GGRNA Home | Help | Advanced search

2024-04-19 09:29:05, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_002817               1757 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens proteasome (prosome, macropain) 26S subunit,
            non-ATPase, 13 (PSMD13), transcript variant 1, mRNA.
ACCESSION   NM_002817
VERSION     NM_002817.3  GI:157502192
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 1757)
  AUTHORS   Gieger,C., Radhakrishnan,A., Cvejic,A., Tang,W., Porcu,E.,
            Pistis,G., Serbanovic-Canic,J., Elling,U., Goodall,A.H.,
            Labrune,Y., Lopez,L.M., Magi,R., Meacham,S., Okada,Y., Pirastu,N.,
            Sorice,R., Teumer,A., Voss,K., Zhang,W., Ramirez-Solis,R.,
            Bis,J.C., Ellinghaus,D., Gogele,M., Hottenga,J.J., Langenberg,C.,
            Kovacs,P., O'Reilly,P.F., Shin,S.Y., Esko,T., Hartiala,J.,
            Kanoni,S., Murgia,F., Parsa,A., Stephens,J., van der Harst,P.,
            Ellen van der Schoot,C., Allayee,H., Attwood,A., Balkau,B.,
            Bastardot,F., Basu,S., Baumeister,S.E., Biino,G., Bomba,L.,
            Bonnefond,A., Cambien,F., Chambers,J.C., Cucca,F., D'Adamo,P.,
            Davies,G., de Boer,R.A., de Geus,E.J., Doring,A., Elliott,P.,
            Erdmann,J., Evans,D.M., Falchi,M., Feng,W., Folsom,A.R.,
            Frazer,I.H., Gibson,Q.D., Glazer,N.L., Hammond,C.,
            Hartikainen,A.L., Heckbert,S.R., Hengstenberg,C., Hersch,M.,
            Illig,T., Loos,R.J., Jolley,J., Khaw,K.T., Kuhnel,B.,
            Kyrtsonis,M.C., Lagou,V., Lloyd-Jones,H., Lumley,T., Mangino,M.,
            Maschio,A., Mateo Leach,I., McKnight,B., Memari,Y., Mitchell,B.D.,
            Montgomery,G.W., Nakamura,Y., Nauck,M., Navis,G., Nothlings,U.,
            Nolte,I.M., Porteous,D.J., Pouta,A., Pramstaller,P.P., Pullat,J.,
            Ring,S.M., Rotter,J.I., Ruggiero,D., Ruokonen,A., Sala,C.,
            Samani,N.J., Sambrook,J., Schlessinger,D., Schreiber,S.,
            Schunkert,H., Scott,J., Smith,N.L., Snieder,H., Starr,J.M.,
            Stumvoll,M., Takahashi,A., Tang,W.H., Taylor,K., Tenesa,A., Lay
            Thein,S., Tonjes,A., Uda,M., Ulivi,S., van Veldhuisen,D.J.,
            Visscher,P.M., Volker,U., Wichmann,H.E., Wiggins,K.L.,
            Willemsen,G., Yang,T.P., Hua Zhao,J., Zitting,P., Bradley,J.R.,
            Dedoussis,G.V., Gasparini,P., Hazen,S.L., Metspalu,A., Pirastu,M.,
            Shuldiner,A.R., Joost van Pelt,L., Zwaginga,J.J., Boomsma,D.I.,
            Deary,I.J., Franke,A., Froguel,P., Ganesh,S.K., Jarvelin,M.R.,
            Martin,N.G., Meisinger,C., Psaty,B.M., Spector,T.D., Wareham,N.J.,
            Akkerman,J.W., Ciullo,M., Deloukas,P., Greinacher,A., Jupe,S.,
            Kamatani,N., Khadake,J., Kooner,J.S., Penninger,J., Prokopenko,I.,
            Stemple,D., Toniolo,D., Wernisch,L., Sanna,S., Hicks,A.A.,
            Rendon,A., Ferreira,M.A., Ouwehand,W.H. and Soranzo,N.
  TITLE     New gene functions in megakaryopoiesis and platelet formation
  JOURNAL   Nature 480 (7376), 201-208 (2011)
   PUBMED   22139419
  REMARK    Publication Status: Online-Only
REFERENCE   2  (bases 1 to 1757)
  AUTHORS   Bellizzi,D., Dato,S., Cavalcante,P., Covello,G., Di Cianni,F.,
            Passarino,G., Rose,G. and De Benedictis,G.
  TITLE     Characterization of a bidirectional promoter shared between two
            human genes related to aging: SIRT3 and PSMD13
  JOURNAL   Genomics 89 (1), 143-150 (2007)
   PUBMED   17059877
  REMARK    GeneRIF: The SIRT3 5' flanking region encompasses the PSMD13 gene
            encoding the p40.5 regulator subunit of the 26S proteasome.
REFERENCE   3  (bases 1 to 1757)
  AUTHORS   Gandhi,T.K., Zhong,J., Mathivanan,S., Karthick,L., Chandrika,K.N.,
            Mohan,S.S., Sharma,S., Pinkert,S., Nagaraju,S., Periaswamy,B.,
            Mishra,G., Nandakumar,K., Shen,B., Deshpande,N., Nayak,R.,
            Sarker,M., Boeke,J.D., Parmigiani,G., Schultz,J., Bader,J.S. and
            Pandey,A.
  TITLE     Analysis of the human protein interactome and comparison with
            yeast, worm and fly interaction datasets
  JOURNAL   Nat. Genet. 38 (3), 285-293 (2006)
   PUBMED   16501559
REFERENCE   4  (bases 1 to 1757)
  AUTHORS   Listovsky,T., Oren,Y.S., Yudkovsky,Y., Mahbubani,H.M., Weiss,A.M.,
            Lebendiker,M. and Brandeis,M.
  TITLE     Mammalian Cdh1/Fzr mediates its own degradation
  JOURNAL   EMBO J. 23 (7), 1619-1626 (2004)
   PUBMED   15029244
REFERENCE   5  (bases 1 to 1757)
  AUTHORS   Bouwmeester,T., Bauch,A., Ruffner,H., Angrand,P.O., Bergamini,G.,
            Croughton,K., Cruciat,C., Eberhard,D., Gagneur,J., Ghidelli,S.,
            Hopf,C., Huhse,B., Mangano,R., Michon,A.M., Schirle,M., Schlegl,J.,
            Schwab,M., Stein,M.A., Bauer,A., Casari,G., Drewes,G., Gavin,A.C.,
            Jackson,D.B., Joberty,G., Neubauer,G., Rick,J., Kuster,B. and
            Superti-Furga,G.
  TITLE     A physical and functional map of the human TNF-alpha/NF-kappa B
            signal transduction pathway
  JOURNAL   Nat. Cell Biol. 6 (2), 97-105 (2004)
   PUBMED   14743216
  REMARK    Erratum:[Nat Cell Biol. 2004 May;6(5):465]
REFERENCE   6  (bases 1 to 1757)
  AUTHORS   Simon,J.H., Gaddis,N.C., Fouchier,R.A. and Malim,M.H.
  TITLE     Evidence for a newly discovered cellular anti-HIV-1 phenotype
  JOURNAL   Nat. Med. 4 (12), 1397-1400 (1998)
   PUBMED   9846577
REFERENCE   7  (bases 1 to 1757)
  AUTHORS   Madani,N. and Kabat,D.
  TITLE     An endogenous inhibitor of human immunodeficiency virus in human
            lymphocytes is overcome by the viral Vif protein
  JOURNAL   J. Virol. 72 (12), 10251-10255 (1998)
   PUBMED   9811770
REFERENCE   8  (bases 1 to 1757)
  AUTHORS   Hori,T., Kato,S., Saeki,M., DeMartino,G.N., Slaughter,C.A.,
            Takeuchi,J., Toh-e,A. and Tanaka,K.
  TITLE     cDNA cloning and functional analysis of p28 (Nas6p) and p40.5
            (Nas7p), two novel regulatory subunits of the 26S proteasome
  JOURNAL   Gene 216 (1), 113-122 (1998)
   PUBMED   9714768
REFERENCE   9  (bases 1 to 1757)
  AUTHORS   Seeger,M., Ferrell,K., Frank,R. and Dubiel,W.
  TITLE     HIV-1 tat inhibits the 20 S proteasome and its 11 S
            regulator-mediated activation
  JOURNAL   J. Biol. Chem. 272 (13), 8145-8148 (1997)
   PUBMED   9079628
REFERENCE   10 (bases 1 to 1757)
  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
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AC136475.7, AB009398.1 and AA931044.1.
            On Sep 25, 2007 this sequence version replaced gi:28872727.
            
            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 a
            non-ATPase subunit of the 19S regulator. Two transcripts encoding
            different isoforms have been described. [provided by RefSeq, Jul
            2008].
            
            Transcript Variant: This variant (1) encodes the longer 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 :: AF083245.1, AB009398.1 [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
            1-173               AC136475.7         21352-21524
            174-1754            AB009398.1         1-1581
            1755-1757           AA931044.1         1-3                 c
FEATURES             Location/Qualifiers
     source          1..1757
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="11"
                     /map="11p15.5"
     gene            1..1757
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /note="proteasome (prosome, macropain) 26S subunit,
                     non-ATPase, 13"
                     /db_xref="GeneID:5719"
                     /db_xref="HGNC:9558"
                     /db_xref="MIM:603481"
     exon            1..337
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /inference="alignment:Splign:1.39.8"
     variation       4
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:519592"
     variation       27
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182895690"
     variation       64
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2272563"
     misc_feature    168..170
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /note="upstream in-frame stop codon"
     variation       184
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149034138"
     variation       195
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200286876"
     variation       201
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:188150985"
     variation       215
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369344513"
     variation       223
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12293349"
     CDS             243..1373
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /note="isoform 1 is encoded by transcript variant 1; 26S
                     proteasome subunit p40.5; 26S proteasome regulatory
                     subunit S11; 26S proteasome non-ATPase regulatory subunit
                     13; 26S proteasome regulatory subunit p40.5; 26S
                     proteasome regulatory subunit RPN9"
                     /codon_start=1
                     /product="26S proteasome non-ATPase regulatory subunit 13
                     isoform 1"
                     /protein_id="NP_002808.3"
                     /db_xref="GI:157502193"
                     /db_xref="CCDS:CCDS7692.1"
                     /db_xref="GeneID:5719"
                     /db_xref="HGNC:9558"
                     /db_xref="MIM:603481"
                     /translation="
MKDVPGFLQQSQNSGPGQPAVWHRLEELYTKKLWHQLTLQVLDFVQDPCFAQGDGLIKLYENFISEFEHRVNPLSLVEIILHVVRQMTDPNVALTFLEKTREKVKSSDEAVILCKTAIGALKLNIGDLQVTKETIEDVEEMLNNLPGVTSVHSRFYDLSSKYYQTIGNHASYYKDALRFLGCVDIKDLPVSEQQERAFTLGLAGLLGEGVFNFGELLMHPVLESLRNTDRQWLIDTLYAFNSGNVERFQTLKTAWGQQPDLAANEAQLLRKIQLLCLMEMTFTRPANHRQLTFEEIAKSAKITVNEVELLVMKALSVGLVKGSIDEVDKRVHMTWVQPRVLDLQQIKGMKDRLEFWCTDVKSMEMLVEHQAHDILT
"
     misc_feature    1041..1310
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /note="PCI/PINT associated module; Region: PAM;
                     smart00753"
                     /db_xref="CDD:197859"
     misc_feature    1134..1136
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="N6-acetyllysine; propagated from
                     UniProtKB/Swiss-Prot (Q9UNM6.2); acetylation site"
     variation       267
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:138214549"
     variation       275
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141263892"
     variation       280
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1045288"
     variation       288
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201217300"
     variation       294
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373557814"
     variation       326
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370974834"
     exon            338..416
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /inference="alignment:Splign:1.39.8"
     exon            417..451
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /inference="alignment:Splign:1.39.8"
     exon            452..507
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /inference="alignment:Splign:1.39.8"
     variation       458
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1128320"
     variation       462
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1128321"
     variation       488
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1128322"
     exon            508..551
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /inference="alignment:Splign:1.39.8"
     variation       543
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372391905"
     variation       544
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376432155"
     exon            552..638
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /inference="alignment:Splign:1.39.8"
     variation       582
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138068479"
     variation       618
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372085323"
     exon            639..810
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /inference="alignment:Splign:1.39.8"
     variation       642
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372670379"
     variation       646
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369255716"
     variation       651
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201907126"
     variation       669
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143016806"
     variation       691
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:28927679"
     variation       692
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372417183"
     variation       702
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190227821"
     variation       703
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370025144"
     variation       739
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140294264"
     variation       740
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142720939"
     variation       749
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147375021"
     variation       751
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200598221"
     variation       774
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148437656"
     exon            811..890
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /inference="alignment:Splign:1.39.8"
     variation       839
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142225853"
     variation       845
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200046358"
     variation       853
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1794108"
     variation       855
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1794109"
     variation       861
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151305149"
     variation       864
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368844853"
     variation       890
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139390743"
     exon            891..1016
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /inference="alignment:Splign:1.39.8"
     variation       894
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146649608"
     variation       905
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201372160"
     variation       920
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375739010"
     variation       931
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141198412"
     variation       975
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369505967"
     variation       982
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184893349"
     variation       986
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201506453"
     variation       1002
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145020061"
     variation       1013
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377054047"
     exon            1017..1079
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /inference="alignment:Splign:1.39.8"
     variation       1034
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372280734"
     variation       1038
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370394564"
     exon            1080..1160
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /inference="alignment:Splign:1.39.8"
     variation       1139
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145743654"
     exon            1161..1277
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /inference="alignment:Splign:1.39.8"
     variation       1163
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372551194"
     variation       1185
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371873059"
     variation       1250
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201183554"
     exon            1278..1757
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /inference="alignment:Splign:1.39.8"
     variation       1296
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148960827"
     variation       1316
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143526107"
     variation       1338
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:199698555"
     variation       1362
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200373903"
     variation       1377
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:192467588"
     variation       1389
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12065"
     variation       1390
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200513693"
     variation       1397
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372882483"
     variation       1422
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6540"
     variation       1506
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1045405"
     variation       1507
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111603100"
     variation       1508
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2948222"
     variation       1551
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:184828985"
     variation       1557
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:7116231"
     variation       1591
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1045502"
     STS             1594..1732
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /standard_name="STS-T99644"
                     /db_xref="UniSTS:62372"
     variation       1611
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372259956"
     variation       1614
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3817635"
     variation       1624
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6541"
     variation       1641
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369873779"
     variation       1661
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:2948223"
     variation       1696
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:186582362"
     variation       1697
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368198844"
     variation       1710
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113652939"
     variation       1714
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6542"
     variation       1715
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1045577"
     variation       1729
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1801807"
     polyA_signal    1734..1739
                     /gene="PSMD13"
                     /gene_synonym="HSPC027; p40.5; Rpn9; S11"
ORIGIN      
tttgacgcctcaatggcacagccaagtgcgcgggaagtgggctgcaaacgccggagagttttgtccggagcgcagagacgcgctgtaaccgagcaaccagcggggcccgcccccggcctgctacggcgctcccagcctgccccgcgccgctcggcgccggaagtgagtgagcatttccggcagccatccccgcggtgctgacatcccggttgttcttctgtgccgggggtcttcctgctgtcatgaaggacgtaccgggcttcctacagcagagccagaactccgggcccgggcagcccgctgtgtggcaccgtctggaggagctctacacgaagaagttgtggcatcagctgacacttcaggtgcttgattttgtgcaggatccgtgctttgcccaaggagatggtctcattaagctttatgaaaactttatcagtgaatttgaacacagggtgaaccctttgtccctcgtggaaatcattcttcatgtagttagacagatgactgatcctaatgtggctcttacttttctggaaaagactcgtgagaaggtgaaaagtagtgatgaggcagtgatcctgtgtaaaacagcaattggagctctaaaattaaacatcggggacctacaggttacaaaggaaacaattgaagatgttgaagaaatgctcaacaaccttcctggtgtgacatcggttcacagtcgtttctatgatctctccagtaaatactatcaaacaatcggaaaccacgcgtcctactacaaagatgctctgcggtttttgggctgtgttgacatcaaggatctaccagtgtctgagcagcaggagagagccttcacgctggggctagcaggacttctcggcgagggagtttttaactttggagaactcctcatgcaccctgtgctggagtccctgaggaatactgaccggcagtggctgattgacaccctctatgccttcaacagtggcaacgtagagcggttccagactctgaagactgcctggggccagcagcctgatttagcagctaatgaagcccagcttctgaggaaaattcagttgttgtgcctcatggagatgactttcacacgacctgccaatcacagacaactcacttttgaagaaattgccaaaagtgctaaaatcacagtgaatgaggtggagcttctggtgatgaaggccctttcggtggggctggtgaaaggcagtatagacgaggtggacaaacgagtccacatgacctgggtgcagccccgagtgttggatttgcaacagatcaagggaatgaaggaccgcctggagttctggtgcacggatgtgaagagcatggagatgctggtggagcaccaggcccatgacatcctcacctagggccccctggttccccgtcgtgtctcctttgactcacctgagagaggcgtttgcagccaatgaagctggctgctcagacggtcgacattgaatttgggtgggggttgggatcctgtctgaagtacagactgttcttgctctaaaaacaggactgtccctgatgggagccaggccacagggaggaggcttctttgtgggtctctcctgcagagggtgggggtctcagggtcttaggtgatacgggagagaaagaacgtgccaggcaggaggccccctgaagtctgtgtactccgaggtggatctccatccccatccacctgtacggacatcttttccgttgcggtttgagaatgttcctataataaacccctctgctttgttctt
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:5719 -> Biological process: GO:0000082 [G1/S transition of mitotic cell cycle] evidence: TAS
            GeneID:5719 -> Biological process: GO:0000209 [protein polyubiquitination] evidence: TAS
            GeneID:5719 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: TAS
            GeneID:5719 -> Biological process: GO:0002474 [antigen processing and presentation of peptide antigen via MHC class I] evidence: TAS
            GeneID:5719 -> Biological process: GO:0002479 [antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent] evidence: TAS
            GeneID:5719 -> Biological process: GO:0006521 [regulation of cellular amino acid metabolic process] evidence: TAS
            GeneID:5719 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
            GeneID:5719 -> Biological process: GO:0006977 [DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest] evidence: TAS
            GeneID:5719 -> Biological process: GO:0007127 [meiosis I] evidence: IEA
            GeneID:5719 -> Biological process: GO:0010467 [gene expression] evidence: TAS
            GeneID:5719 -> Biological process: GO:0016032 [viral process] evidence: TAS
            GeneID:5719 -> Biological process: GO:0016070 [RNA metabolic process] evidence: TAS
            GeneID:5719 -> Biological process: GO:0016071 [mRNA metabolic process] evidence: TAS
            GeneID:5719 -> Biological process: GO:0031145 [anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process] evidence: TAS
            GeneID:5719 -> Biological process: GO:0034641 [cellular nitrogen compound metabolic process] evidence: TAS
            GeneID:5719 -> Biological process: GO:0042590 [antigen processing and presentation of exogenous peptide antigen via MHC class I] evidence: TAS
            GeneID:5719 -> Biological process: GO:0042981 [regulation of apoptotic process] evidence: TAS
            GeneID:5719 -> Biological process: GO:0043066 [negative regulation of apoptotic process] evidence: TAS
            GeneID:5719 -> Biological process: GO:0044281 [small molecule metabolic process] evidence: TAS
            GeneID:5719 -> Biological process: GO:0051436 [negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
            GeneID:5719 -> Biological process: GO:0051437 [positive regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
            GeneID:5719 -> Biological process: GO:0051439 [regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
            GeneID:5719 -> Cellular component: GO:0000502 [proteasome complex] evidence: TAS
            GeneID:5719 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS
            GeneID:5719 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
            GeneID:5719 -> Cellular component: GO:0005838 [proteasome regulatory particle] evidence: IEA
            GeneID:5719 -> Cellular component: GO:0022624 [proteasome accessory complex] evidence: ISS

by @meso_cacase at DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.