LOCUS       NM_194277               3203 bp    mRNA    linear   PRI 12-OCT-2024
DEFINITION  Homo sapiens FERM domain containing 7 (FRMD7), transcript variant
            1, mRNA.
ACCESSION   NM_194277 XM_029570
VERSION     NM_194277.3
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 3203)
  AUTHORS   Su,Y., Zhang,J., Gao,J., Ding,G., Jiang,H., Liu,Y., Li,Y. and
            Yang,G.
  TITLE     Truncated FRMD7 proteins in congenital Nystagmus: novel frameshift
            mutations and proteasomal pathway implications
  JOURNAL   BMC Med Genomics 17 (1), 36 (2024)
   PUBMED   38279119
  REMARK    GeneRIF: Truncated FRMD7 proteins in congenital Nystagmus: novel
            frameshift mutations and proteasomal pathway implications.
            Publication Status: Online-Only
REFERENCE   2  (bases 1 to 3203)
  AUTHORS   Huang,L., Zhou,Y., Chen,W., Lin,P., Xie,Y., He,K., Zhang,S., Wu,Y.
            and Li,N.
  TITLE     Correlations of FRMD7 gene mutations with ocular oscillations
  JOURNAL   Sci Rep 12 (1), 9914 (2022)
   PUBMED   35705619
  REMARK    GeneRIF: Correlations of FRMD7 gene mutations with ocular
            oscillations.
            Publication Status: Online-Only
REFERENCE   3  (bases 1 to 3203)
  AUTHORS   Lee,J., Jeong,H., Won,D., Shin,S., Lee,S.T., Choi,J.R., Byeon,S.H.,
            Kuht,H.J., Thomas,M.G. and Han,J.
  TITLE     Noncanonical Splice Site and Deep Intronic FRMD7 Variants Activate
            Cryptic Exons in X-linked Infantile Nystagmus
  JOURNAL   Transl Vis Sci Technol 11 (6), 25 (2022)
   PUBMED   35762937
  REMARK    GeneRIF: Noncanonical Splice Site and Deep Intronic FRMD7 Variants
            Activate Cryptic Exons in X-linked Infantile Nystagmus.
REFERENCE   4  (bases 1 to 3203)
  AUTHORS   Jiang,L., Li,Y., Yang,K., Wang,Y., Wang,J., Cui,X., Mao,J., Gao,Y.,
            Yi,P., Wang,L. and Liu,J.Y.
  TITLE     FRMD7 Mutations Disrupt the Interaction with GABRA2 and May Result
            in Infantile Nystagmus Syndrome
  JOURNAL   Invest Ophthalmol Vis Sci 61 (5), 41 (2020)
   PUBMED   32446246
  REMARK    GeneRIF: FRMD7 Mutations Disrupt the Interaction with GABRA2 and
            May Result in Infantile Nystagmus Syndrome.
REFERENCE   5  (bases 1 to 3203)
  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   6  (bases 1 to 3203)
  AUTHORS   Guo,X., Li,S., Jia,X., Xiao,X., Wang,P. and Zhang,Q.
  TITLE     Linkage analysis of two families with X-linked recessive congenital
            motor nystagmus
  JOURNAL   J Hum Genet 51 (1), 76-80 (2006)
   PUBMED   16240070
  REMARK    GeneRIF: X-linked recessive congenital motor nystagmus mapped to a
            region overlapped with that for X-linkaged dominant form.
REFERENCE   7  (bases 1 to 3203)
  AUTHORS   Ross,M.T., Grafham,D.V., Coffey,A.J., Scherer,S., McLay,K.,
            Muzny,D., Platzer,M., Howell,G.R., Burrows,C., Bird,C.P.,
            Frankish,A., Lovell,F.L., Howe,K.L., Ashurst,J.L., Fulton,R.S.,
            Sudbrak,R., Wen,G., Jones,M.C., Hurles,M.E., Andrews,T.D.,
            Scott,C.E., Searle,S., Ramser,J., Whittaker,A., Deadman,R.,
            Carter,N.P., Hunt,S.E., Chen,R., Cree,A., Gunaratne,P., Havlak,P.,
            Hodgson,A., Metzker,M.L., Richards,S., Scott,G., Steffen,D.,
            Sodergren,E., Wheeler,D.A., Worley,K.C., Ainscough,R.,
            Ambrose,K.D., Ansari-Lari,M.A., Aradhya,S., Ashwell,R.I.,
            Babbage,A.K., Bagguley,C.L., Ballabio,A., Banerjee,R., Barker,G.E.,
            Barlow,K.F., Barrett,I.P., Bates,K.N., Beare,D.M., Beasley,H.,
            Beasley,O., Beck,A., Bethel,G., Blechschmidt,K., Brady,N.,
            Bray-Allen,S., Bridgeman,A.M., Brown,A.J., Brown,M.J., Bonnin,D.,
            Bruford,E.A., Buhay,C., Burch,P., Burford,D., Burgess,J.,
            Burrill,W., Burton,J., Bye,J.M., Carder,C., Carrel,L., Chako,J.,
            Chapman,J.C., Chavez,D., Chen,E., Chen,G., Chen,Y., Chen,Z.,
            Chinault,C., Ciccodicola,A., Clark,S.Y., Clarke,G., Clee,C.M.,
            Clegg,S., Clerc-Blankenburg,K., Clifford,K., Cobley,V., Cole,C.G.,
            Conquer,J.S., Corby,N., Connor,R.E., David,R., Davies,J., Davis,C.,
            Davis,J., Delgado,O., Deshazo,D., Dhami,P., Ding,Y., Dinh,H.,
            Dodsworth,S., Draper,H., Dugan-Rocha,S., Dunham,A., Dunn,M.,
            Durbin,K.J., Dutta,I., Eades,T., Ellwood,M., Emery-Cohen,A.,
            Errington,H., Evans,K.L., Faulkner,L., Francis,F., Frankland,J.,
            Fraser,A.E., Galgoczy,P., Gilbert,J., Gill,R., Glockner,G.,
            Gregory,S.G., Gribble,S., Griffiths,C., Grocock,R., Gu,Y.,
            Gwilliam,R., Hamilton,C., Hart,E.A., Hawes,A., Heath,P.D.,
            Heitmann,K., Hennig,S., Hernandez,J., Hinzmann,B., Ho,S., Hoffs,M.,
            Howden,P.J., Huckle,E.J., Hume,J., Hunt,P.J., Hunt,A.R.,
            Isherwood,J., Jacob,L., Johnson,D., Jones,S., de Jong,P.J.,
            Joseph,S.S., Keenan,S., Kelly,S., Kershaw,J.K., Khan,Z.,
            Kioschis,P., Klages,S., Knights,A.J., Kosiura,A., Kovar-Smith,C.,
            Laird,G.K., Langford,C., Lawlor,S., Leversha,M., Lewis,L., Liu,W.,
            Lloyd,C., Lloyd,D.M., Loulseged,H., Loveland,J.E., Lovell,J.D.,
            Lozado,R., Lu,J., Lyne,R., Ma,J., Maheshwari,M., Matthews,L.H.,
            McDowall,J., McLaren,S., McMurray,A., Meidl,P., Meitinger,T.,
            Milne,S., Miner,G., Mistry,S.L., Morgan,M., Morris,S., Muller,I.,
            Mullikin,J.C., Nguyen,N., Nordsiek,G., Nyakatura,G., O'Dell,C.N.,
            Okwuonu,G., Palmer,S., Pandian,R., Parker,D., Parrish,J.,
            Pasternak,S., Patel,D., Pearce,A.V., Pearson,D.M., Pelan,S.E.,
            Perez,L., Porter,K.M., Ramsey,Y., Reichwald,K., Rhodes,S.,
            Ridler,K.A., Schlessinger,D., Schueler,M.G., Sehra,H.K.,
            Shaw-Smith,C., Shen,H., Sheridan,E.M., Shownkeen,R., Skuce,C.D.,
            Smith,M.L., Sotheran,E.C., Steingruber,H.E., Steward,C.A.,
            Storey,R., Swann,R.M., Swarbreck,D., Tabor,P.E., Taudien,S.,
            Taylor,T., Teague,B., Thomas,K., Thorpe,A., Timms,K., Tracey,A.,
            Trevanion,S., Tromans,A.C., d'Urso,M., Verduzco,D., Villasana,D.,
            Waldron,L., Wall,M., Wang,Q., Warren,J., Warry,G.L., Wei,X.,
            West,A., Whitehead,S.L., Whiteley,M.N., Wilkinson,J.E.,
            Willey,D.L., Williams,G., Williams,L., Williamson,A.,
            Williamson,H., Wilming,L., Woodmansey,R.L., Wray,P.W., Yen,J.,
            Zhang,J., Zhou,J., Zoghbi,H., Zorilla,S., Buck,D., Reinhardt,R.,
            Poustka,A., Rosenthal,A., Lehrach,H., Meindl,A., Minx,P.J.,
            Hillier,L.W., Willard,H.F., Wilson,R.K., Waterston,R.H., Rice,C.M.,
            Vaudin,M., Coulson,A., Nelson,D.L., Weinstock,G., Sulston,J.E.,
            Durbin,R., Hubbard,T., Gibbs,R.A., Beck,S., Rogers,J. and
            Bentley,D.R.
  TITLE     The DNA sequence of the human X chromosome
  JOURNAL   Nature 434 (7031), 325-337 (2005)
   PUBMED   15772651
REFERENCE   8  (bases 1 to 3203)
  AUTHORS   Cabot,A., Rozet,J.M., Gerber,S., Perrault,I., Ducroq,D., Smahi,A.,
            Souied,E., Munnich,A. and Kaplan,J.
  TITLE     A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to
            chromosome Xp11.4-p11.3
  JOURNAL   Am J Hum Genet 64 (4), 1141-1146 (1999)
   PUBMED   10090899
REFERENCE   9  (bases 1 to 3203)
  AUTHORS   Thomas,M.G., Maconachie,G., Hisaund,M. and Gottlob,I.
  TITLE     FRMD7-Related Infantile Nystagmus
  JOURNAL   (in) Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE and
            Amemiya A (Eds.);
            GENEREVIEWS(R);
            (1993)
   PUBMED   20301748
REFERENCE   10 (bases 1 to 3203)
  AUTHORS   Gutmann,D.H., Brooks,M.L., Emanuel,B.S., McDonald-McGinn,D.M. and
            Zackai,E.H.
  TITLE     Congenital nystagmus in a (46,XX/45,X) mosaic woman from a family
            with X-linked congenital nystagmus
  JOURNAL   Am J Med Genet 39 (2), 167-169 (1991)
   PUBMED   2063919
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AL049792.11, BC114371.1,
            AL161984.1 and AL109749.22.
            
            On Mar 13, 2020 this sequence version replaced NM_194277.2.
            
            Transcript Variant: This variant (1) represents the longer
            transcript and encodes the longer isoform (1).
            
            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 :: AK125336.1, BC114371.1 [ECO:0000332]
            RNAseq introns              :: mixed sample support SAMEA1968189,
                                           SAMEA1968968 [ECO:0006172]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000298542.9/ ENSP00000298542.3
            RefSeq Select criteria :: based on manual assertion, conservation,
                                      expression, longest protein
            ##RefSeq-Attributes-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-31                AL049792.11        28729-28759         c
            32-2456             BC114371.1         1-2425
            2457-3200           AL161984.1         2120-2863
            3201-3203           AL109749.22        117328-117330       c
FEATURES             Location/Qualifiers
     source          1..3203
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="X"
                     /map="Xq26.2"
     gene            1..3203
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /note="FERM domain containing 7"
                     /db_xref="GeneID:90167"
                     /db_xref="HGNC:HGNC:8079"
                     /db_xref="MIM:300628"
     exon            1..233
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /inference="alignment:Splign:2.1.0"
     CDS             177..2321
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /note="isoform 1 is encoded by transcript variant 1; FERM
                     domain-containing protein 7"
                     /codon_start=1
                     /product="FERM domain-containing protein 7 isoform 1"
                     /protein_id="NP_919253.1"
                     /db_xref="CCDS:CCDS35397.1"
                     /db_xref="GeneID:90167"
                     /db_xref="HGNC:HGNC:8079"
                     /db_xref="MIM:300628"
                     /translation="MLHLKVQFLDDSQKIFVVDQKSSGKALFNLSCSHLNLAEKEYFG
                     LEFCSHSGNNVWLELLKPITKQVKNPKEIVFKFMVKFFPVDPGHLREELTRYLFTLQI
                     KKDLALGRLPCSDNCTALMVSHILQSELGDFHEETDRKHLAQTRYLPNQDCLEGKIMH
                     FHQKHIGRSPAESDILLLDIARKLDMYGIRPHPASDGEGMQIHLAVAHMGVLVLRGNT
                     KINTFNWAKIRKLSFKRKHFLIKLHANILVLCKDTLEFTMASRDACKAFWKTCVEYHA
                     FFRLSEEPKSKPKTLLCSKGSSFRYSGRTQRQLLEYGRKGRLKSLPFERKHYPSQYHE
                     RQCRSSPDLLSDVSKQVEDLRLAYGGGYYQNVNGVHASEPVLESRRRNSALEVTFATE
                     LEHSKPEADPTLLHQSQSSSSFPFIYMDPVFNTEPNPNPDPRDIFSERSSLSSFQTSC
                     KFSGNHMSIYSGLTSKVRPAKQLTYTDVPYIPCTGQQVGIMPPQVFFYVDKPPQVPRW
                     SPIRAEERTSPHSYVEPTAMKPAERSPRNIRMKSFQQDLQVLQEAIARTSGRSNINVG
                     LEEEDPNLEDAFVCNIQEQTPKRSQSQSDMKTIRFPFGSEFRPLGPCPALSHKADLFT
                     DMFAEQELPAVLMDQSTAERYVASESSDSESEILKPDYYALYGKEIRSPMARIRLSSG
                     SLQLDEEDEDAYFNTPTAEDRTSLKPCNYFLA"
     exon            234..338
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /inference="alignment:Splign:2.1.0"
     exon            339..381
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /inference="alignment:Splign:2.1.0"
     exon            382..460
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /inference="alignment:Splign:2.1.0"
     exon            461..558
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /inference="alignment:Splign:2.1.0"
     exon            559..673
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /inference="alignment:Splign:2.1.0"
     exon            674..821
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /inference="alignment:Splign:2.1.0"
     exon            822..917
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /inference="alignment:Splign:2.1.0"
     exon            918..1081
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /inference="alignment:Splign:2.1.0"
     exon            1082..1150
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /inference="alignment:Splign:2.1.0"
     exon            1151..1226
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /inference="alignment:Splign:2.1.0"
     exon            1227..3203
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /inference="alignment:Splign:2.1.0"
     regulatory      3182..3187
                     /regulatory_class="polyA_signal_sequence"
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /note="hexamer: ATTAAA"
     polyA_site      3203
                     /gene="FRMD7"
                     /gene_synonym="NYS; NYS1; XIPAN"
                     /note="major polyA site"
ORIGIN      
        1 aaatgccctt gggtgtgcat tacttcaagc aaacggaagt gtgccccgct gacagtggga
       61 atgcctggct gggggtgggg gggcccgagt gcaccacatc cagctgggag tgaaattcct
      121 ggagaaagca cccacagcac tctgagcctg cttgcagccc aacggcctcg ctgagaatgc
      181 tacatttaaa agtgcagttt ttggatgatt cccagaagat ttttgtggtt gatcaaaagt
      241 catccgggaa ggcattgttt aacctgagtt gcagccatct aaatcttgct gaaaaggaat
      301 attttggatt agaattctgc agccattctg gaaataatgt ttggctggag cttttgaagc
      361 ccataacaaa gcaggtaaaa aatcctaagg agattgtttt caaatttatg gtgaaatttt
      421 tcccagtgga ccctggacat ctgcgggaag aacttacaag gtatcttttt actcttcaaa
      481 taaagaagga tttggctcta ggaaggcttc catgcagtga caactgtaca gcgttgatgg
      541 tatctcacat cttacaatca gaacttggag actttcatga agaaacagat aggaagcatc
      601 tggcacaaac tcggtactta ccaaaccaag actgtttaga gggcaagatc atgcactttc
      661 atcagaagca cattggcagg agcccagctg aatctgacat tctgctactg gacatagcaa
      721 ggaagctgga tatgtatggc atcaggcctc accccgccag tgatggtgaa gggatgcaga
      781 ttcacctggc tgttgctcac atgggagtac tggtgttacg gggaaataca aagatcaata
      841 cttttaactg ggctaaaatc cgcaagttga gttttaagag aaagcatttt ctcatcaaac
      901 ttcatgccaa tatcttggtg ttgtgcaagg ataccttgga gttcaccatg gccagccgag
      961 atgcctgcaa ggctttctgg aagacttgtg tggaatacca tgctttcttc aggctttcgg
     1021 aagagcccaa atcaaagccc aaaaccctac tctgcagcaa gggttccagt ttccgctata
     1081 gtggacgaac ccaaaggcaa cttttggaat atgggagaaa agggaggctg aagagcttgc
     1141 catttgaaag gaaacattac ccatctcagt accatgaacg acagtgcagg tcctcaccag
     1201 acctcctctc tgatgtgtca aaacaagtgg aagatttgag actagcatat ggtggtggct
     1261 actaccaaaa tgtgaatgga gtgcacgcat ctgagccagt gctggagagt aggaggagga
     1321 attctgcatt ggaggtgaca tttgcaactg agctggagca ttccaaacca gaggcggatc
     1381 ccacattgct acatcagtcc caaagcagtt cctctttccc ttttatttat atggaccctg
     1441 tctttaacac tgagcccaat cctaaccctg atcccagaga cattttttca gagaggagtt
     1501 ctctaagctc cttccaaaca agctgtaagt tttctggtaa tcacatgagc atatattctg
     1561 gcctcacaag caaagtgcgt ccagcaaagc agctaactta cacggatgtg ccctatattc
     1621 cttgtacagg tcagcaggtt ggtattatgc ctccccaggt ctttttttat gtggacaagc
     1681 caccccaggt gcccagatgg tccccaatta gagcagagga aaggacaagt ccacatagct
     1741 atgtagagcc cactgcaatg aagccagctg aaagaagccc aaggaatatc agaatgaaga
     1801 gctttcagca agacctgcaa gtactccaag aagctatagc caggactagc ggtaggagca
     1861 acatcaatgt aggtctagaa gaggaagacc caaatttgga agatgcattt gtatgtaaca
     1921 ttcaagagca aacccctaaa aggtcccaga gccaatcaga catgaaaact attcgttttc
     1981 cttttgggtc agaatttaga cctttagggc cttgtcctgc tctcagtcat aaagcagacc
     2041 tgtttacgga tatgtttgca gagcaggagt tgccagcagt tctaatggat caaagtacag
     2101 cagaaaggta tgtagctagt gaatccagtg attctgaatc agagattctt aaaccagact
     2161 actatgcttt gtatggcaaa gaaataaggt cacccatggc cagaatccgc ctgtcttctg
     2221 gtagtctaca gttagatgaa gaagatgaag atgcttattt caacacacca actgctgaag
     2281 acaggacttc actaaaacca tgtaattact ttttagctta aaagtgtgaa cctatggaca
     2341 tttctgagcc agttccatgt taccgactta ggcagaaaat aatgaagttg tagaaaccat
     2401 tttcttggtt actacatatt cattggtatt aaggaaatct cattttggat gcctgcctta
     2461 tgaaagatcc agctgttgcc tcattccttg agtttcactc ttccattacc tctgaaggga
     2521 ctttagaaca tgccctctcc tcaccagcac tgtggcaagg caaggtgggt atttgtcatc
     2581 tccactgcat acttcctcat agagacattg tgagtgaagg tcaggctctt caatgctgaa
     2641 gaatggtgac agtatgggtt ggcatatgga attagcgtct aatggcattt agtgatttag
     2701 tagattgtga ctgtgttgat ctttgtgctc ttaaacaaca ctgaacaaat atttcagtct
     2761 ttactatttg tgtggggccc agtagaaatg gtcttgtaat atgctaaata cttccatttt
     2821 tataacatat aaaagcagag catggccctc ctacagcctc aggaaggagg tggtggcata
     2881 gatcctctca agagaataca ggtttagaat taatctagga cttggcagaa ttctaaacct
     2941 aggaaattca tgaattaaat caatttctag agccagacat aaaccagatg aaagtatcat
     3001 gttgttttac ttataacttc tatattctta tctactatat ctagtaaaag agaaacatta
     3061 tcaggtcagt ttgtttatct aatatttcct gccagaattt attttttgtc atagcttctt
     3121 gcatgtatgc aggccaggaa atgaatgtta ttgtaataaa gtgtgatgga aaatccaggt
     3181 aattaaaaaa taaattataa cta
//
