CASP10


Summary: This gene encodes a protein which is a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce two subunits, large and small, that dimerize to form the active enzyme. This protein cleaves and activates caspases 3 and 7, and the protein itself is processed by caspase 8. Mutations in this gene are associated with type IIA autoimmune lymphoproliferative syndrome, non-Hodgkin lymphoma and gastric cancer. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Apr 2011].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location
OMIM IDMIM:601762
PHARMGKB IDPA26084
Map Location2q33.1

Gene Categories:

PROTEASEDRUGGABLE GENOME

GO terms in CASP10


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Term Type
Evidence Type
GO Term ID
GO Des.
CC IBA GO:0005737 cytoplasm
CC TAS GO:0005829 cytosol
CC IDA GO:0031265 CD95 death-inducing signaling complex
CC IDA GO:0097342 ripoptosome
BP IEA GO:0006508 proteolysis
BP IBA GO:0006915 apoptotic process
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Gene expression in normal tissue: CASP10

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in CASP10


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Database
Pathway ID
Pathway Des.
wikipathways WP1772 Apoptosis Modulation and Signaling
wikipathways WP254 Apoptosis
wikipathways WP314 Fas Ligand (FasL) pathway and Stress induction of Heat Shock Proteins (HSP) regulation
wikipathways WP3639 Apoptotic Signaling Pathway
wikipathways WP3802 TP53 Regulates Transcription of Cell Death Genes
wikipathways WP3865 RIG-I-like Receptor Signaling
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD405 PIK-75 3
iGMDRD420 Leucascandrolide A 3
iGMDRD154 NSC23766 1
iGMDRD123 Isoevodiamine 3
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in CASP10

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

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