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2020-10-26 19:08:32, 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
//

Annotations:



by @meso_cacase at DBCLS
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