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2025-05-09 18:23:27, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001199103 2533 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens NT5C1B-RDH14 readthrough (NT5C1B-RDH14), transcript
variant 1, mRNA.
ACCESSION NM_001199103
VERSION NM_001199103.1 GI:312283681
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 2533)
AUTHORS Prakash,T., Sharma,V.K., Adati,N., Ozawa,R., Kumar,N., Nishida,Y.,
Fujikake,T., Takeda,T. and Taylor,T.D.
TITLE Expression of conjoined genes: another mechanism for gene
regulation in eukaryotes
JOURNAL PLoS ONE 5 (10), E13284 (2010)
PUBMED 20967262
REMARK Publication Status: Online-Only
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AC079148.9 and AK307653.1.
Summary: This locus represents naturally occurring read-through
transcription between the neighboring NT5C1B (5'-nucleotidase,
cytosolic IB) and RDH14 (retinol dehydrogenase 14) genes on
chromosome 2. Alternative splicing results in multiple transcript
variants, one of which encodes a fusion protein that shares
sequence identity with the products of each individual gene.
[provided by RefSeq, Nov 2010].
Transcript Variant: This variant (1) represents the shorter
transcript but encodes the longer isoform (1), which is a fusion
protein sharing sequence identity with each individual gene
product.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
##Evidence-Data-START##
Transcript exon combination :: AK307653.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084 [ECO:0000348]
##Evidence-Data-END##
##RefSeq-Attributes-START##
readthrough transcript :: includes exons from GeneID 57665, 93034
##RefSeq-Attributes-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-16 AC079148.9 144228-144243 c
17-995 AK307653.1 1-979
996-996 AC079148.9 138764-138764 c
997-1161 AK307653.1 981-1145
1162-1162 AC079148.9 131536-131536 c
1163-1504 AK307653.1 1147-1488
1505-2533 AC079148.9 109386-110414 c
FEATURES Location/Qualifiers
source 1..2533
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="2"
/map="2p"
gene 1..2533
/gene="NT5C1B-RDH14"
/note="NT5C1B-RDH14 readthrough"
/db_xref="GeneID:100526794"
/db_xref="HGNC:38831"
exon 1..142
/gene="NT5C1B-RDH14"
/inference="alignment:Splign:1.39.8"
misc_feature 8..10
/gene="NT5C1B-RDH14"
/note="upstream in-frame stop codon"
variation complement(92)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="t"
/db_xref="dbSNP:368657100"
variation complement(93)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:375020758"
variation complement(102)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="c"
/db_xref="dbSNP:370091625"
CDS 113..2065
/gene="NT5C1B-RDH14"
/note="isoform 1 is encoded by transcript variant 1;
NT5C1B-RDH14 read-through transcript"
/codon_start=1
/product="NT5C1B-RDH14 protein isoform 1"
/protein_id="NP_001186032.1"
/db_xref="GI:312283682"
/db_xref="GeneID:100526794"
/db_xref="HGNC:38831"
/translation="
MSQTSLKQKKNEPGMRSSKESLEAEKRKESDKTGVRLSNQGSQESSLRKTDSRGYLVRSQWSRISRSPSTKAPSIDEPRSRNTSAKVELPSSSTSSRTPSTSPSLHDSSPPPLSGQPSLQPPASPQLPRSLDSRPPTPPEPDPGSRRSTKMQENPEAWAQGIVREIRQTRDSQPLEYSRTSPTEWKSSSQRRGIYPASTQLDRNSLSEQQQQQREDEDDYEAAYWASMRSFYEKNPSCSRPWPPKPKNAITIALSSCALFNMVDGRKIYEQEGLEKYMEYQLTNENVILTPGPAFRFVKALQYVNARLRDLYPDEQDLFDIVLMTNNHAQVGVRLINSVNHYGLLIDRFCLTGGKDPIGYLKAYLTNLYIAADSEKVQEAIQEGIASATMFDGAKDMAYCDTQLRVAFDGDAVLFSDESEHFTKEHGLDKFFQYDTLCESKPLAQEEPRLDVLINNAGIFQCPYMKTEDGFEMQFGVNHLGHFLLTNLLLGLLKSSAPSRIVVVSSKLYKYGDINFDDLNSEQSYNKSFCYSRSKLANILFTRELARRLEGTNVTVNVLHPGIVRTNLGRHIHIPLLVKPLFNLVSWAFFKTPVEGAQTSIYLASSPEVEGVSGRYFGDCKEEELLPKAMDESVARKLWDISEVMVGLLK
"
misc_feature 947..>1447
/gene="NT5C1B-RDH14"
/note="5'-nucleotidase; Region: 5-nucleotidase; pfam06189"
/db_xref="CDD:148034"
misc_feature <1445..2038
/gene="NT5C1B-RDH14"
/note="Rossmann-fold NAD(P)(+)-binding proteins; Region:
NADB_Rossmann; cl09931"
/db_xref="CDD:213117"
misc_feature order(1478..1486,1640..1648,1703..1705,1715..1717,
1793..1804)
/gene="NT5C1B-RDH14"
/note="NAD(P) binding site [chemical binding]; other site"
/db_xref="CDD:187535"
misc_feature order(1544..1546,1646..1648,1703..1705,1715..1717)
/gene="NT5C1B-RDH14"
/note="active site"
/db_xref="CDD:187535"
variation complement(133)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:17852342"
exon 143..232
/gene="NT5C1B-RDH14"
/inference="alignment:Splign:1.39.8"
variation complement(148)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:139661780"
variation complement(151)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:16985306"
variation complement(152)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:150854562"
variation complement(173)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="t"
/db_xref="dbSNP:142250232"
variation complement(178)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:373948064"
variation complement(219)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:368786487"
exon 233..376
/gene="NT5C1B-RDH14"
/inference="alignment:Splign:1.39.8"
variation complement(241)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:147993928"
variation complement(251)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:201679289"
variation complement(252)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:147855918"
variation complement(254)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:375353460"
variation complement(255)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:142174343"
variation complement(269)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:114622083"
variation complement(270)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:199873248"
variation complement(281)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:200122449"
variation complement(282)
/gene="NT5C1B-RDH14"
/replace="g"
/replace="t"
/db_xref="dbSNP:371760155"
variation complement(285)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:367871143"
variation complement(309)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:202225134"
variation complement(322)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:371117462"
variation complement(329)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:368550960"
variation complement(338)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:201205997"
variation complement(345)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:200286986"
exon 377..841
/gene="NT5C1B-RDH14"
/inference="alignment:Splign:1.39.8"
variation complement(415)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:61741495"
variation complement(430)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:117298882"
variation complement(448)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:200689028"
variation complement(465)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="c"
/db_xref="dbSNP:61742596"
variation complement(498)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:61742608"
variation complement(513)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:368950263"
variation complement(590)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:369345171"
variation complement(595)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="c"
/db_xref="dbSNP:200514864"
variation complement(620)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:373347393"
variation complement(621)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:150624428"
variation complement(633)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:369846764"
variation complement(634)
/gene="NT5C1B-RDH14"
/replace="g"
/replace="t"
/db_xref="dbSNP:200273135"
variation complement(637)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:144486690"
variation complement(651)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:201047201"
variation complement(687)
/gene="NT5C1B-RDH14"
/replace="g"
/replace="t"
/db_xref="dbSNP:76782074"
variation complement(706)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:377296218"
variation complement(713)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:202208251"
variation complement(726)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:146399000"
variation complement(750..752)
/gene="NT5C1B-RDH14"
/replace=""
/replace="agc"
/db_xref="dbSNP:145060005"
variation complement(755)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:200906490"
variation complement(760)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="c"
/db_xref="dbSNP:191446499"
variation complement(776)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:199965310"
variation complement(803)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:113101936"
variation complement(820..821)
/gene="NT5C1B-RDH14"
/replace=""
/replace="a"
/db_xref="dbSNP:34127788"
variation complement(820)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:372417853"
exon 842..1009
/gene="NT5C1B-RDH14"
/inference="alignment:Splign:1.39.8"
variation complement(910)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:151116969"
variation complement(914)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:370362544"
variation complement(919)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:376326986"
variation complement(935)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:372553926"
variation complement(949)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:16985301"
variation complement(953)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:138883415"
variation complement(965)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:140827083"
variation complement(994)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:145994780"
exon 1010..1139
/gene="NT5C1B-RDH14"
/inference="alignment:Splign:1.39.8"
variation complement(1037)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:113497432"
variation complement(1074)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:369708621"
variation complement(1090)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:145263582"
variation complement(1112)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:183534911"
variation complement(1127)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:144184703"
variation complement(1138)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:148193506"
exon 1140..1262
/gene="NT5C1B-RDH14"
/inference="alignment:Splign:1.39.8"
variation complement(1145)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:150673884"
variation complement(1154)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:148419532"
variation complement(1155)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:142671746"
variation complement(1159)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:146130311"
variation complement(1161)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:149545160"
variation complement(1168)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:140315086"
variation complement(1169)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:145698850"
variation complement(1216)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:140510680"
variation complement(1232)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:148789216"
variation complement(1244)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:145414794"
exon 1263..1447
/gene="NT5C1B-RDH14"
/inference="alignment:Splign:1.39.8"
variation complement(1303)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:373568974"
variation complement(1322)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:117487981"
variation complement(1326)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:201567504"
variation complement(1337)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:368221092"
variation complement(1364)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:147377645"
variation complement(1373)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:140280643"
variation complement(1396)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:3902946"
variation complement(1401)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:149286164"
variation complement(1435)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:369771689"
exon 1448..2533
/gene="NT5C1B-RDH14"
/inference="alignment:Splign:1.39.8"
variation complement(1529)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:375822735"
variation complement(1572)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:149867802"
variation complement(1581)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:141384613"
variation complement(1616)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:377520259"
variation complement(1645)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:138658701"
variation complement(1646)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:201424633"
variation complement(1687)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:373055751"
variation complement(1689)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="t"
/db_xref="dbSNP:138843648"
variation complement(1712)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="c"
/db_xref="dbSNP:201455737"
STS 1717..2524
/gene="NT5C1B-RDH14"
/standard_name="RDH14__5475"
/db_xref="UniSTS:463857"
variation complement(1744)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="c"
/db_xref="dbSNP:185675117"
variation complement(1748)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:373938743"
variation complement(1751)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:143289874"
variation complement(1755)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:201623319"
variation complement(1775)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="t"
/db_xref="dbSNP:138173772"
variation complement(1782)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:141886106"
variation complement(1803)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:141569821"
variation complement(1816)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:142589700"
variation complement(1835)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:199868568"
variation complement(1846)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:371846340"
variation complement(1848)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="t"
/db_xref="dbSNP:200669704"
variation complement(1851)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:144461545"
variation complement(1853)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:139953107"
variation complement(1860)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:201317560"
variation complement(1864)
/gene="NT5C1B-RDH14"
/replace="g"
/replace="t"
/db_xref="dbSNP:199674055"
variation complement(1892)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:74378191"
variation complement(1909)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:72775091"
variation complement(1958)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:200234641"
variation complement(2000)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:368455068"
variation complement(2016)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:373588347"
variation complement(2084)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="g"
/db_xref="dbSNP:201282431"
variation complement(2087)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:376900863"
variation complement(2100)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:375620361"
variation complement(2104)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:370947814"
variation complement(2130)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:148385113"
variation complement(2152)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:375607315"
variation complement(2258)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="t"
/db_xref="dbSNP:115362218"
variation complement(2318)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:111233807"
STS 2333..2470
/gene="NT5C1B-RDH14"
/standard_name="RH102895"
/db_xref="UniSTS:97229"
variation complement(2356)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:190845828"
variation complement(2389)
/gene="NT5C1B-RDH14"
/replace="c"
/replace="t"
/db_xref="dbSNP:367551928"
variation complement(2484)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="g"
/db_xref="dbSNP:186442746"
variation complement(2527)
/gene="NT5C1B-RDH14"
/replace="a"
/replace="t"
/db_xref="dbSNP:180786126"
ORIGIN
ataaatttgacattctaaatgcaaagctagactgagcaagggaagtgacaggaaatggagctggggagacaaaaatgtggataacaacaaaagaatttcaacaggtaaaaaaatgagtcaaacatctctcaaacagaaaaagaatgagcctggaatgaggtcctcaaaagagagtctagaagcagaaaaaagaaaggaatctgacaaaacaggagttcgtctgagcaatcagggatcacaagaatcatcactgcggaagacagactctcgagggtaccttgtgcgcagtcaatggtctagaatatcccggagcccatccaccaaggctccatccatagatgagcctagaagcaggaacaccagtgctaaggtagagctccccagcagctccacgagctcccggactccatccacctccccaagcctgcatgactcctcaccgccgccgctgtccgggcagccctcgctccagccacccgcgtcgccccagctgccccggtcgctggactcgcggcctcccacgcccccagagcccgatcctggctcccggcgcagcaccaaaatgcaagagaatccggaggcctgggcccaaggcatcgtgcgggaaatccgccagacccgggactcgcagccgctggaatattcgcgcacgtcccccaccgagtggaagtcctccagccagcgcagggggatctaccccgcctccacccagctggaccgcaactctctgtccgagcagcagcagcagcagcgggaggacgaggacgactacgaggctgcctactgggcatccatgaggtcgttctacgagaagaacccgagctgctcgcgcccctggccgcccaaacccaagaacgccatcaccattgctctctcatcctgcgcgctcttcaacatggtggacggcaggaaaatctacgagcaagagggtctggaaaagtacatggagtatcagctcaccaatgagaacgtcatcctgaccccgggcccggcgttccgcttcgtcaaggcactacagtatgtcaatgctagactccgtgatctatatcctgatgaacaggacttatttgatattgtactgatgactaataaccatgcccaagtgggagtgcggcttataaacagcgtcaatcactacggcttactgattgaccgcttctgtctgaccgggggaaaagaccccattggctatttgaaggcatatcttaccaacttgtatattgctgcagattctgaaaaagtgcaagaggcaatacaagaaggtattgcctctgcgacaatgtttgatggagccaaagacatggcttactgtgacactcagctccgtgtagcctttgatggggatgctgtcctcttctctgatgagtctgaacattttaccaaggagcatgggctcgacaaattcttccagtatgatacattatgtgaaagtaagcctcttgctcaggaagagcctaggctggatgtcttgatcaataacgcagggatcttccagtgcccttacatgaagactgaagatgggtttgagatgcagttcggagtgaaccatctggggcactttctactcaccaatcttctccttggactcctcaaaagttcagctcccagcaggattgtggtagtttcttccaaactttataaatacggagacatcaattttgatgacttgaacagtgaacaaagctataataaaagcttttgttatagccggagcaaactggctaacattctttttaccagggaactagcccgccgcttagaaggcacaaatgtcaccgtcaatgtgttgcatcctggtattgtacggacaaatctggggaggcacatacacattccactgttggtcaaaccactcttcaatttggtgtcatgggcttttttcaaaactccagtagaaggtgcccagacttccatttatttggcctcttcacctgaggtagaaggagtgtcaggaagatactttggggattgtaaagaggaagaactgttgcccaaagctatggatgaatctgttgcaagaaaactctgggatatcagtgaagtgatggttggcctgctaaaataggaacaaggagtaaaagagctgtttataaaactgcatatcagttatatctgtgatcaggaatggtgtggattgagaacttgttacttgaagaaaaagaattttgatattggaatagcctgctaagaggtacatgtgggtattttggagttactgaaaaattatttttgggataagagaatttcagcaaagatgttttaaatatatatagtaagtataatgaataataagtacaatgaaaaatacaattatattgtaaaattataactgggcaagcatggatgacatattaatatttgtcagaattaagtgactcaaagtgctatcgagaggtttttcaagtatctttgagtttcatggccaaagtgttaactagttttactacaatgtttggtgtttgtgtggaaattatctgcctggtgtgtgcacacaagtcttacttggaataaatttactggtacaaattcttaa
//
by
@meso_cacase at
DBCLS
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