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Gene : PINK1 Homo sapiens

Name  ? PTEN induced kinase 1 Cytological Location  1p36.12
Brief Description  PTEN induced kinase 1
description  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]
  • synonyms:
  • Parkinson disease (autosomal recessive) 6,
  • uc001bdm.3,
  • PARK6,
  • AB053323,
  • PARK6,
  • HGNC:14581,
  • OTTHUMG00000002841,
  • PTEN induced putative kinase 1,
  • BRPK,
  • PINK1,
  • NM_032409,
  • BRPK
  • identifiers:
  • 65018,
  • ENSG00000158828,
  • PINK1

Genome feature

Region: gene ? Length: 18054  
Location: 1:20633458-20651511 Cyto location: 1p36.12

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



3756 SN Ps

5 Cross References

18 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results