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2024-04-20 12:02:57, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_080745 1434 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens tripartite motif containing 69 (TRIM69), transcript
variant b, mRNA.
ACCESSION NM_080745
VERSION NM_080745.3 GI:88999602
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 1434)
AUTHORS Han,Y., Li,R., Gao,J., Miao,S. and Wang,L.
TITLE Characterisation of human RING finger protein TRIM69, a novel
testis E3 ubiquitin ligase and its subcellular localisation
JOURNAL Biochem. Biophys. Res. Commun. 429 (1-2), 6-11 (2012)
PUBMED 23131556
REMARK GeneRIF: hTRIM69 is a novel E3 ubiquitin ligase identified from
human testis and may function to ubiquitinate its particular
substrates during spermatogenesis.
REFERENCE 2 (bases 1 to 1434)
AUTHORS Shimada,M., Miyagawa,T., Kawashima,M., Tanaka,S., Honda,Y.,
Honda,M. and Tokunaga,K.
TITLE An approach based on a genome-wide association study reveals
candidate loci for narcolepsy
JOURNAL Hum. Genet. 128 (4), 433-441 (2010)
PUBMED 20677014
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 3 (bases 1 to 1434)
AUTHORS Shyu,H.W., Hsu,S.H., Hsieh-Li,H.M. and Li,H.
TITLE Forced expression of RNF36 induces cell apoptosis
JOURNAL Exp. Cell Res. 287 (2), 301-313 (2003)
PUBMED 12837286
REFERENCE 4 (bases 1 to 1434)
AUTHORS Shyu,H.W., Hsu,S.H., Hsieh-Li,H.M. and Li,H.
TITLE A novel member of the RBCC family, Trif, expressed specifically in
the spermatids of mouse testis
JOURNAL Mech. Dev. 108 (1-2), 213-216 (2001)
PUBMED 11578878
REMARK GeneRIF: Gene and protein analysis of the mouse counterpart.
REFERENCE 5 (bases 1 to 1434)
AUTHORS Venter,J.C., Adams,M.D., Myers,E.W., Li,P.W., Mural,R.J.,
Sutton,G.G., Smith,H.O., Yandell,M., Evans,C.A., Holt,R.A.,
Gocayne,J.D., Amanatides,P., Ballew,R.M., Huson,D.H., Wortman,J.R.,
Zhang,Q., Kodira,C.D., Zheng,X.H., Chen,L., Skupski,M.,
Subramanian,G., Thomas,P.D., Zhang,J., Gabor Miklos,G.L.,
Nelson,C., Broder,S., Clark,A.G., Nadeau,J., McKusick,V.A.,
Zinder,N., Levine,A.J., Roberts,R.J., Simon,M., Slayman,C.,
Hunkapiller,M., Bolanos,R., Delcher,A., Dew,I., Fasulo,D.,
Flanigan,M., Florea,L., Halpern,A., Hannenhalli,S., Kravitz,S.,
Levy,S., Mobarry,C., Reinert,K., Remington,K., Abu-Threideh,J.,
Beasley,E., Biddick,K., Bonazzi,V., Brandon,R., Cargill,M.,
Chandramouliswaran,I., Charlab,R., Chaturvedi,K., Deng,Z., Di
Francesco,V., Dunn,P., Eilbeck,K., Evangelista,C., Gabrielian,A.E.,
Gan,W., Ge,W., Gong,F., Gu,Z., Guan,P., Heiman,T.J., Higgins,M.E.,
Ji,R.R., Ke,Z., Ketchum,K.A., Lai,Z., Lei,Y., Li,Z., Li,J.,
Liang,Y., Lin,X., Lu,F., Merkulov,G.V., Milshina,N., Moore,H.M.,
Naik,A.K., Narayan,V.A., Neelam,B., Nusskern,D., Rusch,D.B.,
Salzberg,S., Shao,W., Shue,B., Sun,J., Wang,Z., Wang,A., Wang,X.,
Wang,J., Wei,M., Wides,R., Xiao,C., Yan,C., Yao,A., Ye,J., Zhan,M.,
Zhang,W., Zhang,H., Zhao,Q., Zheng,L., Zhong,F., Zhong,W., Zhu,S.,
Zhao,S., Gilbert,D., Baumhueter,S., Spier,G., Carter,C.,
Cravchik,A., Woodage,T., Ali,F., An,H., Awe,A., Baldwin,D.,
Baden,H., Barnstead,M., Barrow,I., Beeson,K., Busam,D., Carver,A.,
Center,A., Cheng,M.L., Curry,L., Danaher,S., Davenport,L.,
Desilets,R., Dietz,S., Dodson,K., Doup,L., Ferriera,S., Garg,N.,
Gluecksmann,A., Hart,B., Haynes,J., Haynes,C., Heiner,C.,
Hladun,S., Hostin,D., Houck,J., Howland,T., Ibegwam,C., Johnson,J.,
Kalush,F., Kline,L., Koduru,S., Love,A., Mann,F., May,D.,
McCawley,S., McIntosh,T., McMullen,I., Moy,M., Moy,L., Murphy,B.,
Nelson,K., Pfannkoch,C., Pratts,E., Puri,V., Qureshi,H.,
Reardon,M., Rodriguez,R., Rogers,Y.H., Romblad,D., Ruhfel,B.,
Scott,R., Sitter,C., Smallwood,M., Stewart,E., Strong,R., Suh,E.,
Thomas,R., Tint,N.N., Tse,S., Vech,C., Wang,G., Wetter,J.,
Williams,S., Williams,M., Windsor,S., Winn-Deen,E., Wolfe,K.,
Zaveri,J., Zaveri,K., Abril,J.F., Guigo,R., Campbell,M.J.,
Sjolander,K.V., Karlak,B., Kejariwal,A., Mi,H., Lazareva,B.,
Hatton,T., Narechania,A., Diemer,K., Muruganujan,A., Guo,N.,
Sato,S., Bafna,V., Istrail,S., Lippert,R., Schwartz,R., Walenz,B.,
Yooseph,S., Allen,D., Basu,A., Baxendale,J., Blick,L., Caminha,M.,
Carnes-Stine,J., Caulk,P., Chiang,Y.H., Coyne,M., Dahlke,C.,
Mays,A., Dombroski,M., Donnelly,M., Ely,D., Esparham,S., Fosler,C.,
Gire,H., Glanowski,S., Glasser,K., Glodek,A., Gorokhov,M.,
Graham,K., Gropman,B., Harris,M., Heil,J., Henderson,S., Hoover,J.,
Jennings,D., Jordan,C., Jordan,J., Kasha,J., Kagan,L., Kraft,C.,
Levitsky,A., Lewis,M., Liu,X., Lopez,J., Ma,D., Majoros,W.,
McDaniel,J., Murphy,S., Newman,M., Nguyen,T., Nguyen,N., Nodell,M.,
Pan,S., Peck,J., Peterson,M., Rowe,W., Sanders,R., Scott,J.,
Simpson,M., Smith,T., Sprague,A., Stockwell,T., Turner,R.,
Venter,E., Wang,M., Wen,M., Wu,D., Wu,M., Xia,A., Zandieh,A. and
Zhu,X.
TITLE The sequence of the human genome
JOURNAL Science 291 (5507), 1304-1351 (2001)
PUBMED 11181995
REMARK Erratum:[Science 2001 Jun 5;292(5523):1838]
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DQ232883.1, BC033314.1 and
BC047945.1.
On Feb 28, 2006 this sequence version replaced gi:37595540.
Summary: This gene encodes a member of the RING-B-box-coiled-coil
(RBCC) family and encodes a protein with an N-terminal RING finger
motif, a PRY domain and a C-terminal SPRY domain. The mouse
ortholog of this gene is specifically expressed in germ cells at
the round spermatid stages during spermatogenesis and, when
overexpressed, induces apoptosis. Alternatively spliced transcript
variants encoding distinct isoforms have been described. [provided
by RefSeq, Jul 2008].
Transcript Variant: This variant (b) lacks an alternate in-frame
exon compared to variant a, resulting in a shorter protein (isoform
b) compared to isoform a.
##Evidence-Data-START##
Transcript exon combination :: BC033314.1, BI828755.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025088 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-204 DQ232883.1 519-722
205-1412 BC033314.1 1-1208
1413-1422 DQ232883.1 2408-2417
1423-1434 BC047945.1 1737-1748
FEATURES Location/Qualifiers
source 1..1434
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="15"
/map="15q21.1"
gene 1..1434
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/note="tripartite motif containing 69"
/db_xref="GeneID:140691"
/db_xref="HGNC:17857"
/db_xref="HPRD:11518"
exon 1..349
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/inference="alignment:Splign:1.39.8"
variation 28
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:3759878"
variation 104
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:145414003"
variation 151
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:2470908"
variation 192
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:183738672"
variation 288
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="g"
/replace="t"
/db_xref="dbSNP:370306802"
variation 310
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:202247291"
variation 333
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="g"
/db_xref="dbSNP:200431204"
misc_feature 335..337
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/note="upstream in-frame stop codon"
CDS 344..1369
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/note="isoform b is encoded by transcript variant b;
tripartite motif-containing 69; ring finger protein 36;
tripartite motif-containing protein 69; tripartite motif
protein 69; trimless; RFP-like domain-containing protein
trimless; E3 ubiquitin-protein ligase TRIM69"
/codon_start=1
/product="E3 ubiquitin-protein ligase TRIM69 isoform b"
/protein_id="NP_542783.2"
/db_xref="GI:37595541"
/db_xref="CCDS:CCDS10114.1"
/db_xref="GeneID:140691"
/db_xref="HGNC:17857"
/db_xref="HPRD:11518"
/translation="
MEEELAIQQGQLETTLKELQTLRNMQKEAIAAHKENKLHLQQHVSMEFLKLHQFLHSKEKDILTELREEGKALNEEMELNLSQLQEQCLLAKDMLVSIQAKTEQQNSFDFLKDITTLLHSLEQGMKVLATRELISRKLNLGQYKGPIQYMVWREMQDTLCPGLSPLTLDPKTAHPNLVLSKSQTSVWHGDIKKIMPDDPERFDSSVAVLGSRGFTSGKWYWEVEVAKKTKWTVGVVRESIIRKGSCPLTPEQGFWLLRLRNQTDLKALDLPSFSLTLTNNLDKVGIYLDYEGGQLSFYNAKTMTHIYTFSNTFMEKLYPYFCPCLNDGGENKEPLHILHPQ
"
misc_feature 839..985
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/note="SPRY-associated domain; Region: PRY; pfam13765"
/db_xref="CDD:205938"
misc_feature 989..1312
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/note="Domain in SPla and the RYanodine Receptor; Region:
SPRY; smart00449"
/db_xref="CDD:128725"
variation 344
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:368779908"
exon 350..445
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/inference="alignment:Splign:1.39.8"
variation 351
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:139002192"
variation 356
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="c"
/db_xref="dbSNP:370609382"
variation 370
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="g"
/replace="t"
/db_xref="dbSNP:199697343"
variation 398
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:143209412"
variation 399
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:374508692"
variation 435
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:3759880"
variation 445
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:370797653"
exon 446..679
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/inference="alignment:Splign:1.39.8"
variation 493
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:148227833"
variation 501
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="c"
/db_xref="dbSNP:201306104"
variation 512
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="t"
/db_xref="dbSNP:180922299"
variation 583
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="t"
/db_xref="dbSNP:77414494"
variation 605
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:150729472"
variation 619
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="g"
/replace="t"
/db_xref="dbSNP:372211170"
variation 622
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:138709979"
variation 630
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:375180289"
variation 648
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:139044725"
variation 649
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:148920822"
variation 653
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="c"
/db_xref="dbSNP:201956627"
variation 654
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:143370252"
variation 667
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:147224384"
variation 671
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:201939428"
exon 680..702
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/inference="alignment:Splign:1.39.8"
exon 703..827
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/inference="alignment:Splign:1.39.8"
variation 718
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:202105411"
variation 733
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:140573976"
variation 769
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="g"
/db_xref="dbSNP:144447354"
variation 809
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="c"
/db_xref="dbSNP:145552604"
variation 810
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:201133089"
exon 828..1424
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/inference="alignment:Splign:1.39.8"
variation 839
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:112367336"
variation 854
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:374559258"
variation 878
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:375866898"
variation 913
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:367675407"
variation 919
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:71478342"
variation 922
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:142877382"
variation 938
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:372919928"
variation 978
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:202081848"
variation 987
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:151051317"
variation 1004
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:144953961"
variation 1046
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:375788351"
variation 1061
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="t"
/db_xref="dbSNP:114770697"
variation 1067
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:201166045"
variation 1085
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="g"
/db_xref="dbSNP:371213061"
variation 1144
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:369632375"
variation 1182
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:375025513"
variation 1188
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:140705646"
variation 1189
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:145844765"
variation 1205
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:113204970"
variation 1213
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:115326573"
variation 1223
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:200649837"
variation 1252
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:149919213"
variation 1270
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="c"
/db_xref="dbSNP:201411863"
variation 1291
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="g"
/db_xref="dbSNP:377079867"
variation 1343
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:367855776"
variation 1377
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="c"
/replace="t"
/db_xref="dbSNP:371429122"
variation 1379
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="c"
/db_xref="dbSNP:376529781"
polyA_signal 1402..1407
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
variation 1413
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
/replace="a"
/replace="t"
/db_xref="dbSNP:3100143"
polyA_site 1424
/gene="TRIM69"
/gene_synonym="HSD34; RNF36; Trif"
ORIGIN
ggggagctatgaaccttaagattagaccactaactcgaatctaaatgagctgcccttgtctcctacaaaagaaaagttgggcaggtagggtattctaatgagggtttctctttctcttaagcaaatgatgatcaaagttaactgacaaactgtcacggaatctgccagacctcactctggccttgctgcttctctccagctcctgaacttttctttcttccatcatgctctgagcccattccttgaaaactaaaaggtccctgactcccagtctgcagccatcctgggcctgctgagctctgattcaagtgcctgcctctgccccttggtgggctgaagcttcatggaggaggagcttgccatccaacagggtcaactggagacaactctgaaggagcttcagaccctgaggaacatgcagaaggaagctattgctgctcacaaggaaaacaagctacatctgcagcaacatgtgtccatggagtttctaaagctgcatcagttcctgcacagcaaagaaaaggacattttaactgagctccgggaagaggggaaagccttgaatgaggagatggagttgaatctgagccagcttcaggagcaatgtctcttagccaaggatatgttggtgagcattcaggcaaagacggaacaacagaactccttcgactttctcaaagacatcacaactctcttacatagcttggagcaaggaatgaaggtgctggcaaccagagagcttatttccagaaagctgaacctgggccagtacaaaggtcctatccagtacatggtatggagggaaatgcaggacactctctgcccaggcctgtctccactaactctggaccctaaaacagctcacccaaatctggtgctctccaaaagccaaaccagcgtctggcatggtgacattaagaagataatgcctgatgatcctgagaggtttgactcaagtgtggctgtactgggctcaagaggcttcacctctggaaagtggtactgggaagtagaagtagcaaagaagacaaaatggacagttggagttgtcagagaatccatcattcggaagggcagctgtcctctaactcctgagcaaggattctggcttttaagactaaggaaccaaactgatctaaaggctctggatttgccttctttcagtctgacactgactaacaacctcgacaaggtgggcatatacctggattatgaaggaggacagttgtccttctacaatgctaaaaccatgactcacatttacaccttcagtaacactttcatggagaaactttatccctacttctgcccctgccttaatgatggtggagagaataaagaaccattgcacatcttacatccacagtaatgagtcataatattatacaaattcagagtgttattaaagaggtattgaaatatttaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:140691 -> Molecular function: GO:0004842 [ubiquitin-protein ligase activity] evidence: IDA
GeneID:140691 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA
GeneID:140691 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA
GeneID:140691 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:140691 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
GeneID:140691 -> Cellular component: GO:0016607 [nuclear speck] evidence: IDA
by
@meso_cacase at
DBCLS
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