2024-03-29 11:39:14, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_021253 3354 bp mRNA linear PRI 07-JUL-2013 DEFINITION Homo sapiens tripartite motif containing 39 (TRIM39), transcript variant 1, mRNA. ACCESSION NM_021253 VERSION NM_021253.3 GI:215272322 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 3354) AUTHORS Zhang,L., Huang,N.J., Chen,C., Tang,W. and Kornbluth,S. TITLE Ubiquitylation of p53 by the APC/C inhibitor Trim39 JOURNAL Proc. Natl. Acad. Sci. U.S.A. 109 (51), 20931-20936 (2012) PUBMED 23213260 REMARK GeneRIF: analysis of ubiquitylation of p53 by the APC/C inhibitor Trim39 REFERENCE 2 (bases 1 to 3354) AUTHORS Zhang,L., Mei,Y., Fu,N.Y., Guan,L., Xie,W., Liu,H.H., Yu,C.D., Yin,Z., Yu,V.C. and You,H. TITLE TRIM39 regulates cell cycle progression and DNA damage responses via stabilizing p21 JOURNAL Proc. Natl. Acad. Sci. U.S.A. 109 (51), 20937-20942 (2012) PUBMED 23213251 REMARK GeneRIF: TRIM39 has a role in regulating cell cycle progression and the balance between cytostasis and apoptosis after DNA damage via stabilizing p21 Erratum:[Proc Natl Acad Sci U S A. 2013 Mar 5;110(10):4148] REFERENCE 3 (bases 1 to 3354) AUTHORS Kurata,R., Nakaoka,H., Tajima,A., Hosomichi,K., Shiina,T., Meguro,A., Mizuki,N., Ohono,S., Inoue,I. and Inoko,H. TITLE TRIM39 and RNF39 are associated with Behcet's disease independently of HLA-B *51 and -A *26 JOURNAL Biochem. Biophys. Res. Commun. 401 (4), 533-537 (2010) PUBMED 20875797 REMARK GeneRIF: these findings suggest that RNF39 and TRIM39 are involved in the etiology of Behcet's disease. REFERENCE 4 (bases 1 to 3354) AUTHORS Barcellos,L.F., May,S.L., Ramsay,P.P., Quach,H.L., Lane,J.A., Nititham,J., Noble,J.A., Taylor,K.E., Quach,D.L., Chung,S.A., Kelly,J.A., Moser,K.L., Behrens,T.W., Seldin,M.F., Thomson,G., Harley,J.B., Gaffney,P.M. and Criswell,L.A. TITLE High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions JOURNAL PLoS Genet. 5 (10), E1000696 (2009) PUBMED 19851445 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 5 (bases 1 to 3354) AUTHORS Lee,S.S., Fu,N.Y., Sukumaran,S.K., Wan,K.F., Wan,Q. and Yu,V.C. TITLE TRIM39 is a MOAP-1-binding protein that stabilizes MOAP-1 through inhibition of its poly-ubiquitination process JOURNAL Exp. Cell Res. 315 (7), 1313-1325 (2009) PUBMED 19100260 REMARK GeneRIF: Data suggest that TRIM39 can promote apoptosis signalling through stabilization of MOAP-1. REFERENCE 6 (bases 1 to 3354) AUTHORS Roberts,J.D. Jr., Chiche,J.D., Kolpa,E.M., Bloch,D.B. and Bloch,K.D. TITLE cGMP-dependent protein kinase I interacts with TRIM39R, a novel Rpp21 domain-containing TRIM protein JOURNAL Am. J. Physiol. Lung Cell Mol. Physiol. 293 (4), L903-L912 (2007) PUBMED 17601797 REFERENCE 7 (bases 1 to 3354) AUTHORS Wu,C., Ma,M.H., Brown,K.R., Geisler,M., Li,L., Tzeng,E., Jia,C.Y., Jurisica,I. and Li,S.S. TITLE Systematic identification of SH3 domain-mediated human protein-protein interactions by peptide array target screening JOURNAL Proteomics 7 (11), 1775-1785 (2007) PUBMED 17474147 REFERENCE 8 (bases 1 to 3354) AUTHORS Tao,W.A., Wollscheid,B., O'Brien,R., Eng,J.K., Li,X.J., Bodenmiller,B., Watts,J.D., Hood,L. and Aebersold,R. TITLE Quantitative phosphoproteome analysis using a dendrimer conjugation chemistry and tandem mass spectrometry JOURNAL Nat. Methods 2 (8), 591-598 (2005) PUBMED 16094384 REFERENCE 9 (bases 1 to 3354) AUTHORS Reymond,A., Meroni,G., Fantozzi,A., Merla,G., Cairo,S., Luzi,L., Riganelli,D., Zanaria,E., Messali,S., Cainarca,S., Guffanti,A., Minucci,S., Pelicci,P.G. and Ballabio,A. TITLE The tripartite motif family identifies cell compartments JOURNAL EMBO J. 20 (9), 2140-2151 (2001) PUBMED 11331580 REFERENCE 10 (bases 1 to 3354) AUTHORS Orimo,A., Yamagishi,T., Tominaga,N., Yamauchi,Y., Hishinuma,T., Okada,K., Suzuki,M., Sato,M., Nogi,Y., Suzuki,H., Inoue,S., Yoshimura,K., Shimizu,Y. and Muramatsu,M. TITLE Molecular cloning of testis-abundant finger Protein/Ring finger protein 23 (RNF23), a novel RING-B box-coiled coil-B30.2 protein on the class I region of the human MHC JOURNAL Biochem. Biophys. Res. Commun. 276 (1), 45-51 (2000) PUBMED 11006080 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AI159923.1, AK292512.1, AL662795.5 and BC034985.1. On Nov 27, 2008 this sequence version replaced gi:25777695. Summary: The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The function of this protein has not been identified. This gene lies within the major histocompatibility complex class I region on chromosome 6. Alternate splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]. Transcript Variant: This variant (1) encodes the longer isoform (1) of this protein. ##Evidence-Data-START## Transcript exon combination :: AK292512.1 [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 1-83 AI159923.1 1-83 84-2080 AK292512.1 1-1997 2081-2772 AL662795.5 75824-76515 2773-3354 BC034985.1 2970-3551 FEATURES Location/Qualifiers source 1..3354 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="6" /map="6p21.3" gene 1..3354 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /note="tripartite motif containing 39" /db_xref="GeneID:56658" /db_xref="HGNC:10065" /db_xref="HPRD:09298" /db_xref="MIM:605700" exon 1..152 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /inference="alignment:Splign:1.39.8" exon 153..305 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /inference="alignment:Splign:1.39.8" variation 168 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:5030609" variation 176 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:191524798" variation 190..192 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="" /replace="gga" /db_xref="dbSNP:5030610" variation 224 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="g" /replace="t" /db_xref="dbSNP:376835401" variation 291 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:181517611" exon 306..765 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /inference="alignment:Splign:1.39.8" misc_feature 307..309 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /note="upstream in-frame stop codon" CDS 313..1869 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /note="isoform 1 is encoded by transcript variant 1; ring finger protein 23; tripartite motif-containing 39; testis-abundant finger protein; tripartite motif-containing protein 39; E3 ubiquitin-protein ligase TRIM39" /codon_start=1 /product="E3 ubiquitin-protein ligase TRIM39 isoform 1" /protein_id="NP_067076.2" /db_xref="GI:25777696" /db_xref="CCDS:CCDS34377.1" /db_xref="GeneID:56658" /db_xref="HGNC:10065" /db_xref="HPRD:09298" /db_xref="MIM:605700" /translation="
MAETSLLEAGASAASTAAALENLQVEASCSVCLEYLKEPVIIECGHNFCKACITRWWEDLERDFPCPVCRKTSRYRSLRPNRQLGSMVEIAKQLQAVKRKIRDESLCPQHHEALSLFCYEDQEAVCLICAISHTHRAHTVVPLDDATQEYKEKLQKCLEPLEQKLQEITRCKSSEEKKPGELKRLVESRRQQILREFEELHRRLDEEQQVLLSRLEEEEQDILQRLRENAAHLGDKRRDLAHLAAEVEGKCLQSGFEMLKDVKSTLEKNIPRKFGGSLSTICPRDHKALLGLVKEINRCEKVKTMEVTSVSIELEKNFSNFPRQYFALRKILKQLIADVTLDPETAHPNLVLSEDRKSVKFVETRLRDLPDTPRRFTFYPCVLATEGFTSGRHYWEVEVGDKTHWAVGVCRDSVSRKGELTPLPETGYWRVRLWNGDKYAATTTPFTPLHIKVKPKRVGIFLDYEAGTLSFYNVTDRSHIYTFTDTFTEKLWPLFYPGIRAGRKNAAPLTIRPPTDWE
" misc_feature 394..528 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /note="RING-finger (Really Interesting New Gene) domain, a specialized type of Zn-finger of 40 to 60 residues that binds two atoms of zinc; defined by the 'cross-brace' motif C-X2-C-X(9-39)-C-X(1-3)- H-X(2-3)-(N/C/H)-X2-C-X(4-48)C-X2-C; probably involved in...; Region: RING; cd00162" /db_xref="CDD:29102" misc_feature 394..525 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /note="Zinc finger, C3HC4 type (RING finger); Region: zf-C3HC4_2; pfam13923" /db_xref="CDD:206094" misc_feature order(397..399,406..408,442..444,448..450,457..459, 466..468,508..510,517..519) /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /note="cross-brace motif; other site" /db_xref="CDD:29102" misc_feature 628..741 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /note="B-Box-type zinc finger; zinc binding domain (CHC3H2); often present in combination with other motifs, like RING zinc finger, NHL motif, coiled-coil or RFP domain in functionally unrelated proteins, most likely mediating protein-protein interaction; Region: BBOX; cd00021" /db_xref="CDD:28905" misc_feature order(631..633,640..642,697..699,715..717) /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /note="Zn2+ binding site [ion binding]; other site" /db_xref="CDD:28905" misc_feature 739..>1110 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /note="ATP synthase B/B' CF(0); Region: ATP-synt_B; cl07975" /db_xref="CDD:212286" misc_feature 1327..1476 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /note="SPRY-associated domain; Region: PRY; pfam13765" /db_xref="CDD:205938" misc_feature 1480..1806 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /note="Domain in SPla and the RYanodine Receptor; Region: SPRY; smart00449" /db_xref="CDD:128725" misc_feature 1627..1629 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" /citation=[8] variation 343 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="g" /db_xref="dbSNP:79621337" variation 344 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="g" /db_xref="dbSNP:138653548" variation 492 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:202059196" variation 557 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:372556521" variation 723 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:1264581" variation 730 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:376721046" variation 747 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:2057727" exon 766..861 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /inference="alignment:Splign:1.39.8" variation 821 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:377759954" variation 829 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="g" /replace="t" /db_xref="dbSNP:202142956" variation 833 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:139957931" exon 862..1092 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /inference="alignment:Splign:1.39.8" variation 893 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:145694007" variation 955 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:374179491" variation 1006 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="g" /db_xref="dbSNP:192411663" variation 1030 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:56405317" variation 1054 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:71561373" exon 1093..1115 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /inference="alignment:Splign:1.39.8" exon 1116..1205 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /inference="alignment:Splign:1.39.8" variation 1117 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="c" /db_xref="dbSNP:144233854" variation 1162 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:148705441" exon 1206..1321 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /inference="alignment:Splign:1.39.8" variation 1250 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:61758102" variation 1271 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:151317560" exon 1322..3339 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /inference="alignment:Splign:1.39.8" variation 1341 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:2074474" variation 1363 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="g" /replace="t" /db_xref="dbSNP:115963942" variation 1379 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:199883161" variation 1415 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:146617150" variation 1512 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:201329517" variation 1521 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:182918258" variation 1536 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="t" /db_xref="dbSNP:375516133" variation 1600..1601 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="" /replace="g" /db_xref="dbSNP:138936035" variation 1701 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:368672697" variation 1710 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:140287492" variation 1722 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:368377696" variation 1843 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:200960278" variation 1900 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:375720811" variation 1910 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:367910271" variation 1917 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:6920005" variation 1930 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:116158209" variation 1952 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:186782220" variation 2048..2049 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="" /replace="c" /db_xref="dbSNP:35439125" variation 2127 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:111893696" variation 2288 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:139500656" variation 2296 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:191371462" variation 2333 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:2240058" variation 2386 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:375963757" variation 2413 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:28752116" variation 2460 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="g" /db_xref="dbSNP:143299125" variation 2483 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:183237486" variation 2533 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:187712859" variation 2540 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:146720860" variation 2637..2638 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="" /replace="ct" /db_xref="dbSNP:373545549" variation 2678 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="t" /db_xref="dbSNP:140362243" variation 2765 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="c" /db_xref="dbSNP:115017778" variation 2925 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="g" /db_xref="dbSNP:375533569" variation 3098 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:12100" variation 3315 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="c" /replace="t" /db_xref="dbSNP:145555817" variation 3330 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" /replace="a" /replace="c" /db_xref="dbSNP:1130057" polyA_site 3339 /gene="TRIM39" /gene_synonym="RNF23; TFP; TRIM39B" ORIGIN
cccagcttccactgacacgagcctcggcgcggcttccgcttccggcgagtattgtgtgtcgcgccgcggggcgggggcgaggggaggaggaaggagggaggcagcgctccggcggctccgcgccccgcactcccggacccgaagccgggaagattcctttcttgtctgttagaaacgtatgtcaaacgaggatacagtgtctggaactattggttctaagatataagtggaatgagcctggatcaggagaagtatgctgagctagagttgaaggaagcttctctttctaacaagagaaagcagagttaaattatggcagagacaagtctgttagaggctggggcctctgcagcctctacagctgcggctttggagaacttacaggtggaggcgagctgctctgtgtgcctggagtatctgaaggaacctgtcatcattgagtgtgggcacaacttctgcaaagcttgcatcacccgctggtgggaggacctagagagggacttcccttgtcctgtctgtcgaaagacatcccgctaccgcagtctccgacctaatcggcaactaggcagtatggtggaaattgccaagcagctccaggccgtcaagcggaagatccgggatgagagcctctgcccccaacaccatgaggccctcagccttttctgttatgaggaccaggaggctgtatgcttgatatgtgcaatttcccacacccaccgggcccacaccgttgtgccactggacgatgctacacaggagtacaaggaaaaactgcagaagtgtctggagcccctggaacagaagctgcaggagatcactcgctgcaagtcctctgaggagaagaagcctggtgagctcaagagactagtggaaagtcgccgacagcagatcttgagggagtttgaagagcttcataggcggctggatgaagagcagcaggtgttgctttcacgactggaagaagaggaacaggacattctgcagcgactccgagaaaatgctgctcaccttggggacaagcgccgggacctggcccacttggctgccgaggtggagggcaagtgcttacagtcaggcttcgagatgcttaaggatgtcaaaagtaccctggaaaagaatattcctagaaagttcggaggctcactctcaacgatctgtccacgggatcataaggctctccttggattagtaaaagaaatcaacagatgtgaaaaggtgaagaccatggaggtgacttcagtatccatagagctggaaaagaacttcagcaattttccccgacagtactttgccctaaggaaaatccttaaacagctaattgcggatgtgaccctggaccctgagacagctcatcctaacctagtcctgtcagaggatcgtaagagcgtcaagttcgtggagacaagactccgggatctccctgacacaccaaggcgtttcaccttctacccttgcgtcctggctactgagggtttcacctcaggtcgacactactgggaggtggaggtgggcgacaagacccactgggcagtgggtgtatgccgggactccgtgagccgaaagggcgagttgactccactccctgagactggctactggcgggtgcggctatggaatggggacaaatatgcagccaccaccacaccttttacccctttgcacatcaaggtgaaacccaagcgggtaggcatattcctagactatgaggccggcacactgtctttctacaatgtcacagaccgctctcatatctacaccttcactgatacttttactgagaaactttggcccctcttctacccaggcatccgggctggacggaagaatgctgcaccacttaccatcaggcccccaacagattgggagtgacaggttgggatgtgggaatgactggggtgaggcagggtcaagtgctacgggcctccttcccgtgtcctgctggaacgtcttcgtgtccacctgggtccagtcctgaatcatcttggagaaacaccttggtttctaggatggttttgtgtggagggggaggtaggactgggctggatgagagagcacagctgtgacttcctcctaactgtcagggtggggagctggttcccagaggattgtctaccctgaagtccatcaggttttctgttgcacaaggacgggtcaggaaggaaggagaggcttttccagaaacaaaaaatctgtgagggtctgacttgctcaaaccagaggaggaaacagaaacccctgcacatctttttagggggttctttgacccaggatagtcttgcttcttgaggtagatcacaggggtctgtgtacctctgaattcatgagagatgaatgacagatgctctcatgggtctagatattgaggagtttttctgagggcagagattggacatcaacaaggctagaagggtcagggaagtgggctaaaggaacagattcctagagattaatgaagaggagggaggtttctttggtcttctattccaagggtaaggttgcgattatgggtaagattggccagaggtaggaatgtggggagaaggagaggctgaaaagaaagcagaggagaacccaggtccctgcctcagccttcagcagagttggcttattgcctgcctctataccaataagtcagtcaccttgctcctctccagaggcaaagtggaagagatcctgcaagacacatctatcctttcacagtgttcccaagggaacttggaaaggagagtcaggtattagaggaaagagaagggtatttgtatacaaagccctggccttaaagaatgttacttagtagctactcccaaattgtcagccttcttacctggccaaggtgtccaagccagaaaggaaaaaaggttatggagtctttctcaccctaaggacagggtggaagagggtggtatatagggaagggccagataggcaacttcatttggcttgtgtgcatctggcctggaactggtgttaagccaggcttttgcttgtttgttgccatccctcaccctttgccatttcccttttcagagaatgtaaatgattttcatgttaggccaaaataaacaacttatagggtacatatgttgtcataaaaggtaaaagtgatgcatgccaaaccaaactaaaccaatttggattatctgctattcgggtaatcttcacagaaatgactgagagaagaatctgcagtttactgagggcatttcagttcctcctaccacctcaacaggactttgtccagactctcctcctcttacctttgtgccttgactgtggttctttgtggcaagatactttggttggttaaaataatatggaacaaaggatccactgaagtgaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:56658 -> Molecular function: GO:0003674 [molecular_function] evidence: ND GeneID:56658 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:56658 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA GeneID:56658 -> Molecular function: GO:0016874 [ligase activity] evidence: IEA GeneID:56658 -> Molecular function: GO:0042802 [identical protein binding] evidence: IPI GeneID:56658 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA GeneID:56658 -> Biological process: GO:0008150 [biological_process] evidence: ND GeneID:56658 -> Biological process: GO:0016567 [protein ubiquitination] evidence: IEA GeneID:56658 -> Cellular component: GO:0005575 [cellular_component] evidence: ND GeneID:56658 -> Cellular component: GO:0005739 [mitochondrion] evidence: IEA GeneID:56658 -> Cellular component: GO:0005829 [cytosol] evidence: IEA
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