Homo sapiens Gene: BID
Summary
InnateDB Gene IDBG-1050.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BID
Gene Name BH3 interacting domain death agonist
Synonyms FP497
Species Homo sapiens
Ensembl Gene ENSG00000015475
Encoded Proteins
BH3 interacting domain death agonist
BH3 interacting domain death agonist
BH3 interacting domain death agonist
BH3 interacting domain death agonist
BH3 interacting domain death agonist
BH3 interacting domain death agonist
BH3 interacting domain death agonist
BH3 interacting domain death agonist
BH3 interacting domain death agonist
BH3 interacting domain death agonist
BH3 interacting domain death agonist
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
InnateDB Annotation
Summary
BID is a critical component of the NOD signalling pathway and is crucial for the peptidoglycan inflammation response. BID deficient mice are unresponsive to local or systemic exposure to NOD agonist or their protective effects in experimental colitis. (Demonstrated in murine model)
InnateDB Annotation from Orthologs
Summary
[Mus musculus] Bid is a critical component of the NOD signalling pathway and is crucial for the peptidoglycan inflammation response. Bid deficient mice are unresponsive to local or systemic exposure to NOD agonist or their protective effects in experimental colitis.
Entrez Gene
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]
Gene Information
Type Protein coding
Genomic Location Chromosome 22:17734138-17774770
Strand Reverse strand
Band q11.21
Transcripts
ENST00000317361 ENSP00000318822
ENST00000342111 ENSP00000344594
ENST00000399774 ENSP00000382674
ENST00000399767 ENSP00000382669
ENST00000399765 ENSP00000382667
ENST00000494097
ENST00000473439
ENST00000550946
ENST00000551952 ENSP00000449236
ENST00000552886
ENST00000622694 ENSP00000480414
ENST00000611040 ENSP00000483709
ENST00000615414 ENSP00000483534
ENST00000614949 ENSP00000477773
ENST00000617586 ENSP00000481991
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 99 experimentally validated interaction(s) in this database.
They are also associated with 6 interaction(s) predicted by orthology.
Experimentally validated
Total 99 [view]
Protein-Protein 97 [view]
Protein-DNA 2 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 6 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005123 death receptor binding
GO:0005515 protein binding
GO:0031625 ubiquitin protein ligase binding
Biological Process
GO:0001836 release of cytochrome c from mitochondria
GO:0006626 protein targeting to mitochondrion
GO:0006915 apoptotic process
GO:0006919 activation of cysteine-type endopeptidase activity involved in apoptotic process
GO:0007420 brain development
GO:0008625 extrinsic apoptotic signaling pathway via death domain receptors
GO:0008637 apoptotic mitochondrial changes
GO:0032355 response to estradiol
GO:0032459 regulation of protein oligomerization
GO:0032461 positive regulation of protein oligomerization
GO:0032464 positive regulation of protein homooligomerization
GO:0034349 glial cell apoptotic process
GO:0042127 regulation of cell proliferation
GO:0042770 signal transduction in response to DNA damage
GO:0043065 positive regulation of apoptotic process
GO:0045087 innate immune response (InnateDB)
GO:0051260 protein homooligomerization
GO:0051402 neuron apoptotic process
GO:0090150 establishment of protein localization to membrane
GO:0090200 positive regulation of release of cytochrome c from mitochondria
GO:0097191 extrinsic apoptotic signaling pathway
GO:0097193 intrinsic apoptotic signaling pathway
GO:1900740 positive regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway
GO:1901030 positive regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway
GO:1902108 regulation of mitochondrial membrane permeability involved in apoptotic process
GO:2000045 regulation of G1/S transition of mitotic cell cycle
GO:2001238 positive regulation of extrinsic apoptotic signaling pathway
GO:2001244 positive regulation of intrinsic apoptotic signaling pathway
Cellular Component
GO:0005737 cytoplasm
GO:0005739 mitochondrion
GO:0005741 mitochondrial outer membrane
GO:0005829 cytosol
GO:0016020 membrane
GO:0032592 integral component of mitochondrial membrane
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
TNFalpha pathway
REACTOME
Activation of BAD and translocation to mitochondria pathway
BH3-only proteins associate with and inactivate anti-apoptotic BCL-2 members pathway
Activation, translocation and oligomerization of BAX pathway
Activation, myristolyation of BID and translocation to mitochondria pathway
Activation and oligomerization of BAK protein pathway
Apoptosis pathway
Activation of BH3-only proteins pathway
Intrinsic Pathway for Apoptosis pathway
KEGG
Apoptosis pathway
Alzheimer's disease pathway
Natural killer cell mediated cytotoxicity pathway
p53 signaling pathway pathway
Amyotrophic lateral sclerosis (ALS) pathway
Pathways in cancer pathway
Viral myocarditis pathway
INOH
TNFR1 signaling pathway pathway
Fas signaling pathway pathway
PID NCI
Ceramide signaling pathway
Caspase Cascade in Apoptosis
Direct p53 effectors
ATM pathway
HIV-1 Nef: Negative effector of Fas and TNF-alpha
FAS (CD95) signaling pathway
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.591054
RefSeq NM_001196 NM_001244567 NM_001244569 NM_001244570 NM_001244572 NM_197966 NM_197967
HUGO
OMIM
CCDS CCDS13747 CCDS13748 CCDS13749
HPRD 03590
IMGT
EMBL
GenPept
RNA Seq Atlas