Homo sapiens (human): 637
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Entry
637 CDS
T01001
Symbol
BID, FP497
Name
(RefSeq) BH3 interacting domain death agonist
KO
K04726
BH3 interacting domain death agonist
Organism
hsa
Homo sapiens (human)
Pathway
hsa01524
Platinum drug resistance
hsa04071
Sphingolipid signaling pathway
hsa04115
p53 signaling pathway
hsa04210
Apoptosis
hsa04215
Apoptosis - multiple species
hsa04217
Necroptosis
hsa04650
Natural killer cell mediated cytotoxicity
hsa04932
Non-alcoholic fatty liver disease
hsa05010
Alzheimer disease
hsa05014
Amyotrophic lateral sclerosis
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05152
Tuberculosis
hsa05160
Hepatitis C
hsa05161
Hepatitis B
hsa05162
Measles
hsa05163
Human cytomegalovirus infection
hsa05164
Influenza A
hsa05167
Kaposi sarcoma-associated herpesvirus infection
hsa05168
Herpes simplex virus 1 infection
hsa05169
Epstein-Barr virus infection
hsa05170
Human immunodeficiency virus 1 infection
hsa05200
Pathways in cancer
hsa05416
Viral myocarditis
hsa05417
Lipid and atherosclerosis
Network
nt06161
Human immunodeficiency virus 1 (HIV-1)
nt06162
Hepatitis B virus (HBV)
nt06163
Hepatitis C virus (HCV)
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06165
Epstein-Barr virus (EBV)
nt06167
Human cytomegalovirus (HCMV)
nt06168
Herpes simplex virus 1 (HSV-1)
nt06231
Apoptosis (cancer)
nt06263
Hepatocellular carcinoma
nt06460
Alzheimer disease
nt06466
Pathways of neurodegeneration
nt06524
Apoptosis
Element
N00146
Crosstalk between extrinsic and intrinsic apoptotic pathways
N00449
HIV Tat/Nef to crosstalk between extrinsic and intrinsic apoptotic pathways
N00477
EBV BHRF1 to crosstalk between extrinsic and intrinsic apoptotic pathways
N01005
Mutation-caused aberrant Abeta to crosstalk between extrinsic and intrinsic apoptotic pathways
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04071 Sphingolipid signaling pathway
637 (BID)
09140 Cellular Processes
09143 Cell growth and death
04215 Apoptosis - multiple species
637 (BID)
09150 Organismal Systems
09151 Immune system
04650 Natural killer cell mediated cytotoxicity
637 (BID)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
637 (BID)
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
637 (BID)
05161 Hepatitis B
637 (BID)
05160 Hepatitis C
637 (BID)
05164 Influenza A
637 (BID)
05162 Measles
637 (BID)
05163 Human cytomegalovirus infection
637 (BID)
05167 Kaposi sarcoma-associated herpesvirus infection
637 (BID)
05169 Epstein-Barr virus infection
637 (BID)
09171 Infectious disease: bacterial
05152 Tuberculosis
637 (BID)
09164 Neurodegenerative disease
05010 Alzheimer disease
637 (BID)
05014 Amyotrophic lateral sclerosis
637 (BID)
05022 Pathways of neurodegeneration - multiple diseases
637 (BID)
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
637 (BID)
05416 Viral myocarditis
637 (BID)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
637 (BID)
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
637 (BID)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
BID
Bcl-2
DUF4618
CRM1_C
Motif
Other DBs
NCBI-GeneID:
637
NCBI-ProteinID:
NP_001187
OMIM:
601997
HGNC:
1050
Ensembl:
ENSG00000015475
UniProt:
P55957
A8ASI8
B3KT21
Structure
PDB
PDBj
LinkDB
All DBs
Position
22:complement(17734138..17774665)
Genome browser
AA seq
195 aa
AA seq
DB search
MDCEVNNGSSLRDECITNLLVFGFLQSCSDNSFRRELDALGHELPVLAPQWEGYDELQTD
GNRSSHSRLGRIEADSESQEDIIRNIARHLAQVGDSMDRSIPPGLVNGLALQLRNTSRSE
EDRNRDLATALEQLLQAYPRDMEKEKTMLVLALLLAKKVASHTPSLLRDVFHTTVNFINQ
NLRTYVRSLARNGMD
NT seq
588 nt
NT seq
+upstream
nt +downstream
nt
atggactgtgaggtcaacaacggttccagcctcagggatgagtgcatcacaaacctactg
gtgtttggcttcctccaaagctgttctgacaacagcttccgcagagagctggacgcactg
ggccacgagctgccagtgctggctccccagtgggagggctacgatgagctgcagactgat
ggcaaccgcagcagccactcccgcttgggaagaatagaggcagattctgaaagtcaagaa
gacatcatccggaatattgccaggcacctcgcccaggtcggggacagcatggaccgtagc
atccctccgggcctggtgaacggcctggccctgcagctcaggaacaccagccggtcggag
gaggaccggaacagggacctggccactgccctggagcagctgctgcaggcctaccctaga
gacatggagaaggagaagaccatgctggtgctggccctgctgctggccaagaaggtggcc
agtcacacgccgtccttgctccgtgatgtctttcacacaacagtgaattttattaaccag
aacctacgcacctacgtgaggagcttagccagaaatgggatggactga
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