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Parkinson's UK Annotation Initiative

This initiative focused on the annotation of Parkinson's disease-relevant proteins and was funded by a 3-year Parkinson's UK grant (G-1307) from January 2014 to December 2016.

PARK2 protein structure

The Parkinson's UK-funded GO annotations have facilitated the detailed and high-quality annotation of over 800 Parkinson's disease-relevant genes, providing . There are many ways in with the impact of our curation on data analysis and annotation resources can be demonstrated. Annotations contributed by this project to the GO Consortium dataset are attributed to ParkinsonsUK-UCL.

For this initiative we created two priority gene lists.

  • A high-priority set of 48 Parkinson's disease-relevant genes were selected based on genetic linkage or association studies (see table below).

Our longer Parkinson's-relevant priority list includes 329 gene products. These were chosen based on their interaction with high-priority gene products or because of their role in Parkinson's disease-related biological processes

Priority Parkinson's processes

The following processes were prioritised, following discussions with experts in the field. These processes are considered to have important roles in Parkinson's disease.

High-priority set of Parkinson's disease-relevant genes

Genes in this list were prioritised for comprehensive annotation using GO because variants in these genes have been implicated as having a role in Parkinson's disease, either in published linkage or association studies.

HGNC symbolHGNC namePubMed IdentifierUniProt Identifier (human)
ACMSDaminocarboxymuconate semialdehyde decarboxylase
ATP13A2ATPase type 13A2
BST1bone marrow stromal cell antigen 1
CCDC62coiled-coil domain containing 62
DDRGK1DDRGK domain containing 1
Ìý¶Ù³Ò°­²ÏÌýdiacylglycerol kinase, theta 110kDa
EIF4G1eukaryotic translation initiation factor 4 gamma, 1
FAM47Efamily with sequence similarity 47, member E
FBXO7F-box protein 7
FGF20fibroblast growth factor 20
GAKcyclin G associated kinase
GBAglucosidase, beta, acid
GCH1GTP cyclohydrolase 1
GIGYF2GRB10 interacting GYF protein 2
GPNMBglycoprotein (transmembrane) nmb
HIP1Rhuntingtin interacting protein 1 related
HTRA2HtrA serine peptidase 2
INPP5Finositol polyphosphate-5-phosphatase F
LAMP3lysosomal-associated membrane protein 3
LRRK2leucine-rich repeat kinase 2
MAPTmicrotubule-associated protein tau
MCCC1methylcrotonoyl-CoA carboxylase 1 (alpha)
MMP16matrix metallopeptidase 16 (membrane-inserted)
NMD3NMD3 homolog (S. cerevisiae)
Ìý±·³§¹óÌýN-ethylmaleimide-sensitive factor
NUCKS1nuclear casein kinase and cyclin-dependent kinase substrate 1
PARK2parkin RBR E3 ubiquitin protein ligase
PARK7parkinson protein 7
PINK1PTEN induced putative kinase 1
RAB29RAB29, member RAS oncogene family
Ìý¸é±õ°Õ2ÌýRas-like without CAAX 2
SCARB2scavenger receptor class B, member 2
SETD1ASET domain containing 1A
SIPA1L2signal-induced proliferation-associated 1 like 2
Ìý³§³¢°ä41´¡1Ìýsolute carrier family 41 (magnesium transporter), member 1
Ìý³§³¢°ä45´¡3Ìýsolute carrier family 45, member 3
SNCAsynuclein, alpha (non A4 component of amyloid precursor)
STBD1starch binding domain 1
STK39serine threonine kinase 39
STX1Bsyntaxin 1B
SYNJ1synaptojanin 1
Ìý³§³Û°Õ4Ìýsynaptotagmin IV
SYT11synaptotagmin XI
TAF1TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa
Ìý±«±·°ä13µþÌýunc-13 homolog B (C. elegans)
VPS13Cvacuolar protein sorting 13 homolog C (S. cerevisiae)
VPS35vacuolar protein sorting 35 homolog (S. cerevisiae)
Ìý°Â±·°Õ3Ìýwingless-type MMTV integration site family, member 3ÌýÌý

HUGO Gene Nomenclature Committee (HGNC) approved gene symbols and names are listed, the PubMed identifiers indicate the publication describing the association with Parkinson's disease, and the UniProt IDs link to the QuickGO Gene Ontology annotations for each protein.ÌýGenes identified in genome-wide association studies are those suggested by the authors to be the most likely candidates and genes known to contain causative variants are highlighted inÌýboldÌýfont.

Image credit: By Emw (Own work) [CC BY-SA 3.0 () or GFDL ()], via Wikimedia Commons