori-Daloii,M.R.
  TITLE     Investigating the association of polymorphisms of ANKRD55 and MMEL1
            with susceptibility to multiple sclerosis in Iranian population
  JOURNAL   Int J Neurosci 132 (10), 1037-1042 (2022)
   PUBMED   33491520
  REMARK    GeneRIF: Investigating the association of polymorphisms of ANKRD55
            and MMEL1 with susceptibility to multiple sclerosis in Iranian
            population.
REFERENCE   2  (bases 1 to 2471)
  AUTHORS   Mena,J., Alloza,I., Tulloch Navarro,R., Aldekoa,A., Diez Garcia,J.,
            Villanueva Etxebarria,A., Lindskog,C., Antiguedad,A., Boyero,S.,
            Mendibe-Bilbao,M.D.M., Alvarez de Arcaya,A., Sanchez Menoyo,J.L.,
            Midaglia,L., Villarrubia,N., Malhotra,S., Montalban,X.,
            Villar,L.M., Comabella,M. and Vandenbroeck,K.
  TITLE     Genomic Multiple Sclerosis Risk Variants Modulate the Expression of
            the ANKRD55-IL6ST Gene Region in Immature Dendritic Cells
  JOURNAL   Front Immunol 12, 816930 (2022)
   PUBMED   35111166
  REMARK    GeneRIF: Genomic Multiple Sclerosis Risk Variants Modulate the
            Expression of the ANKRD55-IL6ST Gene Region in Immature Dendritic
            Cells.
            Publication Status: Online-Only
REFERENCE   3  (bases 1 to 2471)
  AUTHORS   Korshunov,A., Okonechnikov,K., Schmitt-Hoffner,F., Ryzhova,M.,
            Sahm,F., Stichel,D., Schrimpf,D., Reuss,D.E., Sievers,P.,
            Suwala,A.K., Kumirova,E., Zheludkova,O., Golanov,A., Jones,D.T.W.,
            Pfister,S.M., Kool,M. and von Deimling,A.
  TITLE     Molecular analysis of pediatric CNS-PNET revealed nosologic
            heterogeneity and potent diagnostic markers for CNS neuroblastoma
            with FOXR2-activation
  JOURNAL   Acta Neuropathol Commun 9 (1), 20 (2021)
   PUBMED   33536079
  REMARK    GeneRIF: Molecular analysis of pediatric CNS-PNET revealed
            nosologic heterogeneity and potent diagnostic markers for CNS
            neuroblastoma with FOXR2-activation.
            Publication Status: Online-Only
REFERENCE   4  (bases 1 to 2471)
  AUTHORS   Luck,K., Kim,D.K., Lambourne,L., Spirohn,K., Begg,B.E., Bian,W.,
            Brignall,R., Cafarelli,T., Campos-Laborie,F.J., Charloteaux,B.,
            Choi,D., Cote,A.G., Daley,M., Deimling,S., Desbuleux,A., Dricot,A.,
            Gebbia,M., Hardy,M.F., Kishore,N., Knapp,J.J., Kovacs,I.A.,
            Lemmens,I., Mee,M.W., Mellor,J.C., Pollis,C., Pons,C.,
            Richardson,A.D., Schlabach,S., Teeking,B., Yadav,A., Babor,M.,
            Balcha,D., Basha,O., Bowman-Colin,C., Chin,S.F., Choi,S.G.,
            Colabella,C., Coppin,G., D'Amata,C., De Ridder,D., De Rouck,S.,
            Duran-Frigola,M., Ennajdaoui,H., Goebels,F., Goehring,L., Gopal,A.,
            Haddad,G., Hatchi,E., Helmy,M., Jacob,Y., Kassa,Y., Landini,S.,
            Li,R., van Lieshout,N., MacWilliams,A., Markey,D., Paulson,J.N.,
            Rangarajan,S., Rasla,J., Rayhan,A., Rolland,T., San-Miguel,A.,
            Shen,Y., Sheykhkarimli,D., Sheynkman,G.M., Simonovsky,E., Tasan,M.,
            Tejeda,A., Tropepe,V., Twizere,J.C., Wang,Y., Weatheritt,R.J.,
            Weile,J., Xia,Y., Yang,X., Yeger-Lotem,E., Zhong,Q., Aloy,P.,
            Bader,G.D., De Las Rivas,J., Gaudet,S., Hao,T., Rak,J.,
            Tavernier,J., Hill,D.E., Vidal,M., Roth,F.P. and Calderwood,M.A.
  TITLE     A reference map of the human binary protein interactome
  JOURNAL   Nature 580 (7803), 402-408 (2020)
   PUBMED   32296183
REFERENCE   5  (bases 1 to 2471)
  AUTHORS   Ugidos,N., Mena,J., Baquero,S., Alloza,I., Azkargorta,M.,
            Elortza,F. and Vandenbroeck,K.
  TITLE     Interactome of the Autoimmune Risk Protein ANKRD55
  JOURNAL   Front Immunol 10, 2067 (2019)
   PUBMED   31620119
  REMARK    GeneRIF: Interactome of the Autoimmune Risk Protein ANKRD55.
            Publication Status: Online-Only
REFERENCE   6  (bases 1 to 2471)
  AUTHORS   Zhernakova,A., Stahl,E.A., Trynka,G., Raychaudhuri,S., Festen,E.A.,
            Franke,L., Westra,H.J., Fehrmann,R.S., Kurreeman,F.A., Thomson,B.,
            Gupta,N., Romanos,J., McManus,R., Ryan,A.W., Turner,G., Brouwer,E.,
            Posthumus,M.D., Remmers,E.F., Tucci,F., Toes,R., Grandone,E.,
            Mazzilli,M.C., Rybak,A., Cukrowska,B., Coenen,M.J., Radstake,T.R.,
            van Riel,P.L., Li,Y., de Bakker,P.I., Gregersen,P.K.,
            Worthington,J., Siminovitch,K.A., Klareskog,L., Huizinga,T.W.,
            Wijmenga,C. and Plenge,R.M.
  TITLE     Meta-analysis of genome-wide association studies in celiac disease
            and rheumatoid arthritis identifies fourteen non-HLA shared loci
  JOURNAL   PLoS Genet 7 (2), e1002004 (2011)
   PUBMED   21383967
REFERENCE   7  (bases 1 to 2471)
  AUTHORS   Teslovich,T.M., Musunuru,K., Smith,A.V., Edmondson,A.C.,
            Stylianou,I.M., Koseki,M., Pirruccello,J.P., Ripatti,S.,
            Chasman,D.I., Willer,C.J., Johansen,C.T., Fouchier,S.W., Isaacs,A.,
            Peloso,G.M., Barbalic,M., Ricketts,S.L., Bis,J.C., Aulchenko,Y.S.,
            Thorleifsson,G., Feitosa,M.F., Chambers,J., Orho-Melander,M.,
            Melander,O., Johnson,T., Li,X., Guo,X., Li,M., Shin Cho,Y., Jin
            Go,M., Jin Kim,Y., Lee,J.Y., Park,T., Kim,K., Sim,X., Twee-Hee
            Ong,R., Croteau-Chonka,D.C., Lange,L.A., Smith,J.D., Song,K., Hua
            Zhao,J., Yuan,X., Luan,J., Lamina,C., Ziegler,A., Zhang,W.,
            Zee,R.Y., Wright,A.F., Witteman,J.C., Wilson,J.F., Willemsen,G.,
            Wichmann,H.E., Whitfield,J.B., Waterworth,D.M., Wareham,N.J.,
            Waeber,G., Vollenweider,P., Voight,B.F., Vitart,V.,
            Uitterlinden,A.G., Uda,M., Tuomilehto,J., Thompson,J.R., Tanaka,T.,
            Surakka,I., Stringham,H.M., Spector,T.D., Soranzo,N., Smit,J.H.,
            Sinisalo,J., Silander,K., Sijbrands,E.J., Scuteri,A., Scott,J.,
            Schlessinger,D., Sanna,S., Salomaa,V., Saharinen,J., Sabatti,C.,
            Ruokonen,A., Rudan,I., Rose,L.M., Roberts,R., Rieder,M.,
            Psaty,B.M., Pramstaller,P.P., Pichler,I., Perola,M., Penninx,B.W.,
            Pedersen,N.L., Pattaro,C., Parker,A.N., Pare,G., Oostra,B.A.,
            O'Donnell,C.J., Nieminen,M.S., Nickerson,D.A., Montgomery,G.W.,
            Meitinger,T., McPherson,R., McCarthy,M.I., McArdle,W., Masson,D.,
            Martin,N.G., Marroni,F., Mangino,M., Magnusson,P.K., Lucas,G.,
            Luben,R., Loos,R.J., Lokki,M.L., Lettre,G., Langenberg,C.,
            Launer,L.J., Lakatta,E.G., Laaksonen,R., Kyvik,K.O., Kronenberg,F.,
            Konig,I.R., Khaw,K.T., Kaprio,J., Kaplan,L.M., Johansson,A.,
            Jarvelin,M.R., Janssens,A.C., Ingelsson,E., Igl,W., Kees
            Hovingh,G., Hottenga,J.J., Hofman,A., Hicks,A.A., Hengstenberg,C.,
            Heid,I.M., Hayward,C., Havulinna,A.S., Hastie,N.D., Harris,T.B.,
            Haritunians,T., Hall,A.S., Gyllensten,U., Guiducci,C., Groop,L.C.,
            Gonzalez,E., Gieger,C., Freimer,N.B., Ferrucci,L., Erdmann,J.,
            Elliott,P., Ejebe,K.G., Doring,A., Dominiczak,A.F., Demissie,S.,
            Deloukas,P., de Geus,E.J., de Faire,U., Crawford,G., Collins,F.S.,
            Chen,Y.D., Caulfield,M.J., Campbell,H., Burtt,N.P.,
            Bonnycastle,L.L., Boomsma,D.I., Boekholdt,S.M., Bergman,R.N.,
            Barroso,I., Bandinelli,S., Ballantyne,C.M., Assimes,T.L.,
            Quertermous,T., Altshuler,D., Seielstad,M., Wong,T.Y., Tai,E.S.,
            Feranil,A.B., Kuzawa,C.W., Adair,L.S., Taylor,H.A. Jr.,
            Borecki,I.B., Gabriel,S.B., Wilson,J.G., Holm,H.,
            Thorsteinsdottir,U., Gudnason,V., Krauss,R.M., Mohlke,K.L.,
            Ordovas,J.M., Munroe,P.B., Kooner,J.S., Tall,A.R., Hegele,R.A.,
            Kastelein,J.J., Schadt,E.E., Rotter,J.I., Boerwinkle,E.,
            Strachan,D.P., Mooser,V., Stefansson,K., Reilly,M.P., Samani,N.J.,
            Schunkert,H., Cupples,L.A., Sandhu,M.S., Ridker,P.M., Rader,D.J.,
            van Duijn,C.M., Peltonen,L., Abecasis,G.R., Boehnke,M. and
            Kathiresan,S.
  TITLE     Biological, clinical and population relevance of 95 loci for blood
            lipids
  JOURNAL   Nature 466 (7307), 707-713 (2010)
   PUBMED   20686565
REFERENCE   8  (bases 1 to 2471)
  AUTHORS   Stahl,E.A., Raychaudhuri,S., Remmers,E.F., Xie,G., Eyre,S.,
            Thomson,B.P., Li,Y., Kurreeman,F.A., Zhernakova,A., Hinks,A.,
            Guiducci,C., Chen,R., Alfredsson,L., Amos,C.I., Ardlie,K.G.,
            Barton,A., Bowes,J., Brouwer,E., Burtt,N.P., Catanese,J.J.,
            Coblyn,J., Coenen,M.J., Costenbader,K.H., Criswell,L.A.,
            Crusius,J.B., Cui,J., de Bakker,P.I., De Jager,P.L., Ding,B.,
            Emery,P., Flynn,E., Harrison,P., Hocking,L.J., Huizinga,T.W.,
            Kastner,D.L., Ke,X., Lee,A.T., Liu,X., Martin,P., Morgan,A.W.,
            Padyukov,L., Posthumus,M.D., Radstake,T.R., Reid,D.M.,
            Seielstad,M., Seldin,M.F., Shadick,N.A., Steer,S., Tak,P.P.,
            Thomson,W., van der Helm-van Mil,A.H., van der Horst-Bruinsma,I.E.,
            van der Schoot,C.E., van Riel,P.L., Weinblatt,M.E., Wilson,A.G.,
            Wolbink,G.J., Wordsworth,B.P., Wijmenga,C., Karlson,E.W.,
            Toes,R.E., de Vries,N., Begovich,A.B., Worthington,J.,
            Siminovitch,K.A., Gregersen,P.K., Klareskog,L. and Plenge,R.M.
  CONSRTM   BIRAC Consortium; YEAR Consortium
  TITLE     Genome-wide association study meta-analysis identifies seven new
            rheumatoid arthritis risk loci
  JOURNAL   Nat Genet 42 (6), 508-514 (2010)
   PUBMED   20453842
REFERENCE   9  (bases 1 to 2471)
  AUTHORS   Xu,J., Zheng,S.L., Isaacs,S.D., Wiley,K.E., Wiklund,F., Sun,J.,
            Kader,A.K., Li,G., Purcell,L.D., Kim,S.T., Hsu,F.C., Stattin,P.,
            Hugosson,J., Adolfsson,J., Walsh,P.C., Trent,J.M., Duggan,D.,
            Carpten,J., Gronberg,H. and Isaacs,W.B.
  TITLE     Inherited genetic variant predisposes to aggressive but not
            indolent prostate cancer
  JOURNAL   Proc Natl Acad Sci U S A 107 (5), 2136-2140 (2010)
   PUBMED   20080650
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   10 (bases 1 to 2471)
  AUTHORS   Schmutz,J., Martin,J., Terry,A., Couronne,O., Grimwood,J.,
            Lowry,S., Gordon,L.A., Scott,D., Xie,G., Huang,W., Hellsten,U.,
            Tran-Gyamfi,M., She,X., Prabhakar,S., Aerts,A., Altherr,M.,
            Bajorek,E., Black,S., Branscomb,E., Caoile,C., Challacombe,J.F.,
            Chan,Y.M., Denys,M., Detter,J.C., Escobar,J., Flowers,D.,
            Fotopulos,D., Glavina,T., Gomez,M., Gonzales,E., Goodstein,D.,
            Grigoriev,I., Groza,M., Hammon,N., Hawkins,T., Haydu,L., Israni,S.,
            Jett,J., Kadner,K., Kimball,H., Kobayashi,A., Lopez,F., Lou,Y.,
            Martinez,D., Medina,C., Morgan,J., Nandkeshwar,R., Noonan,J.P.,
            Pitluck,S., Pollard,M., Predki,P., Priest,J., Ramirez,L.,
            Retterer,J., Rodriguez,A., Rogers,S., Salamov,A., Salazar,A.,
            Thayer,N., Tice,H., Tsai,M., Ustaszewska,A., Vo,N., Wheeler,J.,
            Wu,K., Yang,J., Dickson,M., Cheng,J.F., Eichler,E.E., Olsen,A.,
            Pennacchio,L.A., Rokhsar,D.S., Richardson,P., Lucas,S.M.,
            Myers,R.M. and Rubin,E.M.
  TITLE     The DNA sequence and comparative analysis of human chromosome 5
  JOURNAL   Nature 431 (7006), 268-274 (2004)
   PUBMED   15372022
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AK123389.1, DA292581.1 and AW269928.1.
            
            On Nov 23, 2018 this sequence version replaced NM_024669.2.
            
            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 :: AK123389.1, SRR1803616.37820.1
                                           [ECO:0000332]
            RNAseq introns              :: mixed sample support SAMEA1965299,
                                           SAMEA1966682 [ECO:0006172]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000341048.9/ ENSP00000342295.4
            RefSeq Select criteria :: based on conservation, expression,
                                      longest protein
            ##RefSeq-Attributes-END##
            COMPLETENESS: full length.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-20                AK123389.1         30-49
            21-32               DA292581.1         1-12
            33-2136             AK123389.1         62-2165
            2137-2471           AW269928.1         3-337               c
FEATURES             Location/Qualifiers
     source          1..2471
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="5"
                     /map="5q11.2"
     gene            1..2471
                     /gene="ANKRD55"
                     /note="ankyrin repeat domain 55"
                     /db_xref="GeneID:79722"
                     /db_xref="HGNC:HGNC:25681"
                     /db_xref="MIM:615189"
     exon            1..90
                     /gene="ANKRD55"
                     /inference="alignment:Splign:2.1.0"
     exon            91..181
                     /gene="ANKRD55"
                     /inference="alignment:Splign:2.1.0"
     CDS             124..1968
                     /gene="ANKRD55"
                     /codon_start=1
                     /product="ankyrin repeat domain-containing protein 55"
                     /protein_id="NP_078945.2"
                     /db_xref="CCDS:CCDS34161.1"
                     /db_xref="GeneID:79722"
                     /db_xref="HGNC:HGNC:25681"
                     /db_xref="MIM:615189"
                     /translation="MMRQATMDFSTPSVFDQQRGDSSEEVDLTMVYQAASNGDVNALT
                     AVIREDPSILECCDSEGCTPLMHAVSGRQADTVKLLLKMGANINMQDAYGRTSLCLAT
                     YLGWLEGCVSLLRNGAKHNIPDKNGRLPLHAATAEPDMRLLTVLLQQSNISEINHQDN
                     EGMTPLHWAAFHNQPQHTQMLLKKGADPTLVDKDFKTALHWAVQSGNRILCSIILSHH
                     QGPSIINYDDESGKTCVHIAAAAGFSDIIHELARVPECNLQALDVDDRTPLHWAAAAG
                     KAECVQSLLELGMDSNLRDINESTPLAYALYCGHTACVKLLSQESRTEPTRPPPSQSS
                     RPQKKERRFNVLNQIFCKNKKEEQRAHQKDPSRDRYREEDTSEVNDIITTFDSIVGTN
                     CQEQPGDQVAMVEFKKKTSDNSKYLLPEKKPLARKGLPPIRTQSLPPITLGNNFLTAS
                     HRATSHAGLSSAPHHMAQRSQKSRSEQDLLNNRTGCQMLLDNPWKSDSNQVFSYKVWT
                     VSSSDKLLDRLLSVRPGHQEVSVPPHLRHLHNPSSGQNFQHLSPNRHKIRDLPFTRNN
                     LAPLPDQKFLSGEPLRTNRVLPAIPSQRRHSTAAEESEHSANPTSDEN"
     exon            182..304
                     /gene="ANKRD55"
                     /inference="alignment:Splign:2.1.0"
     exon            305..435
                     /gene="ANKRD55"
                     /inference="alignment:Splign:2.1.0"
     exon            436..545
                     /gene="ANKRD55"
                     /inference="alignment:Splign:2.1.0"
     exon            546..606
                     /gene="ANKRD55"
                     /inference="alignment:Splign:2.1.0"
     exon            607..735
                     /gene="ANKRD55"
                     /inference="alignment:Splign:2.1.0"
     exon            736..920
                     /gene="ANKRD55"
                     /inference="alignment:Splign:2.1.0"
     exon            921..1088
                     /gene="ANKRD55"
                     /inference="alignment:Splign:2.1.0"
     exon            1089..1753
                     /gene="ANKRD55"
                     /inference="alignment:Splign:2.1.0"
     exon            1754..1846
                     /gene="ANKRD55"
                     /inference="alignment:Splign:2.1.0"
     exon            1847..2471
                     /gene="ANKRD55"
                     /inference="alignment:Splign:2.1.0"
     regulatory      2117..2122
                     /regulatory_class="polyA_signal_sequence"
                     /gene="ANKRD55"
                     /note="hexamer: AATAAA"
     polyA_site      2148
                     /gene="ANKRD55"
     regulatory      2202..2207
                     /regulatory_class="polyA_signal_sequence"
                     /gene="ANKRD55"
                     /note="hexamer: ATTAAA"
     polyA_site      2234
                     /gene="ANKRD55"
     regulatory      2448..2453
                     /regulatory_class="polyA_signal_sequence"
                     /gene="ANKRD55"
                     /note="hexamer: AATAAA"
     polyA_site      2471
                     /gene="ANKRD55"
                     /note="major polyA site"
ORIGIN      
        1 actcacccat tcagatttct gttggtgtaa agcgacattc cagctgctga agctccgtga
       61 tctgctgtgt ttttccagcc cagatccaag agacctggat gctttttgcc attctgatgg
      121 taaatgatga gacaggctac catggatttc agcacccctt ctgtgtttga tcagcaaaga
      181 ggtgactcat ctgaggaagt tgacctgacc atggtttatc aagcagcctc taatggagat
      241 gtcaatgctc tgactgcagt gattcgggaa gacccttcta tcctagaatg ctgtgacagt
      301 gaaggatgca cgcccttgat gcatgcggtt tctggacgtc aagcggacac agtgaagctg
      361 ctgttgaaga tgggagccaa tattaacatg caggatgctt atggccgcac aagtttatgc
      421 ctggccacct acctgggctg gcttgaaggc tgtgtgagtc tactcagaaa cggtgccaag
      481 cacaatatcc cagataaaaa tggccgcctg ccactgcatg ctgccactgc tgagcccgat
      541 atgaggctcc tcacggtcct gttgcaacag tcgaacatca gcgagattaa tcaccaggac
      601 aatgagggaa tgacaccact ccactgggcg gctttccaca accagcctca acacacacaa
      661 atgctgctga agaagggggc agaccccacc cttgtggata aagactttaa aaccgctctc
      721 cactgggcag tccagagtgg aaataggatt ctgtgctcca tcattctgag ccatcaccag
      781 gggccgtcca taatcaacta tgatgatgag agtgggaaga catgtgtaca tatcgcagcg
      841 gcagcgggct tcagcgatat tattcatgag ctggcaagag tccctgagtg taacctgcag
      901 gctctggatg tggatgacag gacacctctg cactgggctg cagctgcagg gaaggccgaa
      961 tgtgtccagt cactgctgga gttgggaatg gacagcaacc tgcgggacat caatgagagc
     1021 acgcccttgg cctatgccct gtactgcggt cacacggcgt gtgtcaaact cctctcccaa
     1081 gagagcagaa cagagcctac tcgaccccct ccctcccaga gcagtcggcc ccagaagaag
     1141 gagagacggt tcaacgtgct caaccaaata ttctgcaaaa acaagaaaga agagcagaga
     1201 gcccatcaga aggatcccag cagggaccga tacagagagg aggacacctc agaagtcaat
     1261 gacatcatca ccacctttga tagcatcgtg ggtaccaact gccaagaaca gcctggtgat
     1321 caggtggcta tggttgaatt taagaagaaa acctcagaca attcaaaata tctcttacca
     1381 gaaaagaaac cgctggcccg taaggggctt ccaccaatca gaacgcagag tctcccaccc
     1441 atcaccctgg gcaataactt cctaacagcc tcccataggg ccacttccca tgcaggcctg
     1501 agctctgctc ctcatcatat ggcccagcga tctcagaaaa gtcgaagtga gcaggattta
     1561 ttaaataaca gaactggctg ccagatgtta ctagataacc cctggaagag tgattctaat
     1621 caggtatttt cctacaaagt ttggactgtg tcttcttctg ataagctgct ggacagattg
     1681 ctcagtgtcc ggcctggtca ccaagaggtc tccgtgccac cacaccttcg ccatctacat
     1741 aatccatcat caggacaaaa ttttcagcat ctttccccaa acagacacaa aatcagggat
     1801 cttcctttca ctcggaacaa cctagctccc ctaccagatc aaaaatttct atctggagaa
     1861 cctctgcgga caaaccgagt gcttcctgca attccaagtc aacgaagaca cagcacagca
     1921 gcagaagaga gtgaacattc tgccaacccc accagtgatg aaaattaact gtgggccact
     1981 cgctgcagaa atgtagatga atatgtattt tcaactctca aaggacaaga ttactccagt
     2041 ttgtaagaac gaagaccaat ttagtaagct gcattctata agccatcagt tttataactc
     2101 gaaattcttt attccaaata aagatactcc ctaaataagc acttagaata tttgggtgtg
     2161 catattaagt ctgtgaattt ctgtgacttc cacatgccaa aattaaaaga caaaatatgt
     2221 tatcagtagg aaaactgagc tatgtttggt ttgctttgtg gcatgtgcac tgtttttttg
     2281 ttattgttct ttggttgttt ttttgctgaa tgattttatg ttttgggaaa aaaagtacgc
     2341 tttgctgaat aaaagcaaaa aacaaaacaa aaaaaaaacc acatcccaga caaacatgtc
     2401 ttcacattta ttgtcattct aacttgaact aatgaaacct atttaaaaat aaattcctat
     2461 gatcagtcac a
//
