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2024-04-25 10:01:02, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_002812               1556 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens proteasome (prosome, macropain) 26S subunit,
            non-ATPase, 8 (PSMD8), mRNA.
ACCESSION   NM_002812
VERSION     NM_002812.4  GI:156631004
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 1556)
  AUTHORS   Baglioni,S., Casamenti,F., Bucciantini,M., Luheshi,L.M., Taddei,N.,
            Chiti,F., Dobson,C.M. and Stefani,M.
  TITLE     Prefibrillar amyloid aggregates could be generic toxins in higher
            organisms
  JOURNAL   J. Neurosci. 26 (31), 8160-8167 (2006)
   PUBMED   16885229
  REMARK    GeneRIF: These findings support the hypothesis that
            neurodegenerative disorders result primarily from a generic cell
            dysfunction caused by early misfolded species in the aggregation
            process.
REFERENCE   2  (bases 1 to 1556)
  AUTHORS   Colland,F., Jacq,X., Trouplin,V., Mougin,C., Groizeleau,C.,
            Hamburger,A., Meil,A., Wojcik,J., Legrain,P. and Gauthier,J.M.
  TITLE     Functional proteomics mapping of a human signaling pathway
  JOURNAL   Genome Res. 14 (7), 1324-1332 (2004)
   PUBMED   15231748
REFERENCE   3  (bases 1 to 1556)
  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   4  (bases 1 to 1556)
  AUTHORS   Grimwood,J., Gordon,L.A., Olsen,A., Terry,A., Schmutz,J.,
            Lamerdin,J., Hellsten,U., Goodstein,D., Couronne,O.,
            Tran-Gyamfi,M., Aerts,A., Altherr,M., Ashworth,L., Bajorek,E.,
            Black,S., Branscomb,E., Caenepeel,S., Carrano,A., Caoile,C.,
            Chan,Y.M., Christensen,M., Cleland,C.A., Copeland,A., Dalin,E.,
            Dehal,P., Denys,M., Detter,J.C., Escobar,J., Flowers,D.,
            Fotopulos,D., Garcia,C., Georgescu,A.M., Glavina,T., Gomez,M.,
            Gonzales,E., Groza,M., Hammon,N., Hawkins,T., Haydu,L., Ho,I.,
            Huang,W., Israni,S., Jett,J., Kadner,K., Kimball,H., Kobayashi,A.,
            Larionov,V., Leem,S.H., Lopez,F., Lou,Y., Lowry,S., Malfatti,S.,
            Martinez,D., McCready,P., Medina,C., Morgan,J., Nelson,K.,
            Nolan,M., Ovcharenko,I., Pitluck,S., Pollard,M., Popkie,A.P.,
            Predki,P., Quan,G., Ramirez,L., Rash,S., Retterer,J., Rodriguez,A.,
            Rogers,S., Salamov,A., Salazar,A., She,X., Smith,D., Slezak,T.,
            Solovyev,V., Thayer,N., Tice,H., Tsai,M., Ustaszewska,A., Vo,N.,
            Wagner,M., Wheeler,J., Wu,K., Xie,G., Yang,J., Dubchak,I.,
            Furey,T.S., DeJong,P., Dickson,M., Gordon,D., Eichler,E.E.,
            Pennacchio,L.A., Richardson,P., Stubbs,L., Rokhsar,D.S.,
            Myers,R.M., Rubin,E.M. and Lucas,S.M.
  TITLE     The DNA sequence and biology of human chromosome 19
  JOURNAL   Nature 428 (6982), 529-535 (2004)
   PUBMED   15057824
REFERENCE   5  (bases 1 to 1556)
  AUTHORS   Conticello,S.G., Harris,R.S. and Neuberger,M.S.
  TITLE     The Vif protein of HIV triggers degradation of the human
            antiretroviral DNA deaminase APOBEC3G
  JOURNAL   Curr. Biol. 13 (22), 2009-2013 (2003)
   PUBMED   14614829
REFERENCE   6  (bases 1 to 1556)
  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 1556)
  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 1556)
  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   9  (bases 1 to 1556)
  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   10 (bases 1 to 1556)
  AUTHORS   Kominami,K., DeMartino,G.N., Moomaw,C.R., Slaughter,C.A.,
            Shimbara,N., Fujimuro,M., Yokosawa,H., Hisamatsu,H., Tanahashi,N.,
            Shimizu,Y. et al.
  TITLE     Nin1p, a regulatory subunit of the 26S proteasome, is necessary for
            activation of Cdc28p kinase of Saccharomyces cerevisiae
  JOURNAL   EMBO J. 14 (13), 3105-3115 (1995)
   PUBMED   7621825
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BP369299.1 and BC001164.1.
            On Aug 31, 2007 this sequence version replaced gi:39812361.
            
            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. A pseudogene has been
            identified on chromosome 1. [provided by RefSeq, Jul 2008].
            
            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 :: BC001164.1, AK301771.1 [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
            1-249               BP369299.1         15-263
            250-1556            BC001164.1         1-1307
FEATURES             Location/Qualifiers
     source          1..1556
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="19"
                     /map="19q13.2"
     gene            1..1556
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /note="proteasome (prosome, macropain) 26S subunit,
                     non-ATPase, 8"
                     /db_xref="GeneID:5714"
                     /db_xref="HGNC:9566"
     exon            1..412
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /inference="alignment:Splign:1.39.8"
     variation       20
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369756672"
     variation       26
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:12973506"
     variation       42
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372594226"
     CDS             53..1105
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /note="26S proteasome regulatory subunit p31; 26S
                     proteasome regulatory subunit S14; 26S proteasome
                     regulatory subunit RPN12"
                     /codon_start=1
                     /product="26S proteasome non-ATPase regulatory subunit 8"
                     /protein_id="NP_002803.2"
                     /db_xref="GI:156631005"
                     /db_xref="CCDS:CCDS12515.2"
                     /db_xref="GeneID:5714"
                     /db_xref="HGNC:9566"
                     /translation="
MFIKGRAPRAPPRERRRATRGGLRQVVAPPRALGSTSRPHFRRASVCRRRCRKSGGLLAASRKMAAAAVNGAAGFSSSGPAATSGAVLQAATGMYEQLKGEWNRKSPNLSKCGEELGRLKLVLLELNFLPTTGTKLTKQQLILARDILEIGAQWSILRKDIPSFERYMAQLKCYYFDYKEQLPESAYMHQLLGLNLLFLLSQNRVAEFHTELERLPAKDIQTNVYIKHPVSLEQYLMEGSYNKVFLAKGNIPAESYTFFIDILLDTIRDEIAGCIEKAYEKILFTEATRILFFNTPKKMTDYAKKRGWVLGPNNYYSFASQQQKPEDTTIPSTELAKQVIEYARQLEMIV
"
     misc_feature    653..1030
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /note="COP9 signalosome, subunit CSN8; Region: PCI_Csn8;
                     pfam10075"
                     /db_xref="CDD:204392"
     variation       54
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:376781876"
     variation       99
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375145305"
     variation       191
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:79875980"
     variation       206
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369326461"
     variation       224
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369447667"
     variation       228
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200109220"
     variation       230
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201665089"
     variation       249
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183916438"
     variation       260
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369208449"
     variation       279
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372489810"
     variation       283
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201001430"
     variation       291
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377507303"
     variation       363
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11541762"
     variation       396
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:147693309"
     variation       397
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:28384479"
     exon            413..485
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /inference="alignment:Splign:1.39.8"
     variation       424
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148287182"
     variation       445
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376132803"
     variation       466
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145865086"
     exon            486..588
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /inference="alignment:Splign:1.39.8"
     variation       525
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200403794"
     variation       529
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371805034"
     variation       534..535
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:34950088"
     variation       538
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:11541759"
     exon            589..754
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /inference="alignment:Splign:1.39.8"
     variation       601
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138441628"
     variation       608
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142934372"
     variation       646
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1804245"
     variation       652
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367962688"
     variation       662
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145982766"
     variation       668
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:138444191"
     variation       693
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201667645"
     variation       700
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:149260015"
     variation       712
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376145824"
     variation       721
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368412719"
     STS             729..863
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /standard_name="RH39050"
                     /db_xref="UniSTS:90683"
     variation       736
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11541757"
     exon            755..855
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /inference="alignment:Splign:1.39.8"
     variation       781
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141504927"
     variation       804..805
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:35335693"
     variation       808
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373583013"
     variation       820
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201768988"
     variation       838
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11541756"
     variation       844
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375464238"
     exon            856..967
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /inference="alignment:Splign:1.39.8"
     variation       877
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1131182"
     variation       880
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:199786947"
     variation       913
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141110538"
     variation       946
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:374571539"
     exon            968..1539
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /inference="alignment:Splign:1.39.8"
     variation       969
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367675318"
     variation       982
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371885326"
     variation       1001
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147213822"
     STS             1041..1189
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /standard_name="SGC30294"
                     /db_xref="UniSTS:56979"
     variation       1048
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10828"
     variation       1056
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201308499"
     variation       1083
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:34847046"
     variation       1091
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144402089"
     variation       1100
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151185277"
     variation       1106
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3180566"
     variation       1153
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:377149465"
     variation       1185
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150328547"
     variation       1227
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368351923"
     STS             1289..1428
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /standard_name="RH11793"
                     /db_xref="UniSTS:26303"
     STS             1328..1471
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /standard_name="D19S1131"
                     /db_xref="UniSTS:79288"
     variation       1362..1363
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
                     /replace=""
                     /replace="gccccagcagcactgtggc"
                     /db_xref="dbSNP:374846245"
     polyA_signal    1519..1524
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
     polyA_site      1539
                     /gene="PSMD8"
                     /gene_synonym="HIP6; HYPF; Nin1p; p31; Rpn12; S14"
ORIGIN      
ccaacttccggtcaccatcttgagtgacgacagaggcggagctccaactgacatgttcattaagggcagggctccgagggcgccacctcgagagcgacggcgggctacccggggcgggctgaggcaggttgtagccccgccccgggccttgggctccacctctcggccccacttccgccgggcaagcgtttgtaggcggcgctgccgtaaatcaggcggtctgcttgccgcatcacgcaagatggcggccgcggcggtgaacggggcggcaggcttctcgagctccgggcccgcggcaacctcgggcgctgttctgcaggccgcgaccggcatgtacgagcaactcaagggcgagtggaaccgtaaaagccccaatcttagcaagtgcggggaagagctgggtcgactcaagctagttcttctggagctcaacttcttgccaaccacagggaccaagctgaccaaacagcagctaattctggcccgtgacatactggagatcggggcccaatggagcatcctacgcaaggacatcccctccttcgagcgctacatggcccagctcaaatgctactactttgattacaaggagcagctccccgagtcagcctatatgcaccagctcttgggcctcaacctcctcttcctgctgtcccagaaccgggtggctgagttccacacggagttggagcggctgcctgccaaggacatacagaccaatgtctacatcaagcacccagtgtccctggagcaatacctgatggagggcagctacaacaaagtgttcctggccaagggtaacatccccgccgagagctacaccttcttcattgacatcctgctcgacactatcagggatgagatcgctgggtgcatcgagaaggcctacgagaaaatccttttcactgaggccacccggatcctcttcttcaacacacccaaaaagatgacagactacgccaagaagcgagggtgggtcctgggccccaacaactactacagttttgccagccagcagcagaagccggaagacaccaccattccctccacagaactggccaaacaggtcatcgagtatgcccggcagctggagatgatcgtctgagccccccgggcactgggtggggcagggcacgagttatttaaaacagttacactgcagggtttcgcccaataaaggtggactgacattccctcttccaggcccttgtctccccagttgggacggcagagagacaagttcttatatctgaagaacttggaggttttggggcattcaggagttggagatagcctccaactgggtcagcctctgtctggtgggcattgctcagggtctcaaacatggacgcccactgtggggccccagcagcactgtggcctgcaggagggcatggccccaggtagggggactgttctagccagctgtggacacataggaatgctggaccagggtaccagattttttcaacaaagggggtgaagtgtcctactaaaaagaataaatgttggcagtgaattaaacaatttttcaaatgaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:5714 -> Biological process: GO:0000082 [G1/S transition of mitotic cell cycle] evidence: TAS
            GeneID:5714 -> Biological process: GO:0000209 [protein polyubiquitination] evidence: TAS
            GeneID:5714 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: TAS
            GeneID:5714 -> Biological process: GO:0002474 [antigen processing and presentation of peptide antigen via MHC class I] evidence: TAS
            GeneID:5714 -> Biological process: GO:0002479 [antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent] evidence: TAS
            GeneID:5714 -> Biological process: GO:0006521 [regulation of cellular amino acid metabolic process] evidence: TAS
            GeneID:5714 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
            GeneID:5714 -> Biological process: GO:0006977 [DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest] evidence: TAS
            GeneID:5714 -> Biological process: GO:0010467 [gene expression] evidence: TAS
            GeneID:5714 -> Biological process: GO:0016032 [viral process] evidence: TAS
            GeneID:5714 -> Biological process: GO:0016070 [RNA metabolic process] evidence: TAS
            GeneID:5714 -> Biological process: GO:0016071 [mRNA metabolic process] evidence: TAS
            GeneID:5714 -> Biological process: GO:0031145 [anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process] evidence: TAS
            GeneID:5714 -> Biological process: GO:0034641 [cellular nitrogen compound metabolic process] evidence: TAS
            GeneID:5714 -> Biological process: GO:0042590 [antigen processing and presentation of exogenous peptide antigen via MHC class I] evidence: TAS
            GeneID:5714 -> Biological process: GO:0042981 [regulation of apoptotic process] evidence: TAS
            GeneID:5714 -> Biological process: GO:0043066 [negative regulation of apoptotic process] evidence: TAS
            GeneID:5714 -> Biological process: GO:0044281 [small molecule metabolic process] evidence: TAS
            GeneID:5714 -> Biological process: GO:0051436 [negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
            GeneID:5714 -> Biological process: GO:0051437 [positive regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
            GeneID:5714 -> Biological process: GO:0051439 [regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
            GeneID:5714 -> Cellular component: GO:0000502 [proteasome complex] evidence: TAS
            GeneID:5714 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
            GeneID:5714 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS
            GeneID:5714 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA
            GeneID:5714 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
            GeneID:5714 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
            GeneID:5714 -> Cellular component: GO:0005838 [proteasome regulatory particle] evidence: IEA
            GeneID:5714 -> Cellular component: GO:0022624 [proteasome accessory complex] evidence: ISS

by @meso_cacase at DBCLS
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