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2020-10-26 19:40:56, 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
//

Annotations:



by @meso_cacase at DBCLS
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