LOCUS       NM_001365902            6019 bp    mRNA    linear   PRI 13-DEC-2024
DEFINITION  Homo sapiens nuclear factor I X (NFIX), transcript variant 4, mRNA.
ACCESSION   NM_001365902 XM_005259918
VERSION     NM_001365902.3
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 6019)
  AUTHORS   Liu,G., Shi,H., Zheng,H., Kong,W., Cheng,X. and Deng,L.
  TITLE     Circular RNA NFIX Functions as an Oncogene in Non-Small Cell Lung
            Cancer by Modulating the miR-214-3p/TRIAP1 Axis
  JOURNAL   Clin Respir J 18 (8), e13801 (2024)
   PUBMED   39135128
  REMARK    GeneRIF: Circular RNA NFIX Functions as an Oncogene in Non-Small
            Cell Lung Cancer by Modulating the miR-214-3p/TRIAP1 Axis.
REFERENCE   2  (bases 1 to 6019)
  AUTHORS   Lin,X.Q., Quan,Y.L., He,H.L. and Peng,J.
  TITLE     [NFIX gene mutation causes Marshall-Smith syndrome in a pair of
            identical twins and literature review]
  JOURNAL   Zhongguo Dang Dai Er Ke Za Zhi 26 (7), 750-756 (2024)
   PUBMED   39014953
  REMARK    GeneRIF: [NFIX gene mutation causes Marshall-Smith syndrome in a
            pair of identical twins and literature review].
            Review article
REFERENCE   3  (bases 1 to 6019)
  AUTHORS   Wang,R., Ye,H., Yang,B., Ao,M., Yu,X., Wu,Y., Xi,M. and Hou,M.
  TITLE     m6A-modified circNFIX promotes ovarian cancer progression and
            immune escape via activating IL-6R/JAK1/STAT3 signaling by sponging
            miR-647
  JOURNAL   Int Immunopharmacol 124 (Pt A), 110879 (2023)
   PUBMED   37713785
  REMARK    GeneRIF: m6A-modified circNFIX promotes ovarian cancer progression
            and immune escape via activating IL-6R/JAK1/STAT3 signaling by
            sponging miR-647.
REFERENCE   4  (bases 1 to 6019)
  AUTHORS   Uzman,C.Y., Gursoy,S. and Hazan,F.
  TITLE     A rare cause of intellectual disability: Novel mutations of NFIX
            gene in two patients with clinical features of Marshall-Smith
            syndrome and Malan syndrome
  JOURNAL   Int J Dev Neurosci 83 (5), 479-485 (2023)
   PUBMED   37336770
  REMARK    GeneRIF: A rare cause of intellectual disability: Novel mutations
            of NFIX gene in two patients with clinical features of
            Marshall-Smith syndrome and Malan syndrome.
REFERENCE   5  (bases 1 to 6019)
  AUTHORS   Ribeiro,V., Martins,S.G., Lopes,A.S., Thorsteinsdottir,S.,
            Zilhao,R. and Carlos,A.R.
  TITLE     NFIXing Cancer: The Role of NFIX in Oxidative Stress Response and
            Cell Fate
  JOURNAL   Int J Mol Sci 24 (5), 4293 (2023)
   PUBMED   36901722
  REMARK    GeneRIF: NFIXing Cancer: The Role of NFIX in Oxidative Stress
            Response and Cell Fate.
            Review article
            Publication Status: Online-Only
REFERENCE   6  (bases 1 to 6019)
  AUTHORS   Sumner,C., Shinohara,T., Durham,L., Traub,R., Major,E.O. and
            Amemiya,K.
  TITLE     Expression of multiple classes of the nuclear factor-1 family in
            the developing human brain: differential expression of two classes
            of NF-1 genes
  JOURNAL   J Neurovirol 2 (2), 87-100 (1996)
   PUBMED   8799200
REFERENCE   7  (bases 1 to 6019)
  AUTHORS   Qian,F., Kruse,U., Lichter,P. and Sippel,A.E.
  TITLE     Chromosomal localization of the four genes (NFIA, B, C, and X) for
            the human transcription factor nuclear factor I by FISH
  JOURNAL   Genomics 28 (1), 66-73 (1995)
   PUBMED   7590749
REFERENCE   8  (bases 1 to 6019)
  AUTHORS   Apt,D., Liu,Y. and Bernard,H.U.
  TITLE     Cloning and functional analysis of spliced isoforms of human
            nuclear factor I-X: interference with transcriptional activation by
            NFI/CTF in a cell-type specific manner
  JOURNAL   Nucleic Acids Res 22 (19), 3825-3833 (1994)
   PUBMED   7937100
REFERENCE   9  (bases 1 to 6019)
  AUTHORS   Seisenberger,C., Winnacker,E.L. and Scherthan,H.
  TITLE     Localisation of the human nuclear factor I/X (NFI/X) gene to
            chromosome 19p13 and detection of five other related loci at
            1p21-22, 1q42-43, 5q15, 11p13 and 20q13 by FISH
  JOURNAL   Hum Genet 91 (6), 535-537 (1993)
   PUBMED   8340106
REFERENCE   10 (bases 1 to 6019)
  AUTHORS   Priolo,M.
  TITLE     NFIX-Related Malan Syndrome
  JOURNAL   (in) Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE and
            Amemiya A (Eds.);
            GENEREVIEWS(R);
            (1993)
   PUBMED   39083629
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AC138474.2, AC007787.1 and
            KF456509.1.
            This sequence is a reference standard in the RefSeqGene project.
            
            On Mar 9, 2020 this sequence version replaced NM_001365902.2.
            
            Summary: The protein encoded by this gene is a transcription factor
            that binds the palindromic sequence 5'-TTGGCNNNNNGCCAA-3 in viral
            and cellular promoters. The encoded protein can also stimulate
            adenovirus replication in vitro. Three transcript variants encoding
            different isoforms have been found for this gene. [provided by
            RefSeq, Aug 2012].
            
            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.
            
            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##
            RNAseq introns :: single sample supports all introns SAMEA1968189,
                              SAMEA1968540 [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000592199.6/ ENSP00000467512.1
            RefSeq Select criteria :: based on manual assertion, conservation
            ##RefSeq-Attributes-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-390               AC138474.2         51432-51821         c
            391-922             AC138474.2         21744-22275         c
            923-985             AC007787.1         10643-10705
            986-1060            AC007787.1         11018-11092
            1061-1181           AC007787.1         11502-11622
            1182-1318           AC007787.1         13131-13267
            1319-1441           AC007787.1         16209-16331
            1442-1617           AC007787.1         19276-19451
            1618-1765           AC007787.1         25585-25732
            1766-1857           AC007787.1         27895-27986
            1858-4997           AC007787.1         32231-35370
            4998-5307           KF456509.1         1-310
            5308-6019           AC007787.1         35681-36392
FEATURES             Location/Qualifiers
     source          1..6019
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="19"
                     /map="19p13.13"
     gene            1..6019
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /note="nuclear factor I X"
                     /db_xref="GeneID:4784"
                     /db_xref="HGNC:HGNC:7788"
                     /db_xref="MIM:164005"
     exon            1..390
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /inference="alignment:Splign:2.1.0"
     CDS             364..1872
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /note="isoform 4 is encoded by transcript variant 4;
                     nuclear factor 1/X; TGGCA-binding protein; nuclear factor
                     1 X-type; CCAAT-box-binding transcription factor"
                     /codon_start=1
                     /product="nuclear factor 1 X-type isoform 4"
                     /protein_id="NP_001352831.1"
                     /db_xref="CCDS:CCDS92530.1"
                     /db_xref="GeneID:4784"
                     /db_xref="HGNC:HGNC:7788"
                     /db_xref="MIM:164005"
                     /translation="MYSPYCLTQDEFHPFIEALLPHVRAFSYTWFNLQARKRKYFKKH
                     EKRMSKDEERAVKDELLGEKPEIKQKWASRLLAKLRKDIRPEFREDFVLTITGKKPPC
                     CVLSNPDQKGKIRRIDCLRQADKVWRLDLVMVILFKGIPLESTDGERLYKSPQCSNPG
                     LCVQPHHIGVTIKELDLYLAYFVHTPESGQSDSSNQQGDADIKPLPNGHLSFQDCFVT
                     SGVWNVTELVRVSQTPVATASGPNFSLADLESPSYYNINQVTLGRRSITSPPSTSTTK
                     RPKSIDDSEMESPVDDVFYPGTGRSPAAGSSQSSGWPNDVDAGPASLKKSGKLDFCSA
                     LSSQGSSPRMAFTHHPLPVLAGVRPGSPRATASALHFPSTSIIQQSSPYFTHPTIRYH
                     HHHGQDSLKEFVQFVCSDGSGQATGQPNGSGQGKVPGSFLLPPPPPVARPVPLPMPDS
                     KSTSTAPDGAALTPPSPSFATTGASSANRFVSIGPRDGNFLNIPQQSQSWFL"
     exon            391..922
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /inference="alignment:Splign:2.1.0"
     exon            923..985
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /inference="alignment:Splign:2.1.0"
     exon            986..1060
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /inference="alignment:Splign:2.1.0"
     exon            1061..1181
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /inference="alignment:Splign:2.1.0"
     exon            1182..1318
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /inference="alignment:Splign:2.1.0"
     exon            1319..1441
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /inference="alignment:Splign:2.1.0"
     exon            1442..1617
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /inference="alignment:Splign:2.1.0"
     exon            1618..1765
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /inference="alignment:Splign:2.1.0"
     exon            1766..1857
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /inference="alignment:Splign:2.1.0"
     exon            1858..6019
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /inference="alignment:Splign:2.1.0"
     polyA_site      4578
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
     regulatory      5991..5996
                     /regulatory_class="polyA_signal_sequence"
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /note="hexamer: AATAAA"
     regulatory      5999..6004
                     /regulatory_class="polyA_signal_sequence"
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /note="hexamer: AATAAA"
     polyA_site      6010
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
                     /note="major polyA site"
     polyA_site      6019
                     /gene="NFIX"
                     /gene_synonym="CTF; MALNS; MRSHSS; NF-I/X; NF1-X; NF1A;
                     SOTOS2"
ORIGIN      
        1 gtctaaactt tcactttcac agcgcggcgg ctgcggcggc ggcggcggcg ggcgagggtg
       61 accggccgag cggcggcggc atggagtaga cgcgcggcgg cagcggcggc ggcggcggac
      121 gcgagaggca gcggcgagcg cggcggcggc ggcggcagcg gcggccccgg agccggcggg
      181 gccgagcttg cgagcggcga gcgcggagcg gcgccgggcc gagcgcgggg ccgcgggccg
      241 ggcgggcgca gcgcggcgga ggccggagga gccgagccgg agcccgagcc cgagcgcggc
      301 cgccgcctgc cgggcctccc ctcgccgcgg ccggccgccg cgctcccgcc cgggcgccca
      361 gctatgtact ccccgtactg cctcacccag gatgagttcc acccgttcat cgaggcactg
      421 ctgcctcacg tccgcgcttt ctcctacacc tggttcaacc tgcaggcgcg gaagcgcaag
      481 tacttcaaga agcatgaaaa gcggatgtcg aaggacgagg agcgggcggt gaaggacgag
      541 ctgctgggcg agaagcccga gatcaagcag aagtgggcat cccggctgct ggccaagctg
      601 cgcaaggaca tccggcccga gttccgcgag gacttcgtgc tgaccatcac gggcaagaag
      661 cccccctgct gcgtgctctc caaccccgac cagaagggca agatccggcg gattgactgc
      721 ctgcgccagg ctgacaaggt gtggcggctg gacctggtca tggtgatttt gtttaagggg
      781 atccccctgg aaagtactga tggggagcgg ctctacaagt cgcctcagtg ctcgaacccc
      841 ggcctgtgcg tccagccaca tcacattgga gtcacaatca aagaactgga tctttatctg
      901 gcttactttg tccacactcc ggaatccgga caatcagata gttcaaacca gcaaggagat
      961 gcggacatca aaccactgcc caacgggcac ttaagtttcc aggactgttt tgtgacttcc
     1021 ggggtctgga atgtgacgga gctggtgaga gtatcacaga ctcctgttgc aacagcatca
     1081 gggcccaact tctccctggc ggacctggag agtcccagct actacaacat caaccaggtg
     1141 accctggggc ggcggtccat cacctcccct ccttccacca gcaccaccaa gcgccccaag
     1201 tccatcgatg acagtgagat ggagagccct gttgatgacg tgttctatcc cgggacaggc
     1261 cgttccccag cagctggcag cagccagtcc agcgggtggc ccaacgatgt ggatgcaggc
     1321 ccggcttctc taaagaagtc aggaaagctg gacttctgca gtgccctctc ctctcagggc
     1381 agctccccgc gcatggcttt cacccaccac ccgctgcctg tgcttgctgg agtcagacca
     1441 gggagccccc gggccacagc atcagccctg cacttcccct ccacgtccat catccagcag
     1501 tcgagcccgt atttcacgca cccgaccatc cgctaccacc accaccacgg gcaggactca
     1561 ctgaaggagt ttgtgcagtt tgtgtgctcg gatggctcgg gccaggccac cggacagccc
     1621 aacggtagcg gccagggcaa agtcccgggg tcatttttgc taccgccgcc gcctccagtg
     1681 gccagacctg tgccccttcc tatgcctgat tccaaatcca ccagcactgc cccagacggc
     1741 gccgccttga ctcctccatc accttcattc gcaacgacag gcgcctcctc tgccaaccgg
     1801 tttgtcagca tcggaccccg ggacggcaac tttctgaaca tcccacagca gtctcagtcc
     1861 tggttcctct gataagatcg acaaaagaaa caacaaaatg agaagaagag gttcctcgaa
     1921 aggggggaga agaaattttg agaatggaaa aatcccccag cccagcccag ccccaccgaa
     1981 aagcaaaaat tacacgtcgt cagccactca gcccttctct cctccagccc ggggaccccc
     2041 gcgggcccca gaagcagccc agttctcaga gagcccttgg aaggggtctc ggtggagctg
     2101 tgcaccagca gccaagcaga aagaaacacg cgacatggac tctgtcaagt agaggacaga
     2161 aagcaagaaa ggatgcagaa ctgccttcct ccccctgacc ccgccccggc cttctgggga
     2221 aggaacaaag tccccaaaca aagcaaccag cacaattctg aaggggcctg gcctccaccc
     2281 tcaccccttc ctaggggaac cccaccctcc acacagccgg agctgcccta gggagcctgg
     2341 agggccagct tgtaaagatg atggggttta gatccctcag gctctcccct ccagactccg
     2401 cccttccctc cctccctccc tccctccctc tctgccaagg ctccagcttc ttcccccagc
     2461 tgctcccgac caggaggggg agagcagcct ccacttaccc caccccaccc ttgggctaaa
     2521 agcccccagg cgggcagggg gtgacccctg gagctagttg cgtgtcccag aatggagggt
     2581 gttctgacac cccaccctga gccgcaagag cagtcctggg gccctggacc cctctgtaca
     2641 gtccgtagga aaaagtcgga atgctctcga cggcctcgtc ccagcctggg acaggccccc
     2701 tttcccctct ctctgcaggc caggagggcc tccttcctgc cacgagggag gggagtcggg
     2761 ccccaggtcg cccccgcccc cagccctgca tgcaggtgcc ctcgctccgc cccatcagtt
     2821 cctgcccctg cccctcatgc agactgccct gctggggccg ggccggaggg tggagcagaa
     2881 aggggacccc ggagccgagc gaggaggacc aggcagccgc cgctgccgcg ctaagccacc
     2941 acctgcgctt aggtaggcgt cctgctcgcc gactttcagt tccttgggag ggtgttgggt
     3001 gtcgtccttt tcaaaagtgt tttggagctt tctgtgcccc ccgactttcc cccgcctccc
     3061 cgccccccac gtggccactt ttctctggat tttagctgta atgtctttac tctttattta
     3121 ggggtggggc attcattgtt tgggtctttt gctgttggaa tgggaactcc tcctccattt
     3181 gagcaacttg ggaacaattt ggtaacacac cacaggaagt agctctcccc cccagccccc
     3241 tcctccctca agggagggtt ggggggcctg tccagagggt cttcagaagc ccccctggga
     3301 gggaggggag gatgagcacg cccagctccc ctccagggtg tgacttggcc cctctggctt
     3361 gtctttctgt gccttactcc tcctcctgcg tctcccgttc ctggcccctt cttgagtcct
     3421 tgtgcctctc tctttctctc tctttcttaa ttgtatgaaa acacaaagca caggtcagga
     3481 tcctctgaga gaaaatcaac attgcaccac gtaggggtgg gctatgggct gtatttattg
     3541 tgaatctagt ttgtgaggct gtggccccga gctggcggag ggagggaaga ggagggagtg
     3601 acgggagggg aggaggtcag cgacctgggg ccgtagcggc aggcgaacgg tgcctgctac
     3661 ccagctggaa gccacaaggt ggctggctcc aggggcggct tttgttggaa gttgagtgaa
     3721 gccctccccc tgtcctcagc gtgcagccct agaggacccc agggctgagg ggcagtggat
     3781 cctgcgggag tctcccgggg cgtggggagt aaggccccgg gggtgggggg ccgggtgggc
     3841 cgggcgtgac gcgcggtcaa agtgcaatga tttttcagtt cggttggcta aacagggtca
     3901 gagctgagag cgaagcagaa ggggctccct gtccggccca cgtgcccttt ccctcgacga
     3961 cagtcgaggg ctcgggctct gtgggactgt gggagctagg gtctgcgggg cgcctgcccg
     4021 ggcgaggtcg gaagctgcag gccagctggg cccgggccgg agcgtgcccg gcggggctgc
     4081 ccgggcgggc agggggtggg ggctgctcct ttcccaagtg gtgttgtgag gggcaatgag
     4141 ggcaacagga gatgtgggga cgtgttagga gagaaaaaaa aaaaaacaaa aatatatatg
     4201 ggggaaatta actttttttt ttcattgaac caagtgcaat gcatcagaga gttttcctat
     4261 ctttgtatgt taagagatta agaaaaaaaa attctatttt tgttgtaatg tcctcgcggc
     4321 tctggggacg ctaaaagaac cgggcctgcc ccgccctgcg cggggataac gaaagctgag
     4381 tgtttttccc ttttttttgt tcgtttttag tttttttttt tttaagtcgt tttcctgcgt
     4441 tgacgaggat gatctggggt ttttatttgt ttcgtcgttc gttctgtttc ggtgggaggg
     4501 ctgaaggaaa cgttcacatt ttagagttta aaaaaaacac ctcgacattt aaaaaatcaa
     4561 ccaacacaag atcaaaaagg aaaaggacga gagaaaaatt atttttaaga taattaaaca
     4621 taaaaccctg gtgcttctta cattataaag tacgttttaa agaacccaca aactattata
     4681 cataagttta tgaatcaatt aaatatcctg cacttgttag gaatacgcat atcccttctt
     4741 tgttgagttt aacggaacgg gacagcggcg tgcccccggc ggctggactg ctccggccgc
     4801 gggtctcccc gggcgcccct ccctggggcc cagcacccct cctcgcccca tccccgtccg
     4861 ggtacggggg cgcggcaggg gtccccggcc cctcccccgc agaggtcaat gccaacgaac
     4921 aaacgtcccc tccctccctc cctctccgcc ccgagcgccc ttctttgagc cagacgccaa
     4981 cttgaccctc accagcatta tcaggagcgc gctcagcaag ttggtagttt cctcccccct
     5041 ttcccggcgc ccctcccgcc cccattcaac atctctcatc ctatccccga ccccctccgg
     5101 ggaacaccgg gaaggctcga cgctccagga caggaccagc cacgctgaca ggtcgatttg
     5161 cccaggcccg cgcccgcacg cacgcacgca cacggccccg cacacagccc cgccccaccc
     5221 cgcaaccagc cctgtcgact gccttataca cccgcccccg cgctggccgg ccgacctagt
     5281 gccttgttct cacccccgtg ctggcggagc ggacgccgcg ctctgggtcc cagaggggcc
     5341 gggtggctca gacgacccac cactccccca ccctgaccgt gctgaacaga cccccccaca
     5401 cgagagaaaa taaaggagca ataaagtcac gagaactttc gtcccccaat cgagagcccg
     5461 aggggcaccc cagccccgcc tctgctcccc cccaccccac ccaccctcgg ggcgcccccc
     5521 tccccccgca agccagcctg ggccagcccc gcttcggccc ctcccgggag atccgtgcgc
     5581 ccgaccagca ccagcatcgc ggaccgcaaa ggccgcccgt cccgtcaaac aagtttcttc
     5641 ttaggctaag aaacgcagta tatacgagta tctctatata tagtactaat ggatttggtg
     5701 tgcttccccc ttagcgtccc cctccctctg ctcctcctcc ttcagcctgg tctccccctc
     5761 ttctctgccc tccacccccg tctctgcact gagatacata agaaacaagg gtagtttact
     5821 gtctgttttg ttttctgggt tttcagtgtc ctagcggaat gcaagtaggc agccagcccg
     5881 tctgttccct ctccgccccg ccccgccccg cccccgtcac tgcgcttctg ttataccatc
     5941 tttgcctgac tctctccggc ttctccattg aatggctaat gtgtatgtga aataaagaaa
     6001 taaagaaaaa caaacgcga
//
