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2024-04-20 18:54:20, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001102366 3164 bp mRNA linear PRI 18-APR-2013
DEFINITION Homo sapiens chromosome 14 open reading frame 159 (C14orf159),
transcript variant 1, mRNA.
ACCESSION NM_001102366
VERSION NM_001102366.1 GI:156139130
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 3164)
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 3164)
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 3164)
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, BC065558.1, AL121784.5, DR003467.1 and
BX642394.1.
##Evidence-Data-START##
Transcript exon combination :: BC065558.1 [ECO:0000332]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-50 DA296867.1 1-50
51-377 AL602721.1 1-327
378-1073 BC065558.1 1-696
1074-1074 AL121784.5 56759-56759 c
1075-2795 BC065558.1 698-2418
2796-3124 DR003467.1 272-600
3125-3164 BX642394.1 1-40 c
FEATURES Location/Qualifiers
source 1..3164
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="14"
/map="14q32.11"
gene 1..3164
/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..609
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
exon 610..687
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 653
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:183774665"
exon 688..739
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 733
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116583933"
misc_feature 736..738
/gene="C14orf159"
/note="upstream in-frame stop codon"
exon 740..871
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 744
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375444718"
variation 767
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:140356090"
CDS 769..2619
/gene="C14orf159"
/note="isoform a is encoded by transcript variant 1;
UPF0317 protein C14orf159, mitochondrial"
/codon_start=1
/product="UPF0317 protein C14orf159, mitochondrial isoform
a"
/protein_id="NP_001095836.1"
/db_xref="GI:156139131"
/db_xref="CCDS:CCDS32141.1"
/db_xref="GeneID:80017"
/db_xref="HGNC:20498"
/translation="
MPFTLHLRSRLPSAIRSLILQKKPNIRNTSSMAGELRPASLVVLPRSLAPAFERFCQVNTGPLPLLGQSEPEKWMLPPQGAISETRMGHPQFWKYEFGACTGSLASLEQYSEQLKDMVAFFLGCSFSLEEALEKAGLPRRDPAGHSQTTVPCVTHAGFCCPLVVTMRPIPKDKLEGLVRACCSLGGEQGQPVHMGDPELLGIKELSKPAYGDAMVCPPGEVPVFWPSPLTSLGAVSSCETPLAFASIPGCTVMTDLKDAKAPPGCLTPERIPEVHHISQDPLHYSIASVSASQKIRELESMIGIDPGNRGIGHLLCKDELLKASLSLSHARSVLITTGFPTHFNHEPPEETDGPPGAVALVAFLQALEKEVAIIVDQRAWNLHQKIVEDAVEQGVLKTQIPILTYQGGSVEAAQAFLCKNGDPQTPRFDHLVAIERAGRAADGNYYNARKMNIKHLVDPIDDLFLAAKKIPGISSTGVGDGGNELGMGKVKEAVRRHIRHGDVIACDVEADFAVIAGVSNWGGYALACALYILYSCAVHSQYLRKAVGPSRAPGDQAWTQALPSVIKEEKMLGILVQHKVRSGVSGIVGMEVDGLPFHNTHAEMIQKLVDVTTAQV
"
transit_peptide 769..852
/gene="C14orf159"
/inference="non-experimental evidence, no additional
details recorded"
/note="Mitochondrion (Potential); propagated from
UniProtKB/Swiss-Prot (Q7Z3D6.2)"
mat_peptide 853..2616
/gene="C14orf159"
/product="UPF0317 protein C14orf159, mitochondrial"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q7Z3D6.2)"
misc_feature 1120..1533
/gene="C14orf159"
/note="Protein of unknown function (DUF1445); Region:
DUF1445; pfam07286"
/db_xref="CDD:148727"
misc_feature 1657..2598
/gene="C14orf159"
/note="Domain of unknown function (DUF4392); Region:
DUF4392; pfam14336"
/db_xref="CDD:206504"
variation 796
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:10142502"
variation 805
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147625749"
variation 848
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:200397505"
exon 872..1025
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 894
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:199766208"
variation 903
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:61990138"
variation 921
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:186462130"
variation 924
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:142153831"
variation 948
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:372209590"
variation 1010
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:375074402"
variation 1023
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:146611491"
exon 1026..1209
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1041
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:376028632"
variation 1071
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199942166"
variation 1072
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:201040091"
variation 1074
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:4900071"
variation 1097
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:148932665"
variation 1100
/gene="C14orf159"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201623410"
variation 1143
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:150590185"
variation 1173
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:200698102"
exon 1210..1360
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1230
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147006834"
variation 1249
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:148167595"
variation 1263
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:374015135"
variation 1268
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142032807"
variation 1321
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:146149732"
variation 1331
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:377730215"
variation 1353
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:138979726"
variation 1354
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:193008696"
exon 1361..1483
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1406
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:376295292"
variation 1417
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:142118168"
variation 1423
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:75931548"
variation 1429
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:114448340"
variation 1452
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:149668017"
variation 1464
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115154303"
variation 1471
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:148400411"
variation 1478
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34302825"
exon 1484..1687
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1502
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116685038"
variation 1519
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:80178223"
variation 1526
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116659399"
variation 1534
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147905616"
variation 1556
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:368308336"
variation 1576
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:140473581"
variation 1602
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:113182111"
variation 1628
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:150428305"
variation 1658
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:377123244"
variation 1665
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:115448574"
variation 1673
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116314762"
variation 1674
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:138171068"
exon 1688..1948
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1694
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:145176315"
variation 1714
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:111868616"
variation 1723
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:139000129"
variation 1768
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:199690106"
variation 1802
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:372940671"
variation 1806
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:142154756"
variation 1820
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200668165"
variation 1826
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375680070"
variation 1827
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:145749941"
variation 1838
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:201585097"
variation 1882
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:12895348"
variation 1889
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:374084163"
variation 1892
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:117996584"
variation 1903
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34196107"
variation 1911
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:115077193"
variation 1944
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:201673633"
variation 1946
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:150741072"
exon 1949..2048
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 1950
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200416806"
variation 1962
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:139055044"
variation 1963
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199874947"
variation 1970
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114141780"
variation 1971
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:147223382"
variation 2021
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375027427"
variation 2023
/gene="C14orf159"
/replace=""
/replace="a"
/db_xref="dbSNP:72237815"
variation 2036
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:367665781"
variation 2037
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34942357"
variation 2045
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:185064362"
exon 2049..2197
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 2059
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:145589579"
variation 2071
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:375771695"
variation 2075
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:138297457"
variation 2079
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:28481732"
variation 2085
/gene="C14orf159"
/replace="a"
/replace="c"
/db_xref="dbSNP:151056692"
variation 2106
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:141238498"
variation 2110
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:114411077"
variation 2146
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:373641510"
variation 2168
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114579097"
variation 2194
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:370829084"
variation 2196
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:28715808"
exon 2198..2317
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 2217
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:371519362"
variation 2218
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:367885678"
variation 2223
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:201859863"
variation 2245
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:138293042"
variation 2263
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:149609125"
variation 2264
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:143509911"
variation 2271
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:147998815"
variation 2272
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:2295524"
variation 2280
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:147127627"
variation 2286
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:114953496"
variation 2287
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34523602"
variation 2290
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:200155995"
variation 2307
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:150793173"
variation 2308
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:77771949"
variation 2310
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:149923448"
variation 2311
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:145255200"
variation 2314
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:112112803"
exon 2318..2469
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 2319
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200859829"
variation 2320
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:372220357"
variation 2352
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:146936755"
variation 2353
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:115874122"
variation 2373
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:113735532"
variation 2387
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:140494499"
variation 2403
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:35511234"
variation 2405
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:199970083"
variation 2457
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34424078"
variation 2459
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:368952726"
exon 2470..3145
/gene="C14orf159"
/inference="alignment:Splign:1.39.8"
variation 2479
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:114678661"
variation 2481
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:150235234"
variation 2491
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:116271183"
variation 2509
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:142112616"
variation 2513
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:114316258"
variation 2516
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:34748911"
variation 2517
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:138685998"
variation 2518
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:377731545"
variation 2529
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:200494277"
variation 2530
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:371396745"
variation 2572..2573
/gene="C14orf159"
/replace=""
/replace="c"
/db_xref="dbSNP:5810531"
variation 2574
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:373378972"
variation 2575
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142686008"
variation 2597
/gene="C14orf159"
/replace="a"
/replace="t"
/db_xref="dbSNP:144631642"
variation 2599
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:148051089"
variation 2601
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145141"
variation 2604
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:377043453"
variation 2606
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:35798893"
variation 2607
/gene="C14orf159"
/replace="g"
/replace="t"
/db_xref="dbSNP:200556528"
variation 2655
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:374821767"
variation 2671
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:374622711"
variation 2735
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:187712668"
variation 2744
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:1801590"
STS 2771..3035
/gene="C14orf159"
/standard_name="WI-19880"
/db_xref="UniSTS:52015"
variation 2796
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285859"
variation 2806..2809
/gene="C14orf159"
/replace=""
/replace="ggac"
/db_xref="dbSNP:374263197"
STS 2879..3009
/gene="C14orf159"
/standard_name="G62042"
/db_xref="UniSTS:139136"
variation 2913
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:6562"
variation 2926
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:80181220"
variation 2942
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:112671362"
variation 2964
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:141359028"
variation 3009
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:150364186"
variation 3038
/gene="C14orf159"
/replace="c"
/replace="g"
/db_xref="dbSNP:139087658"
variation 3066
/gene="C14orf159"
/replace="c"
/replace="t"
/db_xref="dbSNP:375228523"
variation 3067
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:142988629"
variation 3103
/gene="C14orf159"
/replace="a"
/replace="g"
/db_xref="dbSNP:183187504"
ORIGIN
aagaactggggcgggctagctgccgaggagaccacgctgctgcatgggccacgtgagctcaggctgtgggagcggatggagctgctacagtcagcgcttggggctggcctcagcttgtagacccgagccctgcagaacaaccccccgtggcgcaggagagcagaagaaagggggcctttatgcccttttgagggaagcacacattctgcaaggccgtggaaacaaagggaggaactgtttgtagccctcgtccagacgccccaaacaaacagtaagtcagaagggaacagagcacagcacagtccctccctccgccccaggcagtatccaccttgccccgccccacctaaggagcccaagggtattctgggagcccaccccaggacaatggcagggcaaaaccagtgagcaaggcagaaaattcctgaaattctccactgaggcccagctgttcctctccttgaaaagtcaaggcttggttcaagccagatagcacctgaggacagaacatatcagatggagaaggaaaggcaagtgacttgtccagagccactctgtcaaaaggggacttgagtcctcagggctgttgactccaaagctgacaagcaggtggcattcttcttcagagcagggcaagtgtaattctggaccaatgtgtgattctgagaccagaccaaccaactgaaggagccaagttacaccctgtttaaccctgccttcaaagggacgactctgtaagattctctgctacttattcaagttgacacgatgcccttcacactccacctgaggtcccgccttccctctgccataaggagtttgattctacaaaagaaaccaaacatcagaaatacatccagcatggctggagagctccgaccagccagcctggtggtcctgcccaggtcccttgctccagcttttgaaagattctgccaggtcaacactggtcctctacccctgctgggccagagtgagccagaaaagtggatgctgccccctcaaggtgctatctcagagaccaggatgggccatccccagttctggaaatacgagttcggtgcctgcaccggcagcctggcttcgctggagcagtactcggagcagctgaaggacatggtggccttcttcctgggctgcagcttctccctggaggaggccttggagaaagcggggctccccagaagagacccagcaggtcacagccagacaacagtgccttgtgttacccatgctggcttctgctgccctctggtggtcacgatgaggcccattcccaaggacaagctggaagggctggtgcgggcctgctgctccctcggaggtgagcaggggcaacctgttcacatgggcgacccagaactgttgggaatcaaagagctttccaaacctgcctacggggatgccatggtgtgtcccccaggggaggttccagtgttctggccttctccgctgaccagtctcggagctgtcagcagctgtgagaccccactggcttttgccagcatcccaggctgcacagttatgactgacctgaaggatgcaaaggctccacctggttgtctcaccccagagagaattccagaggtccatcacatttcccaagatcctctgcactacagcatcgcgtcagtctctgcttctcagaagatcagagaactagagtctatgatcggcatagacccagggaaccgggggattgggcacctgctctgtaaagatgagctgctgaaggcctctctctcgctgtcccatgcccgctcagtgctcatcaccactgggttccccacacatttcaatcatgagcctccagaagagacagatggcccaccaggagctgttgctctggttgccttcctgcaggccttggagaaggaggtcgccataatcgttgaccagagagcctggaacttgcaccagaagattgttgaagatgctgttgagcaaggtgttctgaagacgcagatcccgatattaacttaccaaggtggatcagtggaagctgctcaggcattcctgtgcaaaaatggggacccgcagacacctagatttgaccacctggtggccatagagcgtgccggaagagctgctgatggcaattactacaatgcaaggaagatgaacatcaagcacttggttgaccccattgacgatctttttcttgctgcgaagaagattcctggaatctcatcaactggagtcggtgatggaggcaacgagcttgggatgggtaaagtcaaggaggctgtgaggaggcacatacggcacggggatgtcatcgcctgcgacgtggaggctgactttgccgtcattgctggtgtttctaactggggaggctatgccctggcctgcgcactctacatcctgtactcatgtgctgtccacagtcagtacctgaggaaagcagtcggaccctccagggcacctggagatcaggcctggactcaggccctcccgtcggtcattaaggaagaaaaaatgctgggcatcttggtgcagcacaaagtccggagtggcgtctcgggcatcgtgggcatggaggtggatgggctgcccttccacaacacccacgccgagatgatccagaagctggtggacgtcaccacggcacaggtgtaaccgtccatgttccgtgtgagcagagtccctaccaacgggcaggtctgcatccggggagaatgcagctgcttctggcgacaatcctgctagtaaacactggtcttcggtgagcaacgaacactcgcctggcctgggaaactgcatgcccactttctgggaggggttagtgcaggtgctgtggacaaaggacaacatttctctggggctttttaacttttattcctaagactctaaaggcgttgatttcaaccctccttcactctggcttcttcaggcaacccacgtggtctcctgtgagaatcttctcgacagttacttatggggacacttgtgaacaattaactgccaggcagagcatgagaacaaacattcccaggccatgtaggataggatactccagactccagtcatcctcccccatccatggtttctgttactcatggtttcagttactcatagccaactgcagaccgaaaatactaaatgaaaaatttcagaaataaacaactcttaagttttaaattgtaaaaaaaaaaaaaaaaaaa
//
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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