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2025-05-09 18:26:09, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_144999 2639 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens leucine rich repeat containing 45 (LRRC45), mRNA.
ACCESSION NM_144999 XM_938258
VERSION NM_144999.2 GI:34147703
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 2639)
AUTHORS Gerhard,D.S., Wagner,L., Feingold,E.A., Shenmen,C.M., Grouse,L.H.,
Schuler,G., Klein,S.L., Old,S., Rasooly,R., Good,P., Guyer,M.,
Peck,A.M., Derge,J.G., Lipman,D., Collins,F.S., Jang,W., Sherry,S.,
Feolo,M., Misquitta,L., Lee,E., Rotmistrovsky,K., Greenhut,S.F.,
Schaefer,C.F., Buetow,K., Bonner,T.I., Haussler,D., Kent,J.,
Kiekhaus,M., Furey,T., Brent,M., Prange,C., Schreiber,K.,
Shapiro,N., Bhat,N.K., Hopkins,R.F., Hsie,F., Driscoll,T.,
Soares,M.B., Casavant,T.L., Scheetz,T.E., Brown-stein,M.J.,
Usdin,T.B., Toshiyuki,S., Carninci,P., Piao,Y., Dudekula,D.B.,
Ko,M.S., Kawakami,K., Suzuki,Y., Sugano,S., Gruber,C.E.,
Smith,M.R., Simmons,B., Moore,T., Waterman,R., Johnson,S.L.,
Ruan,Y., Wei,C.L., Mathavan,S., Gunaratne,P.H., Wu,J., Garcia,A.M.,
Hulyk,S.W., Fuh,E., Yuan,Y., Sneed,A., Kowis,C., Hodgson,A.,
Muzny,D.M., McPherson,J., Gibbs,R.A., Fahey,J., Helton,E.,
Ketteman,M., Madan,A., Rodrigues,S., Sanchez,A., Whiting,M.,
Madari,A., Young,A.C., Wetherby,K.D., Granite,S.J., Kwong,P.N.,
Brinkley,C.P., Pearson,R.L., Bouffard,G.G., Blakesly,R.W.,
Green,E.D., Dickson,M.C., Rodriguez,A.C., Grimwood,J., Schmutz,J.,
Myers,R.M., Butterfield,Y.S., Griffith,M., Griffith,O.L.,
Krzywinski,M.I., Liao,N., Morin,R., Palmquist,D., Petrescu,A.S.,
Skalska,U., Smailus,D.E., Stott,J.M., Schnerch,A., Schein,J.E.,
Jones,S.J., Holt,R.A., Baross,A., Marra,M.A., Clifton,S.,
Makowski,K.A., Bosak,S. and Malek,J.
CONSRTM MGC Project Team
TITLE The status, quality, and expansion of the NIH full-length cDNA
project: the Mammalian Gene Collection (MGC)
JOURNAL Genome Res. 14 (10B), 2121-2127 (2004)
PUBMED 15489334
REMARK Erratum:[Genome Res. 2006 Jun;16(6):804. Morrin, Ryan [corrected to
Morin, Ryan]]
COMMENT PROVISIONAL REFSEQ: This record has not yet been subject to final
NCBI review. The reference sequence was derived from BC014109.2.
On or before Mar 4, 2006 this sequence version replaced
gi:89065899, gi:21450704.
##Evidence-Data-START##
Transcript exon combination :: BC014109.2 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025083, ERS025085 [ECO:0000348]
##Evidence-Data-END##
FEATURES Location/Qualifiers
source 1..2639
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="17"
/map="17q25.3"
gene 1..2639
/gene="LRRC45"
/note="leucine rich repeat containing 45"
/db_xref="GeneID:201255"
/db_xref="HGNC:28302"
/db_xref="HPRD:14476"
exon 1..460
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 37
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:4072801"
misc_feature 58..60
/gene="LRRC45"
/note="upstream in-frame stop codon"
variation 104
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:189382460"
variation 144
/gene="LRRC45"
/replace="g"
/replace="t"
/db_xref="dbSNP:182249942"
variation 196
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:11552878"
variation 217
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:368905004"
CDS 241..2253
/gene="LRRC45"
/codon_start=1
/product="leucine-rich repeat-containing protein 45"
/protein_id="NP_659436.1"
/db_xref="GI:21450705"
/db_xref="CCDS:CCDS11797.1"
/db_xref="GeneID:201255"
/db_xref="HGNC:28302"
/db_xref="HPRD:14476"
/translation="
MEEFRRSYSRLCRESGAEPQEAVLQQLHQLPRGRLDLATQSLTVETCRALGKLLPRETLCTELVLSDCMLSEEGATLLLRGLCANTVLRFLDLKGNNLRAAGAEALGKLLQQNKSIQSLTLEWNSLGTWDDAFATFCGGLAANGALQRLDLRNNQISHKGAEELALALKGNTTLQQLDLRWNNVGLLGGRALMNCLPSNRTLWRLDLAGNNIPGDVLRAVEQAMGHSQDRLTTFQENQARTHVLSKEVQHLREEKSKQFLDLMETIDKQREEMAKSSRASAARVGQLQEALNERHSIINALKAKLQMTEAALALSEQKAQDLGELLATAEQEQLSLSQRQAKELKLEQQEAAERESKLLRDLSAANEKNLLLQNQVDELERKFRCQQEQLFQTRQEMTSMSAELKMRAIQAEERLDMEKRRCRQSLEDSESLRIKEVEHMTRHLEESEKAMQERVQRLEAARLSLEEELSRVKAAALSERGQAEEELIKAKSQARLEEQQRLAHLEDKLRLLAQARDEAQGACLQQKQVVAEAQTRVSQLGLQVEGLRRRLEELQQELSLKDQERVAEVSRVRVELQEQNGRLQAELAAQEALREKAAALERQLKVMASDHREALLDRESENASLREKLRLREAEIARIRDEEAQRASFLQNAVLAYVQASPVRTLSPPK
"
misc_feature 259..261
/gene="LRRC45"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 262..264
/gene="LRRC45"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature <379..876
/gene="LRRC45"
/note="Leucine-rich repeats (LRRs), ribonuclease inhibitor
(RI)-like subfamily. LRRs are 20-29 residue sequence
motifs present in many proteins that participate in
protein-protein interactions and have different functions
and cellular locations. LRRs correspond...; Region:
LRR_RI; cl15309"
/db_xref="CDD:199167"
misc_feature 412..480
/gene="LRRC45"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96CN5.1);
Region: LRR 1"
misc_feature order(418..420,427..429,433..435,442..444,448..450,
502..504,511..513,517..519,526..528,532..534,586..588,
595..597,601..603,610..612,616..618,676..678,685..687,
691..693,700..702,706..708,760..762,769..771,775..777,
784..786,790..792,844..846,853..855,859..861,868..870,
874..876)
/gene="LRRC45"
/note="Leucine-rich repeats; other site"
/db_xref="CDD:29015"
misc_feature order(439..441,523..525,697..699,772..774,778..780,
856..858)
/gene="LRRC45"
/note="Substrate binding site [chemical binding]; other
site"
/db_xref="CDD:29015"
misc_feature 499..561
/gene="LRRC45"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96CN5.1);
Region: LRR 2"
misc_feature 583..648
/gene="LRRC45"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96CN5.1);
Region: LRR 3"
misc_feature 673..738
/gene="LRRC45"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96CN5.1);
Region: LRR 4"
misc_feature 676..876
/gene="LRRC45"
/note="Leucine rich repeat; Region: LRR_8; pfam13855"
/db_xref="CDD:206026"
misc_feature 757..822
/gene="LRRC45"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96CN5.1);
Region: LRR 5"
misc_feature 841..876
/gene="LRRC45"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96CN5.1);
Region: LRR 6"
variation 254
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:200245445"
variation 292
/gene="LRRC45"
/replace="c"
/replace="g"
/db_xref="dbSNP:376086300"
variation 312
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:370680911"
variation 335
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:375184869"
variation 340
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:368576582"
variation 422
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:372848486"
exon 461..522
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 472
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:374049967"
variation 498
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:150032877"
exon 523..593
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 523
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:370110836"
variation 549
/gene="LRRC45"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201106510"
variation 565
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:181786492"
variation 576
/gene="LRRC45"
/replace="c"
/replace="g"
/db_xref="dbSNP:369785505"
exon 594..772
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 633
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:200038956"
variation 683
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:372551546"
variation 722
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:375834199"
variation 723
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:142588114"
variation 771
/gene="LRRC45"
/replace="g"
/replace="t"
/db_xref="dbSNP:202058881"
exon 773..901
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 790
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:373267378"
variation 792
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:145781567"
variation 807
/gene="LRRC45"
/replace="a"
/replace="c"
/db_xref="dbSNP:368208586"
variation 814
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:376227945"
variation 835
/gene="LRRC45"
/replace="a"
/replace="t"
/db_xref="dbSNP:200231075"
variation 837
/gene="LRRC45"
/replace="a"
/replace="c"
/db_xref="dbSNP:201220781"
variation 847
/gene="LRRC45"
/replace="g"
/replace="t"
/db_xref="dbSNP:138621912"
variation 867
/gene="LRRC45"
/replace="c"
/replace="g"
/db_xref="dbSNP:141253038"
variation 877
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:202169133"
variation 882
/gene="LRRC45"
/replace="a"
/replace="t"
/db_xref="dbSNP:372034528"
variation 883
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:143513889"
variation 885
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:117200853"
variation 897
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:72861735"
exon 902..1014
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 910
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:376916119"
variation 928
/gene="LRRC45"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:202017922"
variation 944
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:367923406"
variation 967
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:372389389"
variation 970
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:199547820"
variation 979
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:375847680"
variation 992
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:191536932"
exon 1015..1073
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 1020
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:371301942"
variation 1037
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:150139842"
variation 1047
/gene="LRRC45"
/replace="g"
/replace="t"
/db_xref="dbSNP:372860535"
variation 1049
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:375781595"
exon 1074..1151
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 1075
/gene="LRRC45"
/replace="g"
/replace="t"
/db_xref="dbSNP:369430248"
variation 1077
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:372810970"
variation 1080
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:138761482"
variation 1087
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:199704096"
variation 1104
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:181723391"
variation 1137
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:141814848"
exon 1152..1287
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 1167
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:200171991"
variation 1185
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:147028558"
variation 1227
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:78172878"
variation 1276
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:372185907"
variation 1284
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:377589998"
exon 1288..1365
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 1334
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:72861736"
exon 1366..1477
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 1366
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:140038062"
variation 1371
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:372453379"
variation 1374
/gene="LRRC45"
/replace="g"
/replace="t"
/db_xref="dbSNP:376967468"
variation 1382
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:201659216"
variation 1405
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:141938156"
variation 1409
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:200341016"
variation 1410
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:144753610"
variation 1431
/gene="LRRC45"
/replace="g"
/replace="t"
/db_xref="dbSNP:368338209"
variation 1434
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:148532776"
variation 1467
/gene="LRRC45"
/replace="a"
/replace="c"
/db_xref="dbSNP:370876125"
variation 1474
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:375556400"
exon 1478..1548
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 1499
/gene="LRRC45"
/replace="c"
/replace="g"
/db_xref="dbSNP:202210266"
variation 1527
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:114763314"
variation 1546
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:151078179"
exon 1549..1641
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 1554
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:75426455"
variation 1556
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:371710964"
variation 1565
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:374888203"
variation 1588
/gene="LRRC45"
/replace="g"
/replace="t"
/db_xref="dbSNP:369576962"
variation 1605
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:373025228"
variation 1620
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:376728810"
variation 1632
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:200279065"
exon 1642..1734
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 1664
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:373302486"
variation 1679
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:150638074"
variation 1715
/gene="LRRC45"
/replace="c"
/replace="g"
/db_xref="dbSNP:372010624"
variation 1721
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:144900467"
variation 1724
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:117249618"
exon 1735..1908
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 1742
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:199942624"
variation 1778
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:377433201"
variation 1788
/gene="LRRC45"
/replace="g"
/replace="t"
/db_xref="dbSNP:369942853"
variation 1797
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:372994313"
variation 1841
/gene="LRRC45"
/replace="a"
/replace="c"
/db_xref="dbSNP:112189312"
variation 1881
/gene="LRRC45"
/replace="c"
/replace="g"
/db_xref="dbSNP:376511672"
exon 1909..2056
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 1995
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:375643806"
variation 2018
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:201110968"
variation 2030
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:201677781"
exon 2057..2599
/gene="LRRC45"
/inference="alignment:Splign:1.39.8"
variation 2106
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:371038984"
variation 2139
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:373409333"
variation 2149
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:375643032"
variation 2184
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:367669168"
variation 2224
/gene="LRRC45"
/replace="c"
/replace="t"
/db_xref="dbSNP:112357165"
variation 2233
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:116028054"
variation 2297
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:368020301"
variation 2327
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:187487212"
variation 2369
/gene="LRRC45"
/replace="a"
/replace="g"
/db_xref="dbSNP:114642087"
ORIGIN
ctgcttcctgcacgggtggtccccaagcactgcgggaccccagcccaaagcggaccttgactaccgcccagccccgcgctcccaggacctcccgcccgcggagcccactcggattgctctccgcccgggtcggcggaggccccgtctcctgtacccggcgctgggactgctccgcaccgcgcggctccctttcagcagctgcgggagcatgcggaggaggccctgccggccccgcgggtcatggaggagttccggcgctcctacagccgcctgtgcagggagagtggggccgagccccaggaggctgtcctgcagcagctgcaccagcttcccaggggccggctggacctggccacgcaaagcctgacggtggagacctgcagggccctgggcaagctgctgccgagggagacgctgtgcacggagctggtcctgagtgactgcatgctcagcgaggaaggggccacactgctgctccgaggcctgtgtgccaacaccgtgctgcgctttctggacttaaagggcaacaaccttcgggctgcaggggccgaggctctgggaaaactcctccaacagaacaagtccattcagagcctcacgctggagtggaacagcctgggcacgtgggacgatgccttcgccaccttctgcgggggcctggcggccaacggcgccctgcagcggctggacctccgcaacaaccagatcagtcacaagggcgcggaggagctggccctagccctgaagggcaacaccaccctccagcagctggacctgcgctggaataacgttggcctcctggggggccgggccctcatgaactgtctccccagcaacagaaccctgtggagactggacctggctgggaacaacatccctggagacgtcctcagagccgtggagcaagccatgggccacagccaggaccggctcaccaccttccaggagaaccaagcccgcactcacgtcctcagcaaggaggtccagcacctccgggaggagaagtccaagcagttcctcgacttgatggagactattgataagcagcgagaagagatggccaagagcagcagggcgtcggcagcccgtgtagggcagcttcaggaagccctgaatgagaggcactccatcatcaacgctctcaaggccaagctgcagatgacagaggccgccctggctctgtcggagcagaaggcccaggacctgggggagctcctggccacagcggagcaggagcagctgagcctgtcacagaggcaggccaaggagctcaagctggagcagcaggaagctgcagagcgggagtctaaactcctcagagacttgtctgctgccaatgaaaagaacctgcttctgcaaaaccaggtagacgagttggagcggaagttcaggtgtcagcaggagcagctgttccagaccaggcaggagatgaccagcatgtcagctgagctgaagatgcgggccatccaggccgaggagcgcctggacatggagaagagaagatgcagacagagcctggaggactccgaaagcctgcgcatcaaggaggtggagcatatgacccgtcacctggaggagagtgagaaggccatgcaggagcgggtgcagaggctggaggcggcgcggctgtccctggaggaggagctgagccgagtgaaagcagcggcactcagcgagcgtggccaggctgaggaggagctgatcaaggccaagagccaggcccgcctggaggagcaacagcgcctggctcacctggaggacaagctgagactgctggcgcaggcacgggacgaggcgcagggcgcttgcctacagcagaagcaggtggtggccgaggcccagacccgggtcagccagctgggcctgcaagttgagggcctgcggcggcgcctggaagagctgcagcaggagctgagcctcaaggaccaggaaagggtggccgaggtgagcagggtgcgcgtggagctgcaggagcagaacggccggctgcaggcggagctggcggctcaggaggcgctgagggagaaggcggcggccctggagcgccagctgaaagtgatggcgagcgaccaccgagaggcgctgctggacagggagagcgagaacgcgtctctccgggagaagctgcggctccgggaggcggagatcgcccgcatccgggacgaggaggcccagagggcgagcttcctgcagaacgccgtcctggcttacgtgcaggcgtcccccgtgaggaccctgagccccccaaagtgagacaggccgggaggacccgggcgcagtaggagtgcatcaggcggcgcccgagatggaccaggggctgcgtcccgcccgcgccgcctctttgagacccgggtcgtctgttccacgcggcggttgcggcgactgttggtggtgtcgcggctgcgggggaaccccgtgggaggcgcctgggaagggctccctaccggccccttcttcccggtcgacgccacgtgggagcacaccgggaaggggtcccgcgggcgcgtctccccctcgccttttgcgatgtcaccgtgaacgctgcggccgcctgcgcgcggcggggtttggaaatacagcgcgtttgcactttgtgataaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:201255 -> Cellular component: GO:0005813 [centrosome] evidence: IDA
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@meso_cacase at
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