GGRNA Home | Help | Advanced search

2024-04-27 06:55:09, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_004330               2533 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens BCL2/adenovirus E1B 19kDa interacting protein 2
            (BNIP2), mRNA.
ACCESSION   NM_004330
VERSION     NM_004330.2  GI:168480079
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 2533)
  AUTHORS   Park,G., Jeong,J.W. and Kim,J.E.
  TITLE     SIRT1 deficiency attenuates MPP+-induced apoptosis in dopaminergic
            cells
  JOURNAL   FEBS Lett. 585 (1), 219-224 (2011)
   PUBMED   21130087
  REMARK    GeneRIF: Data imply that SIRT1 may mediate MPP(+)-induced
            cytotoxicity, possibly through the regulation of BNIP2.
REFERENCE   2  (bases 1 to 2533)
  AUTHORS   Scott,G.B., Bowles,P.A., Wilson,E.B., Meade,J.L., Low,B.C.,
            Davison,A., Blair,G.E. and Cook,G.P.
  TITLE     Identification of the BCL2/adenovirus E1B-19K protein-interacting
            protein 2 (BNIP-2) as a granzyme B target during human natural
            killer cell-mediated killing
  JOURNAL   Biochem. J. 431 (3), 423-431 (2010)
   PUBMED   20704564
  REMARK    GeneRIF: Inhibition of BNIP-2 expression did not affect the
            susceptibility to NK cell-mediated killing.
REFERENCE   3  (bases 1 to 2533)
  AUTHORS   Kelly,J.L., Novak,A.J., Fredericksen,Z.S., Liebow,M., Ansell,S.M.,
            Dogan,A., Wang,A.H., Witzig,T.E., Call,T.G., Kay,N.E.,
            Habermann,T.M., Slager,S.L. and Cerhan,J.R.
  TITLE     Germline variation in apoptosis pathway genes and risk of
            non-Hodgkin's lymphoma
  JOURNAL   Cancer Epidemiol. Biomarkers Prev. 19 (11), 2847-2858 (2010)
   PUBMED   20855536
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   4  (bases 1 to 2533)
  AUTHORS   Shimada,M., Miyagawa,T., Kawashima,M., Tanaka,S., Honda,Y.,
            Honda,M. and Tokunaga,K.
  TITLE     An approach based on a genome-wide association study reveals
            candidate loci for narcolepsy
  JOURNAL   Hum. Genet. 128 (4), 433-441 (2010)
   PUBMED   20677014
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   5  (bases 1 to 2533)
  AUTHORS   Valencia,C.A., Cotten,S.W. and Liu,R.
  TITLE     Cleavage of BNIP-2 and BNIP-XL by caspases
  JOURNAL   Biochem. Biophys. Res. Commun. 364 (3), 495-501 (2007)
   PUBMED   17961507
  REMARK    GeneRIF: Our results suggest that the caspase-mediated cleavage of
            BNIP-2 and BNIP-XL could result in the release of the BCH domain or
            smaller fragments that are crucial for their proapoptotic
            activities.
REFERENCE   6  (bases 1 to 2533)
  AUTHORS   Low,B.C., Seow,K.T. and Guy,G.R.
  TITLE     The BNIP-2 and Cdc42GAP homology domain of BNIP-2 mediates its
            homophilic association and heterophilic interaction with Cdc42GAP
  JOURNAL   J. Biol. Chem. 275 (48), 37742-37751 (2000)
   PUBMED   10954711
REFERENCE   7  (bases 1 to 2533)
  AUTHORS   Low,B.C., Seow,K.T. and Guy,G.R.
  TITLE     Evidence for a novel Cdc42GAP domain at the carboxyl terminus of
            BNIP-2
  JOURNAL   J. Biol. Chem. 275 (19), 14415-14422 (2000)
   PUBMED   10799524
REFERENCE   8  (bases 1 to 2533)
  AUTHORS   Low,B.C., Lim,Y.P., Lim,J., Wong,E.S. and Guy,G.R.
  TITLE     Tyrosine phosphorylation of the Bcl-2-associated protein BNIP-2 by
            fibroblast growth factor receptor-1 prevents its binding to
            Cdc42GAP and Cdc42
  JOURNAL   J. Biol. Chem. 274 (46), 33123-33130 (1999)
   PUBMED   10551883
REFERENCE   9  (bases 1 to 2533)
  AUTHORS   Ohi,N., Tokunaga,A., Tsunoda,H., Nakano,K., Haraguchi,K., Oda,K.,
            Motoyama,N. and Nakajima,T.
  TITLE     A novel adenovirus E1B19K-binding protein B5 inhibits apoptosis
            induced by Nip3 by forming a heterodimer through the C-terminal
            hydrophobic region
  JOURNAL   Cell Death Differ. 6 (4), 314-325 (1999)
   PUBMED   10381623
REFERENCE   10 (bases 1 to 2533)
  AUTHORS   Boyd,J.M., Malstrom,S., Subramanian,T., Venkatesh,L.K.,
            Schaeper,U., Elangovan,B., D'Sa-Eipper,C. and Chinnadurai,G.
  TITLE     Adenovirus E1B 19 kDa and Bcl-2 proteins interact with a common set
            of cellular proteins
  JOURNAL   Cell 79 (2), 341-351 (1994)
   PUBMED   7954800
  REMARK    Erratum:[Cell. 1994 Dec 16;79(6):1121. PMID: 8001138]
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from DC425485.1, BC002461.2 and
            BX378770.2.
            This sequence is a reference standard in the RefSeqGene project.
            On Feb 22, 2008 this sequence version replaced gi:4757855.
            
            Summary: This gene is a member of the BCL2/adenovirus E1B 19
            kd-interacting protein (BNIP) family. It interacts with the E1B 19
            kDa protein, which protects cells from virally-induced cell death.
            The encoded protein also interacts with E1B 19 kDa-like sequences
            of BCL2, another apoptotic protector. [provided by RefSeq, Mar
            2011].
            
            Sequence Note: The translation start codon selected for this RefSeq
            is conserved in human and Rhesus macaque. A possible downstream
            start codon, which shows better cross-species conservation, would
            shorten the protein by 121 aa. The shorter protein is described in
            the literature, including PMID:7954800. No experimental evidence
            exists to show which start codon is used in vivo.
            
            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 :: BC002461.2, U15173.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-124               DC425485.1         1-124
            125-1927            BC002461.2         1-1803
            1928-2487           BX378770.2         1-560               c
            2488-2533           BC002461.2         2364-2409
FEATURES             Location/Qualifiers
     source          1..2533
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="15"
                     /map="15q22.2"
     gene            1..2533
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /note="BCL2/adenovirus E1B 19kDa interacting protein 2"
                     /db_xref="GeneID:663"
                     /db_xref="HGNC:1083"
                     /db_xref="MIM:603292"
     exon            1..309
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /inference="alignment:Splign:1.39.8"
     CDS             4..1311
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /codon_start=1
                     /product="BCL2/adenovirus E1B 19 kDa protein-interacting
                     protein 2"
                     /protein_id="NP_004321.2"
                     /db_xref="GI:168480080"
                     /db_xref="CCDS:CCDS10174.2"
                     /db_xref="GeneID:663"
                     /db_xref="HGNC:1083"
                     /db_xref="MIM:603292"
                     /translation="
MLCGFQEDATPPPPPRPRRLHRRLPRPEEVGMLSLPPGLLTVSGSAAAADAVPLRPGDWAGVSTADRGERAPLGPAFCDLAVSPTSPAWRGEEDEGAKASSGDIGSLDYQEFVVDIESRLRMEGVELKEEWQDEDFPIPLPEDDSIEADILAITGPEDQPGSLEVNGNKVRKKLMAPDISLTLDPSDGSVLSDDLDESGEIDLDGLDTPSENSNEFEWEDDLPKPKTTEVIRKGSITEYTAAEEKEDGRRWRMFRIGEQDHRVDMKAIEPYKKVISHGGYYGDGLNAIVVFAVCFMPESSQPNYRYLMDNLFKYVIGTLELLVAENYMIVYLNGATTRRKMPSLGWLRKCYQQIDRRLRKNLKSLIIVHPSWFIRTLLAVTRPFISSKFSQKIRYVFNLAELAELVPMEYVGIPECIKQVDQELNGKQDEPKNEQ
"
     misc_feature    505..855
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /note="Bcl2-/adenovirus E1B nineteen kDa-interacting
                     protein 2; Region: BNIP2; pfam12496"
                     /db_xref="CDD:204941"
     misc_feature    805..1236
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /note="Sec14p-like lipid-binding domain. Found in
                     secretory proteins, such as S. cerevisiae
                     phosphatidylinositol transfer protein (Sec14p), and in
                     lipid regulated proteins such as RhoGAPs, RhoGEFs and
                     neurofibromin (NF1). SEC14 domain of Dbl is known to...;
                     Region: SEC14; cd00170"
                     /db_xref="CDD:29115"
     misc_feature    order(868..870,874..876,880..882,967..969,997..999,
                     1042..1044,1054..1056,1066..1068,1078..1080,1087..1089,
                     1096..1098,1102..1104,1123..1125,1144..1146,1180..1182)
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /note="phospholipid binding pocket [chemical binding];
                     other site"
                     /db_xref="CDD:29115"
     misc_feature    order(1081..1083,1177..1179)
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /note="salt bridge; other site"
                     /db_xref="CDD:29115"
     variation       7
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6151434"
     variation       128
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3087328"
     variation       132
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3087330"
     variation       133
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:3087329"
     variation       161
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3087331"
     variation       170
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3087332"
     exon            310..416
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /inference="alignment:Splign:1.39.8"
     exon            417..484
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /inference="alignment:Splign:1.39.8"
     variation       437
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:6151509"
     exon            485..661
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /inference="alignment:Splign:1.39.8"
     exon            662..838
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /inference="alignment:Splign:1.39.8"
     exon            839..941
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /inference="alignment:Splign:1.39.8"
     variation       873
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1057058"
     exon            942..1073
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /inference="alignment:Splign:1.39.8"
     variation       967
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1135148"
     exon            1074..1160
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /inference="alignment:Splign:1.39.8"
     exon            1161..1259
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /inference="alignment:Splign:1.39.8"
     exon            1260..2518
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /inference="alignment:Splign:1.39.8"
     variation       1323
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6151583"
     STS             1349..1490
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /standard_name="D15S1347"
                     /db_xref="UniSTS:70896"
     variation       1474
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6151584"
     variation       1911
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1057059"
     variation       1928
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2306355"
     STS             2034..2186
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /standard_name="D15S703E"
                     /db_xref="UniSTS:151610"
     variation       2041
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1057061"
     variation       2055
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1057062"
     variation       2209
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6151585"
     polyA_signal    2494..2499
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
     polyA_site      2518
                     /gene="BNIP2"
                     /gene_synonym="BNIP-2; NIP2"
ORIGIN      
gggatgctgtgtgggtttcaagaagacgccacgcctccgccgccgccacgcccccgccgcctccaccgccggctgccgcgcccggaggaggtcgggatgttatcacttccgccggggcttctcactgtgtccgggtcagctgctgccgccgacgccgtaccgctgcggccgggggattgggccggggtctccaccgccgaccgaggggagcgggctccgctcggccctgctttttgcgacctggccgtcagccccacgtcgccggcctggaggggcgaagaggacgagggggccaaggcttcctccggggacattggctccctggattatcaagagtttgtagttgacattgaatccaggctgaggatggaaggtgtggaacttaaagaagaatggcaagatgaagattttccgatacctttaccagaagatgatagtattgaagcagatatactagctataactggaccagaggaccagcctggctcactagaagttaatggaaataaagtgagaaagaaactaatggctccagacattagcctgacactggatcctagtgatggctctgtattgtcagatgatttggatgaaagtggggagattgacttagatggcttagacacaccgtcagagaatagtaatgagtttgagtgggaagatgatcttccaaaacccaagactactgaagtaattaggaaaggctcaattactgaatacacagcagcagaggaaaaagaagatggacgacgctggcgtatgttcaggattggagaacaggaccacagggttgatatgaaggcaattgaaccctataaaaaagttatcagccatgggggatattatggggatggattaaatgccattgttgtgtttgctgtctgtttcatgcctgaaagtagtcagcctaactatagatacctgatggacaatctttttaaatatgttattggcactttggagctattagtagcagaaaactacatgatagtttatttaaatggtgcaacaactcgaagaaaaatgcccagtctgggatggctcaggaaatgttatcagcaaattgatagaaggttacggaaaaatctaaaatccctaatcattgtacatccttcttggtttatcagaacacttctggctgttacaagaccatttattagctcgaaattcagccaaaaaattagatacgtgtttaatttggcagaactagcagaacttgtccccatggaatacgttggcataccagaatgcataaaacaagttgatcaagaacttaatggaaaacaagatgaaccgaaaaatgaacagtaagtttggcatctagtccaaacaagactgaagaatgtgctgatggagcagtgctgtttctgcattcataatgcatttattggcccatatttttatgtaacctgttacaaaatagacttgactttttcataatggacttttgtattatacaagggactgttcactgctgtactggtttgcaaatttcttgaatttagctctttaatagctaactgtattattatcgttttatattttatattgctaaatagagaaccacactttatataaagtagtttttgcatttgtttattgaatgatgcatcttcttcggtgaaatatttatatgcataaatggcaaaggaaagaaataatatatatttttatgtcattgagcaatattttttaatgtgtacctgtcttatggaagaaatatgcaggtatataagaccacgattttctaaagtgcatattagaatttttgtttttgtaaatggttaaatacatttcctgggtaacttaggaaattaagtttttcataaggcaacagatggttaaactgattgtcatgaatacccaaagatcatgtatataatcgaagtgtattagtaccatcccaaggtttttttctcatttaacatatttgtttcataattcagcaagtacagatgcaagcgcattgcacactttttcctttctaaacttaaagacaagtcaaaaagccattcttagaactagaggatttaagagggtaggaattagggtttgtatatatgtatatatgggacattttatcttctggcccaaagtcagaactttataaaaatcttgagtttgttcactaatgtgaaataagctatgtgtccagggtattgctcccctgagtgtatatgagtgctgagtagtattgcagagaatgtgatgagttattcactgtcacaactttttctatagaaaacaggggctgctttttaaactctcactatgggcactttaccaaaatacttccatatcaattatttgaactcggtagttgtttgacctagttagatgtggtgtttattcaagtttgtatgaaatcatgtttgacaatactgtaaattaggttaattttgtaagtcttagcatcatcatattgtgctgttttggataacacgtttgttacaagcatttaaactgtttcatttggtagtacctttacattgaaataaattgtgtttgtgcctccaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:663 -> Molecular function: GO:0005096 [GTPase activator activity] evidence: TAS
            GeneID:663 -> Molecular function: GO:0005509 [calcium ion binding] evidence: TAS
            GeneID:663 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:663 -> Biological process: GO:0006915 [apoptotic process] evidence: IPI
            GeneID:663 -> Biological process: GO:0042692 [muscle cell differentiation] evidence: TAS
            GeneID:663 -> Biological process: GO:0043066 [negative regulation of apoptotic process] evidence: TAS
            GeneID:663 -> Biological process: GO:0043547 [positive regulation of GTPase activity] evidence: TAS
            GeneID:663 -> Biological process: GO:0051149 [positive regulation of muscle cell differentiation] evidence: TAS
            GeneID:663 -> Cellular component: GO:0005635 [nuclear envelope] evidence: IDA
            GeneID:663 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
            GeneID:663 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
            GeneID:663 -> Cellular component: GO:0043231 [intracellular membrane-bounded organelle] evidence: IDA
            GeneID:663 -> Cellular component: GO:0048471 [perinuclear region of cytoplasm] evidence: IEA

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