Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
637
Gene name Gene Name - the full gene name approved by the HGNC.
BH3 interacting domain death agonist
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
BID
Synonyms (NCBI Gene) Gene synonyms aliases
FP497
Chromosome Chromosome number
22
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q11.21
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a death agonist that heterodimerizes with either agonist BAX or antagonist BCL2, and thus regulate apoptosis. The encoded protein is a member of the BCL-2 family of cell death regulators. It is a mediator of mitochondrial damage induced
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT006072 hsa-miR-492 Microarray, qRT-PCR 21319197
MIRT006072 hsa-miR-492 Microarray, qRT-PCR 21319197
MIRT006072 hsa-miR-492 Microarray, qRT-PCR 21319197
MIRT049655 hsa-miR-92a-3p CLASH 23622248
MIRT045661 hsa-miR-149-5p CLASH 23622248
Transcription factors
Transcription factor Regulation Reference
HIF1A Repression 15024076
ZBTB16 Repression 20731660
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001836 Process Release of cytochrome c from mitochondria IDA 17052454
GO:0001836 Process Release of cytochrome c from mitochondria IEA
GO:0005123 Function Death receptor binding TAS 8918887
GO:0005515 Function Protein binding IPI 9463381, 12624108, 14963330, 15694340, 16697956, 17052454, 17123957, 17289999, 17485524, 19074266, 19074440, 20956295, 21036904, 21382479, 23374347, 23604079, 23782464, 24814347, 25241761, 25416956, 29531808, 32296183, 33961781
GO:0005737 Component Cytoplasm IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601997 1050 ENSG00000015475
Protein
UniProt ID P55957
Protein name BH3-interacting domain death agonist (p22 BID) (BID) [Cleaved into: BH3-interacting domain death agonist p15 (p15 BID); BH3-interacting domain death agonist p13 (p13 BID); BH3-interacting domain death agonist p11 (p11 BID)]
Protein function Induces caspases and apoptosis (PubMed:14583606). Counters the protective effect of BCL2 (By similarity). ; [BH3-interacting domain death agonist p15]: Induces caspase activat
PDB 1ZY3 , 2BID , 2KBW , 2M5B , 2M5I , 4BD2 , 4QVE , 4ZEQ , 4ZIG , 4ZII , 5AJJ , 5C3F , 7M5A , 7M5B , 7P33 , 7QTW , 8SM5
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06393 BID 3 192 BH3 interacting domain (BID) Domain
Tissue specificity TISSUE SPECIFICITY: [Isoform 2]: Expressed in spleen, pancreas and placenta (at protein level). {ECO:0000269|PubMed:14583606}.; TISSUE SPECIFICITY: [Isoform 3]: Expressed in lung, pancreas and spleen (at protein level). {ECO:0000269|PubMed:14583606}.; TIS
Sequence
Sequence length 195
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Platinum drug resistance
Sphingolipid signaling pathway
p53 signaling pathway
Apoptosis
Apoptosis - multiple species
Necroptosis
Natural killer cell mediated cytotoxicity
Non-alcoholic fatty liver disease
Alzheimer disease
Amyotrophic lateral sclerosis
Pathways of neurodegeneration - multiple diseases
Tuberculosis
Hepatitis C
Hepatitis B
Measles
Human cytomegalovirus infection
Influenza A
Kaposi sarcoma-associated herpesvirus infection
Herpes simplex virus 1 infection
Epstein-Barr virus infection
Human immunodeficiency virus 1 infection
Pathways in cancer
Viral myocarditis
Lipid and atherosclerosis
  Activation of BAD and translocation to mitochondria
Activation and oligomerization of BAK protein
BH3-only proteins associate with and inactivate anti-apoptotic BCL-2 members
Activation, translocation and oligomerization of BAX
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release
Activation, myristolyation of BID and translocation to mitochondria
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