LOCUS       NM_001304438            5806 bp    mRNA    linear   PRI 10-FEB-2025
DEFINITION  Homo sapiens transmembrane protein 132E (TMEM132E), mRNA.
ACCESSION   NM_001304438
VERSION     NM_001304438.2
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 5806)
  AUTHORS   Gu,S., Knowland,D., Matta,J.A., O'Carroll,M.L., Davini,W.B.,
            Dhara,M., Kweon,H.J. and Bredt,D.S.
  TITLE     Hair cell alpha9alpha10 nicotinic acetylcholine receptor functional
            expression regulated by ligand binding and deafness gene products
  JOURNAL   Proc Natl Acad Sci U S A 117 (39), 24534-24544 (2020)
   PUBMED   32929005
  REMARK    GeneRIF: Hair cell alpha9alpha10 nicotinic acetylcholine receptor
            functional expression regulated by ligand binding and deafness gene
            products.
REFERENCE   2  (bases 1 to 5806)
  AUTHORS   Liaqat,K., Hussain,S., Bilal,M., Nasir,A., Acharya,A., Ali,R.H.,
            Nawaz,S., Umair,M., Schrauwen,I., Ahmad,W. and Leal,S.M.
  TITLE     Further evidence of involvement of TMEM132E in autosomal recessive
            nonsyndromic hearing impairment
  JOURNAL   J Hum Genet 65 (2), 187-192 (2020)
   PUBMED   31656313
  REMARK    GeneRIF: The authors present a second Autosomal-recessive (AR)
            nonsyndromic hearing impairment (NSHI) family with TMEM132E
            variants which strengthens the evidence of the involvement of this
            gene in the etiology of ARNSHI.
            Erratum:[J Hum Genet. 2022 Mar;67(3):181. doi:
            10.1038/s10038-021-00951-9.. PMID: 34526652]
REFERENCE   3  (bases 1 to 5806)
  AUTHORS   Sanchez-Pulido,L. and Ponting,C.P.
  TITLE     TMEM132: an ancient architecture of cohesin and immunoglobulin
            domains define a new family of neural adhesion molecules
  JOURNAL   Bioinformatics 34 (5), 721-724 (2018)
   PUBMED   29088312
REFERENCE   4  (bases 1 to 5806)
  AUTHORS   Lane,J.M., Liang,J., Vlasac,I., Anderson,S.G., Bechtold,D.A.,
            Bowden,J., Emsley,R., Gill,S., Little,M.A., Luik,A.I., Loudon,A.,
            Scheer,F.A., Purcell,S.M., Kyle,S.D., Lawlor,D.A., Zhu,X.,
            Redline,S., Ray,D.W., Rutter,M.K. and Saxena,R.
  TITLE     Genome-wide association analyses of sleep disturbance traits
            identify new loci and highlight shared genetics with
            neuropsychiatric and metabolic traits
  JOURNAL   Nat Genet 49 (2), 274-281 (2017)
   PUBMED   27992416
REFERENCE   5  (bases 1 to 5806)
  AUTHORS   Li,J., Zhao,X., Xin,Q., Shan,S., Jiang,B., Jin,Y., Yuan,H., Dai,P.,
            Xiao,R., Zhang,Q., Xiao,J., Shao,C., Gong,Y. and Liu,Q.
  TITLE     Whole-exome sequencing identifies a variant in TMEM132E causing
            autosomal-recessive nonsyndromic hearing loss DFNB99
  JOURNAL   Hum Mutat 36 (1), 98-105 (2015)
   PUBMED   25331638
  REMARK    GeneRIF: Whole-exome sequencing revealed a homozygous missense
            mutation (c.1259G>A, p.Arg420Gln) in the gene-encoding
            transmembrane protein 132E (TMEM132E) as the causative variant of
            autosomal-recessive nonsyndromic hearing loss.
REFERENCE   6  (bases 1 to 5806)
  AUTHORS   Xie,T., Deng,L., Mei,P., Zhou,Y., Wang,B., Zhang,J., Lin,J.,
            Wei,Y., Zhang,X. and Xu,R.
  TITLE     Genome-wide association study combining pathway analysis for
            typical sporadic amyotrophic lateral sclerosis in Chinese Han
            populations
  JOURNAL   Neurobiol Aging 35 (7), 1778 (2014)
   PUBMED   24529757
REFERENCE   7  (bases 1 to 5806)
  AUTHORS   Gregersen,N.O., Buttenschon,H.N., Hedemand,A., Dahl,H.A.,
            Kristensen,A.S., Clementsen,B., Woldbye,D.P., Koefoed,P.,
            Erhardt,A., Kruse,T.A., Wang,A.G., Borglum,A.D. and Mors,O.
  TITLE     Are TMEM genes potential candidate genes for panic disorder?
  JOURNAL   Psychiatr Genet 24 (1), 37-41 (2014)
   PUBMED   24362369
REFERENCE   8  (bases 1 to 5806)
  AUTHORS   Rudolph,A., Hein,R., Lindstrom,S., Beckmann,L., Behrens,S., Liu,J.,
            Aschard,H., Bolla,M.K., Wang,J., Truong,T., Cordina-Duverger,E.,
            Menegaux,F., Bruning,T., Harth,V., Severi,G., Baglietto,L.,
            Southey,M., Chanock,S.J., Lissowska,J., Figueroa,J.D., Eriksson,M.,
            Humpreys,K., Darabi,H., Olson,J.E., Stevens,K.N., Vachon,C.M.,
            Knight,J.A., Glendon,G., Mulligan,A.M., Ashworth,A., Orr,N.,
            Schoemaker,M., Webb,P.M., Guenel,P., Brauch,H., Giles,G.,
            Garcia-Closas,M., Czene,K., Chenevix-Trench,G., Couch,F.J.,
            Andrulis,I.L., Swerdlow,A., Hunter,D.J., Flesch-Janys,D.,
            Easton,D.F., Hall,P., Nevanlinna,H., Kraft,P. and Chang-Claude,J.
  CONSRTM   GENICA Network; kConFab Investigators; AOCS Management Group;
            Breast Cancer Association Consortium
  TITLE     Genetic modifiers of menopausal hormone replacement therapy and
            breast cancer risk: a genome-wide interaction study
  JOURNAL   Endocr Relat Cancer 20 (6), 875-887 (2013)
   PUBMED   24080446
  REMARK    Publication Status: Online-Only
REFERENCE   9  (bases 1 to 5806)
  AUTHORS   Kim,H.N., Roh,S.J., Sung,Y.A., Chung,H.W., Lee,J.Y., Cho,J.,
            Shin,H. and Kim,H.L.
  TITLE     Genome-wide association study of the five-factor model of
            personality in young Korean women
  JOURNAL   J Hum Genet 58 (10), 667-674 (2013)
   PUBMED   23903073
  REMARK    Erratum:[J Hum Genet. 2015 Aug;60(8):463. doi:
            10.1038/jhg.2015.67.. PMID: 26303433]
REFERENCE   10 (bases 1 to 5806)
  AUTHORS   Kehrer-Sawatzki,H., Tinschert,S. and Jenne,D.E.
  TITLE     Heterogeneity of breakpoints in non-LCR-mediated large
            constitutional deletions of the 17q11.2 NF1 tumour suppressor
            region
  JOURNAL   J Med Genet 40 (10), e116 (2003)
   PUBMED   14569139
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AC005691.1.
            This sequence is a reference standard in the RefSeqGene project.
            
            On Aug 5, 2019 this sequence version replaced NM_001304438.1.
            
            Sequence Note: The RefSeq transcript and protein were derived from
            genomic sequence to make the sequence consistent with the reference
            genome assembly. The genomic coordinates used for the transcript
            record were based on alignments.
            
            ##Evidence-Data-START##
            RNAseq introns :: single sample supports all introns SAMEA1970526,
                              SAMEA2159080 [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000631683.2/ ENSP00000487800.2
            RefSeq Select criteria :: based on single protein-coding transcript
            ##RefSeq-Attributes-END##
            COMPLETENESS: full length.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-1562              AC005691.1         67069-68630         c
            1563-2493           AC005691.1         21155-22085         c
            2494-2640           AC005691.1         19503-19649         c
            2641-2833           AC005691.1         19008-19200         c
            2834-2977           AC005691.1         18061-18204         c
            2978-3183           AC005691.1         15303-15508         c
            3184-3472           AC005691.1         13125-13413         c
            3473-3664           AC005691.1         12014-12205         c
            3665-5806           AC005691.1         8894-11035          c
FEATURES             Location/Qualifiers
     source          1..5806
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="17"
                     /map="17q12"
     gene            1..5806
                     /gene="TMEM132E"
                     /gene_synonym="DFNB99"
                     /note="transmembrane protein 132E"
                     /db_xref="GeneID:124842"
                     /db_xref="HGNC:HGNC:26991"
                     /db_xref="MIM:616178"
     exon            1..1562
                     /gene="TMEM132E"
                     /gene_synonym="DFNB99"
                     /inference="alignment:Splign:2.1.0"
     CDS             1496..4720
                     /gene="TMEM132E"
                     /gene_synonym="DFNB99"
                     /codon_start=1
                     /product="transmembrane protein 132E precursor"
                     /protein_id="NP_001291367.1"
                     /db_xref="CCDS:CCDS11283.2"
                     /db_xref="GeneID:124842"
                     /db_xref="HGNC:HGNC:26991"
                     /db_xref="MIM:616178"
                     /translation="MAPGMSGRGGAALLCLSALLAHASGRSHPASPSPPGPQASPVLP
                     VSYRLSHTRLAFFLREARPPSPAVANSSLQRSEPFVVFQTKELPVLNVSLGPFSTSQV
                     VARELLQPSSTLDIPERLTVNWKVRAFIVRSHVPASQPVVQVLFYVAGRDWDDFGVTE
                     RLPCVRLHAFRDAREVKSSCRLSGGLATCLVRAELPLAWFGPPAPAAPPTARRKSPDG
                     LEPEATGESQQAELYYTLHAPDASGGCGGSRRGAGPGVGARAESPTQHPLLRIGSISL
                     FRPPPRRTLQEHRLDSNLMIRLPDRPLKPGEVLSILLYLAPNSSSPSSPSVEHFTLRV
                     KAKKGVTLLGTKSRSGQWHVTSELLTGAKHSTATVDVAWAQSTPLPPREGQGPLEILQ
                     LDFEMENFTSQSVKRRIMWHIDYRGHGALPDLERAVTELTVIQRDVQAILPLAMDTEI
                     INTAILTGRTVAIPVKVIAIEVNGLVLDISALVECESDNEDIIKVSSSCDYVFVSGKE
                     SRGSMNARVTFRYDVLNAPLEMTVWVPKLPLHIELSDARLSQVKGWRVPILPDRRSVR
                     ESEDEDEEEEERRQSASRGCTLQYQHATLQVFTQFHTTSSEGTDQVVTMLGPDWLVEV
                     TDLVSDFMRVGDPRVAHMVDSSTLAGLEPGTTPFKVVSPLTEAVLGETLLTVTEEKVS
                     ITQLQAQVVASLALSLRPSPGSSHTILATTAAQQTLSFLKQEALLSLWLSYSDGTTAP
                     LSLYSPRDYGLLVSSLDEHVATVTQDRAFPLVVAEAEGSGELLRAELTIAESCQKTKR
                     KSVLATTPVGLRVHFGRDEEDPTYDYPGPSQPGPGGGEDEARGAGPPGSALPAPEAPG
                     PGTASPVVPPTEDFLPLPTGFLQVPRGLTDLEIGMYALLGVFCLAILVFLINCIVFVL
                     RYRHKRIPPEGQTSMDHSHHWVFLGNGQPLRVQGELSPPAGNPLETVPAFCHGDHHSS
                     GSSQTSVQSQVHGRGDGSSGGSARDQAEDPASSPTSKRKRVKFTTFTTLPSEELAYDS
                     VPAGEEDEEEEEDLGWGCPDVAGPTRPTAPPDLHNYMRRIKEIA"
     exon            1563..2493
                     /gene="TMEM132E"
                     /gene_synonym="DFNB99"
                     /inference="alignment:Splign:2.1.0"
     exon            2494..2640
                     /gene="TMEM132E"
                     /gene_synonym="DFNB99"
                     /inference="alignment:Splign:2.1.0"
     exon            2641..2833
                     /gene="TMEM132E"
                     /gene_synonym="DFNB99"
                     /inference="alignment:Splign:2.1.0"
     exon            2834..2977
                     /gene="TMEM132E"
                     /gene_synonym="DFNB99"
                     /inference="alignment:Splign:2.1.0"
     exon            2978..3183
                     /gene="TMEM132E"
                     /gene_synonym="DFNB99"
                     /inference="alignment:Splign:2.1.0"
     exon            3184..3472
                     /gene="TMEM132E"
                     /gene_synonym="DFNB99"
                     /inference="alignment:Splign:2.1.0"
     exon            3473..3664
                     /gene="TMEM132E"
                     /gene_synonym="DFNB99"
                     /inference="alignment:Splign:2.1.0"
     exon            3665..5806
                     /gene="TMEM132E"
                     /gene_synonym="DFNB99"
                     /inference="alignment:Splign:2.1.0"
     polyA_site      5806
                     /gene="TMEM132E"
                     /gene_synonym="DFNB99"
                     /note="major polyA site"
ORIGIN      
        1 agtcatttac ggcggagcag ccggcgcgag cgccgaggag gcggcgacgg cggcggcggc
       61 tgcttcgtgc aactgtggct tcccccacct cctcttcctt tttgctcctc gattcttctt
      121 cttcccccac acacgtccat ggggagccgg ctcccctgcc agcacctcct ctcctctcgg
      181 ccccgtaggc accagctgcc gcttccctgg ccgcaagctg cgcaggtgcc ggctgccctg
      241 gcccctggcg ccgcgcccgc gtctcaccgc ccgcagcccg gactggcgcg gcgatccgct
      301 cgcccaaact gactcggagg gagcgggagc cgatgcccgg cagcatcgag acagcgggcg
      361 aacgggcgtc cggggacagg gtgggggcgg cggggaggag gcgtcggaga ctctgaaccc
      421 cagaaaagtt caaggtttgt gcaggttccc ccagggaagg cgaggagcga ggcggggcag
      481 cgcgcctctc tgccgagaca gcgagacctt agcggggtgg cccggagctg ccgtgagctg
      541 caggagcccc tctgcatctt acagcgttta tggtcatcaa gctggagtcg acgtcctggg
      601 caggaagggc tcggggcagg gcgcattagc cggctttctc gctccctcgc ttctccaagc
      661 cccatctaca tggggcagcc cgttctggcc gcgccaccct tgccccagcc gccgagcggc
      721 tgcctgggca ggaggcgctg agccggcctg tgtggagcct gggccctgat ccagactgga
      781 gaaagcgcgc tggagcggag gagcgagcct tgcgagggga caaacatctg gccgcccgcc
      841 tcgggcatcc ggtctgggcg tcgcctaggg tggtggcgac cggcgtcgcc agtttcagca
      901 ccgcacggaa acttttcctt ctccagatgg attaaagttg tctggatttt ctctttcttt
      961 gagaaagaca gcattcattt gcacctgacc tgggattttt atgctgggct gctgcagggg
     1021 cttggaggaa gaaagcggcg ctatccatgt gcggttacta ccgaaaccga ggaaactggg
     1081 gattgcgttg gaagtcggca ccctcgagtg agttcggatt cgagctgggc cgtgaggccg
     1141 ggagattcag cactgggctc taggtagccc ccgggacgcc cgcggccacc gggctccgga
     1201 ctgcacgtgc agctcccccc gcgcctcgca gatcctgcag ggggcaccag ctgggggagg
     1261 tggaggctcc tcccgcccgg agctgcgccc ccaccggctc cgagggtgta gccgccagcg
     1321 cctgggacgc cccctccccg caaagtgtcc ccgaattgca ctctctggtc ccggagctgc
     1381 atctgagaca gccgggcgcc acggcagccc tgagttggat gtgaccaagc ccagcctggg
     1441 gccaagtcgt cgtcgactgt tgctctctcg gacccctccc gcccccgcct cggccatggc
     1501 cccggggatg tcgggccgcg gcggcgccgc cctgctctgc ctctcagcgc tactcgccca
     1561 cgcctctggc cgctcccacc cggccagccc cagcccgccg gggccgcagg ccagcccggt
     1621 gctgccagtc agctaccgcc tgtcgcacac gcggctggcc ttcttcctgc gggaggcgcg
     1681 gcccccgtca cccgcggtcg ccaacagctc tctgcagcgc tccgagccct tcgtggtgtt
     1741 ccagaccaag gagctgccgg tcctcaacgt ctctctgggg cccttcagca ccagccaggt
     1801 ggtggcgcgg gagctcctgc agccgtccag caccctggac atccccgagc gcctgacggt
     1861 gaactggaag gtgcgggcct tcatcgtccg ctcgcacgtg cccgcctcgc agcccgtggt
     1921 ccaggtgctg ttctacgtag ccggccggga ctgggacgac ttcggcgtca ccgagcggct
     1981 gccctgtgtc cgcctgcatg ccttccggga tgcccgggaa gtcaagagct cctgccgcct
     2041 cagcgggggc ctggccactt gtctggtgcg ggcagagctg cccctggcct ggttcgggcc
     2101 cccagccccc gctgcgccac ccacggcccg ccgcaagtcc ccggacgggc tggagcccga
     2161 ggcgacgggg gagagccagc aggccgagct ctactacacg ctccacgccc ctgatgcgtc
     2221 ggggggctgc gggggctccc gccggggggc cgggcccggg gtgggggccc gagcggaaag
     2281 ccctacccag caccccctgc tgcgcatcgg gagcatcagc ctgttccgcc cgccccccag
     2341 gaggaccctg caggagcaca ggctggacag caacctgatg atccgcctgc cagaccggcc
     2401 cctcaagccc ggggaagtgc tcagcatcct cctctatctg gcccccaact cctcctcgcc
     2461 ctccagcccc agcgtggagc acttcacact cagggtgaag gccaagaagg gtgtgaccct
     2521 tttaggtacc aagtcacgga gtggccagtg gcatgtgacc tcggagctgc tgactggggc
     2581 aaagcactca acagccaccg tggatgtggc ctgggctcag agcacacccc tgccccccag
     2641 ggagggccag ggccccttgg agatcttgca gctggacttt gaaatggaga acttcaccag
     2701 ccagtcagtc aagcggagga tcatgtggca cattgactac cgtggccacg gcgccctgcc
     2761 tgacctggag cgggcagtca ctgagctgac ggtcattcag cgggatgtgc aagccatcct
     2821 gcccctggcc atggacacag agatcatcaa cacggccatt ctgactggcc ggacagtggc
     2881 catccctgtc aaggtcattg ccatcgaggt gaatggcctc gtcctggaca tctccgccct
     2941 agtggaatgc gagtctgaca atgaagacat catcaaggta tccagcagct gtgactacgt
     3001 gtttgtgagt ggaaaagagt ctcgagggtc catgaacgcc agggtcacct tccgctacga
     3061 cgtcctcaat gctcccctgg aaatgacagt ctgggtcccc aagctgccct tgcacattga
     3121 gctctcagat gcccgcctca gccaagtgaa gggctggagg gtacctatcc tccccgaccg
     3181 gaggtcagtc cgggaaagcg aggatgagga tgaggaggag gaggagcggc ggcagagtgc
     3241 aagccgtggc tgcaccctgc agtaccagca tgccaccctg caggtcttca cccagttcca
     3301 cacgacatca tccgagggca ctgaccaggt ggtcaccatg ttaggcccgg actggctggt
     3361 ggaggtcacc gacctagtca gtgacttcat gcgggtgggc gatccccgag tggcacacat
     3421 ggtggacagc agcacgctgg caggactgga gccaggcacc acccccttta aggtggtgtc
     3481 tccgctgacg gaggctgtgc tcggggagac gctgctgacg gtgactgagg agaaggtcag
     3541 catcacacag cttcaggccc aggtggtggc cagcctggcc ctctccctgc ggcccagccc
     3601 tgggagcagc cacaccatcc tagccaccac agctgcccaa cagaccttga gcttcctcaa
     3661 gcaggaagcc ctactgagcc tctggctctc ctacagtgat ggcaccacag ccccactctc
     3721 cctctacagc ccacgagact atggactgct agtgagcagc ctggatgagc atgtggccac
     3781 tgtgacccag gaccgggcct tccctctggt agtggctgag gccgaggggt caggggagct
     3841 gcttcgcgca gagctaacca tcgctgagag ctgccagaaa accaaacgca agagtgtgct
     3901 cgccacgacc cctgtgggcc tgcgggtgca ctttgggagg gacgaggagg accccactta
     3961 tgactacccg ggccccagcc aaccagggcc cggcgggggc gaggacgagg cccggggagc
     4021 tggcccgccg ggctctgcgc tacccgcacc ggaggctcca ggcccgggca ccgccagccc
     4081 cgtcgtgcca cccacagaag acttcctgcc gctgcccacc ggcttcctgc aggtgccacg
     4141 gggtctgaca gacctggaga tcggcatgta cgcgctgctg ggcgtcttct gcctcgccat
     4201 cctcgtcttc ctcatcaact gcatcgtttt tgtgctgcgc taccggcaca agcgcatccc
     4261 gcccgagggc cagaccagca tggaccactc tcaccactgg gtgttcctgg gcaacgggca
     4321 gccgctgcgg gtgcaaggag agctgtcgcc gccagcaggc aacccgctgg aaaccgtgcc
     4381 cgccttctgc cacggcgacc accacagcag cggcagctcg cagaccagcg tccagagcca
     4441 ggtgcacggc aggggcgacg gctcctcggg cggctcagcc cgagaccaag ccgaggaccc
     4501 cgccagctcg cccacctcca agcgcaagcg ggtcaagttc accaccttca ccacgctgcc
     4561 gtcagaggag ctggcctatg actcggtgcc cgcgggcgaa gaggacgagg aggaggaaga
     4621 ggacctgggt tggggctgcc cggatgtggc gggccccacg cggcccactg cacccccgga
     4681 cctgcacaat tacatgcgca gaatcaaaga gattgcatag aggcgccagc cggagtagca
     4741 gggacccccc cccccaacgg ggtcagctcg gggtaggaca cagccgggac cccggttcac
     4801 actgactctg ggcggctgaa ttgattttgt actccctgcc cctgcagctt ggctccgtgc
     4861 ggagcgggcc gcctcagtgt ctgggccttc cctcgcctca cgccattacc ctcttctgcc
     4921 ccctgcaggt ggagggctct tcctccagtg gctcgtaagg aggaaagcaa ccccagcctc
     4981 tgttctgccc tttccaaacc tcctcccatc ttaagcaacc ccctgcccca agagtgaggc
     5041 aaggaggtcc agcttggggt caggtgggcc cacgctgtgt cccgggcccg cctcccgtcc
     5101 cccgtgtcgt ccccctgtgc agggggttct gtgggggtct tgtgtcacag gctgcacaaa
     5161 gactttcctc aaactaatat tcagggattt ctgtcctgca gggtggggag gtggcagctg
     5221 cctgccctgc caaggatctt gctgtggacg aaatatctgg gggttagggg gacagttgta
     5281 gcatctgctg gcattcgggt gcctcccagg acctgggagc tgactctaca gagaggtctg
     5341 gtgccaagcc aggcaccttc ctgagttctc aggactccca cctctgcccc aagggctttg
     5401 ggcagggacc taaaggggaa agagtcctgg atccatctct agccaaatca caccccagag
     5461 ccagaggcct ggggacctcc ttgccttccc cgtcccccac agcaaggtca acactactac
     5521 gccttagcca cccgtcaccc tgctgactgc gacttccctc tgcagcacag ggcaggcagc
     5581 cacctatgcc ccacaagacg gaacccggga ggggagtaga gggcaccagg gaatgctgtg
     5641 agggacttca gggtgggcaa atgcagaagg gagccagtgt cgcccctacc ccatcccaca
     5701 gccatttttc tctcgggttc tacccaccac tgtgtcggat ttttcttaaa taaatggaag
     5761 cggtcagact ggaggtgggg gcagcagctc ccatgaacag agagta
//
