2024-04-27 11:33:41, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_181777 2678 bp mRNA linear PRI 22-JUN-2013 DEFINITION Homo sapiens ubiquitin-conjugating enzyme E2A (UBE2A), transcript variant 3, mRNA. ACCESSION NM_181777 VERSION NM_181777.1 GI:32967277 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 2678) AUTHORS Jahanshad,N., Rajagopalan,P., Hua,X., Hibar,D.P., Nir,T.M., Toga,A.W., Jack,C.R. Jr., Saykin,A.J., Green,R.C., Weiner,M.W., Medland,S.E., Montgomery,G.W., Hansell,N.K., McMahon,K.L., de Zubicaray,G.I., Martin,N.G., Wright,M.J. and Thompson,P.M. CONSRTM Alzheimer's Disease Neuroimaging Initiative TITLE Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity JOURNAL Proc. Natl. Acad. Sci. U.S.A. 110 (12), 4768-4773 (2013) PUBMED 23471985 REFERENCE 2 (bases 1 to 2678) AUTHORS Shchebet,A., Karpiuk,O., Kremmer,E., Eick,D. and Johnsen,S.A. TITLE Phosphorylation by cyclin-dependent kinase-9 controls ubiquitin-conjugating enzyme-2A function JOURNAL Cell Cycle 11 (11), 2122-2127 (2012) PUBMED 22592529 REMARK GeneRIF: UBE2A specifically interacts with CDK9, but not CDK2 and is phosphorylated by CDK9 in vitro. REFERENCE 3 (bases 1 to 2678) AUTHORS Chen,S., Wang,D.L., Liu,Y., Zhao,L. and Sun,F.L. TITLE RAD6 regulates the dosage of p53 by a combination of transcriptional and posttranscriptional mechanisms JOURNAL Mol. Cell. Biol. 32 (2), 576-587 (2012) PUBMED 22083959 REMARK GeneRIF: RAD6 can form a ternary complex with MDM2 and p53 that contributes to the degradation of p53. REFERENCE 4 (bases 1 to 2678) AUTHORS de Leeuw,N., Bulk,S., Green,A., Jaeckle-Santos,L., Baker,L.A., Zinn,A.R., Kleefstra,T., van der Smagt,J.J., Vianne Morgante,A.M., de Vries,B.B., van Bokhoven,H. and de Brouwer,A.P. TITLE UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients JOURNAL Am. J. Med. Genet. A 152A (12), 3084-3090 (2010) PUBMED 21108393 REMARK GeneRIF: UBE2A deficiency syndrome is reported in two male patients. REFERENCE 5 (bases 1 to 2678) AUTHORS Park,H.K., Wang,H., Zhang,J., Datta,S. and Fei,P. TITLE Convergence of Rad6/Rad18 and Fanconi anemia tumor suppressor pathways upon DNA damage JOURNAL PLoS ONE 5 (10), E13313 (2010) PUBMED 20967207 REMARK GeneRIF: showed that the function of FA signaling pathway is at least partly mediated through coupling with hRad6/hRad18 signaling (HHR6 pathway) Publication Status: Online-Only REFERENCE 6 (bases 1 to 2678) AUTHORS Xin,H., Lin,W., Sumanasekera,W., Zhang,Y., Wu,X. and Wang,Z. TITLE The human RAD18 gene product interacts with HHR6A and HHR6B JOURNAL Nucleic Acids Res. 28 (14), 2847-2854 (2000) PUBMED 10908344 REFERENCE 7 (bases 1 to 2678) AUTHORS Tateishi,S., Sakuraba,Y., Masuyama,S., Inoue,H. and Yamaizumi,M. TITLE Dysfunction of human Rad18 results in defective postreplication repair and hypersensitivity to multiple mutagens JOURNAL Proc. Natl. Acad. Sci. U.S.A. 97 (14), 7927-7932 (2000) PUBMED 10884424 REFERENCE 8 (bases 1 to 2678) AUTHORS Kato,S., Sekine,S., Oh,S.W., Kim,N.S., Umezawa,Y., Abe,N., Yokoyama-Kobayashi,M. and Aoki,T. TITLE Construction of a human full-length cDNA bank JOURNAL Gene 150 (2), 243-250 (1994) PUBMED 7821789 REFERENCE 9 (bases 1 to 2678) AUTHORS Koken,M.H., Smit,E.M., Jaspers-Dekker,I., Oostra,B.A., Hagemeijer,A., Bootsma,D. and Hoeijmakers,J.H. TITLE Localization of two human homologs, HHR6A and HHR6B, of the yeast DNA repair gene RAD6 to chromosomes Xq24-q25 and 5q23-q31 JOURNAL Genomics 12 (3), 447-453 (1992) PUBMED 1559696 REFERENCE 10 (bases 1 to 2678) AUTHORS Koken,M.H., Reynolds,P., Jaspers-Dekker,I., Prakash,L., Prakash,S., Bootsma,D. and Hoeijmakers,J.H. TITLE Structural and functional conservation of two human homologs of the yeast DNA repair gene RAD6 JOURNAL Proc. Natl. Acad. Sci. U.S.A. 88 (20), 8865-8869 (1991) PUBMED 1717990 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from BC042021.1. Summary: The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. This enzyme is required for post-replicative DNA damage repair. Multiple alternatively spliced transcript variants have been found for this gene and they encode distinct isoforms. [provided by RefSeq, Jul 2008]. Transcript Variant: This variant (3) lacks several 5' exons but has an alternate 5' segment, as compared to variant 1. It uses a downstream in-frame start codon and encodes isoform 3, which has a shorter N-terminus than that of isoform 1. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: BC042021.1, CB127128.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025081, ERS025082 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-2678 BC042021.1 2-2679 FEATURES Location/Qualifiers source 1..2678 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="X" /map="Xq24" gene 1..2678 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /note="ubiquitin-conjugating enzyme E2A" /db_xref="GeneID:7319" /db_xref="HGNC:12472" /db_xref="HPRD:02422" /db_xref="MIM:312180" exon 1..1262 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /inference="alignment:Splign:1.39.8" variation 244 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="a" /replace="c" /db_xref="dbSNP:184389323" variation 285 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="c" /replace="g" /db_xref="dbSNP:189298647" variation 419 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="a" /replace="g" /db_xref="dbSNP:112788267" variation 420..421 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="" /replace="a" /db_xref="dbSNP:66553683" variation 531 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="a" /replace="g" /db_xref="dbSNP:73637860" variation 619 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="c" /replace="t" /db_xref="dbSNP:34146345" variation 635 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="a" /replace="t" /db_xref="dbSNP:374702937" variation 647 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="g" /replace="t" /db_xref="dbSNP:180956632" variation 694 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="a" /replace="t" /db_xref="dbSNP:368755207" variation 803 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="a" /replace="g" /db_xref="dbSNP:184789804" variation 987..988 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="" /replace="a" /db_xref="dbSNP:66943262" misc_feature 1106..1108 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /note="upstream in-frame stop codon" variation 1123 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="c" /replace="t" /db_xref="dbSNP:34138874" CDS 1247..1480 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /EC_number="6.3.2.19" /note="isoform 3 is encoded by transcript variant 3; ubiquitin-conjugating enzyme E2A (RAD6 homolog); ubiquitin-protein ligase A; ubiquitin carrier protein A; HR6A; RAD6 homolog A" /codon_start=1 /product="ubiquitin-conjugating enzyme E2 A isoform 3" /protein_id="NP_861442.1" /db_xref="GI:32967278" /db_xref="CCDS:CCDS14582.1" /db_xref="GeneID:7319" /db_xref="HGNC:12472" /db_xref="HPRD:02422" /db_xref="MIM:312180" /translation="
MFHPNVYADGSICLDILQNRWSPTYDVSSILTSIQSLLDEPNPNSPANSQAAQLYQENKREYEKRVSAIVEQSWRDC
" misc_feature <1247..1444 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /note="Ubiquitin-conjugating enzyme E2, catalytic (UBCc) domain. This is part of the ubiquitin-mediated protein degradation pathway in which a thiol-ester linkage forms between a conserved cysteine and the C-terminus of ubiquitin and complexes with ubiquitin...; Region: UBCc; cd00195" /db_xref="CDD:238117" misc_feature order(1247..1249,1259..1264,1268..1270,1280..1288, 1292..1297,1307..1312,1319..1321,1334..1336,1343..1345, 1352..1354,1361..1366,1370..1372,1376..1381) /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /note="Ub thioester intermediate interaction residues; other site" /db_xref="CDD:238117" misc_feature 1283..1285 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /note="active site cysteine" /db_xref="CDD:238117" misc_feature 1379..1381 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" /db_xref="HPRD:00302" misc_feature 1379..1381 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" /db_xref="HPRD:00310" exon 1263..1351 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /inference="alignment:Splign:1.39.8" variation 1328 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="c" /replace="t" /db_xref="dbSNP:111885581" variation 1342 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="a" /replace="g" /db_xref="dbSNP:61757566" exon 1352..2643 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /inference="alignment:Splign:1.39.8" variation 1403 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="c" /replace="t" /db_xref="dbSNP:104894952" STS 1423..1545 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /standard_name="G44726" /db_xref="UniSTS:95201" variation 1462 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="a" /replace="g" /db_xref="dbSNP:4234" variation 1483 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="c" /replace="t" /db_xref="dbSNP:376065272" variation 1499 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="g" /replace="t" /db_xref="dbSNP:1803725" variation 1518..1521 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="" /replace="atat" /db_xref="dbSNP:370058300" polyA_signal 1570..1575 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" variation 1574 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="a" /replace="g" /db_xref="dbSNP:190231807" polyA_site 1590 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /experiment="experimental evidence, no additional details recorded" variation 1599 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="g" /replace="t" /db_xref="dbSNP:143338897" variation 1638 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="c" /replace="t" /db_xref="dbSNP:35554236" variation 2004 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="a" /replace="c" /db_xref="dbSNP:35570533" variation 2015 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="g" /replace="t" /db_xref="dbSNP:1803724" variation 2060 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="a" /replace="t" /db_xref="dbSNP:35068848" variation 2075 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="c" /replace="t" /db_xref="dbSNP:181367972" variation 2165..2166 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="" /replace="g" /db_xref="dbSNP:35317457" variation 2172 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="c" /replace="t" /db_xref="dbSNP:368813411" variation 2185 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="g" /replace="t" /db_xref="dbSNP:1803723" variation 2186 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="c" /replace="t" /db_xref="dbSNP:186621711" STS 2267..2510 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /standard_name="STS-M74524" /db_xref="UniSTS:58149" variation 2368 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="c" /replace="g" /db_xref="dbSNP:190671903" STS 2391..2527 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /standard_name="A009F17" /db_xref="UniSTS:62018" STS 2391..2527 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /standard_name="G32504" /db_xref="UniSTS:117089" variation 2521 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="a" /replace="t" /db_xref="dbSNP:1803722" variation 2527 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="a" /replace="g" /db_xref="dbSNP:14982" variation 2542 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="c" /replace="t" /db_xref="dbSNP:1803726" variation 2587 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" /replace="c" /replace="t" /db_xref="dbSNP:368008641" polyA_signal 2625..2630 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" polyA_site 2643 /gene="UBE2A" /gene_synonym="HHR6A; MRXS30; MRXSN; RAD6A; UBC2" ORIGIN
tagtcttctctctttcttaagcagtgataaaccttttaatgagaacaaaaaggaaataaattgctaactctgaaggaaccagtaagaaatacactgaagtatggtctgttgttttagaataatttgttaaatggaccagagtaatatagtggaacatgcatcaccttataccatatagtaactgattcttctaagtttacttgaacagatttcagtcaggaaaaaacattgctcaattgtgttcttcaatttattcaacaaacaattgaaaataatattttaaaggacataatctcttcatatcacatcttaacaattcttgaatgagatccagtttgtccatgccttgtaagtaagtttataacctactatgctttagggcctcctgctaccttaggttgacatatatttaagaaaaataatttcatttcaatagtagcataaacattagaaaaataaatttgctggaaacatgaatgcaatctaaaccaaatgtgattttaaaattatttctgccattaattccctccatatgtgtgaataattgagttgattttatagtgaagtaccttatgagccatacttaagggtttctgagagggactatgaagtttttcctggcttaaattcaattaagttttcattatagggtcactatgacatgaaaaggaaccagtatgaacacttttatacttattcccttctattttaaaaataacttgattatggatttgtattctggcattggtttttgaaccattgtgctttcattctttctagtctgtctaaaaatcactggagcgtttaagatggcagctgactaacataggcctttgaggtcttttggtcttctaaaggaagaaggccaaattttgggcccagtttcttaaggatgttttcaaaatgtacagtggctaaaatcttgtaagcagtaattttgtgtttatgatggctgtctccaagtttgggggaaaataatggcaaaacaaaaaatcacatttgagtagttcttagagcaattcctagagatgtatttcttacctggcctttcctctctaccctgtatctttgcattatttaatacttggaaaaacccacatagcattaaaaacaaagtactactgaacaaagtgataaatacattttcttaaatctttcttttctaaccacaggaacatttaaacttacaatagaattcactgaagaatatccaaataaaccacctacagttagatttgtctctaagatgttccatccaaatgtctatgcagatggtagtatatgtctggacatacttcagaaccgttggagtccaacctatgatgtgtcttccattctaacatccatacagtctctgttggatgaacccaatcccaatagtccagcaaacagccaggctgctcagctgtaccaggagaacaaacgggaatatgaaaagcgtgtttctgcaatagtagaacaaagctggcgtgattgttgaccccgggtacagtttaaagaagctggccataagaaaaatatatattgatgtgtttgtcacctccctactcctgtcattacatttactttattaaaagcaaaataactgttgtgctgtttccatcttccttgccaagttttcctaccccttctaccctctccttaaacatcagaaaacaccctctatgaaatcaaatgtactgtacctgggttacttgcaaaaattactaatgcttcagtttttctgttgtatttcatttccagttttcaggcagttatttttattattgtactttaagcttttaagatgaattgttatacaagaggtgcttatgcttagcttgatgaccaggatgttatttttaacaaaatgattgctgaagtgtttcatcctggctggtccttcacttgtgttggatttagaagtgaatgtgtttggaatatggcctacagagaatagaaacaaatccatgtaaacaattttgaaggaggcatgggagctaaaaatcctgtgatactaagatctcagtcatatgaattacaacgtagtatttactggcaagaaggagaaagttgaaggactcagctaaaggagtacagcaattgtagtaactgacacatcctctctttgcaagctgctgactgggcacactcatgccaagtttcagaattattggtcttctgggtttttgctttttaaaagaggtgtgggagcagaggaatggaaacaatcgtgagtttttgagctagggaaagttggagctcctttaatctttttaaaggatcagtgctgccctaagtgaataaactcaattgtccatctttattttagagttttaatgaattcaaggaagggagcatagcatatctgtggcaaactattttccactcaaatcctgagttattgctgcatgctttaatttcttccctttcagcatctgagaaccttaaagccaatgtctgcgatctttttttggatatttatacttttagatatatagtacctttaagtagcagtatgggacaaggcttgtaaatgttttgtctaatgttctattgtcaccttttatgcatttatcacttccaaatctaactttgcacaagtaacccatgtaaaaaaaaatgtacatttttcaaaagttgtaaataaaaataaccttaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:7319 -> Molecular function: GO:0004842 [ubiquitin-protein ligase activity] evidence: IDA GeneID:7319 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:7319 -> Molecular function: GO:0005524 [ATP binding] evidence: IEA GeneID:7319 -> Molecular function: GO:0031625 [ubiquitin protein ligase binding] evidence: IPI GeneID:7319 -> Biological process: GO:0000209 [protein polyubiquitination] evidence: TAS GeneID:7319 -> Biological process: GO:0001701 [in utero embryonic development] evidence: IEA GeneID:7319 -> Biological process: GO:0002474 [antigen processing and presentation of peptide antigen via MHC class I] evidence: TAS GeneID:7319 -> Biological process: GO:0006281 [DNA repair] evidence: IGI GeneID:7319 -> Biological process: GO:0006301 [postreplication repair] evidence: NAS GeneID:7319 -> Biological process: GO:0006511 [ubiquitin-dependent protein catabolic process] evidence: NAS GeneID:7319 -> Biological process: GO:0008284 [positive regulation of cell proliferation] evidence: IDA GeneID:7319 -> Biological process: GO:0009411 [response to UV] evidence: IGI GeneID:7319 -> Biological process: GO:0033522 [histone H2A ubiquitination] evidence: IDA GeneID:7319 -> Biological process: GO:0051865 [protein autoubiquitination] evidence: IDA GeneID:7319 -> Biological process: GO:0060135 [maternal process involved in female pregnancy] evidence: IEA GeneID:7319 -> Biological process: GO:0070936 [protein K48-linked ubiquitination] evidence: IDA GeneID:7319 -> Biological process: GO:0070979 [protein K11-linked ubiquitination] evidence: IDA GeneID:7319 -> Cellular component: GO:0000785 [chromatin] evidence: ISS GeneID:7319 -> Cellular component: GO:0000790 [nuclear chromatin] evidence: IEA GeneID:7319 -> Cellular component: GO:0001741 [XY body] evidence: IEA GeneID:7319 -> Cellular component: GO:0005829 [cytosol] evidence: TAS GeneID:7319 -> Cellular component: GO:0033503 [HULC complex] evidence: IDA ANNOTATIONS from NCBI Entrez Gene (20130726): NP_861442 -> EC 6.3.2.19
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