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Gene : DNAJC13 Homo sapiens

Name  ? DnaJ heat shock protein family (Hsp40) member C13 Cytological Location  3q22.1
Brief Description  DnaJ heat shock protein family (Hsp40) member C13
Description  This gene encodes a member of the Dnaj protein family whose members act as co-chaperones of a partner heat-shock protein by binding to the latter and stimulating ATP hydrolysis. The encoded protein associates with the heat-shock protein Hsc70 and plays a role in clathrin-mediated endocytosis. It may also be involved in post-endocytic transport mechanisms via its associations with other proteins, including the sorting nexin SNX1. Mutations in this gene are associated with Parkinson's disease. [provided by RefSeq, Jun 2016]
  • synonyms:
  • PARK21,
  • KIAA0678,
  • NM_015268,
  • HGNC:30343,
  • DnaJ (Hsp40) homolog, subfamily C, member 13,
  • OTTHUMG00000159674,
  • uc003eor.4,
  • RME8,
  • AB014578,
  • RME8,
  • DNAJC13
  • identifiers:
  • 23317,
  • ENSG00000138246,
  • DNAJC13

Genome feature

Region: gene ? Length: 121531  
Location: 3:132417502-132539032 Cyto location: 3q22.1

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

Gene Ontology

Gene --> GO terms.



3753 SN Ps

5 Cross References

17 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results