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Gene : PINK1 Homo sapiens

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

Genome feature

Region: gene ? Length: 18057  
Location: 1:20633455-20651511 Cyto location: 1p36.12


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Function

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Gene --> GO terms.

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

729 SN Ps

5 Cross References

19 Data Sets

7 Homologues

0 Located Features

90 Rna Seq Results