Genes in panel
STRs in panel
Prev Next
Regions in panel
Prev Next

Prepair 1000+

Gene: DNAJC6

Green List (high evidence)

DNAJC6 (DnaJ heat shock protein family (Hsp40) member C6)
EnsemblGeneIds (GRCh38): ENSG00000116675
EnsemblGeneIds (GRCh37): ENSG00000116675
OMIM: 608375, Gene2Phenotype
DNAJC6 is in 6 panels

1 review

Karina Sandoval (Victorian Clinical Genetics Services)

Green List (high evidence)

Parkinson disease 19a, juvenile-onset, MIM#615528 characterized by onset of parkinsonism in the first or second decade. Parkinson disease 19b, early-onset, MIM#615528 is characterised by onset of parkinsonism between the third and fifth decades.

This is a well-established Parkinson's disease gene

Multiple unrelated families with early-onset Parkinson disease reported.
Created: 11 Mar 2025, 4:15 a.m. | Last Modified: 11 Mar 2025, 4:15 a.m.
Panel Version: 1.1568

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Parkinson disease 19a, juvenile-onset, MIM#615528

Publications

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Parkinson disease 19, juvenile-onset, 615528 (3)
OMIM
608375
Clinvar variants
Variants in DNAJC6
Penetrance
None
Panels with this gene

History Filter Activity

1 Jun 2022, Gel status: 3

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: DNAJC6 was added gene: DNAJC6 was added to Reproductive Carrier Screen_VCGS. Sources: Mackenzie's Mission,Expert Review Green Mode of inheritance for gene: DNAJC6 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: DNAJC6 were set to Parkinson disease 19, juvenile-onset, 615528 (3)