Homo sapiens (human): 5366
Help
Entry
5366 CDS
T01001
Symbol
PMAIP1, APR, NOXA
Name
(RefSeq) phorbol-12-myristate-13-acetate-induced protein 1
KO
K10131
phorbol-12-myristate-13-acetate-induced protein 1
Organism
hsa
Homo sapiens (human)
Pathway
hsa01524
Platinum drug resistance
hsa04115
p53 signaling pathway
hsa04210
Apoptosis
hsa04215
Apoptosis - multiple species
hsa05200
Pathways in cancer
hsa05203
Viral carcinogenesis
hsa05210
Colorectal cancer
Network
nt06161
Human immunodeficiency virus 1 (HIV-1)
nt06165
Epstein-Barr virus (EBV)
nt06166
Human papillomavirus (HPV)
nt06168
Herpes simplex virus 1 (HSV-1)
nt06170
Influenza A virus (IAV)
nt06231
Apoptosis (cancer)
nt06260
Colorectal cancer
nt06267
Small cell lung cancer
nt06463
Parkinson disease
nt06464
Amyotrophic lateral sclerosis
nt06466
Pathways of neurodegeneration
nt06524
Apoptosis
Element
N00098
Intrinsic apoptotic pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
5366 (PMAIP1)
04215 Apoptosis - multiple species
5366 (PMAIP1)
04115 p53 signaling pathway
5366 (PMAIP1)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
5366 (PMAIP1)
05203 Viral carcinogenesis
5366 (PMAIP1)
09162 Cancer: specific types
05210 Colorectal cancer
5366 (PMAIP1)
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
5366 (PMAIP1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PMAIP1
Motif
Other DBs
NCBI-GeneID:
5366
NCBI-ProteinID:
NP_066950
OMIM:
604959
HGNC:
9108
Ensembl:
ENSG00000141682
UniProt:
Q13794
A0A0S2Z490
Structure
PDB
PDBj
LinkDB
All DBs
Position
18:59899996..59904305
Genome browser
AA seq
54 aa
AA seq
DB search
MPGKKARKNAQPSPARAPAELEVECATQLRRFGDKLNFRQKLLNLISKLFCSGT
NT seq
165 nt
NT seq
+upstream
nt +downstream
nt
atgcctgggaagaaggcgcgcaagaacgctcaaccgagccccgcgcgggctccagcagag
ctggaagtcgagtgtgctactcaactcaggagatttggagacaaactgaacttccggcag
aaacttctgaatctgatatccaaactcttctgctcaggaacctga
Homo sapiens (human): 27113
Help
Entry
27113 CDS
T01001
Symbol
BBC3, JFY-1, JFY1, PUMA
Name
(RefSeq) BCL2 binding component 3
KO
K10132
Bcl-2-binding component 3
Organism
hsa
Homo sapiens (human)
Pathway
hsa01524
Platinum drug resistance
hsa04115
p53 signaling pathway
hsa04210
Apoptosis
hsa04215
Apoptosis - multiple species
hsa04390
Hippo signaling pathway
hsa05016
Huntington disease
hsa05162
Measles
hsa05200
Pathways in cancer
hsa05210
Colorectal cancer
Network
nt06161
Human immunodeficiency virus 1 (HIV-1)
nt06165
Epstein-Barr virus (EBV)
nt06166
Human papillomavirus (HPV)
nt06168
Herpes simplex virus 1 (HSV-1)
nt06169
Measles virus (MV)
nt06170
Influenza A virus (IAV)
nt06231
Apoptosis (cancer)
nt06260
Colorectal cancer
nt06267
Small cell lung cancer
nt06461
Huntington disease
nt06463
Parkinson disease
nt06464
Amyotrophic lateral sclerosis
nt06466
Pathways of neurodegeneration
nt06524
Apoptosis
Element
N00098
Intrinsic apoptotic pathway
N00695
MV V to p73-mediated transcription
N00982
Mutation-caused aberrant Htt to p53-mediated transcription
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04390 Hippo signaling pathway
27113 (BBC3)
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
27113 (BBC3)
04215 Apoptosis - multiple species
27113 (BBC3)
04115 p53 signaling pathway
27113 (BBC3)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
27113 (BBC3)
09162 Cancer: specific types
05210 Colorectal cancer
27113 (BBC3)
09172 Infectious disease: viral
05162 Measles
27113 (BBC3)
09164 Neurodegenerative disease
05016 Huntington disease
27113 (BBC3)
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
27113 (BBC3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Other DBs
NCBI-GeneID:
27113
NCBI-ProteinID:
NP_001120712
OMIM:
605854
HGNC:
17868
Ensembl:
ENSG00000105327
UniProt:
Q96PG8
Q9BXH1
Structure
PDB
PDBj
LinkDB
All DBs
Position
19:complement(47220824..47232860)
Genome browser
AA seq
261 aa
AA seq
DB search
MKFGMGSAQACPCQVPRAASTTWVPCQICGPRERHGPRTPGGQLPGARRGPGPRRPAPLP
ARPPGALGSVLRPLRARPGCRPRRPHPAARCLPLRPHRPTRRHRRPGGFPLAWGSPQPAP
RPAPGRSSALALAGGAAPGVARAQRPGGSGGRSHPGGPGSPRGGGTVGPGDRGPAAADGG
RPQRTVRAAETRGAAAAPPLTLEGPVQSHHGTPALTQGPQSPRDGAQLGACTRPVDVRDS
GGRPLPPPDTLASAGDFLCTM
NT seq
786 nt
NT seq
+upstream
nt +downstream
nt
atgaaatttggcatggggtctgcccaggcatgtccatgccaggtgcccagggctgcttcc
acgacgtgggtcccctgccagatttgtggccccagggagcgccatggcccgcgcacgcca
ggagggcagctccccggagcccgtagagggcctggcccgcgacggcccgcgccccttccc
gctcggccgcctggtgccctcggcagtgtcctgcggcctctgcgagcccggcctggctgc
cgcccccgccgcccccaccctgctgcccgctgcctacctctgcgcccccaccgccccacc
cgccgtcaccgccgccctggggggttcccgctggcctgggggtccccgcagccggccccg
aggcccgcgcccggacggtcctcagccctcgctctcgctggcggagcagcacctggagtc
gcccgtgcccagcgccccgggggctctggcgggcggtcccacccaggcggccccgggagt
ccgcggggaggaggaacagtgggcccgggagatcggggcccagctgcggcggatggcgga
cgacctcaacgcacagtacgagcggcggagacaagaggagcagcagcggcaccgcccctc
accctggagggtcctgtacaatctcatcatgggactcctgcccttacccaggggccacag
agcccccgagatggagcccaattaggtgcctgcacccgcccggtggacgtcagggactcg
gggggcaggcccctcccacctcctgacaccctggccagcgcgggggactttctctgcacc
atgtag
Homo sapiens (human): 572
Help
Entry
572 CDS
T01001
Symbol
BAD, BBC2, BCL2L8
Name
(RefSeq) BCL2 associated agonist of cell death
KO
K02158
Bcl-2-antagonist of cell death
Organism
hsa
Homo sapiens (human)
Pathway
hsa01521
EGFR tyrosine kinase inhibitor resistance
hsa01522
Endocrine resistance
hsa01524
Platinum drug resistance
hsa04012
ErbB signaling pathway
hsa04014
Ras signaling pathway
hsa04022
cGMP-PKG signaling pathway
hsa04024
cAMP signaling pathway
hsa04062
Chemokine signaling pathway
hsa04140
Autophagy - animal
hsa04151
PI3K-Akt signaling pathway
hsa04210
Apoptosis
hsa04370
VEGF signaling pathway
hsa04510
Focal adhesion
hsa04722
Neurotrophin signaling pathway
hsa04910
Insulin signaling pathway
hsa04919
Thyroid hormone signaling pathway
hsa05010
Alzheimer disease
hsa05014
Amyotrophic lateral sclerosis
hsa05020
Prion disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05145
Toxoplasmosis
hsa05152
Tuberculosis
hsa05160
Hepatitis C
hsa05161
Hepatitis B
hsa05162
Measles
hsa05165
Human papillomavirus infection
hsa05168
Herpes simplex virus 1 infection
hsa05170
Human immunodeficiency virus 1 infection
hsa05200
Pathways in cancer
hsa05203
Viral carcinogenesis
hsa05207
Chemical carcinogenesis - receptor activation
hsa05208
Chemical carcinogenesis - reactive oxygen species
hsa05210
Colorectal cancer
hsa05211
Renal cell carcinoma
hsa05212
Pancreatic cancer
hsa05213
Endometrial cancer
hsa05215
Prostate cancer
hsa05218
Melanoma
hsa05220
Chronic myeloid leukemia
hsa05221
Acute myeloid leukemia
hsa05223
Non-small cell lung cancer
hsa05225
Hepatocellular carcinoma
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)
nt06166
Human papillomavirus (HPV)
nt06168
Herpes simplex virus 1 (HSV-1)
nt06170
Influenza A virus (IAV)
nt06214
PI3K signaling (cancer)
nt06231
Apoptosis (cancer)
nt06260
Colorectal cancer
nt06261
Gastric cancer
nt06262
Pancreatic cancer
nt06263
Hepatocellular carcinoma
nt06264
Renal cell carcinoma
nt06266
Non-small cell lung cancer
nt06267
Small cell lung cancer
nt06268
Melanoma
nt06270
Breast cancer
nt06272
Prostate cancer
nt06273
Glioma
nt06275
Acute myeloid leukemia
nt06276
Chronic myeloid leukemia
nt06463
Parkinson disease
nt06464
Amyotrophic lateral sclerosis
nt06466
Pathways of neurodegeneration
nt06524
Apoptosis
Element
N00030
EGF-EGFR-RAS-PI3K signaling pathway
N00031
Duplication or mutation-activated FLT3 to RAS-PI3K signaling pathway
N00032
Mutation-activated KRAS/NRAS to PI3K signaling pathway
N00033
EGF-EGFR-PI3K signaling pathway
N00036
Mutation-activated EGFR to PI3K signaling pathway
N00043
HGF-MET-PI3K signaling pathway
N00044
Mutation-activated MET to PI3K signaling pathway
N00046
Mutation-activated KIT to PI3K signaling pathway
N00047
EML4-ALK fusion kinase to PI3K signaling pathway
N00048
BCR-ABL fusion kinase to PI3K signaling pathway
N00082
Loss of NKX3-1 to PI3K signaling pathway
N00098
Intrinsic apoptotic pathway
N00247
HGF-overexpression to PI3K signaling pathway
N00249
MET-overexpression to PI3K signaling pathway
N00384
HPV E6 to intrinsic apoptotic pathway
N00430
CXCR4-GNAI-PI3K-BAD signaling pathway
N00452
HIV Nef to intrinsic apoptotic pathway
N00514
Mutation-activated EGFR to PI3K signaling pathway
N00585
HSV US3 to intrinsic apoptotic pathway
N01348
Nicotine/NNK to PI3K signaling pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04012 ErbB signaling pathway
572 (BAD)
04014 Ras signaling pathway
572 (BAD)
04370 VEGF signaling pathway
572 (BAD)
04024 cAMP signaling pathway
572 (BAD)
04022 cGMP-PKG signaling pathway
572 (BAD)
04151 PI3K-Akt signaling pathway
572 (BAD)
09140 Cellular Processes
09141 Transport and catabolism
04140 Autophagy - animal
572 (BAD)
09143 Cell growth and death
04210 Apoptosis
572 (BAD)
09144 Cellular community - eukaryotes
04510 Focal adhesion
572 (BAD)
09150 Organismal Systems
09151 Immune system
04062 Chemokine signaling pathway
572 (BAD)
09152 Endocrine system
04910 Insulin signaling pathway
572 (BAD)
04919 Thyroid hormone signaling pathway
572 (BAD)
09156 Nervous system
04722 Neurotrophin signaling pathway
572 (BAD)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
572 (BAD)
05207 Chemical carcinogenesis - receptor activation
572 (BAD)
05208 Chemical carcinogenesis - reactive oxygen species
572 (BAD)
05203 Viral carcinogenesis
572 (BAD)
09162 Cancer: specific types
05210 Colorectal cancer
572 (BAD)
05212 Pancreatic cancer
572 (BAD)
05225 Hepatocellular carcinoma
572 (BAD)
05221 Acute myeloid leukemia
572 (BAD)
05220 Chronic myeloid leukemia
572 (BAD)
05218 Melanoma
572 (BAD)
05211 Renal cell carcinoma
572 (BAD)
05215 Prostate cancer
572 (BAD)
05213 Endometrial cancer
572 (BAD)
05223 Non-small cell lung cancer
572 (BAD)
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
572 (BAD)
05161 Hepatitis B
572 (BAD)
05160 Hepatitis C
572 (BAD)
05162 Measles
572 (BAD)
05168 Herpes simplex virus 1 infection
572 (BAD)
05165 Human papillomavirus infection
572 (BAD)
09171 Infectious disease: bacterial
05152 Tuberculosis
572 (BAD)
09174 Infectious disease: parasitic
05145 Toxoplasmosis
572 (BAD)
09164 Neurodegenerative disease
05010 Alzheimer disease
572 (BAD)
05014 Amyotrophic lateral sclerosis
572 (BAD)
05020 Prion disease
572 (BAD)
05022 Pathways of neurodegeneration - multiple diseases
572 (BAD)
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
572 (BAD)
09176 Drug resistance: antineoplastic
01521 EGFR tyrosine kinase inhibitor resistance
572 (BAD)
01524 Platinum drug resistance
572 (BAD)
01522 Endocrine resistance
572 (BAD)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Bcl-2_BAD
Bclx_interact
Motif
Other DBs
NCBI-GeneID:
572
NCBI-ProteinID:
NP_004313
OMIM:
603167
HGNC:
936
Ensembl:
ENSG00000002330
UniProt:
Q92934
Structure
PDB
PDBj
LinkDB
All DBs
Position
11:complement(64269828..64284704)
Genome browser
AA seq
168 aa
AA seq
DB search
MFQIPEFEPSEQEDSSSAERGLGPSPAGDGPSGSGKHHRQAPGLLWDASHQQEQPTSSSH
HGGAGAVEIRSRHSSYPAGTEDDEGMGEEPSPFRGRSRSAPPNLWAAQRYGRELRRMSDE
FVDSFKKGLPRPKSAGTATQMRQSSSWTRVFQSWWDRNLGRGSSAPSQ
NT seq
507 nt
NT seq
+upstream
nt +downstream
nt
atgttccagatcccagagtttgagccgagtgagcaggaagactccagctctgcagagagg
ggcctgggccccagccccgcaggggacgggccctcaggctccggcaagcatcatcgccag
gccccaggcctcctgtgggacgccagtcaccagcaggagcagccaaccagcagcagccat
catggaggcgctggggctgtggagatccggagtcgccacagctcctaccccgcggggacg
gaggacgacgaagggatgggggaggagcccagcccctttcggggccgctcgcgctcggcg
ccccccaacctctgggcagcacagcgctatggccgcgagctccggaggatgagtgacgag
tttgtggactcctttaagaagggacttcctcgcccgaagagcgcgggcacagcaacgcag
atgcggcaaagctccagctggacgcgagtcttccagtcctggtgggatcggaacttgggc
aggggaagctccgccccctcccagtga
Homo sapiens (human): 10018
Help
Entry
10018 CDS
T01001
Symbol
BCL2L11, BAM, BIM, BOD
Name
(RefSeq) BCL2 like 11
KO
K16341
Bcl-2-like protein 11
Organism
hsa
Homo sapiens (human)
Pathway
hsa01521
EGFR tyrosine kinase inhibitor resistance
hsa04068
FoxO signaling pathway
hsa04151
PI3K-Akt signaling pathway
hsa04210
Apoptosis
hsa04215
Apoptosis - multiple species
hsa04932
Non-alcoholic fatty liver disease
hsa05169
Epstein-Barr virus infection
hsa05200
Pathways in cancer
hsa05206
MicroRNAs in cancer
hsa05210
Colorectal cancer
Network
nt06161
Human immunodeficiency virus 1 (HIV-1)
nt06165
Epstein-Barr virus (EBV)
nt06166
Human papillomavirus (HPV)
nt06168
Herpes simplex virus 1 (HSV-1)
nt06170
Influenza A virus (IAV)
nt06231
Apoptosis (cancer)
nt06260
Colorectal cancer
nt06267
Small cell lung cancer
nt06463
Parkinson disease
nt06464
Amyotrophic lateral sclerosis
nt06466
Pathways of neurodegeneration
nt06524
Apoptosis
Element
N00098
Intrinsic apoptotic pathway
N00262
EBV EBNA3C to intrinsic apoptotic pathway
N00474
EBV BHRF1 to intrinsic apoptotic pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04068 FoxO signaling pathway
10018 (BCL2L11)
04151 PI3K-Akt signaling pathway
10018 (BCL2L11)
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
10018 (BCL2L11)
04215 Apoptosis - multiple species
10018 (BCL2L11)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
10018 (BCL2L11)
05206 MicroRNAs in cancer
10018 (BCL2L11)
09162 Cancer: specific types
05210 Colorectal cancer
10018 (BCL2L11)
09172 Infectious disease: viral
05169 Epstein-Barr virus infection
10018 (BCL2L11)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
10018 (BCL2L11)
09176 Drug resistance: antineoplastic
01521 EGFR tyrosine kinase inhibitor resistance
10018 (BCL2L11)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Bclx_interact
Bim_N
Phage_blade
Motif
Other DBs
NCBI-GeneID:
10018
NCBI-ProteinID:
NP_619527
OMIM:
603827
HGNC:
994
Ensembl:
ENSG00000153094
UniProt:
O43521
Structure
PDB
PDBj
LinkDB
All DBs
Position
2:111120914..111168445
Genome browser
AA seq
198 aa
AA seq
DB search
MAKQPSDVSSECDREGRQLQPAERPPQLRPGAPTSLQTEPQGNPEGNHGGEGDSCPHGSP
QGPLAPPASPGPFATRSPLFIFMRRSSLLSRSSSGYFSFDTDRSPAPMSCDKSTQTPSPP
CQAFNHYLSAMASMRQAEPADMRPEIWIAQELRRIGDEFNAYYARRVFLNNYQAAEDHPR
MVILRLLRYIVRLVWRMH
NT seq
597 nt
NT seq
+upstream
nt +downstream
nt
atggcaaagcaaccttctgatgtaagttctgagtgtgaccgagaaggtagacaattgcag
cctgcggagaggcctccccagctcagacctggggcccctacctccctacagacagagcca
caaggtaatcctgaaggcaatcacggaggtgaaggggacagctgcccccacggcagccct
cagggcccgctggccccacctgccagccctggcccttttgctaccagatccccgcttttc
atctttatgagaagatcctccctgctgtctcgatcctccagtgggtatttctcttttgac
acagacaggagcccagcacccatgagttgtgacaaatcaacacaaaccccaagtcctcct
tgccaggccttcaaccactatctcagtgcaatggcttccatgaggcaggctgaacctgca
gatatgcgcccagagatatggatcgcccaagagttgcggcgtattggagacgagtttaac
gcttactatgcaaggagggtatttttgaataattaccaagcagccgaagaccacccacga
atggttatcttacgactgttacgttacattgtccgcctggtgtggagaatgcattga
DBGET
integrated database retrieval system