GGRNA Home | Help | Advanced search

2024-04-19 23:54:11, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_138764                849 bp    mRNA    linear   PRI 07-JUL-2013
DEFINITION  Homo sapiens BCL2-associated X protein (BAX), transcript variant
            sigma, mRNA.
ACCESSION   NM_138764 NM_138765
VERSION     NM_138764.4  GI:242117892
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 849)
  AUTHORS   Li,Y., Zhao,Y., Cheng,Z., Zhan,J., Sun,X., Qian,H., Zhu,W. and
            Xu,W.
  TITLE     Mesenchymal stem cell-like cells from children foreskin inhibit the
            growth of SGC-7901 gastric cancer cells
  JOURNAL   Exp. Mol. Pathol. 94 (3), 430-437 (2013)
   PUBMED   23421973
  REMARK    GeneRIF: Human mesenchymal stem cell-like cells from foreskin
            derived conditioned medium inhibited the expression of BCL-2 while
            increased the expression of BAX and caspase-3 in gastric cancer
            cells.
REFERENCE   2  (bases 1 to 849)
  AUTHORS   Zhang,A., Hildreth,R.L. and Colberg-Poley,A.M.
  TITLE     Human cytomegalovirus inhibits apoptosis by proteasome-mediated
            degradation of Bax at endoplasmic reticulum-mitochondrion contacts
  JOURNAL   J. Virol. 87 (10), 5657-5668 (2013)
   PUBMED   23487455
  REMARK    GeneRIF: Authors establish that the UL37 exon 1 protein retargets
            Bax to the mitochondrion-associated membranes as well as to the
            outer mitochondrial membrane from immediate early through late
            times of infection.
REFERENCE   3  (bases 1 to 849)
  AUTHORS   Nayak,M.K., Kulkarni,P.P. and Dash,D.
  TITLE     Regulatory role of proteasome in determination of platelet life
            span
  JOURNAL   J. Biol. Chem. 288 (10), 6826-6834 (2013)
   PUBMED   23329846
  REMARK    GeneRIF: Data indicate a critical role of proteasome in delimiting
            platelet life span ostensibly through constitutive elimination of
            the conformationally active Bax.
REFERENCE   4  (bases 1 to 849)
  AUTHORS   Kim,M.S., Kim,S.S., Yoo,N.J. and Lee,S.H.
  TITLE     Rare somatic mutation of pro-apoptotic BAX and BAK genes in common
            human cancers
  JOURNAL   Tumori 98 (6), 149E-151E (2012)
   PUBMED   23389372
  REMARK    GeneRIF: data indicate that somatic mutation of BAX and BAK genes
            are rare in the common cancers (besides the cancers with high
            microsatellite instability) and suggest that neither BAX nor BAK
            mutation may causally be implicated in their tumorigenesis
REFERENCE   5  (bases 1 to 849)
  AUTHORS   Kopinski,P., Dyczek,A., Chorostowska-Wynimko,J., Marszalek,A.,
            Balicka-Slusarczyk,B., Kubiszewska,I., Szablowska,K., Polgesek,E.
            and Szpechcinski,A.
  TITLE     [Higher incidence of alveolar lymphocytes (AL) apoptosis in smokers
            depends on BCL-2 expression and specific response to tumor necrosis
            factor alpha (TNFalpha). Bronchoalveolar lavage (BAL) material
            analysis from selected interstitial lung diseases (ILD) and healthy
            controls]
  JOURNAL   Prz. Lek. 69 (10), 731-736 (2012)
   PUBMED   23421021
  REMARK    GeneRIF: The most likely mechanisms involve down-regulation of
            BCL-2 expression and altered alveolar lymphocyte susceptibility to
            TNFalpha in smokers with idiopathic pulmonary ibrosis and pulmonary
            sarcoidosis.
REFERENCE   6  (bases 1 to 849)
  AUTHORS   Chittenden,T., Flemington,C., Houghton,A.B., Ebb,R.G., Gallo,G.J.,
            Elangovan,B., Chinnadurai,G. and Lutz,R.J.
  TITLE     A conserved domain in Bak, distinct from BH1 and BH2, mediates cell
            death and protein binding functions
  JOURNAL   EMBO J. 14 (22), 5589-5596 (1995)
   PUBMED   8521816
REFERENCE   7  (bases 1 to 849)
  AUTHORS   Adams,M.D., Kerlavage,A.R., Fleischmann,R.D., Fuldner,R.A.,
            Bult,C.J., Lee,N.H., Kirkness,E.F., Weinstock,K.G., Gocayne,J.D.,
            White,O. et al.
  TITLE     Initial assessment of human gene diversity and expression patterns
            based upon 83 million nucleotides of cDNA sequence
  JOURNAL   Nature 377 (6547 SUPPL), 3-174 (1995)
   PUBMED   7566098
REFERENCE   8  (bases 1 to 849)
  AUTHORS   Apte,S.S., Mattei,M.G. and Olsen,B.R.
  TITLE     Mapping of the human BAX gene to chromosome 19q13.3-q13.4 and
            isolation of a novel alternatively spliced transcript, BAX delta
  JOURNAL   Genomics 26 (3), 592-594 (1995)
   PUBMED   7607685
REFERENCE   9  (bases 1 to 849)
  AUTHORS   Miyashita,T. and Reed,J.C.
  TITLE     Tumor suppressor p53 is a direct transcriptional activator of the
            human bax gene
  JOURNAL   Cell 80 (2), 293-299 (1995)
   PUBMED   7834749
REFERENCE   10 (bases 1 to 849)
  AUTHORS   Oltvai,Z.N., Milliman,C.L. and Korsmeyer,S.J.
  TITLE     Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that
            accelerates programmed cell death
  JOURNAL   Cell 74 (4), 609-619 (1993)
   PUBMED   8358790
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BE396495.1, BC014175.2 and
            AI565203.1.
            On or before Jun 26, 2009 this sequence version replaced
            gi:163659850, gi:163659851.
            
            Summary: The protein encoded by this gene belongs to the BCL2
            protein family. BCL2 family members form hetero- or homodimers and
            act as anti- or pro-apoptotic regulators that are involved in a
            wide variety of cellular activities. This protein forms a
            heterodimer with BCL2, and functions as an apoptotic activator.
            This protein is reported to interact with, and increase the opening
            of, the mitochondrial voltage-dependent anion channel (VDAC), which
            leads to the loss in membrane potential and the release of
            cytochrome c. The expression of this gene is regulated by the tumor
            suppressor P53 and has been shown to be involved in P53-mediated
            apoptosis. Multiple alternatively spliced transcript variants,
            which encode different isoforms, have been reported for this gene.
            [provided by RefSeq, Jul 2008].
            
            Transcript Variant: This variant (sigma) contains a distinct 3'
            coding region and 3' UTR when compared to variant beta. It encodes
            an isoform (sigma) that has a shorter and different C terminus, as
            compared to isoform beta.
            
            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 :: AF247393.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025084 [ECO:0000350]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-17                BE396495.1         1-17
            18-543              BC014175.2         1-526
            544-686             BC014175.2         566-708
            687-687             AI565203.1         91-91               c
            688-849             BC014175.2         710-871
FEATURES             Location/Qualifiers
     source          1..849
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="19"
                     /map="19q13.3-q13.4"
     gene            1..849
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /note="BCL2-associated X protein"
                     /db_xref="GeneID:581"
                     /db_xref="HGNC:959"
                     /db_xref="MIM:600040"
     exon            1..103
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /inference="alignment:Splign:1.39.8"
     variation       53
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200532779"
     STS             69..610
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /standard_name="GDB:632822"
                     /db_xref="UniSTS:158495"
     CDS             70..609
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /note="isoform sigma is encoded by transcript variant
                     sigma; apoptosis regulator BAX; bcl2-L-4; bcl-2-like
                     protein 4; BCL2-associated X protein omega;
                     BCL2-associated X protein transcript variant delta2"
                     /codon_start=1
                     /product="apoptosis regulator BAX isoform sigma"
                     /protein_id="NP_620119.2"
                     /db_xref="GI:242117893"
                     /db_xref="CCDS:CCDS12745.2"
                     /db_xref="GeneID:581"
                     /db_xref="HGNC:959"
                     /db_xref="MIM:600040"
                     /translation="
MDGSGEQPRGGGPTSSEQIMKTGALLLQGFIQDRAGRMGGEAPELALDPVPQDASTKKLSECLKRIGDELDSNMELQRMIAAVDTDSPREVFFRVAADMFSDGNFNWGRVVALFYFASKLVLKALCTKVPELIRTIMGWTLDFLRERLLGWIQDQGGWTVTIFVAGVLTASLTIWKKMG
"
     misc_feature    82..606
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /note="apoptosis regulator; Region: bcl-2; TIGR00865"
                     /db_xref="CDD:162075"
     misc_feature    142..543
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /note="Apoptosis regulator proteins of the Bcl-2 family,
                     named after B-cell lymphoma 2. This alignment model spans
                     what have been described as Bcl-2 homology regions BH1,
                     BH2, BH3, and BH4. Many members of this family have an
                     additional C-terminal transmembrane...; Region:
                     Bcl-2_like; cd06845"
                     /db_xref="CDD:132900"
     misc_feature    142..171
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /note="BH4; other site"
                     /db_xref="CDD:132900"
     misc_feature    256..282
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /note="BH3; other site"
                     /db_xref="CDD:132900"
     misc_feature    order(265..270,274..279,295..297,304..309,337..342,
                     349..354,361..366,385..387,391..396,400..405,415..417,
                     427..429)
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /note="BH3-homology region binding site; other site"
                     /db_xref="CDD:132900"
     misc_feature    order(361..369,382..420)
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /note="BH1; other site"
                     /db_xref="CDD:132900"
     misc_feature    517..543
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /note="BH2; other site"
                     /db_xref="CDD:132900"
     variation       95
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:74422693"
     exon            104..155
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /inference="alignment:Splign:1.39.8"
     variation       105
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200327680"
     variation       106..107
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:67198826"
     STS             110..609
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /standard_name="PMC114802P1"
                     /db_xref="UniSTS:270279"
     variation       110
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144179827"
     variation       112
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151036634"
     STS             117..574
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /standard_name="BARC0009"
                     /db_xref="UniSTS:255299"
     variation       125
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:374123839"
     variation       138
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140986746"
     exon            156..302
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /inference="alignment:Splign:1.39.8"
     STS             157..302
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /standard_name="PMC230316P5"
                     /db_xref="UniSTS:272183"
     STS             160..253
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /standard_name="PMC27116P1"
                     /db_xref="UniSTS:272373"
     variation       171
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145555385"
     variation       174
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:4645885"
     variation       183
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:141306106"
     variation       184
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:36017265"
     variation       185
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:147630961"
     STS             227..392
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /standard_name="Bax"
                     /db_xref="UniSTS:265693"
     variation       229
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200153051"
     variation       263
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:142278713"
     variation       273
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145765277"
     variation       295
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376911304"
     exon            303..438
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /inference="alignment:Splign:1.39.8"
     variation       315
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370634054"
     variation       333
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374052135"
     variation       335
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202190487"
     variation       375
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148204524"
     variation       388
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:367558446"
     variation       402
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201578495"
     variation       407..408
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:66527050"
     exon            439..543
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /inference="alignment:Splign:1.39.8"
     variation       439
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376997564"
     variation       458
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369660551"
     variation       459
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371947281"
     variation       469
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375291870"
     variation       470
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369570399"
     variation       502
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372506919"
     variation       508
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375752615"
     variation       509
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190602136"
     exon            544..771
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /inference="alignment:Splign:1.39.8"
     variation       547
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377294979"
     variation       582
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1057369"
     variation       600
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370817149"
     variation       687
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:704243"
     variation       723..724
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:72215802"
     variation       727
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373416805"
     polyA_signal    750..755
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
     polyA_site      771
                     /gene="BAX"
                     /gene_synonym="BCL2L4"
ORIGIN      
tcacgtgacccgggcgcgctgcggccgcccgcgcggacccggcgagaggcggcggcgggagcggcggtgatggacgggtccggggagcagcccagaggcggggggcccaccagctctgagcagatcatgaagacaggggcccttttgcttcagggtttcatccaggatcgagcagggcgaatggggggggaggcacccgagctggccctggacccggtgcctcaggatgcgtccaccaagaagctgagcgagtgtctcaagcgcatcggggacgaactggacagtaacatggagctgcagaggatgattgccgccgtggacacagactccccccgagaggtctttttccgagtggcagctgacatgttttctgacggcaacttcaactggggccgggttgtcgcccttttctactttgccagcaaactggtgctcaaggccctgtgcaccaaggtgccggaactgatcagaaccatcatgggctggacattggacttcctccgggagcggctgttgggctggatccaagaccagggtggttggaccgtgaccatctttgtggcgggagtgctcaccgcctcactcaccatctggaagaagatgggctgaggcccccagctgccttggactgtgtttttcctccataaattatggcatttttctgggaggggtggggattgggggacgtgggcatttttcttacttttgtaattattggggggtgtggggaagagtggtcttgagggggtaataaacctccttcgggacacaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:581 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:581 -> Molecular function: GO:0008289 [lipid binding] evidence: IDA
            GeneID:581 -> Molecular function: GO:0015267 [channel activity] evidence: IDA
            GeneID:581 -> Molecular function: GO:0042802 [identical protein binding] evidence: IPI
            GeneID:581 -> Molecular function: GO:0042803 [protein homodimerization activity] evidence: IDA
            GeneID:581 -> Molecular function: GO:0042803 [protein homodimerization activity] evidence: IPI
            GeneID:581 -> Molecular function: GO:0046982 [protein heterodimerization activity] evidence: IPI
            GeneID:581 -> Molecular function: GO:0051434 [BH3 domain binding] evidence: IDA
            GeneID:581 -> Molecular function: GO:0051434 [BH3 domain binding] evidence: IPI
            GeneID:581 -> Biological process: GO:0001101 [response to acid] evidence: IEA
            GeneID:581 -> Biological process: GO:0001541 [ovarian follicle development] evidence: IEA
            GeneID:581 -> Biological process: GO:0001764 [neuron migration] evidence: IEA
            GeneID:581 -> Biological process: GO:0001777 [T cell homeostatic proliferation] evidence: IEA
            GeneID:581 -> Biological process: GO:0001782 [B cell homeostasis] evidence: IEA
            GeneID:581 -> Biological process: GO:0001783 [B cell apoptotic process] evidence: IDA
            GeneID:581 -> Biological process: GO:0001822 [kidney development] evidence: IEA
            GeneID:581 -> Biological process: GO:0001836 [release of cytochrome c from mitochondria] evidence: IDA
            GeneID:581 -> Biological process: GO:0001844 [protein insertion into mitochondrial membrane involved in apoptotic signaling pathway] evidence: IEA
            GeneID:581 -> Biological process: GO:0001974 [blood vessel remodeling] evidence: IEA
            GeneID:581 -> Biological process: GO:0002262 [myeloid cell homeostasis] evidence: IEA
            GeneID:581 -> Biological process: GO:0002352 [B cell negative selection] evidence: IEA
            GeneID:581 -> Biological process: GO:0002358 [B cell homeostatic proliferation] evidence: IEA
            GeneID:581 -> Biological process: GO:0002904 [positive regulation of B cell apoptotic process] evidence: IEA
            GeneID:581 -> Biological process: GO:0006309 [apoptotic DNA fragmentation] evidence: IMP
            GeneID:581 -> Biological process: GO:0006687 [glycosphingolipid metabolic process] evidence: IEA
            GeneID:581 -> Biological process: GO:0006808 [regulation of nitrogen utilization] evidence: IEA
            GeneID:581 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
            GeneID:581 -> Biological process: GO:0006917 [induction of apoptosis] evidence: NAS
            GeneID:581 -> Biological process: GO:0006919 [activation of cysteine-type endopeptidase activity involved in apoptotic process] evidence: IDA
            GeneID:581 -> Biological process: GO:0006919 [activation of cysteine-type endopeptidase activity involved in apoptotic process] evidence: IMP
            GeneID:581 -> Biological process: GO:0006922 [cleavage of lamin involved in execution phase of apoptosis] evidence: IMP
            GeneID:581 -> Biological process: GO:0006927 [transformed cell apoptotic process] evidence: IMP
            GeneID:581 -> Biological process: GO:0006974 [response to DNA damage stimulus] evidence: IEA
            GeneID:581 -> Biological process: GO:0007281 [germ cell development] evidence: IEA
            GeneID:581 -> Biological process: GO:0008053 [mitochondrial fusion] evidence: IDA
            GeneID:581 -> Biological process: GO:0008635 [activation of cysteine-type endopeptidase activity involved in apoptotic process by cytochrome c] evidence: IDA
            GeneID:581 -> Biological process: GO:0008637 [apoptotic mitochondrial changes] evidence: IDA
            GeneID:581 -> Biological process: GO:0009566 [fertilization] evidence: IEA
            GeneID:581 -> Biological process: GO:0009636 [response to toxic substance] evidence: IDA
            GeneID:581 -> Biological process: GO:0009651 [response to salt stress] evidence: IEA
            GeneID:581 -> Biological process: GO:0010248 [establishment or maintenance of transmembrane electrochemical gradient] evidence: IDA
            GeneID:581 -> Biological process: GO:0010332 [response to gamma radiation] evidence: IEA
            GeneID:581 -> Biological process: GO:0019048 [modulation by virus of host morphology or physiology] evidence: IEA
            GeneID:581 -> Biological process: GO:0021854 [hypothalamus development] evidence: IEA
            GeneID:581 -> Biological process: GO:0021987 [cerebral cortex development] evidence: IEA
            GeneID:581 -> Biological process: GO:0030264 [nuclear fragmentation involved in apoptotic nuclear change] evidence: IMP
            GeneID:581 -> Biological process: GO:0032091 [negative regulation of protein binding] evidence: IDA
            GeneID:581 -> Biological process: GO:0032461 [positive regulation of protein oligomerization] evidence: IDA
            GeneID:581 -> Biological process: GO:0032471 [reduction of endoplasmic reticulum calcium ion concentration] evidence: IEA
            GeneID:581 -> Biological process: GO:0032976 [release of matrix enzymes from mitochondria] evidence: IDA
            GeneID:581 -> Biological process: GO:0033137 [negative regulation of peptidyl-serine phosphorylation] evidence: IEA
            GeneID:581 -> Biological process: GO:0033599 [regulation of mammary gland epithelial cell proliferation] evidence: IEA
            GeneID:581 -> Biological process: GO:0034644 [cellular response to UV] evidence: IEA
            GeneID:581 -> Biological process: GO:0035108 [limb morphogenesis] evidence: IEA
            GeneID:581 -> Biological process: GO:0035234 [germ cell programmed cell death] evidence: IEA
            GeneID:581 -> Biological process: GO:0042475 [odontogenesis of dentin-containing tooth] evidence: IEA
            GeneID:581 -> Biological process: GO:0043065 [positive regulation of apoptotic process] evidence: IMP
            GeneID:581 -> Biological process: GO:0043496 [regulation of protein homodimerization activity] evidence: IDA
            GeneID:581 -> Biological process: GO:0043497 [regulation of protein heterodimerization activity] evidence: IPI
            GeneID:581 -> Biological process: GO:0043524 [negative regulation of neuron apoptotic process] evidence: IEA
            GeneID:581 -> Biological process: GO:0043525 [positive regulation of neuron apoptotic process] evidence: IDA
            GeneID:581 -> Biological process: GO:0043653 [mitochondrial fragmentation involved in apoptotic process] evidence: IDA
            GeneID:581 -> Biological process: GO:0045136 [development of secondary sexual characteristics] evidence: IEA
            GeneID:581 -> Biological process: GO:0046666 [retinal cell programmed cell death] evidence: IEA
            GeneID:581 -> Biological process: GO:0048087 [positive regulation of developmental pigmentation] evidence: IEA
            GeneID:581 -> Biological process: GO:0048147 [negative regulation of fibroblast proliferation] evidence: IEA
            GeneID:581 -> Biological process: GO:0048515 [spermatid differentiation] evidence: IEA
            GeneID:581 -> Biological process: GO:0048597 [post-embryonic camera-type eye morphogenesis] evidence: IEA
            GeneID:581 -> Biological process: GO:0048678 [response to axon injury] evidence: IEA
            GeneID:581 -> Biological process: GO:0048873 [homeostasis of number of cells within a tissue] evidence: IEA
            GeneID:581 -> Biological process: GO:0051259 [protein oligomerization] evidence: IDA
            GeneID:581 -> Biological process: GO:0051260 [protein homooligomerization] evidence: IDA
            GeneID:581 -> Biological process: GO:0051281 [positive regulation of release of sequestered calcium ion into cytosol] evidence: IEA
            GeneID:581 -> Biological process: GO:0051402 [neuron apoptotic process] evidence: IEA
            GeneID:581 -> Biological process: GO:0051726 [regulation of cell cycle] evidence: IEA
            GeneID:581 -> Biological process: GO:0051881 [regulation of mitochondrial membrane potential] evidence: IDA
            GeneID:581 -> Biological process: GO:0060011 [Sertoli cell proliferation] evidence: IEA
            GeneID:581 -> Biological process: GO:0060041 [retina development in camera-type eye] evidence: IEA
            GeneID:581 -> Biological process: GO:0060058 [positive regulation of apoptotic process involved in mammary gland involution] evidence: IEA
            GeneID:581 -> Biological process: GO:0060068 [vagina development] evidence: IEA
            GeneID:581 -> Biological process: GO:0070059 [intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress] evidence: IMP
            GeneID:581 -> Biological process: GO:0071310 [cellular response to organic substance] evidence: IEA
            GeneID:581 -> Biological process: GO:0090200 [positive regulation of release of cytochrome c from mitochondria] evidence: IDA
            GeneID:581 -> Biological process: GO:0097190 [apoptotic signaling pathway] evidence: IDA
            GeneID:581 -> Biological process: GO:0097191 [extrinsic apoptotic signaling pathway] evidence: IDA
            GeneID:581 -> Biological process: GO:0097193 [intrinsic apoptotic signaling pathway] evidence: IDA
            GeneID:581 -> Biological process: GO:0097193 [intrinsic apoptotic signaling pathway] evidence: TAS
            GeneID:581 -> Biological process: GO:1900103 [positive regulation of endoplasmic reticulum unfolded protein response] evidence: IMP
            GeneID:581 -> Biological process: GO:1901030 [positive regulation of mitochondrial outer membrane permeabilization] evidence: TAS
            GeneID:581 -> Biological process: GO:1990009 [retinal cell apoptotic process] evidence: IMP
            GeneID:581 -> Biological process: GO:2001244 [positive regulation of intrinsic apoptotic signaling pathway] evidence: IMP
            GeneID:581 -> Cellular component: GO:0005634 [nucleus] evidence: IMP
            GeneID:581 -> Cellular component: GO:0005739 [mitochondrion] evidence: IDA
            GeneID:581 -> Cellular component: GO:0005741 [mitochondrial outer membrane] evidence: TAS
            GeneID:581 -> Cellular component: GO:0005757 [mitochondrial permeability transition pore complex] evidence: IDA
            GeneID:581 -> Cellular component: GO:0005783 [endoplasmic reticulum] evidence: IDA
            GeneID:581 -> Cellular component: GO:0005789 [endoplasmic reticulum membrane] evidence: IDA
            GeneID:581 -> Cellular component: GO:0005829 [cytosol] evidence: IDA
            GeneID:581 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
            GeneID:581 -> Cellular component: GO:0046930 [pore complex] evidence: IDA
            GeneID:581 -> Cellular component: GO:0097136 [Bcl-2 family protein complex] evidence: IDA

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