LOCUS       NM_001385030            5717 bp    mRNA    linear   PRI 07-APR-2024
DEFINITION  Homo sapiens multiple EGF like domains 11 (MEGF11), transcript
            variant 4, mRNA.
ACCESSION   NM_001385030
VERSION     NM_001385030.1
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 5717)
  AUTHORS   Lee,J., Kim,J., Zinia,S.S., Park,J., Won,S. and Kim,W.J.
  TITLE     Prenatal phthalate exposure and cord blood DNA methylation
  JOURNAL   Sci Rep 13 (1), 7046 (2023)
   PUBMED   37120575
  REMARK    GeneRIF: Prenatal phthalate exposure and cord blood DNA
            methylation.
            Publication Status: Online-Only
REFERENCE   2  (bases 1 to 5717)
  AUTHORS   Huang,C.P., Tsai,Y.F., Lin,Y.S., Liu,C.Y., Huang,T.T., Huang,C.C.,
            Chiu,J.H. and Tseng,L.M.
  TITLE     Overexpression of multiple epidermal growth factor like domains 11
            rescues anoikis survival through tumor cells-platelet interaction
            in triple negative breast Cancer cells
  JOURNAL   Life Sci 299, 120541 (2022)
   PUBMED   35398017
  REMARK    GeneRIF: Overexpression of multiple epidermal growth factor like
            domains 11 rescues anoikis survival through tumor cells-platelet
            interaction in triple negative breast Cancer cells.
REFERENCE   3  (bases 1 to 5717)
  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   4  (bases 1 to 5717)
  AUTHORS   Yoshida,T., Kato,K., Yokoi,K., Oguri,M., Watanabe,S., Metoki,N.,
            Yoshida,H., Satoh,K., Aoyagi,Y., Nozawa,Y. and Yamada,Y.
  TITLE     Association of genetic variants with hemorrhagic stroke in Japanese
            individuals
  JOURNAL   Int J Mol Med 25 (4), 649-656 (2010)
   PUBMED   20198315
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   5  (bases 1 to 5717)
  AUTHORS   Oguri,M., Kato,K., Yokoi,K., Yoshida,T., Watanabe,S., Metoki,N.,
            Yoshida,H., Satoh,K., Aoyagi,Y., Nozawa,Y. and Yamada,Y.
  TITLE     Assessment of a polymorphism of SDK1 with hypertension in Japanese
            Individuals
  JOURNAL   Am J Hypertens 23 (1), 70-77 (2010)
   PUBMED   19851296
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   6  (bases 1 to 5717)
  AUTHORS   Suzuki,E. and Nakayama,M.
  TITLE     The mammalian Ced-1 ortholog MEGF10/KIAA1780 displays a novel
            adhesion pattern
  JOURNAL   Exp Cell Res 313 (11), 2451-2464 (2007)
   PUBMED   17498693
REFERENCE   7  (bases 1 to 5717)
  AUTHORS   Lim,J., Hao,T., Shaw,C., Patel,A.J., Szabo,G., Rual,J.F.,
            Fisk,C.J., Li,N., Smolyar,A., Hill,D.E., Barabasi,A.L., Vidal,M.
            and Zoghbi,H.Y.
  TITLE     A protein-protein interaction network for human inherited ataxias
            and disorders of Purkinje cell degeneration
  JOURNAL   Cell 125 (4), 801-814 (2006)
   PUBMED   16713569
REFERENCE   8  (bases 1 to 5717)
  AUTHORS   Clark,H.F., Gurney,A.L., Abaya,E., Baker,K., Baldwin,D., Brush,J.,
            Chen,J., Chow,B., Chui,C., Crowley,C., Currell,B., Deuel,B.,
            Dowd,P., Eaton,D., Foster,J., Grimaldi,C., Gu,Q., Hass,P.E.,
            Heldens,S., Huang,A., Kim,H.S., Klimowski,L., Jin,Y., Johnson,S.,
            Lee,J., Lewis,L., Liao,D., Mark,M., Robbie,E., Sanchez,C.,
            Schoenfeld,J., Seshagiri,S., Simmons,L., Singh,J., Smith,V.,
            Stinson,J., Vagts,A., Vandlen,R., Watanabe,C., Wieand,D., Woods,K.,
            Xie,M.H., Yansura,D., Yi,S., Yu,G., Yuan,J., Zhang,M., Zhang,Z.,
            Goddard,A., Wood,W.I., Godowski,P. and Gray,A.
  TITLE     The secreted protein discovery initiative (SPDI), a large-scale
            effort to identify novel human secreted and transmembrane proteins:
            a bioinformatics assessment
  JOURNAL   Genome Res 13 (10), 2265-2270 (2003)
   PUBMED   12975309
  REMARK    Erratum:[Genome Res. 2003 Dec;13(12):2759]
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AC087382.11, AC011847.9 and AC084854.11.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AB058677.1 [ECO:0000332]
            RNAseq introns              :: partial sample support SAMEA1965299,
                                           SAMEA1968189 [ECO:0000350]
            ##Evidence-Data-END##
            COMPLETENESS: full length.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-146               AC087382.11        31069-31214
            147-248             AC087382.11        160819-160920
            249-341             AC087382.11        190325-190417
            342-588             AC011847.9         102264-102510
            589-709             AC011847.9         103854-103974
            710-846             AC011847.9         114063-114199
            847-1059            AC011847.9         119632-119844
            1060-1234           AC011847.9         127031-127205
            1235-1355           AC011847.9         153809-153929
            1356-1519           AC011847.9         154869-155032
            1520-1622           AC011847.9         156225-156327
            1623-1769           AC011847.9         161783-161929
            1770-1904           AC011847.9         162280-162414
            1905-2033           AC011847.9         166658-166786
            2034-2162           AC011847.9         167796-167924
            2163-2291           AC011847.9         168476-168604
            2292-2420           AC011847.9         169154-169282
            2421-2657           AC011847.9         170779-171015
            2658-2714           AC084854.11        143104-143160       c
            2715-2921           AC084854.11        135747-135953       c
            2922-5717           AC084854.11        132318-135113       c
FEATURES             Location/Qualifiers
     source          1..5717
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="15"
                     /map="15q22.31"
     gene            1..5717
                     /gene="MEGF11"
                     /note="multiple EGF like domains 11"
                     /db_xref="GeneID:84465"
                     /db_xref="HGNC:HGNC:29635"
                     /db_xref="MIM:612454"
     exon            1..146
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            147..248
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     CDS             173..3082
                     /gene="MEGF11"
                     /note="isoform 4 is encoded by transcript variant 4;
                     multiple epidermal growth factor-like domains protein 11;
                     multiple EGF-like domains protein 11"
                     /codon_start=1
                     /product="multiple epidermal growth factor-like domains
                     protein 11 isoform 4"
                     /protein_id="NP_001371959.1"
                     /db_xref="CCDS:CCDS92026.1"
                     /db_xref="GeneID:84465"
                     /db_xref="HGNC:HGNC:29635"
                     /db_xref="MIM:612454"
                     /translation="MHTPSIRSITHDAQTSSTGSSAPGTALCTEECVHGRCVSPDTCH
                     CEPGWGGPDCSSGCDSDHWGPHCSNRCQCQNGALCNPITGACVCAAGFRGWRCEELCA
                     PGTHGKGCQLPCQCRHGASCDPRAGECLCAPGYTGVYCEELCPPGSHGAHCELRCPCQ
                     NGGTCHHITGECACPPGWTGAVCAQPCPPGTFGQNCSQDCPCHHGGQCDHVTGQCHCT
                     AGYMGDRCQEECPFGSFGFQCSQHCDCHNGGQCSPTTGACECEPGYKGPRCQERLCPE
                     GLHGPGCTLPCPCDADNTISCHPVTGACTCQPGWSGHHCNESCPVGYYGDGCQLPCTC
                     QNGADCHSITGGCTCAPGFMGEVCAVSCAAGTYGPNCSSICSCNNGGTCSPVDGSCTC
                     KEGWQGLDCTLPCPSGTWGLNCNESCTCANGAACSPIDGSCSCTPGWLGDTCELPCPD
                     GTFGLNCSEHCDCSHADGCDPVTGHCCCLAGWTGIRCDSTCPPGRWGPNCSVSCSCEN
                     GGSCSPEDGSCECAPGFRGPLCQRICPPGFYGHGCAQPCPLCVHSSRPCHHISGICEC
                     LPGFSGALCNQVCAGGYFGQDCAQLCSCANNGTCSPIDGSCQCFPGWIGKDCSQACPP
                     GFWGPACFHACSCHNGASCSAEDGACHCTPGWTGLFCTQRCPAAFFGKDCGRVCQCQN
                     GASCDHISGKCTCRTGFTGQHCEQRCAPGTFGYGCQQLCECMNNSTCDHVTGTCYCSP
                     GFKGIRCDQAALMMEELNPYTKISPALGAERHSVGAVTGIMLLLFLIVVLLGLFAWHR
                     RRQKEKGRDLAPRVSYTPAMRMTSTDYSLSGACGMDRRQNTYIMDKGFKDYMKESVCS
                     SSTCSLNSSENPYATIKDPPILTCKLPESSYVEMKSPVHMGSPYTDVPSLSTSNKNIY
                     EVEPTVSVVQEGCGHNSSYIQNAYDLPRNSHIPGHYDLLPVRQSPANGPSQDKQS"
     exon            249..341
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            342..588
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            589..709
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            710..846
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            847..1059
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            1060..1234
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            1235..1355
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            1356..1519
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            1520..1622
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            1623..1769
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            1770..1904
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            1905..2033
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            2034..2162
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            2163..2291
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            2292..2420
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            2421..2657
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            2658..2714
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            2715..2921
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     exon            2922..5717
                     /gene="MEGF11"
                     /inference="alignment:Splign:2.1.0"
     regulatory      5699..5704
                     /regulatory_class="polyA_signal_sequence"
                     /gene="MEGF11"
                     /note="hexamer: AACAAA"
     polyA_site      5717
                     /gene="MEGF11"
                     /note="major polyA site"
ORIGIN      
        1 agtcgctccc ggtgcccgct gcccgccgcc cggctcccgg ctgctcgcgg ccccctgctc
       61 ctgcctggcg ctctggccag gctcgggctc cggaggacag gaccgcgcga ctggccggcc
      121 gatccctggg ccggccgcgg gagcagctat gctgtgactg tccaggaatc gtatgcacac
      181 cccttcgatc agatctatta cacacgatgc acagacatcc tcaactggtt caagtgcacc
      241 aggcaccgcc ctgtgtacgg aggagtgtgt gcacggccgc tgcgtttccc cggacacctg
      301 ccactgcgag cctggctggg gagggcccga ctgctccagc ggctgcgaca gcgaccactg
      361 ggggccccac tgcagcaacc ggtgccagtg ccagaacggc gccctgtgta accccatcac
      421 aggcgcctgc gtgtgcgccg ccggcttccg tggatggcgc tgcgaggagc tctgcgcacc
      481 tggcacccac ggcaagggat gccagctgcc gtgccagtgc cgacacggtg ccagctgcga
      541 cccccgcgcc ggcgagtgcc tctgcgcacc tggctacacc ggcgtctact gcgaggagct
      601 gtgccctcct gggagccatg gagctcactg tgagctgcgc tgcccctgtc agaatggggg
      661 cacctgccac cacatcactg gcgagtgtgc ctgcccccca ggctggacgg gagcagtgtg
      721 tgcccagccc tgcccaccag ggacatttgg ccagaactgc agccaggatt gtccttgcca
      781 ccatggaggg cagtgtgacc acgtgactgg acagtgccac tgtacagctg gatacatggg
      841 ggacaggtgc caagaggagt gccccttcgg gtccttcggc ttccagtgct cacagcactg
      901 tgactgccac aatggggggc agtgttcacc caccacgggt gcctgcgagt gtgagcctgg
      961 ctacaagggc ccacgctgcc aggagcgact gtgcccggag ggcctgcatg gcccaggctg
     1021 caccctgccc tgcccctgtg acgctgacaa caccatcagc tgccacccag taactggagc
     1081 ttgtacctgc cagccaggct ggtctggtca ccactgcaat gaatcctgcc ctgttggcta
     1141 ctatggcgat ggctgccagc tgccttgcac ctgtcagaat ggcgccgact gccacagcat
     1201 cactgggggc tgcacttgtg ctccgggctt catgggagag gtctgtgccg tttcctgtgc
     1261 agcagggacc tatggcccca actgctcgtc catctgtagc tgtaacaatg gtggcacctg
     1321 ctccccagta gatggctcct gtacctgcaa ggaagggtgg cagggcctgg actgcaccct
     1381 gccatgtccc agtgggacgt ggggcctgaa ctgcaacgag agctgcacct gtgccaatgg
     1441 ggcagcctgc agccccatag acggctcctg ctcctgcact cctggctggc tgggagacac
     1501 ctgtgagctg ccttgcccgg atggcacatt tgggctgaac tgcagtgaac actgtgactg
     1561 cagccatgct gatggatgtg accccgtcac aggccactgc tgctgcctgg ccggatggac
     1621 aggcatccgc tgtgacagca cgtgtccacc tggccgctgg ggccccaact gctctgtctc
     1681 ctgcagctgt gagaatggag gctcctgctc cccagaggat gggagctgcg agtgtgcccc
     1741 tggcttccga ggacccttat gccagagaat ctgcccccct gggttctatg gccacggctg
     1801 cgcccagcca tgccccctct gcgtgcacag cagcaggccc tgccaccaca tcagcggcat
     1861 ctgtgagtgc ctcccaggat tctctggagc tctctgcaac caagtgtgtg ctggaggata
     1921 ctttgggcag gactgtgccc agctctgctc ctgtgccaac aacgggacct gcagccctat
     1981 cgatggctcc tgccagtgct ttcctggatg gattggcaag gactgctcac aggcttgccc
     2041 acccgggttc tggggccccg cctgcttcca cgcatgcagc tgccacaacg gggcgagctg
     2101 cagcgccgag gacggggcct gccactgcac ccctggctgg actggactct tctgcacaca
     2161 gcgctgccca gcagcatttt ttgggaagga ctgtgggcgc gtatgccagt gtcagaatgg
     2221 cgccagctgt gaccacatca gtggcaagtg cacctgccgc acaggcttca ccgggcaaca
     2281 ctgtgagcag agatgtgccc caggaacctt tggctatggg tgtcagcagc tatgtgagtg
     2341 catgaacaac tccacctgtg accatgtcac cggcacctgt tactgcagcc ctggcttcaa
     2401 aggaatcagg tgtgaccaag ctgccctcat gatggaggag ctgaatccct acaccaagat
     2461 cagcccagca ctgggtgcag agcggcactc ggtgggtgct gtcacaggca tcatgctcct
     2521 gttattcctc attgtggtgc tgctgggcct atttgcctgg catcggcggc ggcagaaaga
     2581 gaagggccga gacctggctc cccgtgtctc ctacacacct gccatgagga tgaccagcac
     2641 cgactactcc ctctcaggtg cttgtggaat ggatagacgt cagaacacat acattatgga
     2701 caaaggcttc aaagattaca tgaaagaatc cgtgtgcagt tctagtactt gttccttgaa
     2761 tagcagtgaa aacccttacg ccacaattaa ggacccaccc atcctcacct gcaagcttcc
     2821 agaaagcagc tatgtagaaa tgaagtcgcc tgtgcacatg gggtctccgt acacagatgt
     2881 gccatccttg tcgacatcta ataaaaatat atatgaagtt gagcccacag tcagtgtggt
     2941 ccaagaaggt tgcggtcata actccagcta tatccagaat gcatacgacc tacctaggaa
     3001 cagccatatt cctggtcatt atgacctcct cccagtaaga cagagccctg ccaatgggcc
     3061 gtcccaggac aagcaatctt aagagggata agcttctctc ttgcagtgtg ctctactgaa
     3121 tattctgact ctgaaagaag acagtccctt gacttgaagt aatggtacag actggctcca
     3181 gctgcatgtt agttattacg ttcacctgga actaaagaag agcgtccagg tgggactggg
     3241 ataattgttc aaggaattgt gttctcaaag gcaaatccta tcacccactc agccccaaat
     3301 gccctggatt atatgatttt taaaacattt taagatacag ctactcatca acatcagcta
     3361 aatatagctg atatatatat atatatttat ctgaaacgtg atattttaaa aacatgtagg
     3421 tttaacaaac cttcctagga caaaaaggag actggggagg gaagaggatt actttaaagc
     3481 acctgaaacg tatatgtact tttggttgct gttaccatca acatctgttt tattaccgaa
     3541 gacaattagt acacagacat gaactgttct taaacagaac agtcttaaaa tgtctgtaca
     3601 tatctgtctg gtccatcaaa ttacaacagc caagattaca gaatctatat agtctaatgc
     3661 tgacaacttc tattttaaaa aacaagactt tactttcttc tgccccctaa gtgataggtt
     3721 taaacacaca gagacacaca cacacgtttc caaagtgcag cagtgtctct ttcagtctac
     3781 aataagattc ctagggcagc tttatcaaat tttgccaatt caaagttcaa ggacattaca
     3841 agttagtcct ggctttgtca tatctactta gtccatccga cacctgaatc attccatgta
     3901 aaacagagct ctaagatgat cctttaagca agcagtcata gactggtcgg gattaagtaa
     3961 aagacggcta gttggcctcc tcattttatt tggtcagcat cccttgactc aagagtactt
     4021 gctttcaagt tcttcataaa tcttgagatt gacgtagtat gaaacctaaa agtatacagg
     4081 aaattggaca aatgtggata cagcaagttt acactgctta aagtacatta tgctttttaa
     4141 tggaactaaa tgatcaaaaa aagaatggac tgtaaccagt tgctgtaacg tgatgtaaaa
     4201 acgttactgt aaacagcatg aggatatgaa gtccttccac cttctatctt aaaactacta
     4261 cttactgagc tagcccaata tgcattacaa tgagctaatg ctccagatcc cagtattcag
     4321 atgtgtctat accttccact atgaacacag ataaactgag gctcagataa gtccaaatga
     4381 aatgaaatca actcccaagc cctaaagaga accttctcac aagaattaaa aacaaaaagg
     4441 gcaaacctag gaagctaacg gctactcctg taccactcta ttcactggta cagtccagcc
     4501 agtaaaaaac acttccaaaa agatacacag aagaggaact aaatgactgc gaagctggaa
     4561 tactgctaca ggaagtatga gagttctgaa acccttgata gaaactggaa gcctgccatg
     4621 gaacacaata ctttgggcaa taatcagaaa aagcaaaaaa ataaataaat gagtacatct
     4681 ccccttccca catcactcaa ggcataagca gattttactg ttagaggaaa atatgtaata
     4741 cttacatgaa tgttgcatgt gtgcatggga gcaactgagt agcaatagta aatttacttt
     4801 ccaaaaaagc cttattaaaa tataaatatt agaaaattac tttggagacc caagtaaata
     4861 tttctcatac atatgtagaa agaaatatag gtaagcagct tacctcagta tttcagggca
     4921 gcaagtgttt gtgaagcaag gatgagcagc atgaagatgt cagatcagca aggagaaact
     4981 tcaactcaat cccaggtttt ctcttcttcc cttatcctgc atgtacaata actgctgcct
     5041 ggcaaactgc aaacaagcag catcactcaa gtttgaagtt tcgccgcttt tgtcaactat
     5101 cctctgggca aaggtattca gcaagaggtg gaatggctag acactgaatc aagagatttc
     5161 agtgttactc tggtcaagtt agtcgccctc tctgggctcc cttttttcct atgcataaaa
     5221 aggggagaag cagagagtgg gaagacagct ctactaaccc ttcagctcta gcagtccatg
     5281 actttttaag gaaatgtaat acaagtcaaa ccaggcaata cagaggagaa gggaaaggca
     5341 gagggtgtga ttatggtgac aatagctgcc ttcccctatc gaacagttat cagtaaaaga
     5401 catttcaatc ttacaaagca actgttagaa acttctgtct aacaccatca caaataggtt
     5461 catggtcagc ctaaacatgt atactgtgca ttttatgggt gactttgaaa gatctgttca
     5521 attatttttc agaaactaaa ttttcaaaaa attaatatgt gtacaattaa aatgaatgaa
     5581 agaaaaacca ttattgtaca gaggtattaa tgagactatg aaacggcaat acttttttaa
     5641 atcacagatt tgtaatatat gttcactgtg cagagggatt gtaccttgta caaaataaaa
     5701 caaatttctc aaactaa
//
