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2025-05-09 17:21:08, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001102369 2763 bp mRNA linear PRI 18-APR-2013
DEFINITION Homo sapiens chromosome 14 open reading frame 159 (C14orf159),
transcript variant 5, mRNA.
ACCESSION NM_001102369
VERSION NM_001102369.1 GI:156139136
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, DA641301.1, AK023200.1, AL121784.5, BC065558.1,
DR003467.1 and BX642394.1.
##Evidence-Data-START##
Transcript exon combination :: AK023200.1 [ECO:0000332]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-52 DA296867.1 1-52
53-291 DA641301.1 1-239
292-828 AK023200.1 90-626
829-829 AL121784.5 56759-56759 c
830-2342 AK023200.1 628-2140
2343-2394 BC065558.1 2367-2418
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..364
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
exon 365..442
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 408
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:183774665"
exon 443..494
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 488
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116583933"
misc_feature 491..493
/gene="C14orf159"
/note="upstream in-frame stop codon"
exon 495..626
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 499
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375444718"
variation 522
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:140356090"
CDS 524..2218
/gene="C14orf159"
/note="isoform c is encoded by transcript variant 5;
UPF0317 protein C14orf159, mitochondrial"
/codon_start=1
/product="UPF0317 protein C14orf159, mitochondrial isoform
c"
/protein_id="NP_001095839.1"
/db_xref="GI:156139137"
/db_xref="CCDS:CCDS45150.1"
/db_xref="GeneID:80017"
/db_xref="HGNC:20498"
/translation="
MPFTLHLRSRLPSAIRSLILQKKPNIRNTSSMAGELRPASLVVLPRSLAPAFERFCQVNTGPLPLLGQSEPEKWMLPPQGAISETRMGHPQFWKYEFGACTGSLASLEQYSEQLKDMVAFFLGCSFSLEEALEKAGLPRRDPAGHSQTTVPCVTHAGFCCPLVVTMRPIPKDKLEGLVRACCSLGELLGIKELSKPAYGDAMVCPPGEVPVFWPSPLTSLGAVSSCETPLAFASIPGCTVMTDLKDAKAPPGCLTPERIPEVHHISQDPLHYSIASVSASQKIRELESMIGIDPGNRGIGHLLCKDELLKASLSLSHARSVLITTGFPTHFNHEPPEETDGPPGAVALVAFLQALEKEVAIIVDQRAWNLHQKIVEDAVEQGVLKTQIPILTYQGGSVEAAQAFLCKNGDPQTPRFDHLVAIERAGRAADGNYYNARKMNIKHLVDPIDDLFLAAKKIPGISSTGVSNWGGYALACALYILYSCAVHSQYLRKAVGPSRAPGDQAWTQALPSVIKEEKMLGILVQHKVRSGVSGIVGMEVDGLPFHNTHAEMIQKLVDVTTAQV
"
misc_feature 875..1252
/gene="C14orf159"
/note="Protein of unknown function (DUF1445); Region:
DUF1445; cl01790"
/db_xref="CDD:186475"
misc_feature 1376..2197
/gene="C14orf159"
/note="Domain of unknown function (DUF4392); Region:
DUF4392; pfam14336"
/db_xref="CDD:206504"
variation 551
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:10142502"
variation 560
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147625749"
variation 603
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:200397505"
exon 627..780
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 649
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:199766208"
variation 658
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:61990138"
variation 676
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:186462130"
variation 679
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:142153831"
variation 703
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:372209590"
variation 765
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:375074402"
variation 778
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:146611491"
exon 781..964
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 796
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:376028632"
variation 826
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199942166"
variation 827
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:201040091"
variation 829
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:4900071"
variation 852
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:148932665"
variation 855
/gene="C14orf159"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201623410"
variation 898
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:150590185"
variation 928
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:200698102"
exon 965..1079
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 985
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147006834"
variation 1004
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:148167595"
variation 1018
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374015135"
variation 1023
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142032807"
variation 1076
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:146149732"
exon 1080..1202
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1125
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:376295292"
variation 1136
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:142118168"
variation 1142
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:75931548"
variation 1148
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:114448340"
variation 1171
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:149668017"
variation 1183
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115154303"
variation 1190
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:148400411"
variation 1197
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34302825"
exon 1203..1406
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1221
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116685038"
variation 1238
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:80178223"
variation 1245
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116659399"
variation 1253
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147905616"
variation 1275
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:368308336"
variation 1295
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:140473581"
variation 1321
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:113182111"
variation 1347
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:150428305"
variation 1377
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:377123244"
variation 1384
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:115448574"
variation 1392
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116314762"
variation 1393
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:138171068"
exon 1407..1667
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1413
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:145176315"
variation 1433
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:111868616"
variation 1442
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:139000129"
variation 1487
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:199690106"
variation 1521
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372940671"
variation 1525
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:142154756"
variation 1539
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200668165"
variation 1545
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375680070"
variation 1546
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:145749941"
variation 1557
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:201585097"
variation 1601
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:12895348"
variation 1608
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:374084163"
variation 1611
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:117996584"
variation 1622
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34196107"
variation 1630
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115077193"
variation 1663
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:201673633"
variation 1665
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:150741072"
exon 1668..1767
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1669
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200416806"
variation 1681
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:139055044"
variation 1682
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199874947"
variation 1689
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114141780"
variation 1690
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:147223382"
variation 1740
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375027427"
variation 1742
/gene="C14orf159"
/replace=""
/replace="a"
/db_xref="dbSNP:72237815"
variation 1755
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:367665781"
variation 1756
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34942357"
variation 1764
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:185064362"
exon 1768..1916
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1778
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:145589579"
variation 1790
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375771695"
variation 1794
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:138297457"
variation 1798
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:28481732"
variation 1804
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:151056692"
variation 1825
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:141238498"
variation 1829
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:114411077"
variation 1865
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:373641510"
variation 1887
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114579097"
variation 1913
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:370829084"
variation 1915
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:28715808"
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
aagaactggggcgggctagctgccgaggagaccacgctgctgcatgggccacgtgagctcaggctgtgggagcggatggagctgctacagtcagcgcttggggctggcctcagcttgtagacccgagccctgcagaacaaccccccgtggcgcaggagagcagaagaaagggggcctttatgcccttttgagggaagcacacattctgcaaggccgtggaaacaaagggaggaactgtttgtagccctcgtccagacgccccaaacaaacaatggagaaggaaaggcaagtgacttgtccagagccactctgtcaaaaggggacttgagtcctcagggctgttgactccaaagctgacaagcaggtggcattcttcttcagagcagggcaagtgtaattctggaccaatgtgtgattctgagaccagaccaaccaactgaaggagccaagttacaccctgtttaaccctgccttcaaagggacgactctgtaagattctctgctacttattcaagttgacacgatgcccttcacactccacctgaggtcccgccttccctctgccataaggagtttgattctacaaaagaaaccaaacatcagaaatacatccagcatggctggagagctccgaccagccagcctggtggtcctgcccaggtcccttgctccagcttttgaaagattctgccaggtcaacactggtcctctacccctgctgggccagagtgagccagaaaagtggatgctgccccctcaaggtgctatctcagagaccaggatgggccatccccagttctggaaatacgagttcggtgcctgcaccggcagcctggcttcgctggagcagtactcggagcagctgaaggacatggtggccttcttcctgggctgcagcttctccctggaggaggccttggagaaagcggggctccccagaagagacccagcaggtcacagccagacaacagtgccttgtgttacccatgctggcttctgctgccctctggtggtcacgatgaggcccattcccaaggacaagctggaagggctggtgcgggcctgctgctccctcggagaactgttgggaatcaaagagctttccaaacctgcctacggggatgccatggtgtgtcccccaggggaggttccagtgttctggccttctccgctgaccagtctcggagctgtcagcagctgtgagaccccactggcttttgccagcatcccaggctgcacagttatgactgacctgaaggatgcaaaggctccacctggttgtctcaccccagagagaattccagaggtccatcacatttcccaagatcctctgcactacagcatcgcgtcagtctctgcttctcagaagatcagagaactagagtctatgatcggcatagacccagggaaccgggggattgggcacctgctctgtaaagatgagctgctgaaggcctctctctcgctgtcccatgcccgctcagtgctcatcaccactgggttccccacacatttcaatcatgagcctccagaagagacagatggcccaccaggagctgttgctctggttgccttcctgcaggccttggagaaggaggtcgccataatcgttgaccagagagcctggaacttgcaccagaagattgttgaagatgctgttgagcaaggtgttctgaagacgcagatcccgatattaacttaccaaggtggatcagtggaagctgctcaggcattcctgtgcaaaaatggggacccgcagacacctagatttgaccacctggtggccatagagcgtgccggaagagctgctgatggcaattactacaatgcaaggaagatgaacatcaagcacttggttgaccccattgacgatctttttcttgctgcgaagaagattcctggaatctcatcaactggtgtttctaactggggaggctatgccctggcctgcgcactctacatcctgtactcatgtgctgtccacagtcagtacctgaggaaagcagtcggaccctccagggcacctggagatcaggcctggactcaggccctcccgtcggtcattaaggaagaaaaaatgctgggcatcttggtgcagcacaaagtccggagtggcgtctcgggcatcgtgggcatggaggtggatgggctgcccttccacaacacccacgccgagatgatccagaagctggtggacgtcaccacggcacaggtgtaaccgtccatgttccgtgtgagcagagtccctaccaacgggcaggtctgcatccggggagaatgcagctgcttctggcgacaatcctgctagtaaacactggtcttcggtgagcaacgaacactcgcctggcctgggaaactgcatgcccactttctgggaggggttagtgcaggtgctgtggacaaaggacaacatttctctggggctttttaacttttattcctaagactctaaaggcgttgatttcaaccctccttcactctggcttcttcaggcaacccacgtggtctcctgtgagaatcttctcgacagttacttatggggacacttgtgaacaattaactgccaggcagagcatgagaacaaacattcccaggccatgtaggataggatactccagactccagtcatcctcccccatccatggtttctgttactcatggtttcagttactcatagccaactgcagaccgaaaatactaaatgaaaaatttcagaaataaacaactcttaagttttaaattgtaaaaaaaaaaaaaaaaaaa
//
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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DBCLS
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