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2024-04-19 21:02:39, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001135993 5253 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens tetratricopeptide repeat domain 39C (TTC39C),
transcript variant 1, mRNA.
ACCESSION NM_001135993
VERSION NM_001135993.1 GI:209862742
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 5253)
AUTHORS Nusbaum,C., Zody,M.C., Borowsky,M.L., Kamal,M., Kodira,C.D.,
Taylor,T.D., Whittaker,C.A., Chang,J.L., Cuomo,C.A., Dewar,K.,
FitzGerald,M.G., Yang,X., Abouelleil,A., Allen,N.R., Anderson,S.,
Bloom,T., Bugalter,B., Butler,J., Cook,A., DeCaprio,D., Engels,R.,
Garber,M., Gnirke,A., Hafez,N., Hall,J.L., Norman,C.H., Itoh,T.,
Jaffe,D.B., Kuroki,Y., Lehoczky,J., Lui,A., Macdonald,P.,
Mauceli,E., Mikkelsen,T.S., Naylor,J.W., Nicol,R., Nguyen,C.,
Noguchi,H., O'Leary,S.B., O'Neill,K., Piqani,B., Smith,C.L.,
Talamas,J.A., Topham,K., Totoki,Y., Toyoda,A., Wain,H.M.,
Young,S.K., Zeng,Q., Zimmer,A.R., Fujiyama,A., Hattori,M.,
Birren,B.W., Sakaki,Y. and Lander,E.S.
TITLE DNA sequence and analysis of human chromosome 18
JOURNAL Nature 437 (7058), 551-555 (2005)
PUBMED 16177791
REMARK Erratum:[Nature. 2005 Dec 1;438(7068):696. O'Neill, Keith [added]]
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
BC016833.2, AC010754.10, BC032684.1, AC090772.9 and BM069557.1.
Transcript Variant: This variant (1) represents the longest
transcript and encodes the longest isoform (1).
##Evidence-Data-START##
Transcript exon combination :: BC032684.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025088 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-187 BC016833.2 1-187
188-188 AC010754.10 123040-123040
189-562 BC016833.2 189-562
563-2658 BC032684.1 12-2107
2659-4833 AC090772.9 121051-123225 c
4834-5253 BM069557.1 1-420 c
FEATURES Location/Qualifiers
source 1..5253
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="18"
/map="18q11.2"
gene 1..5253
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/note="tetratricopeptide repeat domain 39C"
/db_xref="GeneID:125488"
/db_xref="HGNC:26595"
exon 1..619
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 62
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:372727628"
variation 75
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:28503640"
variation 119
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:144517169"
variation 185
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:145670244"
variation 188
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:28608904"
CDS 453..2204
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/note="isoform 1 is encoded by transcript variant 1;
tetratricopeptide repeat protein 39C; TPR repeat protein
39C"
/codon_start=1
/product="tetratricopeptide repeat protein 39C isoform 1"
/protein_id="NP_001129465.1"
/db_xref="GI:209862743"
/db_xref="CCDS:CCDS45839.1"
/db_xref="GeneID:125488"
/db_xref="HGNC:26595"
/translation="
MAGSEQQRPRRRDDGDSDAAAAAAAPLQDAELALAGINMLLNNGFRESDQLFKQYRNHSPLMSFGASFVSFLNAMMTFEEEKMQLACDDLKTTEKLCESEEAGVIETIKNKIKKNVDVRKSAPSMVDRLQRQIIIADCQVYLAVLSFVKQELSAYIKGGWILRKAWKIYNKCYLDINALQELYQKKLTEESLTSDAANDNHIVAEGVSEESLNRLKGAVSFGYGLFHLCISMVPPNLLKIINLLGFPGDRLQGLSSLMYASESKDMKAPLATLALLWYHTVVRPFFALDGSDNKAGLDEAKEILLKKEAAYPNSSLFMFFKGRIQRLECQINSALTSFHTALELAVDQREIQHVCLYEIGWCSMIELNFKDAFDSFERLKNESRWSQCYYAYLTAVCQGATGDVDGAQIVFKEVQKLFKRKNNQIEQFSVKKAERFRKQTPTKALCVLASIEVLYLWKALPNCSFPNLQRMSQACHEVDDSSVVGLKYLLLGAIHKCLGNSEDAVQYFQRAVKDELCRQNNLYVQPYACYELGCLLLDKPETVGRGRALLLQAKEDFSGYDFENRLHVRIHAALASLRELVPQ
"
misc_feature 558..1946
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/note="Protein of unknown function (DUF3808); Region:
DUF3808; pfam10300"
/db_xref="CDD:192523"
misc_feature 1395..1496
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q8N584.2);
Region: TPR 1"
misc_feature 1509..1610
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q8N584.2);
Region: TPR 2"
misc_feature 1905..2006
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q8N584.2);
Region: TPR 3"
variation 469
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:371876007"
exon 620..668
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
exon 669..797
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 703
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:201044353"
variation 710
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:149349073"
variation 731
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:151171824"
variation 752
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:138298971"
variation 782
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:8083357"
variation 797
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:61734884"
exon 798..912
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 814
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:146129310"
variation 815
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:376106417"
variation 823
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:767931"
variation 825
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:186767900"
variation 848
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:1386548"
exon 913..1267
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 987
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:200601152"
variation 999
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:368153817"
variation 1000
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:201690284"
variation 1140
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:140104738"
variation 1205
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:377300367"
variation 1228
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:369896831"
variation 1235
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:142253813"
exon 1268..1436
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1271
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:146357922"
variation 1277
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:371743578"
variation 1284
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:376510552"
variation 1299
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:150902504"
variation 1303
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:368898208"
variation 1304
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:139065111"
variation 1343
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:376392818"
variation 1362
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:376352864"
variation 1400
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:149872526"
variation 1408
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:75214464"
variation 1420
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:144967797"
variation 1424
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:140420514"
variation 1427
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:144279445"
exon 1437..1530
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1440
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:147825390"
variation 1441
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:201906825"
variation 1460
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:140346851"
variation 1479
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:200673106"
variation 1493
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:149428949"
exon 1531..1638
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1560
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:62089609"
variation 1570
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:200696364"
variation 1637
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:200046547"
exon 1639..1748
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1645
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:201467118"
exon 1749..1872
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1755
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:140461929"
variation 1787
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:150406754"
variation 1798
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:72881750"
variation 1840
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:375333859"
variation 1870
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:201589709"
exon 1873..1970
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1892
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:199694307"
variation 1922
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:201908092"
variation 1946
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:370538816"
variation 1960
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:138187993"
variation 1961
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:142854411"
exon 1971..2075
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1983
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:377264490"
variation 2005
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:145032259"
variation 2015
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:12970083"
variation 2030
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:149403354"
variation 2071
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:200139722"
exon 2076..2114
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
exon 2115..5240
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 2145
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:112708978"
variation 2158
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:147210803"
variation 2212
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:202129133"
variation 2220
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:76450357"
variation 2221
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:201275114"
variation 2226
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:371932283"
variation 2232
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:369918334"
variation 2243
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:187918854"
variation 2246
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:368148244"
variation 2276
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:62089641"
variation 2345
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:191858324"
STS 2437..2566
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="RH68668"
/db_xref="UniSTS:76706"
variation 2443
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:184154616"
variation 2481
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:112907260"
variation 2624
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:372937960"
variation 2670
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:376328546"
variation 2692
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:188327629"
variation 2802
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:9965422"
variation 2817
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:193197493"
variation 2943
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:372960180"
variation 2979
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:9957536"
variation 3122
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:960745"
variation 3187
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:140597970"
variation 3204
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:144562327"
variation 3316
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:79103214"
variation 3362
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:59530034"
variation 3375
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:11877735"
variation 3439
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:182522157"
variation 3442
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:186842784"
variation 3468
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:148878010"
variation 3497
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:142542703"
variation 3527..3529
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="atg"
/db_xref="dbSNP:72352648"
variation 3529..3531
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="gat"
/db_xref="dbSNP:34468889"
variation 3673
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:191726117"
variation 3845
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:183510548"
variation 3848
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:1663514"
variation 3884
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:150961977"
variation 3890
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:112724867"
variation 3892
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="tg"
/db_xref="dbSNP:139665498"
variation 3893
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="ac"
/db_xref="dbSNP:71163663"
variation 3894
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:4800548"
variation 3915
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:113195287"
STS 3931..4083
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="D11S3732"
/db_xref="UniSTS:152962"
STS 3952..4770
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="PMC156606P1"
/db_xref="UniSTS:271408"
STS 3952..4041
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="PMC156606P1"
/db_xref="UniSTS:271408"
STS 3967..4049
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="L18426"
/db_xref="UniSTS:34648"
STS 3971..4866
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="G35510"
/db_xref="UniSTS:44150"
STS 3976..4045
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="D1S1423"
/db_xref="UniSTS:149619"
variation 3985
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:140771873"
STS 3999..4103
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="D8S2278"
/db_xref="UniSTS:473906"
STS 4007..4098
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="D8S2279"
/db_xref="UniSTS:473907"
variation 4012
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:189545085"
variation 4029
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:193058781"
variation 4067
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:4800549"
variation 4107
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:367876859"
variation 4121
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:144591403"
variation 4127
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:189970186"
variation 4156
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:181442264"
variation 4198
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:374081519"
variation 4204
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:138543523"
variation 4261
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:186124004"
variation 4264..4265
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="gggg"
/db_xref="dbSNP:142253449"
variation 4400..4402
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="tat"
/db_xref="dbSNP:143884966"
variation 4457
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:11082962"
variation 4459
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:188533599"
variation 4491
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:77892285"
variation 4562
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:375168052"
variation 4600
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:34452859"
variation 4677
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:372423478"
variation 4750
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:12607257"
variation 4828
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:1133162"
variation 4863
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:140711593"
variation 4879
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:181339583"
variation 4930..4931
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="t"
/db_xref="dbSNP:375658371"
variation 4935
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:373336972"
variation 4990
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:185855791"
STS 5068..5207
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="STS-T03922"
/db_xref="UniSTS:68856"
variation 5121
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:369195459"
variation 5169
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:138246384"
ORIGIN
gtctcgcgtgcgtgtgtccgagcagtcctgggcggtgggcgaaggcgcggcttggggacccgggaggggccggggcgcgggggctgcaggaagtggaggcggccgccgctcggggaccggcttggcggggtgagagacacccggaaacggattccgcttcggggcccgcgcgagttgggtgcttcggagggcgcgagaggagcgggcgggtgctgctgagtaatccccgcggcggcggccggacgcccacctcccacgccgcgccgcagccgggccgcggctcctccctccgcggtccttccctcctcttccctcccgtcttctcccctcccctcccctcccctcccggctccgcttggctccgggcaggtagagccgggctccgggcgcgcgcggggccgcagcagctgctcccgatctcgcctcggcccagcgcagggcctcgcacgcccatggccggctcggagcagcagcggccgcggcggcgggacgacggagactcggacgcggcagcggcggcggcggcgcccctgcaggacgcggagctggccctggccggcatcaacatgctgctcaacaacggcttcagggagtcggaccagcttttcaaacaatacagaaatcatagcccactaatgagttttggagccagctttgtcagttttttgaatgccatgatgacatttgaggaagaaaaaatgcagttggcatgtgatgacttaaaaaccacagaaaaactgtgtgaaagtgaagaggctggagtaattgaaacaatcaagaataaaattaagaagaacgttgatgtccgaaaatccgccccctctatggttgatcggcttcagaggcagataatcatagctgactgccaggtttacctggctgtgctttcatttgtaaaacaagaattgtcagcttatatcaaaggtgggtggatccttaggaaagcctggaagatttacaataaatgctatctggacatcaatgcccttcaggagctgtatcagaagaagctaactgaagagtccttgacttctgatgctgcaaatgataatcacattgtggctgaaggggtgtctgaggagtctctgaacagactgaaaggtgctgttagctttggatatggcctttttcacctttgcatatccatggtgcccccaaacctgctcaaaatcatcaacctgctgggttttcctggagaccgcctacaggggctttcttcactgatgtatgcaagcgaaagtaaggacatgaaggcccctttagctacattagctctgctctggtatcatactgtagtccgcccgttttttgccttggatggcagtgataacaaggcaggcctggatgaagctaaggaaattctccttaaaaaagaagctgcttatccaaattcttccctctttatgtttttcaagggacggatacaacgactagagtgtcaaatcaacagtgccttgacatctttccacactgctttggaacttgcagtagaccagagagaaattcaacatgtctgtctgtatgaaattggttggtgcagcatgatagagctcaatttcaaggatgcatttgattcctttgagaggctaaaaaatgagtccaggtggtcccagtgctattatgcctacttgactgcagtttgtcagggagccactggtgatgtggatggggcacagattgtctttaaagaagttcagaaactcttcaaaaggaaaaacaatcagattgaacagttctcggtgaaaaaggcagagcgatttcggaagcaaaccccaaccaaagcgctctgtgtgttggcgtctattgaagtgttgtacttgtggaaagctcttccaaactgttccttccccaacctgcagaggatgagtcaagcttgccatgaagtggatgactcatctgttgttggattaaagtatttgcttcttggtgccatacacaaatgtctaggaaactcagaagatgctgttcagtacttccagcgagctgttaaagatgaattgtgtcgtcagaataatttatatgttcagccgtatgcctgttatgaacttggctgtcttctattagacaaaccagagactgtaggaagaggcagagctctacttcttcaagcaaaggaggatttctctggctacgactttgaaaacagattgcatgtccgcatccatgctgctctggcctctctgagggaattggttcctcagtgacagacccggaacacccgctccgtccctccccacccagggtccgcactttaaaataaaagcagaggacaaagctcttgtgaagatgggcttttcttctgaaaaccacctgtgccagggacacattttcccagttaagctgacatattaaagatctcctcttttaaacatgtagctgaaaagtaataatgatgttgaggaggatgatgatggtaataataactaaccacctggggagagggttaagtgaccttgctcaaacgttttagttttgtgatttattatttttaaaataaaatcaaacggaacatccaacccaagatcctgtaggaacacctaccttaagcacatatctgaatgggtaacatgatgaggtacctgtaaaattattaacaatatcatgacatagcatttatatttgtgttttgaaaaaataaaagtgctttctagtgttttactttatcctcaaaatactccagtgaataacatagcacagatattcttaaccccactttgcagacagtgaaactcaggcacaaaaaggcaaattgacttatcccaattaattattcctgttatcagcagagcaatgaatagaaagcagatctcctgaccaccaactgacttttattgtaaaaataattcatgttaataggccagaattccatgttttacttattaaaagaacaaaatcttcagctgaagttatgtcaccagaaatagtcatctccagattgtctacagaatgtttcaaagcgatggacactctttttcctttgaaagccaaccaagtaagagcaaatattaatagaagataattttacaactaaaagtgtgactcttttgctaatctattagcctagtctatagattagacaaacagtatctacattttaggagtttacctttctttgtgaaaattgtcaaattaccaacttttggaaatcttttgacacattacttgaaaaggttattcgtgaatgaacatagattttggcctcaaaatatttgctggtggaacatttgctgggctacacagtgccaggatttaatcattttccccttagctcaggttatttagatattatacaaggaattcaaagttatttttttattcttcattgctaatttttgtcatttaatttacctccatgcccggtactgcaaacctgtggttttgaagaatctaaatacctcagtcacttttaagaatctctgccataatttggctcaatgtttaaggttagatttttaaagaaatttttattgagctaaaggatatcattttagggtatcgtttatttacaaattcttttggctgaaacatgatctcatattaatattttaatatttcttttcaaaataaaacagaaaagcaagtagaatgttggcaaattttatctgatttgaccttgttttgagggaatagtcataatttctttgaaagaagttatttctcactgattttggctaaacagtattcatatttcttcatctctgttactgaccacttttcagtagactgtttccaaaatgtgtattcacattgactttctccctgatgtgaattccgtgtgggttttagataatagtaagagagaagagattgctctcctatattcagtgaatgagaagggaacttttttctgaagagcaaaattggtgcccaaaaatattggacatctgttttttgtttttttttttttttttttttttttttgagacggagtctcgctctgtcacccaggctggagtgcagtggcgtgatcttggctcactgcaacctctgcctcctgggttcacaccattctcctgcctcagcctcccaagtagctgggactacaggcacccgcaaccacacccggctaattttttttgtatttttagtagagatggggtttcaccatgttagccaggattgtctccatctcctgacctcgtgatccacccgccttggcctcccaaagagctgggattactggtgtgagccaccgtgcccggcctggacatctggttttaactagatggaagggaagaacattatgaatctttaaaatacggctgttgccatttttctctcttcttaacatgcagcataggtgacaagcttttctgtcatcatcatggagcattctgaatcatgacatttttgtttgagagttcattcttgaattttcagttcaaaatattgtttgaactattattccacattcaaagattatataaggtcctgtgcttttgaatctttttcaaaacatttatttctgcctgcttaaaaaaaatacttttatttccccacagagagttcaggacttcagattagtttgtgttcagctcacttaactggatagacaattttgcgttttgcaacaccatcctgtaggttttctttactagtcaaagtgtaggtctttttaaaatttttaatctttatttttatttttattttgaaacagagtctcactctgttgcccaggctggagtgcagtggtgtgatctgtgctcactgcaacctctgtcacccgggtttaagcgattcttctgcctgagcctcccaagtagctgggattacaagttcctgccaccgtgcctggctaatttttgcagttttagtagaggcagggttccaccaccttggccaggctggtcttgaactcctgacctcatgatccacccaccttgtcctctcaaaatgcttacaggcatgaaccactgtgaccggccaggtctttttttttttaaagagtctatcctaggcttggtacagatggcgcctgtggtaaatctgtgttaacatggtggtagaccatggagaatgggtagatggagcttctagactccaaaacaacaaaaccacagtgtgagtacactgtcccattaggttgactgaagtctgagtacattttctggcctgcgtgccgtgacttatccaacctgtgaactgattgtgatctgcttggtaacttggtttggtgtaaactgctcttaaccctttgctgatgaagaaaataatcatataagtggaactatttgcatctaaaaaaaaaaaaaa
//
by
@meso_cacase at
DBCLS
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