PINK1


Summary: This gene encodes a serine/threonine protein kinase that localizes to mitochondria. It is thought to protect cells from stress-induced mitochondrial dysfunction. Mutations in this gene cause one form of autosomal recessive early-onset Parkinson disease. [provided by RefSeq, Jul 2008].

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OMIM ID
Ensembl ID
HGNC ID
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GO terms in PINK1


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Term Type
Evidence Type
GO Term ID
GO Des.
BP IBA GO:0000422 autophagy of mitochondrion
BP IMP GO:0000422 autophagy of mitochondrion
BP IDA GO:0001934 positive regulation of protein phosphorylation
BP IDA GO:0002082 regulation of oxidative phosphorylation
BP IEA GO:0002931 response to ischemia
BP IBA GO:0006468 protein phosphorylation
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Gene expression in normal tissue: PINK1

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in PINK1


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Database
Pathway ID
Pathway Des.
reactome R-HSA-5205647 Mitophagy
reactome R-HSA-5205685 Pink/Parkin Mediated Mitophagy
kegg hsa04137 Mitophagy - animal - Homo sapiens (human)
kegg hsa05012 Parkinson,s disease - Homo sapiens (human)
wikipathways WP2371 Parkinsons Disease Pathway
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD121 GMX1778 4
iGMDRD474 Avrainvillamide 3
iGMDRD512 nutlin 3 1
iGMDRD780 PP-30 3
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in PINK1

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

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