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2024-04-20 03:46:36, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001244569            2006 bp    mRNA    linear   PRI 07-JUL-2013
DEFINITION  Homo sapiens BH3 interacting domain death agonist (BID), transcript
            variant 5, mRNA.
ACCESSION   NM_001244569
VERSION     NM_001244569.1  GI:347300415
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 2006)
  AUTHORS   Moldoveanu,T., Grace,C.R., Llambi,F., Nourse,A., Fitzgerald,P.,
            Gehring,K., Kriwacki,R.W. and Green,D.R.
  TITLE     BID-induced structural changes in BAK promote apoptosis
  JOURNAL   Nat. Struct. Mol. Biol. 20 (5), 589-597 (2013)
   PUBMED   23604079
  REMARK    GeneRIF: BAK activation follows a 'hit-and-run' mechanism whereby
            BID dissociates from the trigger site, which allows BAK
            oligomerization at an overlapping interface.
REFERENCE   2  (bases 1 to 2006)
  AUTHORS   Santiveri,C.M., Sborgi,L. and de Alba,E.
  TITLE     Nuclear magnetic resonance study of protein-protein interactions
            involving apoptosis regulator Diva (Boo) and the BH3 domain of
            proapoptotic Bcl-2 members
  JOURNAL   J. Mol. Recognit. 25 (12), 665-673 (2012)
   PUBMED   23192964
  REMARK    GeneRIF: Diva binds peptides derived from the BH3 domain of several
            other proapoptotic Bcl-2 proteins, including mouse Harakiri, Bid,
            Bak and Bmf.
REFERENCE   3  (bases 1 to 2006)
  AUTHORS   Jiang,H., He,P., Adler,C.H., Shill,H., Beach,T.G., Li,R. and
            Shen,Y.
  TITLE     Bid signal pathway components are identified in the temporal cortex
            with Parkinson disease
  JOURNAL   Neurology 79 (17), 1767-1773 (2012)
   PUBMED   23019260
  REMARK    GeneRIF: Patients with Parkinson disease have an activated
            Bid-mediated destructive signal pathway via tumor necrosis factor
            death receptor I (TNFRI) in the temporal cortex.
REFERENCE   4  (bases 1 to 2006)
  AUTHORS   Aranovich,A., Liu,Q., Collins,T., Geng,F., Dixit,S., Leber,B. and
            Andrews,D.W.
  TITLE     Differences in the mechanisms of proapoptotic BH3 proteins binding
            to Bcl-XL and Bcl-2 quantified in live MCF-7 cells
  JOURNAL   Mol. Cell 45 (6), 754-763 (2012)
   PUBMED   22464442
  REMARK    GeneRIF: mechanism of proapoptotic BH3 proteins Bad and Bid binding
            to Bcl-XL and Bcl-2 in breast cancer cells
REFERENCE   5  (bases 1 to 2006)
  AUTHORS   Appelqvist,H., Johansson,A.C., Linderoth,E., Johansson,U.,
            Antonsson,B., Steinfeld,R., Kagedal,K. and Ollinger,K.
  TITLE     Lysosome-mediated apoptosis is associated with cathepsin D-specific
            processing of bid at Phe24, Trp48, and Phe183
  JOURNAL   Ann. Clin. Lab. Sci. 42 (3), 231-242 (2012)
   PUBMED   22964611
  REMARK    GeneRIF: Three cathepsin D-specific cleavage sites in Bid, Phe24,
            Trp48, and Phe183, were identified.
REFERENCE   6  (bases 1 to 2006)
  AUTHORS   Footz,T.K., Birren,B., Minoshima,S., Asakawa,S., Shimizu,N.,
            Riazi,M.A. and McDermid,H.E.
  TITLE     The gene for death agonist BID maps to the region of human 22q11.2
            duplicated in cat eye syndrome chromosomes and to mouse chromosome
            6
  JOURNAL   Genomics 51 (3), 472-475 (1998)
   PUBMED   9721221
REFERENCE   7  (bases 1 to 2006)
  AUTHORS   Huang,D.C., Adams,J.M. and Cory,S.
  TITLE     The conserved N-terminal BH4 domain of Bcl-2 homologues is
            essential for inhibition of apoptosis and interaction with CED-4
  JOURNAL   EMBO J. 17 (4), 1029-1039 (1998)
   PUBMED   9463381
REFERENCE   8  (bases 1 to 2006)
  AUTHORS   Wang,K., Yin,X.M., Chao,D.T., Milliman,C.L. and Korsmeyer,S.J.
  TITLE     BID: a novel BH3 domain-only death agonist
  JOURNAL   Genes Dev. 10 (22), 2859-2869 (1996)
   PUBMED   8918887
REFERENCE   9  (bases 1 to 2006)
  AUTHORS   Amagai,M., Wang,Y., Minoshima,S., Kawamura,K., Green,K.J.,
            Nishikawa,T. and Shimizu,N.
  TITLE     Assignment of the human genes for desmocollin 3 (DSC3) and
            desmocollin 4 (DSC4) to chromosome 18q12
  JOURNAL   Genomics 25 (1), 330-332 (1995)
   PUBMED   7774948
REFERENCE   10 (bases 1 to 2006)
  AUTHORS   Kawamura,K., Watanabe,K., Suzuki,T., Yamakawa,T., Kamiyama,T.,
            Nakagawa,H. and Tsurufuji,S.
  TITLE     cDNA cloning and expression of a novel human desmocollin
  JOURNAL   J. Biol. Chem. 269 (42), 26295-26302 (1994)
   PUBMED   7929347
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from DA158889.1, CN277529.1,
            AK094795.1, AC006285.13 and BC036364.1.
            
            Summary: This gene encodes a death agonist that heterodimerizes
            with either agonist BAX or antagonist BCL2. The encoded protein is
            a member of the BCL-2 family of cell death regulators. It is a
            mediator of mitochondrial damage induced by caspase-8 (CASP8);
            CASP8 cleaves this encoded protein, and the COOH-terminal part
            translocates to mitochondria where it triggers cytochrome c
            release. Multiple alternatively spliced transcript variants have
            been found, but the full-length nature of some variants has not
            been defined. [provided by RefSeq, Jul 2008].
            
            Transcript Variant: This variant (5) has an alternate 5' exon and
            uses a downstream in-frame start codon, as compared to variant 1.
            The encoded isoform 3 thus has a shorter N-terminus, as compared to
            isoform 1.
            
            Publication Note:  This RefSeq record includes a subset of the
            publications that are available for this gene. Please see the Gene
            record to access additional publications.
            
            ##Evidence-Data-START##
            Transcript exon combination :: BU168412.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025088 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-35                DA158889.1         1-35
            36-506              CN277529.1         6-476
            507-610             AK094795.1         977-1080
            611-611             AC006285.13        123432-123432       c
            612-1966            AK094795.1         1082-2436
            1967-1967           AC006285.13        122076-122076       c
            1968-1988           AK094795.1         2438-2458
            1989-2006           BC036364.1         2495-2512
FEATURES             Location/Qualifiers
     source          1..2006
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="22"
                     /map="22q11.1"
     gene            1..2006
                     /gene="BID"
                     /gene_synonym="FP497"
                     /note="BH3 interacting domain death agonist"
                     /db_xref="GeneID:637"
                     /db_xref="HGNC:1050"
                     /db_xref="MIM:601997"
     exon            1..115
                     /gene="BID"
                     /gene_synonym="FP497"
                     /inference="alignment:Splign:1.39.8"
     exon            116..185
                     /gene="BID"
                     /gene_synonym="FP497"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    182..184
                     /gene="BID"
                     /gene_synonym="FP497"
                     /note="upstream in-frame stop codon"
     exon            186..325
                     /gene="BID"
                     /gene_synonym="FP497"
                     /inference="alignment:Splign:1.39.8"
     CDS             251..550
                     /gene="BID"
                     /gene_synonym="FP497"
                     /note="isoform 3 is encoded by transcript variant 5;
                     BH3-interacting domain death agonist; apoptic death
                     agonist; Human BID coding sequence; desmocollin type 4;
                     BID isoform ES(1b); BID isoform L(2); BID isoform Si6; p22
                     BID"
                     /codon_start=1
                     /product="BH3-interacting domain death agonist isoform 3"
                     /protein_id="NP_001231498.1"
                     /db_xref="GI:347300416"
                     /db_xref="CCDS:CCDS13749.1"
                     /db_xref="GeneID:637"
                     /db_xref="HGNC:1050"
                     /db_xref="MIM:601997"
                     /translation="
MDRSIPPGLVNGLALQLRNTSRSEEDRNRDLATALEQLLQAYPRDMEKEKTMLVLALLLAKKVASHTPSLLRDVFHTTVNFINQNLRTYVRSLARNGMD
"
     misc_feature    <251..538
                     /gene="BID"
                     /gene_synonym="FP497"
                     /note="BH3 interacting domain (BID); Region: BID;
                     pfam06393"
                     /db_xref="CDD:203434"
     exon            326..538
                     /gene="BID"
                     /gene_synonym="FP497"
                     /inference="alignment:Splign:1.39.8"
     variation       490
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11538"
     exon            539..1990
                     /gene="BID"
                     /gene_synonym="FP497"
                     /inference="alignment:Splign:1.39.8"
     variation       585
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:8190354"
     STS             609..683
                     /gene="BID"
                     /gene_synonym="FP497"
                     /standard_name="SHGC-36512"
                     /db_xref="UniSTS:4995"
     variation       701
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1802194"
     variation       716
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1061200"
     polyA_site      768
                     /gene="BID"
                     /gene_synonym="FP497"
     STS             960..1121
                     /gene="BID"
                     /gene_synonym="FP497"
                     /standard_name="RH92974"
                     /db_xref="UniSTS:89764"
     variation       1012
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:8190355"
     variation       1099..1100
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:201806962"
     variation       1099
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:8190357"
     variation       1508
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:8190358"
     variation       1814..1817
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace=""
                     /replace="cttt"
                     /db_xref="dbSNP:78336589"
     variation       1816..1817
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace=""
                     /replace="cttt"
                     /db_xref="dbSNP:201965650"
     variation       1817
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace=""
                     /replace="cttt"
                     /db_xref="dbSNP:8190359"
     variation       1820
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace=""
                     /replace="aa"
                     /db_xref="dbSNP:25591"
     variation       1944
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:8190360"
     variation       1945
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:8190361"
     variation       1951
                     /gene="BID"
                     /gene_synonym="FP497"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:8190362"
     polyA_signal    1970..1975
                     /gene="BID"
                     /gene_synonym="FP497"
     polyA_site      1990
                     /gene="BID"
                     /gene_synonym="FP497"
ORIGIN      
gaaggaggaagcgcgcggggcgccataaggaggaagcgggtagtcgaccgtgtccgcgcgcctgggagacgctgcctcggcccggacgcgcccgcgcccccgcggctggagggtggtcgccactgggacactgtgaaccaggagtgagtcggagctgccgcgctgcccaggccatggactgtgagattctgaaagtcaagaagacatcatccggaatattgccaggcacctcgcccaggtcggggacagcatggaccgtagcatccctccgggcctggtgaacggcctggccctgcagctcaggaacaccagccggtcggaggaggaccggaacagggacctggccactgccctggagcagctgctgcaggcctaccctagagacatggagaaggagaagaccatgctggtgctggccctgctgctggccaagaaggtggccagtcacacgccgtccttgctccgtgatgtctttcacacaacagtgaattttattaaccagaacctacgcacctacgtgaggagcttagccagaaatgggatggactgaacggacagttccagaagtgtgactggctaaagctcgatgtggtcacagctgtatagctgcttccagtgtagacggagccctggcatgtcaacagcgttcctagagaagacaggctggaagatagctgtgacttctattttaaagacaatgttaaacttataacccactttaaaatatctacattaatatacttgaatgaaaatgtccatttacacgtatttgaatggccttcatatcatccacacatgaatctgcacatctgtaaatctacacacggtgcctttatttccactgtgcaggttcccacttaaaaattaaattggaaagcaggtttcaaggaagtagaaacaaaatacaatttttttggtaaaaaaaaattactgtttattaaagtacaaccatagaggatggtcttacagcaggcagtatcctgtttgaggaaagcaagaatcagagaaggaacataccccttacaaatgaaaaattccactcaaaatagggactatctatcttaatactaaggaaccaacaatcttcctgtttaaaaaaccacatggcacagagattctgaactaaagtgctgcactcaaatgatgggaagtccggccccagtacacaggggcttgactttttcaacttcgtttcctttgttggagtcaaaaagaaccacttgtggttctaaaaggtgtgaaggtgatttaagggcccaggtcagccactgtttgtttacaaaatcaggtaactaactgcatacactttttctctttccatgacatcaagactttgctaaagacatgaagccacgggtgccagaagctactgcgatgccccgggagttagccccctggtaatagctgtaaacttccaatttctagccatacgctcagctcatccatgcctcagaagtgcatctggagagaacaggtttctaagcataaaagatgaaagagcagttggactttttaaaaattcagcaaagtggttccctctcttagggacagtcaaaaccaagtcacttaggtagtaccaaaataaataaggaaaagcttagctttagaaacagtgcaacactggtctgctgttccagtggtaagctatgtcccaggaatcagtttaaaagcacgacagtggatgctgggtccatatcacacacattgctgtgaacaggaaactcctgtgaccacaacatgaggccactggagacgcatatgagtaagggcactgacggactcatgatttcttcttaccagatgctttcctgttctttaagagtttaaaatcatcagaaaggaaaaacaaactctatattgttcagcatgcaatacataccacgctagggctggctcaattgaaagtgggcaaaagcttacaaatactaaaaagaagtgctgccgcgcagtgtggaggccactgtttggaaataaatcttcctaacactacaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:637 -> Molecular function: GO:0005123 [death receptor binding] evidence: TAS
            GeneID:637 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:637 -> Molecular function: GO:0031625 [ubiquitin protein ligase binding] evidence: IEA
            GeneID:637 -> Biological process: GO:0001836 [release of cytochrome c from mitochondria] evidence: IDA
            GeneID:637 -> Biological process: GO:0006626 [protein targeting to mitochondrion] evidence: IEA
            GeneID:637 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
            GeneID:637 -> Biological process: GO:0007420 [brain development] evidence: IEA
            GeneID:637 -> Biological process: GO:0008625 [extrinsic apoptotic signaling pathway via death domain receptors] evidence: TAS
            GeneID:637 -> Biological process: GO:0008637 [apoptotic mitochondrial changes] evidence: TAS
            GeneID:637 -> Biological process: GO:0032355 [response to estradiol stimulus] evidence: IEA
            GeneID:637 -> Biological process: GO:0032461 [positive regulation of protein oligomerization] evidence: IDA
            GeneID:637 -> Biological process: GO:0032464 [positive regulation of protein homooligomerization] evidence: IDA
            GeneID:637 -> Biological process: GO:0034349 [glial cell apoptotic process] evidence: IEA
            GeneID:637 -> Biological process: GO:0042127 [regulation of cell proliferation] evidence: IEA
            GeneID:637 -> Biological process: GO:0043065 [positive regulation of apoptotic process] evidence: IMP
            GeneID:637 -> Biological process: GO:0046902 [regulation of mitochondrial membrane permeability] evidence: IEA
            GeneID:637 -> Biological process: GO:0051260 [protein homooligomerization] evidence: IEA
            GeneID:637 -> Biological process: GO:0051402 [neuron apoptotic process] evidence: TAS
            GeneID:637 -> Biological process: GO:0090150 [establishment of protein localization to membrane] evidence: IDA
            GeneID:637 -> Biological process: GO:0090200 [positive regulation of release of cytochrome c from mitochondria] evidence: IGI
            GeneID:637 -> Biological process: GO:0090200 [positive regulation of release of cytochrome c from mitochondria] evidence: IMP
            GeneID:637 -> Biological process: GO:0097193 [intrinsic apoptotic signaling pathway] evidence: TAS
            GeneID:637 -> Biological process: GO:1900740 [positive regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway] evidence: TAS
            GeneID:637 -> Biological process: GO:1901030 [positive regulation of mitochondrial outer membrane permeabilization] evidence: TAS
            GeneID:637 -> Biological process: GO:2000045 [regulation of G1/S transition of mitotic cell cycle] evidence: IEA
            GeneID:637 -> Biological process: GO:2001238 [positive regulation of extrinsic apoptotic signaling pathway] evidence: IMP
            GeneID:637 -> Biological process: GO:2001244 [positive regulation of intrinsic apoptotic signaling pathway] evidence: TAS
            GeneID:637 -> Cellular component: GO:0005739 [mitochondrion] evidence: TAS
            GeneID:637 -> Cellular component: GO:0005741 [mitochondrial outer membrane] evidence: TAS
            GeneID:637 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
            GeneID:637 -> Cellular component: GO:0016020 [membrane] evidence: TAS
            GeneID:637 -> Cellular component: GO:0032592 [integral to mitochondrial membrane] evidence: IEA

by @meso_cacase at DBCLS
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