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2024-04-19 03:11:31, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001102367 2930 bp mRNA linear PRI 18-APR-2013
DEFINITION Homo sapiens chromosome 14 open reading frame 159 (C14orf159),
transcript variant 2, mRNA.
ACCESSION NM_001102367
VERSION NM_001102367.1 GI:156139132
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 2930)
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 2930)
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 2930)
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
DB258432.1, BC010614.2, AL121784.5, DR003467.1 and BX642394.1.
##Evidence-Data-START##
Transcript exon combination :: BC010614.2 [ECO:0000332]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-51 DB258432.1 1-51
52-839 BC010614.2 1-788
840-840 AL121784.5 56759-56759 c
841-2561 BC010614.2 790-2510
2562-2890 DR003467.1 272-600
2891-2930 BX642394.1 1-40 c
FEATURES Location/Qualifiers
source 1..2930
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="14"
/map="14q32.11"
gene 1..2930
/gene="C14orf159"
/note="chromosome 14 open reading frame 159"
/db_xref="GeneID:80017"
/db_xref="HGNC:20498"
exon 1..360
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 62
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:76164842"
variation 65
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:2295529"
variation 80
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:371484772"
variation 112
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:141411347"
variation 115
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:150864470"
variation 154
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116725036"
variation 204
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:374656568"
variation 294
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:41299205"
exon 361..453
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
exon 454..505
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 499
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116583933"
misc_feature 502..504
/gene="C14orf159"
/note="upstream in-frame stop codon"
exon 506..637
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 510
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375444718"
variation 533
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:140356090"
CDS 535..2385
/gene="C14orf159"
/note="isoform a is encoded by transcript variant 2;
UPF0317 protein C14orf159, mitochondrial"
/codon_start=1
/product="UPF0317 protein C14orf159, mitochondrial isoform
a"
/protein_id="NP_001095837.1"
/db_xref="GI:156139133"
/db_xref="CCDS:CCDS32141.1"
/db_xref="GeneID:80017"
/db_xref="HGNC:20498"
/translation="
MPFTLHLRSRLPSAIRSLILQKKPNIRNTSSMAGELRPASLVVLPRSLAPAFERFCQVNTGPLPLLGQSEPEKWMLPPQGAISETRMGHPQFWKYEFGACTGSLASLEQYSEQLKDMVAFFLGCSFSLEEALEKAGLPRRDPAGHSQTTVPCVTHAGFCCPLVVTMRPIPKDKLEGLVRACCSLGGEQGQPVHMGDPELLGIKELSKPAYGDAMVCPPGEVPVFWPSPLTSLGAVSSCETPLAFASIPGCTVMTDLKDAKAPPGCLTPERIPEVHHISQDPLHYSIASVSASQKIRELESMIGIDPGNRGIGHLLCKDELLKASLSLSHARSVLITTGFPTHFNHEPPEETDGPPGAVALVAFLQALEKEVAIIVDQRAWNLHQKIVEDAVEQGVLKTQIPILTYQGGSVEAAQAFLCKNGDPQTPRFDHLVAIERAGRAADGNYYNARKMNIKHLVDPIDDLFLAAKKIPGISSTGVGDGGNELGMGKVKEAVRRHIRHGDVIACDVEADFAVIAGVSNWGGYALACALYILYSCAVHSQYLRKAVGPSRAPGDQAWTQALPSVIKEEKMLGILVQHKVRSGVSGIVGMEVDGLPFHNTHAEMIQKLVDVTTAQV
"
transit_peptide 535..618
/gene="C14orf159"
/inference="non-experimental evidence, no additional
details recorded"
/note="Mitochondrion (Potential); propagated from
UniProtKB/Swiss-Prot (Q7Z3D6.2)"
mat_peptide 619..2382
/gene="C14orf159"
/product="UPF0317 protein C14orf159, mitochondrial"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q7Z3D6.2)"
misc_feature 886..1299
/gene="C14orf159"
/note="Protein of unknown function (DUF1445); Region:
DUF1445; pfam07286"
/db_xref="CDD:148727"
misc_feature 1423..2364
/gene="C14orf159"
/note="Domain of unknown function (DUF4392); Region:
DUF4392; pfam14336"
/db_xref="CDD:206504"
variation 562
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:10142502"
variation 571
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147625749"
variation 614
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:200397505"
exon 638..791
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 660
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:199766208"
variation 669
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:61990138"
variation 687
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:186462130"
variation 690
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:142153831"
variation 714
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:372209590"
variation 776
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:375074402"
variation 789
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:146611491"
exon 792..975
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 807
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:376028632"
variation 837
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199942166"
variation 838
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:201040091"
variation 840
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:4900071"
variation 863
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:148932665"
variation 866
/gene="C14orf159"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201623410"
variation 909
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:150590185"
variation 939
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:200698102"
exon 976..1126
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 996
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147006834"
variation 1015
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:148167595"
variation 1029
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374015135"
variation 1034
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142032807"
variation 1087
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:146149732"
variation 1097
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:377730215"
variation 1119
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:138979726"
variation 1120
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:193008696"
exon 1127..1249
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1172
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:376295292"
variation 1183
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:142118168"
variation 1189
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:75931548"
variation 1195
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:114448340"
variation 1218
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:149668017"
variation 1230
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115154303"
variation 1237
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:148400411"
variation 1244
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34302825"
exon 1250..1453
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1268
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116685038"
variation 1285
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:80178223"
variation 1292
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116659399"
variation 1300
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147905616"
variation 1322
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:368308336"
variation 1342
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:140473581"
variation 1368
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:113182111"
variation 1394
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:150428305"
variation 1424
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:377123244"
variation 1431
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:115448574"
variation 1439
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116314762"
variation 1440
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:138171068"
exon 1454..1714
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1460
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:145176315"
variation 1480
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:111868616"
variation 1489
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:139000129"
variation 1534
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:199690106"
variation 1568
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372940671"
variation 1572
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:142154756"
variation 1586
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200668165"
variation 1592
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375680070"
variation 1593
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:145749941"
variation 1604
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:201585097"
variation 1648
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:12895348"
variation 1655
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:374084163"
variation 1658
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:117996584"
variation 1669
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34196107"
variation 1677
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115077193"
variation 1710
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:201673633"
variation 1712
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:150741072"
exon 1715..1814
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1716
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200416806"
variation 1728
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:139055044"
variation 1729
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199874947"
variation 1736
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114141780"
variation 1737
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:147223382"
variation 1787
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375027427"
variation 1789
/gene="C14orf159"
/replace=""
/replace="a"
/db_xref="dbSNP:72237815"
variation 1802
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:367665781"
variation 1803
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34942357"
variation 1811
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:185064362"
exon 1815..1963
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1825
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:145589579"
variation 1837
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375771695"
variation 1841
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:138297457"
variation 1845
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:28481732"
variation 1851
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:151056692"
variation 1872
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:141238498"
variation 1876
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:114411077"
variation 1912
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:373641510"
variation 1934
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114579097"
variation 1960
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:370829084"
variation 1962
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:28715808"
exon 1964..2083
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1983
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:371519362"
variation 1984
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:367885678"
variation 1989
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:201859863"
variation 2011
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:138293042"
variation 2029
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:149609125"
variation 2030
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:143509911"
variation 2037
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:147998815"
variation 2038
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:2295524"
variation 2046
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147127627"
variation 2052
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114953496"
variation 2053
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34523602"
variation 2056
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:200155995"
variation 2073
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:150793173"
variation 2074
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:77771949"
variation 2076
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:149923448"
variation 2077
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:145255200"
variation 2080
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:112112803"
exon 2084..2235
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 2085
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200859829"
variation 2086
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:372220357"
variation 2118
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:146936755"
variation 2119
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:115874122"
variation 2139
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:113735532"
variation 2153
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:140494499"
variation 2169
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:35511234"
variation 2171
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199970083"
variation 2223
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34424078"
variation 2225
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:368952726"
exon 2236..2911
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 2245
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:114678661"
variation 2247
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:150235234"
variation 2257
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116271183"
variation 2275
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:142112616"
variation 2279
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:114316258"
variation 2282
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34748911"
variation 2283
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:138685998"
variation 2284
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:377731545"
variation 2295
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200494277"
variation 2296
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:371396745"
variation 2338..2339
/gene="C14orf159"
/replace=""
/replace="c"
/db_xref="dbSNP:5810531"
variation 2340
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:373378972"
variation 2341
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142686008"
variation 2363
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:144631642"
variation 2365
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:148051089"
variation 2367
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145141"
variation 2370
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:377043453"
variation 2372
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:35798893"
variation 2373
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:200556528"
variation 2421
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:374821767"
variation 2437
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:374622711"
variation 2501
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:187712668"
variation 2510
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:1801590"
STS 2537..2801
/gene="C14orf159"
/standard_name="WI-19880"
/db_xref="UniSTS:52015"
variation 2562
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285859"
variation 2572..2575
/gene="C14orf159"
/replace=""
/replace="ggac"
/db_xref="dbSNP:374263197"
STS 2645..2775
/gene="C14orf159"
/standard_name="G62042"
/db_xref="UniSTS:139136"
variation 2679
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:6562"
variation 2692
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:80181220"
variation 2708
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:112671362"
variation 2730
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:141359028"
variation 2775
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:150364186"
variation 2804
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:139087658"
variation 2832
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375228523"
variation 2833
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142988629"
variation 2869
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:183187504"
ORIGIN
gaaactgcctttgagccacaggcttgctggggatgaggtgacaaagctaatcgaggtggcaattggggaaggggttctgggctgccgcaggcacacaggccagagcttcgtggatacctgcagggcccaaaggtccctccctgttttgaagagtgagtgatggctatgaggtagcggccaggctgatcacccctgcgttggctggaggcagaattctgtaaatcctcgccaagtctttctccaggccactggttagctcatctcagcctcctctgggagcatcaacaccaacatggcacaggggactgcagtggtgtgctttggacctgtgtacccacccaaggctaaaggcagagccagatggagaaggaaaggcaagtgacttgtccagagccactctgtcaaaaggggacttgagtcctcagggctgttgactccaaagctgacaagcaggagccaagttacaccctgtttaaccctgccttcaaagggacgactctgtaagattctctgctacttattcaagttgacacgatgcccttcacactccacctgaggtcccgccttccctctgccataaggagtttgattctacaaaagaaaccaaacatcagaaatacatccagcatggctggagagctccgaccagccagcctggtggtcctgcccaggtcccttgctccagcttttgaaagattctgccaggtcaacactggtcctctacccctgctgggccagagtgagccagaaaagtggatgctgccccctcaaggtgctatctcagagaccaggatgggccatccccagttctggaaatacgagttcggtgcctgcaccggcagcctggcttcgctggagcagtactcggagcagctgaaggacatggtggccttcttcctgggctgcagcttctccctggaggaggccttggagaaagcggggctccccagaagagacccagcaggtcacagccagacaacagtgccttgtgttacccatgctggcttctgctgccctctggtggtcacgatgaggcccattcccaaggacaagctggaagggctggtgcgggcctgctgctccctcggaggtgagcaggggcaacctgttcacatgggcgacccagaactgttgggaatcaaagagctttccaaacctgcctacggggatgccatggtgtgtcccccaggggaggttccagtgttctggccttctccgctgaccagtctcggagctgtcagcagctgtgagaccccactggcttttgccagcatcccaggctgcacagttatgactgacctgaaggatgcaaaggctccacctggttgtctcaccccagagagaattccagaggtccatcacatttcccaagatcctctgcactacagcatcgcgtcagtctctgcttctcagaagatcagagaactagagtctatgatcggcatagacccagggaaccgggggattgggcacctgctctgtaaagatgagctgctgaaggcctctctctcgctgtcccatgcccgctcagtgctcatcaccactgggttccccacacatttcaatcatgagcctccagaagagacagatggcccaccaggagctgttgctctggttgccttcctgcaggccttggagaaggaggtcgccataatcgttgaccagagagcctggaacttgcaccagaagattgttgaagatgctgttgagcaaggtgttctgaagacgcagatcccgatattaacttaccaaggtggatcagtggaagctgctcaggcattcctgtgcaaaaatggggacccgcagacacctagatttgaccacctggtggccatagagcgtgccggaagagctgctgatggcaattactacaatgcaaggaagatgaacatcaagcacttggttgaccccattgacgatctttttcttgctgcgaagaagattcctggaatctcatcaactggagtcggtgatggaggcaacgagcttgggatgggtaaagtcaaggaggctgtgaggaggcacatacggcacggggatgtcatcgcctgcgacgtggaggctgactttgccgtcattgctggtgtttctaactggggaggctatgccctggcctgcgcactctacatcctgtactcatgtgctgtccacagtcagtacctgaggaaagcagtcggaccctccagggcacctggagatcaggcctggactcaggccctcccgtcggtcattaaggaagaaaaaatgctgggcatcttggtgcagcacaaagtccggagtggcgtctcgggcatcgtgggcatggaggtggatgggctgcccttccacaacacccacgccgagatgatccagaagctggtggacgtcaccacggcacaggtgtaaccgtccatgttccgtgtgagcagagtccctaccaacgggcaggtctgcatccggggagaatgcagctgcttctggcgacaatcctgctagtaaacactggtcttcggtgagcaacgaacactcgcctggcctgggaaactgcatgcccactttctgggaggggttagtgcaggtgctgtggacaaaggacaacatttctctggggctttttaacttttattcctaagactctaaaggcgttgatttcaaccctccttcactctggcttcttcaggcaacccacgtggtctcctgtgagaatcttctcgacagttacttatggggacacttgtgaacaattaactgccaggcagagcatgagaacaaacattcccaggccatgtaggataggatactccagactccagtcatcctcccccatccatggtttctgttactcatggtttcagttactcatagccaactgcagaccgaaaatactaaatgaaaaatttcagaaataaacaactcttaagttttaaattgtaaaaaaaaaaaaaaaaaaa
//
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
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@meso_cacase at
DBCLS
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