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2025-05-09 17:25:25, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_153211 4900 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens tetratricopeptide repeat domain 39C (TTC39C),
transcript variant 2, mRNA.
ACCESSION NM_153211
VERSION NM_153211.3 GI:209862741
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 4900)
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
AK091080.1, BC121034.2, AC090772.9 and BM069557.1.
On Oct 21, 2008 this sequence version replaced gi:116256461.
Transcript Variant: This variant (2) contains a distinct 5' UTR,
lacks an in-frame portion of the 5' coding region, and initiates
translation at a downstream start codon, compared to variant 1. The
resulting isoform (2) has a shorter N-terminus compared to isoform
1.
##Evidence-Data-START##
Transcript exon combination :: AK091080.1, BC121034.2 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025089 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-117 AK091080.1 1-117
118-2168 BC121034.2 1-2051
2169-4480 AC090772.9 121051-123362 c
4481-4900 BM069557.1 1-420 c
FEATURES Location/Qualifiers
source 1..4900
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="18"
/map="18q11.2"
gene 1..4900
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/note="tetratricopeptide repeat domain 39C"
/db_xref="GeneID:125488"
/db_xref="HGNC:26595"
exon 1..266
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 8
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:142649290"
variation 61
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:150596671"
variation 101
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:12327412"
variation 175
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:113565185"
variation 177
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:139567949"
misc_feature 265..267
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/note="upstream in-frame stop codon"
exon 267..315
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
CDS 283..1851
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/note="isoform 2 is encoded by transcript variant 2;
tetratricopeptide repeat protein 39C; TPR repeat protein
39C"
/codon_start=1
/product="tetratricopeptide repeat protein 39C isoform 2"
/protein_id="NP_694943.2"
/db_xref="GI:116256462"
/db_xref="CCDS:CCDS32804.1"
/db_xref="GeneID:125488"
/db_xref="HGNC:26595"
/translation="
MSFGASFVSFLNAMMTFEEEKMQLACDDLKTTEKLCESEEAGVIETIKNKIKKNVDVRKSAPSMVDRLQRQIIIADCQVYLAVLSFVKQELSAYIKGGWILRKAWKIYNKCYLDINALQELYQKKLTEESLTSDAANDNHIVAEGVSEESLNRLKGAVSFGYGLFHLCISMVPPNLLKIINLLGFPGDRLQGLSSLMYASESKDMKAPLATLALLWYHTVVRPFFALDGSDNKAGLDEAKEILLKKEAAYPNSSLFMFFKGRIQRLECQINSALTSFHTALELAVDQREIQHVCLYEIGWCSMIELNFKDAFDSFERLKNESRWSQCYYAYLTAVCQGATGDVDGAQIVFKEVQKLFKRKNNQIEQFSVKKAERFRKQTPTKALCVLASIEVLYLWKALPNCSFPNLQRMSQACHEVDDSSVVGLKYLLLGAIHKCLGNSEDAVQYFQRAVKDELCRQNNLYVQPYACYELGCLLLDKPETVGRGRALLLQAKEDFSGYDFENRLHVRIHAALASLRELVPQ
"
misc_feature 283..1593
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/note="Protein of unknown function (DUF3808); Region:
DUF3808; pfam10300"
/db_xref="CDD:192523"
exon 316..444
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 350
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:201044353"
variation 357
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:149349073"
variation 378
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:151171824"
variation 399
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:138298971"
variation 429
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:8083357"
variation 444
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:61734884"
exon 445..559
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 461
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:146129310"
variation 462
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:376106417"
variation 470
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:767931"
variation 472
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:186767900"
variation 495
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:1386548"
exon 560..914
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 634
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:200601152"
variation 646
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:368153817"
variation 647
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:201690284"
variation 787
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:140104738"
variation 852
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:377300367"
variation 875
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:369896831"
variation 882
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:142253813"
exon 915..1083
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 918
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:146357922"
variation 924
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:371743578"
variation 931
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:376510552"
variation 946
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:150902504"
variation 950
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:368898208"
variation 951
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:139065111"
variation 990
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:376392818"
variation 1009
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:376352864"
variation 1047
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:149872526"
variation 1055
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:75214464"
variation 1067
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:144967797"
variation 1071
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:140420514"
variation 1074
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:144279445"
exon 1084..1177
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1087
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:147825390"
variation 1088
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:201906825"
variation 1107
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:140346851"
variation 1126
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:200673106"
variation 1140
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:149428949"
exon 1178..1285
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1207
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:62089609"
variation 1217
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:200696364"
variation 1284
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:200046547"
exon 1286..1395
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1292
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:201467118"
exon 1396..1519
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1402
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:140461929"
variation 1434
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:150406754"
variation 1445
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:72881750"
variation 1487
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:375333859"
variation 1517
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:201589709"
exon 1520..1617
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1539
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:199694307"
variation 1569
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:201908092"
variation 1593
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:370538816"
variation 1607
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:138187993"
variation 1608
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:142854411"
exon 1618..1722
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1630
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:377264490"
variation 1652
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:145032259"
variation 1662
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:12970083"
variation 1677
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:149403354"
variation 1718
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:200139722"
exon 1723..1761
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
exon 1762..4887
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/inference="alignment:Splign:1.39.8"
variation 1792
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:112708978"
variation 1805
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:147210803"
variation 1859
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:202129133"
variation 1867
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:76450357"
variation 1868
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:201275114"
variation 1873
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:371932283"
variation 1879
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:369918334"
variation 1890
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:187918854"
variation 1893
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:368148244"
variation 1923
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:62089641"
variation 1992
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:191858324"
STS 2084..2213
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="RH68668"
/db_xref="UniSTS:76706"
variation 2090
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:184154616"
variation 2128
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:112907260"
variation 2271
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:372937960"
variation 2317
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:376328546"
variation 2339
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:188327629"
variation 2449
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:9965422"
variation 2464
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:193197493"
variation 2590
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:372960180"
variation 2626
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:9957536"
variation 2769
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:960745"
variation 2834
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:140597970"
variation 2851
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:144562327"
variation 2963
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:79103214"
variation 3009
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:59530034"
variation 3022
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:11877735"
variation 3086
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:182522157"
variation 3089
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:186842784"
variation 3115
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:148878010"
variation 3144
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:142542703"
variation 3174..3176
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="atg"
/db_xref="dbSNP:72352648"
variation 3176..3178
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="gat"
/db_xref="dbSNP:34468889"
variation 3320
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:191726117"
variation 3492
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:183510548"
variation 3495
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:1663514"
variation 3531
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:150961977"
variation 3537
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:112724867"
variation 3539
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="tg"
/db_xref="dbSNP:139665498"
variation 3540
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="ac"
/db_xref="dbSNP:71163663"
variation 3541
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:4800548"
variation 3562
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:113195287"
STS 3578..3730
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="D11S3732"
/db_xref="UniSTS:152962"
STS 3599..4417
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="PMC156606P1"
/db_xref="UniSTS:271408"
STS 3599..3688
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="PMC156606P1"
/db_xref="UniSTS:271408"
STS 3614..3696
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="L18426"
/db_xref="UniSTS:34648"
STS 3618..4513
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="G35510"
/db_xref="UniSTS:44150"
STS 3623..3692
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="D1S1423"
/db_xref="UniSTS:149619"
variation 3632
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:140771873"
STS 3646..3750
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="D8S2278"
/db_xref="UniSTS:473906"
STS 3654..3745
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="D8S2279"
/db_xref="UniSTS:473907"
variation 3659
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:189545085"
variation 3676
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:193058781"
variation 3714
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:4800549"
variation 3754
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:367876859"
variation 3768
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:144591403"
variation 3774
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:189970186"
variation 3803
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:181442264"
variation 3845
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:374081519"
variation 3851
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="g"
/db_xref="dbSNP:138543523"
variation 3908
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:186124004"
variation 3911..3912
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="gggg"
/db_xref="dbSNP:142253449"
variation 4047..4049
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="tat"
/db_xref="dbSNP:143884966"
variation 4104
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:11082962"
variation 4106
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:188533599"
variation 4138
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:77892285"
variation 4209
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:375168052"
variation 4247
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:34452859"
variation 4324
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:372423478"
variation 4397
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="c"
/db_xref="dbSNP:12607257"
variation 4475
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:1133162"
variation 4510
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:140711593"
variation 4526
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="c"
/replace="t"
/db_xref="dbSNP:181339583"
variation 4577..4578
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace=""
/replace="t"
/db_xref="dbSNP:375658371"
variation 4582
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="g"
/replace="t"
/db_xref="dbSNP:373336972"
variation 4637
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="t"
/db_xref="dbSNP:185855791"
STS 4715..4854
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/standard_name="STS-T03922"
/db_xref="UniSTS:68856"
variation 4768
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:369195459"
variation 4816
/gene="TTC39C"
/gene_synonym="C18orf17; HsT2697"
/replace="a"
/replace="g"
/db_xref="dbSNP:138246384"
ORIGIN
aatcatgcttacgcatataggttaaccacagttatgtaagcaggttctgagaaaaggtgagaaagagaatggagagttttgctacaacagaggcaggattctgaatttatttccagctgcccatcttgtccctcctggagacctaacccctccagcacctacacacacagcctctttagaagcaactatcctgccactggctcagaaaggctgagtcctaagaattctaaaatcttgctcctaagaaatctcaagcttcttttgtgaaatcatagcccactaatgagttttggagccagctttgtcagttttttgaatgccatgatgacatttgaggaagaaaaaatgcagttggcatgtgatgacttaaaaaccacagaaaaactgtgtgaaagtgaagaggctggagtaattgaaacaatcaagaataaaattaagaagaacgttgatgtccgaaaatccgccccctctatggttgatcggcttcagaggcagataatcatagctgactgccaggtttacctggctgtgctttcatttgtaaaacaagaattgtcagcttatatcaaaggtgggtggatccttaggaaagcctggaagatttacaataaatgctatctggacatcaatgcccttcaggagctgtatcagaagaagctaactgaagagtccttgacttctgatgctgcaaatgataatcacattgtggctgaaggggtgtctgaggagtctctgaacagactgaaaggtgctgttagctttggatatggcctttttcacctttgcatatccatggtgcccccaaacctgctcaaaatcatcaacctgctgggttttcctggagaccgcctacaggggctttcttcactgatgtatgcaagcgaaagtaaggacatgaaggcccctttagctacattagctctgctctggtatcatactgtagtccgcccgttttttgccttggatggcagtgataacaaggcaggcctggatgaagctaaggaaattctccttaaaaaagaagctgcttatccaaattcttccctctttatgtttttcaagggacggatacaacgactagagtgtcaaatcaacagtgccttgacatctttccacactgctttggaacttgcagtagaccagagagaaattcaacatgtctgtctgtatgaaattggttggtgcagcatgatagagctcaatttcaaggatgcatttgattcctttgagaggctaaaaaatgagtccaggtggtcccagtgctattatgcctacttgactgcagtttgtcagggagccactggtgatgtggatggggcacagattgtctttaaagaagttcagaaactcttcaaaaggaaaaacaatcagattgaacagttctcggtgaaaaaggcagagcgatttcggaagcaaaccccaaccaaagcgctctgtgtgttggcgtctattgaagtgttgtacttgtggaaagctcttccaaactgttccttccccaacctgcagaggatgagtcaagcttgccatgaagtggatgactcatctgttgttggattaaagtatttgcttcttggtgccatacacaaatgtctaggaaactcagaagatgctgttcagtacttccagcgagctgttaaagatgaattgtgtcgtcagaataatttatatgttcagccgtatgcctgttatgaacttggctgtcttctattagacaaaccagagactgtaggaagaggcagagctctacttcttcaagcaaaggaggatttctctggctacgactttgaaaacagattgcatgtccgcatccatgctgctctggcctctctgagggaattggttcctcagtgacagacccggaacacccgctccgtccctccccacccagggtccgcactttaaaataaaagcagaggacaaagctcttgtgaagatgggcttttcttctgaaaaccacctgtgccagggacacattttcccagttaagctgacatattaaagatctcctcttttaaacatgtagctgaaaagtaataatgatgttgaggaggatgatgatggtaataataactaaccacctggggagagggttaagtgaccttgctcaaacgttttagttttgtgatttattatttttaaaataaaatcaaacggaacatccaacccaagatcctgtaggaacacctaccttaagcacatatctgaatgggtaacatgatgaggtacctgtaaaattattaacaatatcatgacatagcatttatatttgtgttttgaaaaaataaaagtgctttctagtgttttactttatcctcaaaatactccagtgaataacatagcacagatattcttaaccccactttgcagacagtgaaactcaggcacaaaaaggcaaattgacttatcccaattaattattcctgttatcagcagagcaatgaatagaaagcagatctcctgaccaccaactgacttttattgtaaaaataattcatgttaataggccagaattccatgttttacttattaaaagaacaaaatcttcagctgaagttatgtcaccagaaatagtcatctccagattgtctacagaatgtttcaaagcgatggacactctttttcctttgaaagccaaccaagtaagagcaaatattaatagaagataattttacaactaaaagtgtgactcttttgctaatctattagcctagtctatagattagacaaacagtatctacattttaggagtttacctttctttgtgaaaattgtcaaattaccaacttttggaaatcttttgacacattacttgaaaaggttattcgtgaatgaacatagattttggcctcaaaatatttgctggtggaacatttgctgggctacacagtgccaggatttaatcattttccccttagctcaggttatttagatattatacaaggaattcaaagttatttttttattcttcattgctaatttttgtcatttaatttacctccatgcccggtactgcaaacctgtggttttgaagaatctaaatacctcagtcacttttaagaatctctgccataatttggctcaatgtttaaggttagatttttaaagaaatttttattgagctaaaggatatcattttagggtatcgtttatttacaaattcttttggctgaaacatgatctcatattaatattttaatatttcttttcaaaataaaacagaaaagcaagtagaatgttggcaaattttatctgatttgaccttgttttgagggaatagtcataatttctttgaaagaagttatttctcactgattttggctaaacagtattcatatttcttcatctctgttactgaccacttttcagtagactgtttccaaaatgtgtattcacattgactttctccctgatgtgaattccgtgtgggttttagataatagtaagagagaagagattgctctcctatattcagtgaatgagaagggaacttttttctgaagagcaaaattggtgcccaaaaatattggacatctgttttttgtttttttttttttttttttttttttttgagacggagtctcgctctgtcacccaggctggagtgcagtggcgtgatcttggctcactgcaacctctgcctcctgggttcacaccattctcctgcctcagcctcccaagtagctgggactacaggcacccgcaaccacacccggctaattttttttgtatttttagtagagatggggtttcaccatgttagccaggattgtctccatctcctgacctcgtgatccacccgccttggcctcccaaagagctgggattactggtgtgagccaccgtgcccggcctggacatctggttttaactagatggaagggaagaacattatgaatctttaaaatacggctgttgccatttttctctcttcttaacatgcagcataggtgacaagcttttctgtcatcatcatggagcattctgaatcatgacatttttgtttgagagttcattcttgaattttcagttcaaaatattgtttgaactattattccacattcaaagattatataaggtcctgtgcttttgaatctttttcaaaacatttatttctgcctgcttaaaaaaaatacttttatttccccacagagagttcaggacttcagattagtttgtgttcagctcacttaactggatagacaattttgcgttttgcaacaccatcctgtaggttttctttactagtcaaagtgtaggtctttttaaaatttttaatctttatttttatttttattttgaaacagagtctcactctgttgcccaggctggagtgcagtggtgtgatctgtgctcactgcaacctctgtcacccgggtttaagcgattcttctgcctgagcctcccaagtagctgggattacaagttcctgccaccgtgcctggctaatttttgcagttttagtagaggcagggttccaccaccttggccaggctggtcttgaactcctgacctcatgatccacccaccttgtcctctcaaaatgcttacaggcatgaaccactgtgaccggccaggtctttttttttttaaagagtctatcctaggcttggtacagatggcgcctgtggtaaatctgtgttaacatggtggtagaccatggagaatgggtagatggagcttctagactccaaaacaacaaaaccacagtgtgagtacactgtcccattaggttgactgaagtctgagtacattttctggcctgcgtgccgtgacttatccaacctgtgaactgattgtgatctgcttggtaacttggtttggtgtaaactgctcttaaccctttgctgatgaagaaaataatcatataagtggaactatttgcatctaaaaaaaaaaaaaa
//
by
@meso_cacase at
DBCLS
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