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2024-04-18 22:06:38, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_024952 2993 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens chromosome 14 open reading frame 159 (C14orf159),
transcript variant 3, mRNA.
ACCESSION NM_024952
VERSION NM_024952.6 GI:156139128
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 2993)
AUTHORS Hendrickson,S.L., Lautenberger,J.A., Chinn,L.W., Malasky,M.,
Sezgin,E., Kingsley,L.A., Goedert,J.J., Kirk,G.D., Gomperts,E.D.,
Buchbinder,S.P., Troyer,J.L. and O'Brien,S.J.
TITLE Genetic variants in nuclear-encoded mitochondrial genes influence
AIDS progression
JOURNAL PLoS ONE 5 (9), E12862 (2010)
PUBMED 20877624
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 2993)
AUTHORS Cheng,J., Kapranov,P., Drenkow,J., Dike,S., Brubaker,S., Patel,S.,
Long,J., Stern,D., Tammana,H., Helt,G., Sementchenko,V.,
Piccolboni,A., Bekiranov,S., Bailey,D.K., Ganesh,M., Ghosh,S.,
Bell,I., Gerhard,D.S. and Gingeras,T.R.
TITLE Transcriptional maps of 10 human chromosomes at 5-nucleotide
resolution
JOURNAL Science 308 (5725), 1149-1154 (2005)
PUBMED 15790807
REFERENCE 3 (bases 1 to 2993)
AUTHORS Clark,H.F., Gurney,A.L., Abaya,E., Baker,K., Baldwin,D., Brush,J.,
Chen,J., Chow,B., Chui,C., Crowley,C., Currell,B., Deuel,B.,
Dowd,P., Eaton,D., Foster,J., Grimaldi,C., Gu,Q., Hass,P.E.,
Heldens,S., Huang,A., Kim,H.S., Klimowski,L., Jin,Y., Johnson,S.,
Lee,J., Lewis,L., Liao,D., Mark,M., Robbie,E., Sanchez,C.,
Schoenfeld,J., Seshagiri,S., Simmons,L., Singh,J., Smith,V.,
Stinson,J., Vagts,A., Vandlen,R., Watanabe,C., Wieand,D., Woods,K.,
Xie,M.H., Yansura,D., Yi,S., Yu,G., Yuan,J., Zhang,M., Zhang,Z.,
Goddard,A., Wood,W.I., Godowski,P. and Gray,A.
TITLE The secreted protein discovery initiative (SPDI), a large-scale
effort to identify novel human secreted and transmembrane proteins:
a bioinformatics assessment
JOURNAL Genome Res. 13 (10), 2265-2270 (2003)
PUBMED 12975309
REMARK Erratum:[Genome Res. 2003 Dec;13(12):2759]
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
DA296867.1, AL602721.1, AK022564.1, AL121784.5, DR003467.1 and
BX642394.1.
On Aug 21, 2007 this sequence version replaced gi:142375327.
##Evidence-Data-START##
Transcript exon combination :: AK022564.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025082, ERS025083 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-50 DA296867.1 1-50
51-429 AL602721.1 1-379
430-902 AK022564.1 1-473
903-903 AL121784.5 56759-56759 c
904-2624 AK022564.1 475-2195
2625-2953 DR003467.1 272-600
2954-2993 BX642394.1 1-40 c
FEATURES Location/Qualifiers
source 1..2993
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="14"
/map="14q32.11"
gene 1..2993
/gene="C14orf159"
/note="chromosome 14 open reading frame 159"
/db_xref="GeneID:80017"
/db_xref="HGNC:20498"
exon 1..516
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 39
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:75331684"
variation 65
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:45549638"
variation 142
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:56175636"
variation 173
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:77221837"
variation 207
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115104184"
variation 250
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:189165079"
variation 308
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:181825270"
variation 467
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:148308026"
variation 491
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:117688873"
exon 517..568
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 562
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116583933"
misc_feature 565..567
/gene="C14orf159"
/note="upstream in-frame stop codon"
exon 569..700
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 573
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375444718"
variation 596
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:140356090"
CDS 598..2448
/gene="C14orf159"
/note="isoform a is encoded by transcript variant 3;
UPF0317 protein C14orf159, mitochondrial"
/codon_start=1
/product="UPF0317 protein C14orf159, mitochondrial isoform
a"
/protein_id="NP_079228.4"
/db_xref="GI:156139129"
/db_xref="CCDS:CCDS32141.1"
/db_xref="GeneID:80017"
/db_xref="HGNC:20498"
/translation="
MPFTLHLRSRLPSAIRSLILQKKPNIRNTSSMAGELRPASLVVLPRSLAPAFERFCQVNTGPLPLLGQSEPEKWMLPPQGAISETRMGHPQFWKYEFGACTGSLASLEQYSEQLKDMVAFFLGCSFSLEEALEKAGLPRRDPAGHSQTTVPCVTHAGFCCPLVVTMRPIPKDKLEGLVRACCSLGGEQGQPVHMGDPELLGIKELSKPAYGDAMVCPPGEVPVFWPSPLTSLGAVSSCETPLAFASIPGCTVMTDLKDAKAPPGCLTPERIPEVHHISQDPLHYSIASVSASQKIRELESMIGIDPGNRGIGHLLCKDELLKASLSLSHARSVLITTGFPTHFNHEPPEETDGPPGAVALVAFLQALEKEVAIIVDQRAWNLHQKIVEDAVEQGVLKTQIPILTYQGGSVEAAQAFLCKNGDPQTPRFDHLVAIERAGRAADGNYYNARKMNIKHLVDPIDDLFLAAKKIPGISSTGVGDGGNELGMGKVKEAVRRHIRHGDVIACDVEADFAVIAGVSNWGGYALACALYILYSCAVHSQYLRKAVGPSRAPGDQAWTQALPSVIKEEKMLGILVQHKVRSGVSGIVGMEVDGLPFHNTHAEMIQKLVDVTTAQV
"
transit_peptide 598..681
/gene="C14orf159"
/inference="non-experimental evidence, no additional
details recorded"
/note="Mitochondrion (Potential); propagated from
UniProtKB/Swiss-Prot (Q7Z3D6.2)"
mat_peptide 682..2445
/gene="C14orf159"
/product="UPF0317 protein C14orf159, mitochondrial"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q7Z3D6.2)"
misc_feature 949..1362
/gene="C14orf159"
/note="Protein of unknown function (DUF1445); Region:
DUF1445; pfam07286"
/db_xref="CDD:148727"
misc_feature 1486..2427
/gene="C14orf159"
/note="Domain of unknown function (DUF4392); Region:
DUF4392; pfam14336"
/db_xref="CDD:206504"
variation 625
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:10142502"
variation 634
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147625749"
variation 677
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:200397505"
exon 701..854
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 723
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:199766208"
variation 732
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:61990138"
variation 750
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:186462130"
variation 753
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:142153831"
variation 777
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:372209590"
variation 839
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:375074402"
variation 852
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:146611491"
exon 855..1038
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 870
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:376028632"
variation 900
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199942166"
variation 901
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:201040091"
variation 903
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:4900071"
variation 926
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:148932665"
variation 929
/gene="C14orf159"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201623410"
variation 972
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:150590185"
variation 1002
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:200698102"
exon 1039..1189
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1059
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147006834"
variation 1078
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:148167595"
variation 1092
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374015135"
variation 1097
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142032807"
variation 1150
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:146149732"
variation 1160
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:377730215"
variation 1182
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:138979726"
variation 1183
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:193008696"
exon 1190..1312
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1235
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:376295292"
variation 1246
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:142118168"
variation 1252
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:75931548"
variation 1258
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:114448340"
variation 1281
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:149668017"
variation 1293
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115154303"
variation 1300
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:148400411"
variation 1307
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34302825"
exon 1313..1516
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1331
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116685038"
variation 1348
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:80178223"
variation 1355
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116659399"
variation 1363
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147905616"
variation 1385
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:368308336"
variation 1405
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:140473581"
variation 1431
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:113182111"
variation 1457
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:150428305"
variation 1487
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:377123244"
variation 1494
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:115448574"
variation 1502
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116314762"
variation 1503
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:138171068"
exon 1517..1777
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1523
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:145176315"
variation 1543
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:111868616"
variation 1552
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:139000129"
variation 1597
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:199690106"
variation 1631
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372940671"
variation 1635
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:142154756"
variation 1649
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200668165"
variation 1655
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375680070"
variation 1656
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:145749941"
variation 1667
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:201585097"
variation 1711
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:12895348"
variation 1718
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:374084163"
variation 1721
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:117996584"
variation 1732
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34196107"
variation 1740
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115077193"
variation 1773
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:201673633"
variation 1775
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:150741072"
exon 1778..1877
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1779
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200416806"
variation 1791
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:139055044"
variation 1792
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199874947"
variation 1799
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114141780"
variation 1800
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:147223382"
variation 1850
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375027427"
variation 1852
/gene="C14orf159"
/replace=""
/replace="a"
/db_xref="dbSNP:72237815"
variation 1865
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:367665781"
variation 1866
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34942357"
variation 1874
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:185064362"
exon 1878..2026
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1888
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:145589579"
variation 1900
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375771695"
variation 1904
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:138297457"
variation 1908
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:28481732"
variation 1914
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:151056692"
variation 1935
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:141238498"
variation 1939
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:114411077"
variation 1975
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:373641510"
variation 1997
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114579097"
variation 2023
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:370829084"
variation 2025
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:28715808"
exon 2027..2146
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 2046
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:371519362"
variation 2047
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:367885678"
variation 2052
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:201859863"
variation 2074
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:138293042"
variation 2092
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:149609125"
variation 2093
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:143509911"
variation 2100
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:147998815"
variation 2101
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:2295524"
variation 2109
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147127627"
variation 2115
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114953496"
variation 2116
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34523602"
variation 2119
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:200155995"
variation 2136
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:150793173"
variation 2137
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:77771949"
variation 2139
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:149923448"
variation 2140
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:145255200"
variation 2143
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:112112803"
exon 2147..2298
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 2148
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200859829"
variation 2149
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:372220357"
variation 2181
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:146936755"
variation 2182
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:115874122"
variation 2202
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:113735532"
variation 2216
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:140494499"
variation 2232
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:35511234"
variation 2234
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199970083"
variation 2286
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34424078"
variation 2288
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:368952726"
exon 2299..2974
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 2308
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:114678661"
variation 2310
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:150235234"
variation 2320
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116271183"
variation 2338
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:142112616"
variation 2342
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:114316258"
variation 2345
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34748911"
variation 2346
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:138685998"
variation 2347
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:377731545"
variation 2358
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200494277"
variation 2359
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:371396745"
variation 2401..2402
/gene="C14orf159"
/replace=""
/replace="c"
/db_xref="dbSNP:5810531"
variation 2403
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:373378972"
variation 2404
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142686008"
variation 2426
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:144631642"
variation 2428
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:148051089"
variation 2430
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145141"
variation 2433
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:377043453"
variation 2435
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:35798893"
variation 2436
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:200556528"
variation 2484
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:374821767"
variation 2500
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:374622711"
variation 2564
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:187712668"
variation 2573
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:1801590"
STS 2600..2864
/gene="C14orf159"
/standard_name="WI-19880"
/db_xref="UniSTS:52015"
variation 2625
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285859"
variation 2635..2638
/gene="C14orf159"
/replace=""
/replace="ggac"
/db_xref="dbSNP:374263197"
STS 2708..2838
/gene="C14orf159"
/standard_name="G62042"
/db_xref="UniSTS:139136"
variation 2742
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:6562"
variation 2755
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:80181220"
variation 2771
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:112671362"
variation 2793
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:141359028"
variation 2838
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:150364186"
variation 2867
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:139087658"
variation 2895
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375228523"
variation 2896
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142988629"
variation 2932
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:183187504"
ORIGIN
aagaactggggcgggctagctgccgaggagaccacgctgctgcatgggccacgtgagctcaggctgtgggagcggatggagctgctacagtcagcgcttggggctggcctcagcttgtagacccgagccctgcagaacaaccccccgtggcgcaggagagcagaagaaagggggcctttatgcccttttgagggaagcacacattctgcaaggccgtggaaacaaagggaggaactgtttgtagccctcgtccagacgccccaaacaaacagtaagtcagaagggaacagagcacagcacagtccctccctccgccccaggcagtatccaccttgccccgccccacctaaggagcccaagggtattctgggagcccaccccaggacaatggcagggcaaaaccagtgagcaaggcagaaaattcctgaaattctccactgaggcccagctgttcctctccttgaaaagtcaaggcttggttcaagccagatagcacctgaggacagaacatatcaggagccaagttacaccctgtttaaccctgccttcaaagggacgactctgtaagattctctgctacttattcaagttgacacgatgcccttcacactccacctgaggtcccgccttccctctgccataaggagtttgattctacaaaagaaaccaaacatcagaaatacatccagcatggctggagagctccgaccagccagcctggtggtcctgcccaggtcccttgctccagcttttgaaagattctgccaggtcaacactggtcctctacccctgctgggccagagtgagccagaaaagtggatgctgccccctcaaggtgctatctcagagaccaggatgggccatccccagttctggaaatacgagttcggtgcctgcaccggcagcctggcttcgctggagcagtactcggagcagctgaaggacatggtggccttcttcctgggctgcagcttctccctggaggaggccttggagaaagcggggctccccagaagagacccagcaggtcacagccagacaacagtgccttgtgttacccatgctggcttctgctgccctctggtggtcacgatgaggcccattcccaaggacaagctggaagggctggtgcgggcctgctgctccctcggaggtgagcaggggcaacctgttcacatgggcgacccagaactgttgggaatcaaagagctttccaaacctgcctacggggatgccatggtgtgtcccccaggggaggttccagtgttctggccttctccgctgaccagtctcggagctgtcagcagctgtgagaccccactggcttttgccagcatcccaggctgcacagttatgactgacctgaaggatgcaaaggctccacctggttgtctcaccccagagagaattccagaggtccatcacatttcccaagatcctctgcactacagcatcgcgtcagtctctgcttctcagaagatcagagaactagagtctatgatcggcatagacccagggaaccgggggattgggcacctgctctgtaaagatgagctgctgaaggcctctctctcgctgtcccatgcccgctcagtgctcatcaccactgggttccccacacatttcaatcatgagcctccagaagagacagatggcccaccaggagctgttgctctggttgccttcctgcaggccttggagaaggaggtcgccataatcgttgaccagagagcctggaacttgcaccagaagattgttgaagatgctgttgagcaaggtgttctgaagacgcagatcccgatattaacttaccaaggtggatcagtggaagctgctcaggcattcctgtgcaaaaatggggacccgcagacacctagatttgaccacctggtggccatagagcgtgccggaagagctgctgatggcaattactacaatgcaaggaagatgaacatcaagcacttggttgaccccattgacgatctttttcttgctgcgaagaagattcctggaatctcatcaactggagtcggtgatggaggcaacgagcttgggatgggtaaagtcaaggaggctgtgaggaggcacatacggcacggggatgtcatcgcctgcgacgtggaggctgactttgccgtcattgctggtgtttctaactggggaggctatgccctggcctgcgcactctacatcctgtactcatgtgctgtccacagtcagtacctgaggaaagcagtcggaccctccagggcacctggagatcaggcctggactcaggccctcccgtcggtcattaaggaagaaaaaatgctgggcatcttggtgcagcacaaagtccggagtggcgtctcgggcatcgtgggcatggaggtggatgggctgcccttccacaacacccacgccgagatgatccagaagctggtggacgtcaccacggcacaggtgtaaccgtccatgttccgtgtgagcagagtccctaccaacgggcaggtctgcatccggggagaatgcagctgcttctggcgacaatcctgctagtaaacactggtcttcggtgagcaacgaacactcgcctggcctgggaaactgcatgcccactttctgggaggggttagtgcaggtgctgtggacaaaggacaacatttctctggggctttttaacttttattcctaagactctaaaggcgttgatttcaaccctccttcactctggcttcttcaggcaacccacgtggtctcctgtgagaatcttctcgacagttacttatggggacacttgtgaacaattaactgccaggcagagcatgagaacaaacattcccaggccatgtaggataggatactccagactccagtcatcctcccccatccatggtttctgttactcatggtttcagttactcatagccaactgcagaccgaaaatactaaatgaaaaatttcagaaataaacaactcttaagttttaaattgtaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:80017 -> Molecular function: GO:0003674 [molecular_function] evidence: ND
GeneID:80017 -> Biological process: GO:0008150 [biological_process] evidence: ND
GeneID:80017 -> Cellular component: GO:0005575 [cellular_component] evidence: ND
GeneID:80017 -> Cellular component: GO:0005739 [mitochondrion] evidence: IEA
by
@meso_cacase at
DBCLS
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