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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:

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

by @meso_cacase at DBCLS
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