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2024-04-20 19:51:19, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001102368 2763 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens chromosome 14 open reading frame 159 (C14orf159),
transcript variant 4, mRNA.
ACCESSION NM_001102368
VERSION NM_001102368.1 GI:156139134
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 2763)
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 2763)
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 2763)
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, AB210031.1, BC065558.1, DR003467.1 and BX642394.1.
##Evidence-Data-START##
Transcript exon combination :: BX537970.1, AK097294.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025082, ERS025084 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-99 DA296867.1 1-99
100-1076 AB210031.1 1-977
1077-2394 BC065558.1 1101-2418
2395-2723 DR003467.1 272-600
2724-2763 BX642394.1 1-40 c
FEATURES Location/Qualifiers
source 1..2763
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="14"
/map="14q32.11"
gene 1..2763
/gene="C14orf159"
/note="chromosome 14 open reading frame 159"
/db_xref="GeneID:80017"
/db_xref="HGNC:20498"
exon 1..271
/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"
exon 272..323
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 317
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116583933"
misc_feature 320..322
/gene="C14orf159"
/note="upstream in-frame stop codon"
exon 324..455
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 328
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375444718"
variation 351
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:140356090"
CDS 353..2218
/gene="C14orf159"
/note="isoform b is encoded by transcript variant 4;
UPF0317 protein C14orf159, mitochondrial"
/codon_start=1
/product="UPF0317 protein C14orf159, mitochondrial isoform
b"
/protein_id="NP_001095838.1"
/db_xref="GI:156139135"
/db_xref="CCDS:CCDS41979.1"
/db_xref="GeneID:80017"
/db_xref="HGNC:20498"
/translation="
MPFTLHLRSRLPSAIRSLILQKKPNIRNTSSMAGELRPASLVVLPRSLAPAFERFCQVNTGPLPLLGQSEPEKWMLPPQGAISETRMGHPQFWKYEFGACTGSLASLEQYSEQLKDMVAFFLGCSFSLEEALEKAGLPRRDPAGHSQAGAYKTTVPCVTHAGFCCPLVVTMRPIPKDKLEGLVRACCSLGGEQGQPVHMGDPELLGIKELSKPAYGDAMVCPPGEVPVFWPSPLTSLGAVSSCETPLAFASIPGCTVMTDLKDAKAPPGCLTPERIPEVHHISQDPLHYSIASVSASQKIRELESMIGIDPGNRGIGHLLCKDELLKASLSLSHARSVLITTGFPTHFNHEPPEETDGPPGAVALVAFLQALEKEVAIIVDQRAWNLHQKIVEDAVEQGVLKTQIPILTYQGGSVEAAQAFLCKNGDPQTPRFDHLVAIERAGRAADGNYYNARKMNIKHLVDPIDDLFLAAKKIPGISSTGVGDGGNELGMGKVKEAVRRHIRHGDVIACDVEADFAVIAGVSNWGGYALACALYILYSCAVHSQYLRKAVGPSRAPGDQAWTQALPSVIKEEKMLGILVQHKVRSGVSGIVGMEVDGLPFHNTHAEMIQKLVDVTTAQV
"
transit_peptide 353..436
/gene="C14orf159"
/inference="non-experimental evidence, no additional
details recorded"
/note="Mitochondrion (Potential); propagated from
UniProtKB/Swiss-Prot (Q7Z3D6.2)"
misc_feature 704..1132
/gene="C14orf159"
/note="Protein of unknown function (DUF1445); Region:
DUF1445; pfam07286"
/db_xref="CDD:148727"
misc_feature 1256..2197
/gene="C14orf159"
/note="Domain of unknown function (DUF4392); Region:
DUF4392; pfam14336"
/db_xref="CDD:206504"
variation 380
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:10142502"
variation 389
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147625749"
variation 432
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:200397505"
exon 456..609
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 478
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:199766208"
variation 487
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:61990138"
variation 505
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:186462130"
variation 508
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:142153831"
variation 532
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:372209590"
variation 594
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:375074402"
variation 607
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:146611491"
exon 610..808
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 625
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:376028632"
variation 655
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199942166"
variation 656
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:201040091"
variation 658
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:4900071"
variation 681
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:148932665"
variation 684
/gene="C14orf159"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201623410"
variation 727
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:150590185"
variation 757
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:200698102"
variation 794
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:181128831"
variation 795
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:4900072"
exon 809..959
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 829
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147006834"
variation 848
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:148167595"
variation 862
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374015135"
variation 867
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142032807"
variation 920
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:146149732"
variation 930
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:377730215"
variation 952
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:138979726"
variation 953
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:193008696"
exon 960..1082
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1005
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:376295292"
variation 1016
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:142118168"
variation 1022
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:75931548"
variation 1028
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:114448340"
variation 1051
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:149668017"
variation 1063
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115154303"
variation 1070
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:148400411"
variation 1077
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34302825"
exon 1083..1286
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1101
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116685038"
variation 1118
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:80178223"
variation 1125
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116659399"
variation 1133
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147905616"
variation 1155
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:368308336"
variation 1175
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:140473581"
variation 1201
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:113182111"
variation 1227
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:150428305"
variation 1257
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:377123244"
variation 1264
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:115448574"
variation 1272
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116314762"
variation 1273
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:138171068"
exon 1287..1547
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1293
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:145176315"
variation 1313
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:111868616"
variation 1322
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:139000129"
variation 1367
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:199690106"
variation 1401
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372940671"
variation 1405
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:142154756"
variation 1419
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200668165"
variation 1425
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375680070"
variation 1426
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:145749941"
variation 1437
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:201585097"
variation 1481
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:12895348"
variation 1488
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:374084163"
variation 1491
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:117996584"
variation 1502
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34196107"
variation 1510
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115077193"
variation 1543
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:201673633"
variation 1545
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:150741072"
exon 1548..1647
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1549
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200416806"
variation 1561
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:139055044"
variation 1562
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199874947"
variation 1569
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114141780"
variation 1570
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:147223382"
variation 1620
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375027427"
variation 1622
/gene="C14orf159"
/replace=""
/replace="a"
/db_xref="dbSNP:72237815"
variation 1635
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:367665781"
variation 1636
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34942357"
variation 1644
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:185064362"
exon 1648..1796
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1658
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:145589579"
variation 1670
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375771695"
variation 1674
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:138297457"
variation 1678
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:28481732"
variation 1684
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:151056692"
variation 1705
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:141238498"
variation 1709
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:114411077"
variation 1745
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:373641510"
variation 1767
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114579097"
variation 1793
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:370829084"
variation 1795
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:28715808"
exon 1797..1916
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1816
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:371519362"
variation 1817
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:367885678"
variation 1822
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:201859863"
variation 1844
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:138293042"
variation 1862
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:149609125"
variation 1863
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:143509911"
variation 1870
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:147998815"
variation 1871
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:2295524"
variation 1879
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147127627"
variation 1885
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114953496"
variation 1886
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34523602"
variation 1889
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:200155995"
variation 1906
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:150793173"
variation 1907
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:77771949"
variation 1909
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:149923448"
variation 1910
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:145255200"
variation 1913
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:112112803"
exon 1917..2068
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1918
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200859829"
variation 1919
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:372220357"
variation 1951
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:146936755"
variation 1952
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:115874122"
variation 1972
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:113735532"
variation 1986
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:140494499"
variation 2002
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:35511234"
variation 2004
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199970083"
variation 2056
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34424078"
variation 2058
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:368952726"
exon 2069..2744
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 2078
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:114678661"
variation 2080
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:150235234"
variation 2090
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116271183"
variation 2108
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:142112616"
variation 2112
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:114316258"
variation 2115
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34748911"
variation 2116
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:138685998"
variation 2117
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:377731545"
variation 2128
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200494277"
variation 2129
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:371396745"
variation 2171..2172
/gene="C14orf159"
/replace=""
/replace="c"
/db_xref="dbSNP:5810531"
variation 2173
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:373378972"
variation 2174
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142686008"
variation 2196
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:144631642"
variation 2198
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:148051089"
variation 2200
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145141"
variation 2203
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:377043453"
variation 2205
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:35798893"
variation 2206
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:200556528"
variation 2254
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:374821767"
variation 2270
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:374622711"
variation 2334
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:187712668"
variation 2343
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:1801590"
STS 2370..2634
/gene="C14orf159"
/standard_name="WI-19880"
/db_xref="UniSTS:52015"
variation 2395
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285859"
variation 2405..2408
/gene="C14orf159"
/replace=""
/replace="ggac"
/db_xref="dbSNP:374263197"
STS 2478..2608
/gene="C14orf159"
/standard_name="G62042"
/db_xref="UniSTS:139136"
variation 2512
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:6562"
variation 2525
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:80181220"
variation 2541
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:112671362"
variation 2563
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:141359028"
variation 2608
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:150364186"
variation 2637
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:139087658"
variation 2665
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375228523"
variation 2666
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142988629"
variation 2702
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:183187504"
ORIGIN
aagaactggggcgggctagctgccgaggagaccacgctgctgcatgggccacgtgagctcaggctgtgggagcggatggagctgctacagtcagcgcttggggctggcctcagcttgtagacccgagccctgcagaacaaccccccgtggcgcaggagagcagaagaaagggggcctttatgcccttttgagggaagcacacattctgcaaggccgtggaaacaaagggaggaactgtttgtagccctcgtccagacgccccaaacaaacagagccaagttacaccctgtttaaccctgccttcaaagggacgactctgtaagattctctgctacttattcaagttgacacgatgcccttcacactccacctgaggtcccgccttccctctgccataaggagtttgattctacaaaagaaaccaaacatcagaaatacatccagcatggctggagagctccgaccagccagcctggtggtcctgcccaggtcccttgctccagcttttgaaagattctgccaggtcaacactggtcctctacccctgctgggccagagtgagccagaaaagtggatgctgccccctcaaggtgctatctcagagaccaggatgggccatccccagttctggaaatacgagttcggtgcctgcaccggcagcctggcttcgctggagcagtactcggagcagctgaaggacatggtggccttcttcctgggctgcagcttctccctggaggaggccttggagaaagcggggctccccagaagagacccagcaggtcacagccaggcgggtgcatacaagacaacagtgccttgtgttacccatgctggcttctgctgccctctggtggtcacgatgaggcccattcccaaggacaagctggaagggctggtgcgggcctgctgctccctcggaggtgagcaggggcaacctgttcacatgggcgacccagaactgttgggaatcaaagagctttccaaacctgcctacggggatgccatggtgtgtcccccaggggaggttccagtgttctggccttctccgctgaccagtctcggagctgtcagcagctgtgagaccccactggcttttgccagcatcccaggctgcacagttatgactgacctgaaggatgcaaaggctccacctggttgtctcaccccagagagaattccagaggtccatcacatttcccaagatcctctgcactacagcatcgcgtcagtctctgcttctcagaagatcagagaactagagtctatgatcggcatagacccagggaaccgggggattgggcacctgctctgtaaagatgagctgctgaaggcctctctctcgctgtcccatgcccgctcagtgctcatcaccactgggttccccacacatttcaatcatgagcctccagaagagacagatggcccaccaggagctgttgctctggttgccttcctgcaggccttggagaaggaggtcgccataatcgttgaccagagagcctggaacttgcaccagaagattgttgaagatgctgttgagcaaggtgttctgaagacgcagatcccgatattaacttaccaaggtggatcagtggaagctgctcaggcattcctgtgcaaaaatggggacccgcagacacctagatttgaccacctggtggccatagagcgtgccggaagagctgctgatggcaattactacaatgcaaggaagatgaacatcaagcacttggttgaccccattgacgatctttttcttgctgcgaagaagattcctggaatctcatcaactggagtcggtgatggaggcaacgagcttgggatgggtaaagtcaaggaggctgtgaggaggcacatacggcacggggatgtcatcgcctgcgacgtggaggctgactttgccgtcattgctggtgtttctaactggggaggctatgccctggcctgcgcactctacatcctgtactcatgtgctgtccacagtcagtacctgaggaaagcagtcggaccctccagggcacctggagatcaggcctggactcaggccctcccgtcggtcattaaggaagaaaaaatgctgggcatcttggtgcagcacaaagtccggagtggcgtctcgggcatcgtgggcatggaggtggatgggctgcccttccacaacacccacgccgagatgatccagaagctggtggacgtcaccacggcacaggtgtaaccgtccatgttccgtgtgagcagagtccctaccaacgggcaggtctgcatccggggagaatgcagctgcttctggcgacaatcctgctagtaaacactggtcttcggtgagcaacgaacactcgcctggcctgggaaactgcatgcccactttctgggaggggttagtgcaggtgctgtggacaaaggacaacatttctctggggctttttaacttttattcctaagactctaaaggcgttgatttcaaccctccttcactctggcttcttcaggcaacccacgtggtctcctgtgagaatcttctcgacagttacttatggggacacttgtgaacaattaactgccaggcagagcatgagaacaaacattcccaggccatgtaggataggatactccagactccagtcatcctcccccatccatggtttctgttactcatggtttcagttactcatagccaactgcagaccgaaaatactaaatgaaaaatttcagaaataaacaactcttaagttttaaattgtaaaaaaaaaaaaaaaaaaa
//
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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