19 Jun 2019
Mitochondrial disorders v1.394
VPS13C
Sarah Leigh Classified gene: VPS13C as Red List (low evidence)
19 Jun 2019
Mitochondrial disorders v1.394
VPS13C
Sarah Leigh Added comment: Comment on list classification: This gene was demoted from Green to Red, based on the reviews of clinical experts.
19 Jun 2019
Mitochondrial disorders v1.394
VPS13C
Sarah Leigh Gene: vps13c has been classified as Red List (Low Evidence).
19 Jun 2019
Mitochondrial disorders v1.388
VPS13C
Anna de Burca reviewed gene: VPS13C: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Parkinson disease 23, autosomal recessive, early onset, 616840; Mode of inheritance:
11 Jun 2019
Mitochondrial disorders v1.384
VPS13C
Carl Fratter reviewed gene: VPS13C: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Parkinson disease 23, autosomal recessive, early onset, 616840; Mode of inheritance:
03 May 2019
Mitochondrial disorders v1.291
VPS13C
Ivone Leong Classified gene: VPS13C as Green List (high evidence)
03 May 2019
Mitochondrial disorders v1.291
VPS13C
Ivone Leong Added comment: Comment on list classification: Promoted from red to green based on expert review. This gene is associated with a phenotype in OMIM but not Gene2Phenotype. There are >3 unrelated cases of patients with different variants in this gene.
03 May 2019
Mitochondrial disorders v1.291
VPS13C
Ivone Leong Gene: vps13c has been classified as Green List (High Evidence).
03 May 2019
Mitochondrial disorders v1.290
VPS13C
Ivone Leong Publications for gene: VPS13C were set to 26942284
03 May 2019
Mitochondrial disorders v1.289
VPS13C
Ivone Leong Mode of inheritance for gene: VPS13C was changed from to BIALLELIC, autosomal or pseudoautosomal
03 May 2019
Mitochondrial disorders v1.288
VPS13C
Ivone Leong Publications for gene: VPS13C were set to 616840
03 May 2019
Mitochondrial disorders v1.287
VPS13C
Ivone Leong Publications for gene: VPS13C were set to
03 May 2019
Mitochondrial disorders v1.286
VPS13C
Ivone Leong Phenotypes for gene: VPS13C were changed from to Parkinson disease 23, autosomal recessive, early onset, 616840
01 Sep 2018
Mitochondrial disorders
VPS13C
Zornitza Stark reviewed gene: VPS13C
28 Aug 2018
Mitochondrial disorders
VPS13C
Sarah Leigh Added gene to panel