Genes in panel

Neurodegenerative disorders - adult onset

Gene: SNCAIP

Red List (low evidence)

SNCAIP (synuclein alpha interacting protein)
EnsemblGeneIds (GRCh38): ENSG00000064692
EnsemblGeneIds (GRCh37): ENSG00000064692
OMIM: 603779, Gene2Phenotype
SNCAIP is in 3 panels

0 reviews

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
Phenotypes
  • Parkinson Disease, Dominant/Recessive
OMIM
603779
Clinvar variants
Variants in SNCAIP
Penetrance
None
Panels with this gene

History Filter Activity

25 Jan 2019, Gel status: 1

Panel promoted to version 1.0

Louise Daugherty (Genomics England Curator)

Rebecca Foulger: Gene awaiting curator evaluati

18 Dec 2018, Gel status: 1

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

Rebecca Foulger (Genomics England curator)

gene: SNCAIP was added gene: SNCAIP was added to Neurodegenerative disorders - adult onset. Sources: Expert Review Red Mode of inheritance for gene: SNCAIP was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SNCAIP were set to Parkinson Disease, Dominant/Recessive