2024-03-29 07:40:28, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_002803 2846 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens proteasome (prosome, macropain) 26S subunit, ATPase, 2 (PSMC2), transcript variant 1, mRNA. ACCESSION NM_002803 VERSION NM_002803.3 GI:325053650 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 2846) AUTHORS Kaneko,T., Hamazaki,J., Iemura,S., Sasaki,K., Furuyama,K., Natsume,T., Tanaka,K. and Murata,S. TITLE Assembly pathway of the Mammalian proteasome base subcomplex is mediated by multiple specific chaperones JOURNAL Cell 137 (5), 914-925 (2009) PUBMED 19490896 REFERENCE 2 (bases 1 to 2846) AUTHORS Tu,L.C., Yan,X., Hood,L. and Lin,B. TITLE Proteomics analysis of the interactome of N-myc downstream regulated gene 1 and its interactions with the androgen response program in prostate cancer cells JOURNAL Mol. Cell Proteomics 6 (4), 575-588 (2007) PUBMED 17220478 REFERENCE 3 (bases 1 to 2846) AUTHORS Guo,D., Han,J., Adam,B.L., Colburn,N.H., Wang,M.H., Dong,Z., Eizirik,D.L., She,J.X. and Wang,C.Y. TITLE Proteomic analysis of SUMO4 substrates in HEK293 cells under serum starvation-induced stress JOURNAL Biochem. Biophys. Res. Commun. 337 (4), 1308-1318 (2005) PUBMED 16236267 REFERENCE 4 (bases 1 to 2846) AUTHORS Oh,J.H., Yang,J.O., Hahn,Y., Kim,M.R., Byun,S.S., Jeon,Y.J., Kim,J.M., Song,K.S., Noh,S.M., Kim,S., Yoo,H.S., Kim,Y.S. and Kim,N.S. TITLE Transcriptome analysis of human gastric cancer JOURNAL Mamm. Genome 16 (12), 942-954 (2005) PUBMED 16341674 REFERENCE 5 (bases 1 to 2846) AUTHORS Bruneel,A., Labas,V., Mailloux,A., Sharma,S., Royer,N., Vinh,J., Pernet,P., Vaubourdolle,M. and Baudin,B. TITLE Proteomics of human umbilical vein endothelial cells applied to etoposide-induced apoptosis JOURNAL Proteomics 5 (15), 3876-3884 (2005) PUBMED 16130169 REFERENCE 6 (bases 1 to 2846) AUTHORS Coux,O., Tanaka,K. and Goldberg,A.L. TITLE Structure and functions of the 20S and 26S proteasomes JOURNAL Annu. Rev. Biochem. 65, 801-847 (1996) PUBMED 8811196 REMARK Review article REFERENCE 7 (bases 1 to 2846) AUTHORS Nacken,W., Kingsman,A.J., Kingsman,S.M., Sablitzky,F. and Sorg,C. TITLE A homologue of the human MSS1 gene, a positive modulator of HIV-1 gene expression, is massively expressed in Xenopus oocytes JOURNAL Biochim. Biophys. Acta 1261 (2), 293-295 (1995) PUBMED 7711076 REFERENCE 8 (bases 1 to 2846) AUTHORS Dubiel,W., Ferrell,K. and Rechsteiner,M. TITLE Peptide sequencing identifies MSS1, a modulator of HIV Tat-mediated transactivation, as subunit 7 of the 26 S protease JOURNAL FEBS Lett. 323 (3), 276-278 (1993) PUBMED 8500623 REFERENCE 9 (bases 1 to 2846) AUTHORS Shibuya,H., Irie,K., Ninomiya-Tsuji,J., Goebl,M., Taniguchi,T. and Matsumoto,K. TITLE New human gene encoding a positive modulator of HIV Tat-mediated transactivation JOURNAL Nature 357 (6380), 700-702 (1992) PUBMED 1377363 REFERENCE 10 (bases 1 to 2846) AUTHORS Dawson,S.J. and White,L.A. TITLE Treatment of Haemophilus aphrophilus endocarditis with ciprofloxacin JOURNAL J. Infect. 24 (3), 317-320 (1992) PUBMED 1602151 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from BE269755.1, BC002589.2, AC093701.4 and BU675889.1. On Mar 2, 2011 this sequence version replaced gi:24430152. Summary: The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes one of the ATPase subunits, a member of the triple-A family of ATPases which have a chaperone-like activity. This subunit has been shown to interact with several of the basal transcription factors so, in addition to participation in proteasome functions, this subunit may participate in the regulation of transcription. This subunit may also compete with PSMC3 for binding to the HIV tat protein to regulate the interaction between the viral protein and the transcription complex. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Mar 2011]. Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1). Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. 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 :: AB075520.1, BC002589.2 [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 1-156 BE269755.1 78-233 157-1645 BC002589.2 1-1489 1646-2540 AC093701.4 15452-16346 2541-2846 BU675889.1 1-306 c FEATURES Location/Qualifiers source 1..2846 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="7" /map="7q22.1-q22.3" gene 1..2846 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /note="proteasome (prosome, macropain) 26S subunit, ATPase, 2" /db_xref="GeneID:5701" /db_xref="HGNC:9548" /db_xref="HPRD:01105" /db_xref="MIM:154365" exon 1..258 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /inference="alignment:Splign:1.39.8" variation 4 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="c" /db_xref="dbSNP:112987408" variation 94 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:144620518" variation 128 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="c" /db_xref="dbSNP:189273862" misc_feature 159..161 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /note="upstream in-frame stop codon" variation 172 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="c" /db_xref="dbSNP:138514927" CDS 189..1490 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /note="isoform 1 is encoded by transcript variant 1; mammalian suppressor of sgv-1 of yeast; protease 26S subunit 7; proteasome 26S subunit, ATPase, 2; 26S protease regulatory subunit 7; putative protein product of Nbla10058; proteasome 26S subunit ATPase 2; 26S proteasome AAA-ATPase subunit RPT1" /codon_start=1 /product="26S protease regulatory subunit 7 isoform 1" /protein_id="NP_002794.1" /db_xref="GI:4506209" /db_xref="CCDS:CCDS5731.1" /db_xref="GeneID:5701" /db_xref="HGNC:9548" /db_xref="HPRD:01105" /db_xref="MIM:154365" /translation="
MPDYLGADQRKTKEDEKDDKPIRALDEGDIALLKTYGQSTYSRQIKQVEDDIQQLLKKINELTGIKESDTGLAPPALWDLAADKQTLQSEQPLQVARCTKIINADSEDPKYIINVKQFAKFVVDLSDQVAPTDIEEGMRVGVDRNKYQIHIPLPPKIDPTVTMMQVEEKPDVTYSDVGGCKEQIEKLREVVETPLLHPERFVNLGIEPPKGVLLFGPPGTGKTLCARAVANRTDACFIRVIGSELVQKYVGEGARMVRELFEMARTKKACLIFFDEIDAIGGARFDDGAGGDNEVQRTMLELINQLDGFDPRGNIKVLMATNRPDTLDPALMRPGRLDRKIEFSLPDLEGRTHIFKIHARSMSVERDIRFELLARLCPNSTGAEIRSVCTEAGMFAIRARRKIATEKDFLEAVNKVIKSYAKFSATPRYMTYN
" misc_feature 285..1478 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /note="ATP-dependent 26S proteasome regulatory subunit [Posttranslational modification, protein turnover, chaperones]; Region: RPT1; COG1222" /db_xref="CDD:224143" misc_feature 534..536 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /experiment="experimental evidence, no additional details recorded" /note="N6-acetyllysine; propagated from UniProtKB/Swiss-Prot (P35998.3); acetylation site" misc_feature 720..1223 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /note="The AAA+ (ATPases Associated with a wide variety of cellular Activities) superfamily represents an ancient group of ATPases belonging to the ASCE (for additional strand, catalytic E) division of the P-loop NTPase fold. The ASCE division also includes ABC; Region: AAA; cd00009" /db_xref="CDD:99707" misc_feature 834..857 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /note="Walker A motif; other site" /db_xref="CDD:99707" misc_feature order(837..860,1011..1013,1152..1154) /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /note="ATP binding site [chemical binding]; other site" /db_xref="CDD:99707" misc_feature 999..1016 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /note="Walker B motif; other site" /db_xref="CDD:99707" misc_feature 1194..1196 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /note="arginine finger; other site" /db_xref="CDD:99707" misc_feature 1452..1454 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /experiment="experimental evidence, no additional details recorded" /note="N6-acetyllysine; propagated from UniProtKB/Swiss-Prot (P35998.3); acetylation site" variation 201 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="g" /db_xref="dbSNP:202147098" variation 203 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:140451125" variation 204 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:61738529" variation 225 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:201035586" variation 239 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:61729405" exon 259..296 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /inference="alignment:Splign:1.39.8" variation 284 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:145606402" exon 297..378 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /inference="alignment:Splign:1.39.8" variation 307 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="g" /db_xref="dbSNP:376614496" variation 314 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:140442131" variation 325 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="t" /db_xref="dbSNP:11545648" variation 329 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="c" /db_xref="dbSNP:369823547" exon 379..478 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /inference="alignment:Splign:1.39.8" variation 416 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="c" /db_xref="dbSNP:201584289" variation 458 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="c" /db_xref="dbSNP:74998067" exon 479..610 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /inference="alignment:Splign:1.39.8" variation 501 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:200658637" variation 503 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:200083313" variation 530 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:146114386" variation 536 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="g" /replace="t" /db_xref="dbSNP:201653763" variation 542 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:138047874" variation 549 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:200242883" variation 556 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:11545647" exon 611..683 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /inference="alignment:Splign:1.39.8" variation 671 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:202202308" exon 684..779 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /inference="alignment:Splign:1.39.8" STS 747..967 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /standard_name="RH80487" /db_xref="UniSTS:85537" exon 780..944 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /inference="alignment:Splign:1.39.8" variation 787 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:374959956" variation 804 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="t" /db_xref="dbSNP:199759890" variation 842 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:61733321" variation 848 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:376164420" variation 857 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:370246510" variation 893 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:144680798" variation 935 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:147608353" exon 945..1032 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /inference="alignment:Splign:1.39.8" variation 960 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="g" /db_xref="dbSNP:6976756" variation 1026 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:183644599" exon 1033..1235 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /inference="alignment:Splign:1.39.8" variation 1040 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:200759691" variation 1122 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="c" /db_xref="dbSNP:4520097" variation 1169 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:141147542" variation 1172 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:199849429" variation 1174 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="c" /db_xref="dbSNP:1803992" variation 1219 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:372290123" variation 1227 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:374218623" variation 1231 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:113265696" exon 1236..1332 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /inference="alignment:Splign:1.39.8" variation 1262 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:144431266" variation 1276 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:1803990" variation 1299 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:201746080" variation 1312 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:371675280" STS 1330..1512 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /standard_name="PSMC2" /db_xref="UniSTS:39107" exon 1333..2831 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /inference="alignment:Splign:1.39.8" variation 1349 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:183253099" variation 1357 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:201353285" STS 1359..1504 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /standard_name="RH11504" /db_xref="UniSTS:44750" variation 1380 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="c" /db_xref="dbSNP:373150287" variation 1402 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:377111119" variation 1424 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:373941772" STS 1448..1580 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /standard_name="SGC32632" /db_xref="UniSTS:13306" variation 1451 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="g" /db_xref="dbSNP:200390723" variation 1471 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:370553048" variation 1527 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:371777406" variation 1535 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="g" /db_xref="dbSNP:373655880" variation 1538 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="c" /db_xref="dbSNP:1803991" polyA_signal 1570..1575 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" variation 1579 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="g" /db_xref="dbSNP:7792404" polyA_site 1591 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" variation 1607..1608 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="" /replace="tctt" /db_xref="dbSNP:202220027" polyA_signal 1622..1627 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" variation 1635 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:78804802" polyA_site 1645 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" variation 1662 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="g" /replace="t" /db_xref="dbSNP:186871457" variation 1786 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="c" /db_xref="dbSNP:190686105" variation 1818 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:183396821" variation 1927 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:75807150" variation 1934 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:79084084" STS 1942..2086 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /standard_name="RH69239" /db_xref="UniSTS:64018" variation 1998 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:12535070" variation 2158 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="t" /db_xref="dbSNP:368075134" variation 2191..2192 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="" /replace="a" /db_xref="dbSNP:199518022" variation 2199 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="t" /db_xref="dbSNP:187932420" variation 2364 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="g" /db_xref="dbSNP:376657341" variation 2366..2367 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="" /replace="ga" /db_xref="dbSNP:71687393" variation 2381 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:115429609" variation 2446 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="c" /db_xref="dbSNP:114269220" variation 2480 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="a" /replace="g" /db_xref="dbSNP:147617940" variation 2682 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="t" /db_xref="dbSNP:200182916" variation 2787 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" /replace="c" /replace="g" /db_xref="dbSNP:193200807" polyA_signal 2803..2808 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" polyA_signal 2807..2812 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" polyA_site 2831 /gene="PSMC2" /gene_synonym="MSS1; Nbla10058; S7" ORIGIN
gtaatcagtccaaaaaccagcgtgccaaagcgtttccccagggctctgtccggactctgaagcactgcataaaggggtctgtctgagcccaatttacttccggtggggaagggaaagggaagacaccaccggaagcaaggaaggtgctgtgtaatcattaaggagcggaggcttttggagctgctaaaatgccggattacctcggtgccgatcagcggaagaccaaagaggatgagaaggacgacaagcccatccgagctctggatgagggggatattgccttgttgaaaacttatggtcagagcacttactctaggcagatcaagcaagttgaagatgacattcagcaacttctcaagaaaattaatgagctcactggtattaaagaatctgacactggcctggccccaccagcactctgggatttggctgcagataagcagacactccagagtgaacagcctttacaggttgccaggtgtacaaagataatcaatgctgattcggaggacccaaaatacattatcaacgtaaagcagtttgccaagtttgtggtggaccttagtgatcaggtggcacctactgacattgaagaagggatgagagtgggcgtggatagaaataaatatcaaattcacattccattgcctcctaagattgacccaacagttaccatgatgcaggtggaagagaaacctgatgtcacatacagtgatgttggtggctgtaaggaacagattgagaaactgcgagaagtagttgaaaccccattacttcatccagagaggtttgtgaaccttggcattgagcctcccaagggcgtgctgctctttggtccacccggtacaggcaagacactctgtgcgcgggcagttgctaatcggactgatgcgtgcttcattcgagttattggatctgagcttgtacagaaatacgtcggtgagggggctcgaatggttcgtgaactctttgaaatggccagaacaaaaaaagcctgccttatcttctttgatgaaattgatgctattggaggggctcgttttgatgatggtgctggaggtgacaatgaagtgcagagaacaatgttggaactgatcaatcagcttgatggttttgatcctcgaggcaatattaaagtgctgatggccactaacagacctgatactttggatccagcactgatgaggccagggagattggatagaaaaattgaatttagcttgcccgatctagagggtcggacccacatatttaagattcacgctcgttcaatgagtgttgaaagagatatcagatttgaactgttagcacgactgtgtccaaatagcactggtgctgagattagaagcgtctgcacagaggctggtatgtttgccatcagagcacggcgaaaaattgctaccgagaaggatttcttggaagctgtaaataaggtcattaagtcttatgccaaattcagtgctactcctcgttacatgacatacaactgaaccctgaaggctttcaagtgaaaactttaaattggaatcctaaccttatatagacttgttaataaccaattcataaacaaataaatggcttcaaaattgtatgcttttttccatatctcttcttgtaatataataaaaggtgatttctaatgttattaggcagaaaagcttgttagaatatattttgactatttttttgacccacacccgtttaaggatttcacatcatacaaagcgcttgcttagatggcttctatcctaggcatatgctggccgggtgctctacatataaattctcattgtatcctcccatctgtccactgaggaagattatcaaatggatcttcatccaatggatgcataaactttcctacttacttgtagtggcaaagctggctttcaagtacaagtttgttggctccattacctatgctcctattatccgcttctgtcccgcaacaaagtagctcacttaggcgtatgaccacatgcattatgatagtttcccaccaccatattgaataataaaagctttggccaaagcttttttaaagtaggagaaacattggatgtatatgttttgcattgccatttgatttcaaattaatcaggaagaattagtgattttaatgagcagtaaagtggtgcaataaagcagaaagaaaaatgttcagccagaagtgaaagactagtaaaaaaagaaaaaaaaatatttgtacatatgatctaatttagaaagtccagaattggcttcatacagaaaagtgattactttcattttacaaattactttaaaattttggtaaagtttctgttaggcttctggtctacagtgaggtattttaaaaataaaggttatattagaatcctcaacatctctttaaaattacctcctgtgtaaccaccaccaaatcctatcttctaccacaattaccccttcccccaatgccaagaccaaagcacaataatgaatatttttattgaagttcgatattcataaataagttgcaaaataagagttggatatatttttaattcacaatagaaaaagttgacaacatagaaaatgctgctttgcactgaaatacttaaaattatgaaagttttcaagtaaagaaattaaagccttttataaaatccaaccaacattcttgatttttcatttttatgaacttgatcagaaaaattcatcttttttaaccctgccctaatttttcttgaggaattaaatagagcaaactattttcaggttatgcttacaataaaatatacttaagaaaatgactgaagatgtatgtttttgaatgttttgattaaataaatgtacacatttagaacacaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:5701 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:5701 -> Molecular function: GO:0005524 [ATP binding] evidence: IEA GeneID:5701 -> Molecular function: GO:0016887 [ATPase activity] evidence: IDA GeneID:5701 -> Biological process: GO:0000082 [G1/S transition of mitotic cell cycle] evidence: TAS GeneID:5701 -> Biological process: GO:0000209 [protein polyubiquitination] evidence: TAS GeneID:5701 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: TAS GeneID:5701 -> Biological process: GO:0002474 [antigen processing and presentation of peptide antigen via MHC class I] evidence: TAS GeneID:5701 -> Biological process: GO:0002479 [antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent] evidence: TAS GeneID:5701 -> Biological process: GO:0006200 [ATP catabolic process] evidence: IDA GeneID:5701 -> Biological process: GO:0006511 [ubiquitin-dependent protein catabolic process] evidence: IDA GeneID:5701 -> Biological process: GO:0006521 [regulation of cellular amino acid metabolic process] evidence: TAS GeneID:5701 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS GeneID:5701 -> Biological process: GO:0006977 [DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest] evidence: TAS GeneID:5701 -> Biological process: GO:0010467 [gene expression] evidence: TAS GeneID:5701 -> Biological process: GO:0016032 [viral process] evidence: TAS GeneID:5701 -> Biological process: GO:0016070 [RNA metabolic process] evidence: TAS GeneID:5701 -> Biological process: GO:0016071 [mRNA metabolic process] evidence: TAS GeneID:5701 -> Biological process: GO:0019048 [modulation by virus of host morphology or physiology] evidence: IEA GeneID:5701 -> Biological process: GO:0031145 [anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process] evidence: TAS GeneID:5701 -> Biological process: GO:0034641 [cellular nitrogen compound metabolic process] evidence: TAS GeneID:5701 -> Biological process: GO:0042590 [antigen processing and presentation of exogenous peptide antigen via MHC class I] evidence: TAS GeneID:5701 -> Biological process: GO:0042981 [regulation of apoptotic process] evidence: TAS GeneID:5701 -> Biological process: GO:0043066 [negative regulation of apoptotic process] evidence: TAS GeneID:5701 -> Biological process: GO:0044281 [small molecule metabolic process] evidence: TAS GeneID:5701 -> Biological process: GO:0051436 [negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS GeneID:5701 -> Biological process: GO:0051437 [positive regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS GeneID:5701 -> Biological process: GO:0051439 [regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS GeneID:5701 -> Cellular component: GO:0000502 [proteasome complex] evidence: IDA GeneID:5701 -> Cellular component: GO:0000932 [cytoplasmic mRNA processing body] evidence: ISS GeneID:5701 -> Cellular component: GO:0005634 [nucleus] evidence: IDA GeneID:5701 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS GeneID:5701 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA GeneID:5701 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA GeneID:5701 -> Cellular component: GO:0005737 [cytoplasm] evidence: TAS GeneID:5701 -> Cellular component: GO:0005739 [mitochondrion] evidence: IDA GeneID:5701 -> Cellular component: GO:0005829 [cytosol] evidence: TAS GeneID:5701 -> Cellular component: GO:0022624 [proteasome accessory complex] evidence: ISS
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