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2024-04-26 07:17:18, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001190481            8292 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens claspin (CLSPN), transcript variant 2, mRNA.
ACCESSION   NM_001190481
VERSION     NM_001190481.1  GI:299522983
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 8292)
  AUTHORS   Sato,K., Sundaramoorthy,E., Rajendra,E., Hattori,H.,
            Jeyasekharan,A.D., Ayoub,N., Schiess,R., Aebersold,R.,
            Nishikawa,H., Sedukhina,A.S., Wada,H., Ohta,T. and
            Venkitaraman,A.R.
  TITLE     A DNA-damage selective role for BRCA1 E3 ligase in claspin
            ubiquitylation, CHK1 activation, and DNA repair
  JOURNAL   Curr. Biol. 22 (18), 1659-1666 (2012)
   PUBMED   22863316
  REMARK    GeneRIF: findings identify claspin as an in vivo substrate for the
            BRCA1 E3 ligase and suggest that its modification selectively
            triggers CHK1 activation for the homology-directed repair of a
            subset of genotoxic lesions
REFERENCE   2  (bases 1 to 8292)
  AUTHORS   Liu,S., Song,N. and Zou,L.
  TITLE     The conserved C terminus of Claspin interacts with Rad9 and
            promotes rapid activation of Chk1
  JOURNAL   Cell Cycle 11 (14), 2711-2716 (2012)
   PUBMED   22732499
  REMARK    GeneRIF: The conserved C terminus of Claspin interacts with Rad9
            and ensures timely activation of the ATR-Chk1 pathway.
REFERENCE   3  (bases 1 to 8292)
  AUTHORS   Benevolo,M., Musio,A., Vocaturo,A., Dona,M.G., Rollo,F.,
            Terrenato,I., Carosi,M., Pescarmona,E., Vocaturo,G. and
            Mottolese,M.
  TITLE     Claspin as a biomarker of human papillomavirus-related high grade
            lesions of uterine cervix
  JOURNAL   J Transl Med 10, 132 (2012)
   PUBMED   22731782
  REMARK    GeneRIF: analysis of claspin expression could be clinically
            relevant in the diagnosis of HPV-related cervical lesions, in
            particular when applied to cervico-vaginal cytology
            Publication Status: Online-Only
REFERENCE   4  (bases 1 to 8292)
  AUTHORS   Yoshimura,A., Akita,M., Hosono,Y., Abe,T., Kobayashi,M.,
            Yamamoto,K., Tada,S., Seki,M. and Enomoto,T.
  TITLE     Functional relationship between Claspin and Rad17
  JOURNAL   Biochem. Biophys. Res. Commun. 414 (2), 298-303 (2011)
   PUBMED   21945441
  REMARK    GeneRIF: the functions of Claspin and the functional relationship
            between Claspin and Rad17 were studied.
REFERENCE   5  (bases 1 to 8292)
  AUTHORS   Izawa,N., Wu,W., Sato,K., Nishikawa,H., Kato,A., Boku,N., Itoh,F.
            and Ohta,T.
  TITLE     HERC2 Interacts with Claspin and regulates DNA origin firing and
            replication fork progression
  JOURNAL   Cancer Res. 71 (17), 5621-5625 (2011)
   PUBMED   21775519
  REMARK    GeneRIF: In the presence of BRCA1, endogenous HERC2 interacts with
            Claspin, a protein essential for G(2)-M checkpoint activation and
            replication fork stability.
REFERENCE   6  (bases 1 to 8292)
  AUTHORS   Sorensen,C.S., Syljuasen,R.G., Lukas,J. and Bartek,J.
  TITLE     ATR, Claspin and the Rad9-Rad1-Hus1 complex regulate Chk1 and
            Cdc25A in the absence of DNA damage
  JOURNAL   Cell Cycle 3 (7), 941-945 (2004)
   PUBMED   15190204
REFERENCE   7  (bases 1 to 8292)
  AUTHORS   Lin,S.Y., Li,K., Stewart,G.S. and Elledge,S.J.
  TITLE     Human Claspin works with BRCA1 to both positively and negatively
            regulate cell proliferation
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 101 (17), 6484-6489 (2004)
   PUBMED   15096610
  REMARK    GeneRIF: determination of properties of both a tumor suppressor and
            an oncogene
REFERENCE   8  (bases 1 to 8292)
  AUTHORS   Chini,C.C. and Chen,J.
  TITLE     Human claspin is required for replication checkpoint control
  JOURNAL   J. Biol. Chem. 278 (32), 30057-30062 (2003)
   PUBMED   12766152
  REMARK    GeneRIF: Claspin has a potentially critical role in replication
            checkpoint control in mammalian cells
REFERENCE   9  (bases 1 to 8292)
  AUTHORS   Zou,L. and Elledge,S.J.
  TITLE     Sensing DNA damage through ATRIP recognition of RPA-ssDNA complexes
  JOURNAL   Science 300 (5625), 1542-1548 (2003)
   PUBMED   12791985
REFERENCE   10 (bases 1 to 8292)
  AUTHORS   Kumagai,A. and Dunphy,W.G.
  TITLE     Claspin, a novel protein required for the activation of Chk1 during
            a DNA replication checkpoint response in Xenopus egg extracts
  JOURNAL   Mol. Cell 6 (4), 839-849 (2000)
   PUBMED   11090622
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AF297866.1, BC115025.1,
            BC137279.1 and AL354864.16.
            
            Summary: The product of this gene is an essential upstream
            regulator of checkpoint kinase 1 and triggers a checkpoint arrest
            of the cell cycle in response to replicative stress or DNA damage.
            The protein is also required for efficient DNA replication during a
            normal S phase. Multiple transcript variants encoding different
            isoforms have been found for this gene. [provided by RefSeq, Jun
            2010].
            
            Transcript Variant: This variant (2) lacks an alternate in-frame
            exon in the central coding region, compared to variant 1. The
            resulting isoform (2) lacks an internal segment, compared to
            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 :: BC115025.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025081, ERS025082 [ECO:0000350]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-1417              AF297866.1         1-1417
            1418-2678           BC115025.1         1411-2671
            2679-4109           BC137279.1         2850-4280
            4110-8292           AL354864.16        77956-82138
FEATURES             Location/Qualifiers
     source          1..8292
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="1"
                     /map="1p34.2"
     gene            1..8292
                     /gene="CLSPN"
                     /note="claspin"
                     /db_xref="GeneID:63967"
                     /db_xref="HGNC:19715"
                     /db_xref="MIM:605434"
     exon            1..104
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    54..56
                     /gene="CLSPN"
                     /note="upstream in-frame stop codon"
     CDS             81..3908
                     /gene="CLSPN"
                     /note="isoform 2 is encoded by transcript variant 2;
                     hClaspin; claspin homolog"
                     /codon_start=1
                     /product="claspin isoform 2"
                     /protein_id="NP_001177410.1"
                     /db_xref="GI:299522984"
                     /db_xref="CCDS:CCDS53297.1"
                     /db_xref="GeneID:63967"
                     /db_xref="HGNC:19715"
                     /db_xref="MIM:605434"
                     /translation="
MTGEVGSEVHLEINDPNVISQEEADSPSDSGQGSYETIGPLSEGDSDEEIFVSKKLKNRKVLQDSDSETEDTNASPEKTTYDSAEEENKENLYAGKNTKIKRIYKTVADSDESYMEKSLYQENLEAQVKPCLELSLQSGNSTDFTTDRKSSKKHIHDKEGTAGKAKVKSKRRLEKEERKMEKIRQLKKKETKNQEDDVEQPFNDSGCLLVDKDLFETGLEDENNSPLEDEESLESIRAAVKNKVKKHKKKEPSLESGVHSFEEGSELSKGTTRKERKAARLSKEALKQLHSETQRLIRESALNLPYHMPENKTIHDFFKRKPRPTCHGNAMALLKSSKYQSSHHKEIIDTANTTEMNSDHHSKGSEQTTGAENEVETNALPVVSKETQIITGSDESCRKDLVKNEELEIQEKQKQSDIRPSPGDSSVLQQESNFLGNNHSEECQVGGLVAFEPHALEGEGPQNPEETDEKVEEPEQQNKSSAVGPPEKVRRFTLDRLKQLGVDVSIKPRLGADEDSFVILEPETNRGEKLQVLKAKLQEAMKLRRFEERQKRQALFKLDNEDGFEEEEEEEEEMTDESEEDGEEKVEKEEKEEELEEEEEKEEEEEEEGNQETAEFLLSSEEIETKDEKEMDKENNDGSSEIGKAVGFLSVPKSLSSDSTLLLFKDSSSKMGYFPTEEKSETDENSGKQPSKLDEDDSCSLLTKESSHNSSFELIGSTIPSYQPCNRQTGRGTSFFPTAGGFRSPSPGLFRASLVSSASKSSGKLSEPSLPIEDSQDLYNASPEPKTLFLGAGDFQFCLEDDTQSQLLDADGFLNVRNHRNQYQALKPRLPLASMDENAMDANMDELLDLCTGKFTSQAEKHLPRKSDKKENMEELLNLCSGKFTSQDASTPASSELNKQEKESSMGDPMEEALALCSGSFPTDKEEEDEEEEFGDFRLVSNDNEFDSDEDEHSDSGNDLALEDHEDDDEEELLKRSEKLKRQMRLRKYLEDEAEVSGSDVGSEDEYDGEEIDEYEEDVIDEVLPSDEELQSQIKKIHMKTMLDDDKRQLRLYQERYLADGDLHSDGPGRMRKFRWKNIDDASQMDLFHRDSDDDQTEEQLDESEARWRKERIEREQWLRDMAQQGKITAEEEEEIGEDSQFMILAKKVTAKALQKNASRPMVIQESKSLLRNPFEAIRPGSAQQVKTGSLLNQPKAVLQKLAALSDHNPSAPRNSRNFVFHTLSPVKAEAAKESSKSQVKKRGPSFMTSPSPKHLKTDDSTSGLTRSIFKYLES
"
     exon            105..213
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            214..662
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            663..824
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            825..902
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     variation       852
                     /gene="CLSPN"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35435909"
     exon            903..975
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            976..1084
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            1085..1659
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            1660..1916
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            1917..2095
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            2096..2160
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            2161..2360
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            2361..2515
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            2516..2742
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     variation       2562
                     /gene="CLSPN"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:34390044"
     exon            2743..2854
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            2855..2930
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            2931..3031
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            3032..3196
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            3197..3318
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            3319..3446
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            3447..3552
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            3553..3635
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     exon            3636..3797
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     variation       3727
                     /gene="CLSPN"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:35490896"
     exon            3798..8292
                     /gene="CLSPN"
                     /inference="alignment:Splign:1.39.8"
     STS             4217..4816
                     /gene="CLSPN"
                     /standard_name="PMC156606P1"
                     /db_xref="UniSTS:271408"
     STS             4298..5758
                     /gene="CLSPN"
                     /standard_name="GDB:312794"
                     /db_xref="UniSTS:30247"
     STS             4353..5756
                     /gene="CLSPN"
                     /standard_name="L17971"
                     /db_xref="UniSTS:43966"
     STS             4378..4799
                     /gene="CLSPN"
                     /standard_name="G38154"
                     /db_xref="UniSTS:53341"
     variation       4657
                     /gene="CLSPN"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1062047"
     STS             4751..4820
                     /gene="CLSPN"
                     /standard_name="D1S1423"
                     /db_xref="UniSTS:149619"
     STS             5128..5251
                     /gene="CLSPN"
                     /standard_name="RH91339"
                     /db_xref="UniSTS:88492"
     STS             5280..5419
                     /gene="CLSPN"
                     /standard_name="SHGC-37119"
                     /db_xref="UniSTS:32226"
     polyA_signal    5414..5419
                     /gene="CLSPN"
     STS             5426..6474
                     /gene="CLSPN"
                     /standard_name="D11S1910"
                     /db_xref="UniSTS:149174"
     polyA_site      5436
                     /gene="CLSPN"
     variation       5615
                     /gene="CLSPN"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:609070"
     STS             5738..5859
                     /gene="CLSPN"
                     /standard_name="G44334"
                     /db_xref="UniSTS:95121"
     variation       5771
                     /gene="CLSPN"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:620296"
     STS             5800..6579
                     /gene="CLSPN"
                     /standard_name="RH36905"
                     /db_xref="UniSTS:87932"
     STS             7020..7167
                     /gene="CLSPN"
                     /standard_name="L17791"
                     /db_xref="UniSTS:42740"
     STS             7298..7367
                     /gene="CLSPN"
                     /standard_name="D1S1423"
                     /db_xref="UniSTS:149619"
     polyA_signal    8270..8275
                     /gene="CLSPN"
     polyA_site      8292
                     /gene="CLSPN"
ORIGIN      
gacggcgggagccgctgctctccggctgagggaatcagagacagctccgtccctagtggagcgcaggggaggcagaagtcatgacaggcgaggtgggttctgaggttcacctagaaatcaatgacccaaacgtcatttcacaagaggaagcagatagtccttcagatagtggacagggcagctatgaaacaattggacccttgagtgaaggagattcagatgaagagatatttgtaagtaagaagttgaaaaacaggaaggttctacaagacagtgattccgaaacagaggacacaaatgcctctccagagaaaactacctatgacagtgccgaggaggaaaataaagagaatttatatgctgggaaaaatacaaaaatcaaaaggatttacaaaactgtggcagacagtgatgaaagttacatggaaaagtctttgtatcaggaaaatcttgaagcgcaagtgaaaccttgcttagagctgagtcttcagtctggaaactctacagactttaccactgacagaaagagttccaaaaagcacatacatgataaagaaggaactgcaggaaaagcaaaagtaaaatcaaaaagaagacttgagaaagaggagagaaaaatggaaaaaattagacagctaaaaaagaaggaaacaaaaaaccaggaagatgatgtagaacagccatttaatgacagtggctgtcttcttgtggataaagacctttttgaaactgggttggaggatgaaaataactctccattggaagatgaagagtcattagaatcaataagagcagctgtaaaaaacaaagtaaaaaagcacaagaaaaaagaaccatctttggagagtggggtccattcatttgaggaaggaagtgagttatcaaaaggaaccacgaggaaggaaagaaaggcagccagattaagtaaagaagcattaaaacaactgcatagtgagactcagcgccttattcgagagtctgcactgaaccttccatatcatatgcctgagaataaaaccattcatgatttcttcaaacgtaaaccccggcccacttgccacggaaatgccatggcactattgaagtcatctaaatatcagtcaagccatcacaaagaaatcatagacactgcaaatactactgaaatgaacagtgatcaccatagtaaaggttctgagcagacaacaggtgcagaaaatgaagtggaaactaatgcactccctgtagtttcaaaggaaacccagatcattactggatcagatgagtcttgcaggaaggatttggtaaaaaatgaagagctagaaattcaggagaaacagaagcagagtgacattagaccttcacctggggacagctcagtgttgcaacaggaatccaacttcctcgggaacaatcacagtgaggaatgtcaggttggagggcttgtagcatttgaacctcatgccctggagggtgaaggcccccaaaatccagaagaaacagatgagaaagtggaagagcctgagcagcaaaataaatcatcagcagttgggccacctgaaaaagtgagacggtttactctggatagacttaagcaactgggagtagatgtttccattaaaccacggctaggtgctgatgaagattcctttgtgatacttgaacctgaaaccaacagaggtgaaaagcttcaggtgttaaaagctaaactgcaagaagcaatgaaactccgaaggtttgaggagcgccagaagcgccaagcactgtttaaattagataatgaagatgggtttgaggaagaggaggaggaagaggaagaaatgacagatgagtctgaggaagatggagaagagaaggtagagaaagaagagaaagaggaagaactagaggaagaggaggagaaagaagaggaggaggaagaagaaggaaatcaggagactgcagaattccttcttagtagtgaagaaatagaaacaaaagatgaaaaagaaatggataaagaaaataatgatggcagtagtgaaattggcaaggcagttggcttcctctctgttcccaagtctctctcatcagattctactttacttctgtttaaggacagctcttccaagatgggttactttcctactgaagaaaaatcagaaacagatgaaaactcaggcaagcagcctagcaaactggatgaggatgattcatgttcattgctaacaaaggagagcagccacaatagcagctttgagctgattggctccacgattccatcctatcagccttgcaacagacaaacaggccgtgggaccagttttttccctacagcaggaggattcagatctccttcccctgggctatttcgagccagtttggtcagctcagcttctaagagttcagggaaactgtctgagccttcacttcccatagaggattcccaggatctgtataacgcctccccagagcctaagacacttttcctaggagcaggagacttccagttctgtttagaagatgacactcagagccaactgttggatgcagatgggttcttaaatgttagaaaccacaggaatcagtaccaagctttgaagcctcgattgccattggccagtatggatgagaatgccatggatgccaacatggatgagctgttggatttgtgtactggaaagttcacatctcaggctgaaaaacatctacccaggaagagtgacaagaaagagaacatggaggaacttctgaacctttgttcaggaaaattcacttctcaggatgcctccactccagcctcatcagagttaaataaacaggagaaggagagcagcatgggtgatccaatggaagaagcacttgctctttgctcaggctcttttcccacagacaaggaagaggaagacgaggaggaggaatttggagactttcggcttgtttcaaatgataatgagtttgatagtgatgaggatgaacacagtgactctggtaatgatctggcactggaagaccatgaagatgatgatgaagaagaactcctgaagcgatctgagaagttgaaaaggcaaatgaggttgaggaaatacctggaggatgaggcagaggtgtcaggaagtgatgtgggaagcgaagatgagtatgatggggaagaaattgatgaatatgaagaggacgtaattgatgaagtacttccttctgatgaggaactgcagagtcaaatcaagaaaatacacatgaaaactatgttggatgatgataagcgacagctacgtttataccaagagaggtaccttgctgatggggatctgcacagcgatggtcctgggcgaatgaggaagtttcgatggaaaaacatagatgatgcttcccagatggacttgttccacagagactctgatgatgatcagactgaagaacagcttgatgagtcagaagccaggtggaggaaggagcgaattgaacgagagcagtggcttcgggacatggcacagcaggggaaaattacagctgaagaagaagaagaaattggggaggacagtcagtttatgatactggccaagaaagttacagccaaagcactgcagaagaatgccagtcgccctatggttattcaggaatcaaagtctttgctcagaaatccttttgaagccatcagaccaggaagtgctcaacaggtgaagacaggctcactgctaaaccagcccaaagctgtgcttcagaaactggctgctctctctgaccataaccccagtgctcctcgaaattcaagaaactttgtctttcatacactttctcctgtcaaggctgaggcggcaaaggaatcgtctaagtctcaggtaaagaaaaggggtccatctttcatgacttctccttcacctaagcacctcaaaacagatgatagcacttcaggattgacgcgaagcatcttcaaatatttggagagctaacaccatcaaaggtgccaaaatctacattgagactgctttgagaagtttctagcactgaaagttggaattgacactccagccaatgatccttccttctttcataatcaatgcaataagattgcagacagaaattccagtgatttctactgcacagctctggacatctcttttcctagtattattccctgaattggccactgatttcaattctgcagtatttacaacatcaacaactcatggaatacttgggtgaggtttcctttttttttttttttttaagatgggagtctcactctgttgcccagcttggagtgcagtggcgtgatctcggctcaccacaatctctgcctcccaggttcaagcgattctcctccttcagcctcccgagtagctgggattacaggcatgtgccaatacgcccagctaatttttgtatttttagtagagacggggtttcaccatgttggccaggctggtcttgaactcctgacctcaaatgatccatccacctcggccccacaaagtgctggtcacatgcatgagtcactgcacctggccttgggttaggtttcacttcctccattagacatttgacattttattgtagcagctttctgggttaatatctctttgtgattgatagaagtggttggaagaggaagagtagggaaaagtgtgacattacagattaaacagtgaaaatcagtaccataatgactcctttacacccatgagatacgtaccatgatgaccagggctcggtgaaagaaagatttctttttttttttttgagatagtctcactttgttgcccagtctggagtgcagtggcgcaatctcggctcacggcaacctctgcctcccgggttcaagtgattctcctgtctcagcctcccaagtagctgggactacaggtgcatgccaccacacctggctaatttttgtatttttagtggagacagggagtcaccatgttggccaggctggtctcgatctcctgacctcaagtgatccagctgcctcagcctcccaaagtgctgagattacaggcgtgagccactgtgcccagccaaaagaacgatttcttagatgg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//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:63967 -> Molecular function: GO:0003677 [DNA binding] evidence: IEA
            GeneID:63967 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:63967 -> Molecular function: GO:0010997 [anaphase-promoting complex binding] evidence: IPI
            GeneID:63967 -> Biological process: GO:0000077 [DNA damage checkpoint] evidence: IMP
            GeneID:63967 -> Biological process: GO:0006260 [DNA replication] evidence: TAS
            GeneID:63967 -> Biological process: GO:0006281 [DNA repair] evidence: IEA
            GeneID:63967 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
            GeneID:63967 -> Biological process: GO:0006921 [cellular component disassembly involved in execution phase of apoptosis] evidence: TAS
            GeneID:63967 -> Biological process: GO:0007049 [cell cycle] evidence: IEA
            GeneID:63967 -> Biological process: GO:0018105 [peptidyl-serine phosphorylation] evidence: IDA
            GeneID:63967 -> Biological process: GO:0031572 [G2 DNA damage checkpoint] evidence: IDA
            GeneID:63967 -> Biological process: GO:0032147 [activation of protein kinase activity] evidence: IDA
            GeneID:63967 -> Biological process: GO:0033314 [mitotic DNA replication checkpoint] evidence: IMP
            GeneID:63967 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS

by @meso_cacase at DBCLS
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