Parkinson's disease 23

Summary
Synonym
  • autosomal recessive early-onset Parkinson disease 23
  • autosomal recessive early-onset Parkinson's disease 23
Definition
An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22.
Super Class
autosomal recessive disease early-onset Parkinson's disease
External Links
Disease Ontology
DOID:0060896
Mondo Disease Ontology
OMIM
Related Genes
Displaying entries 61 - 70 of 164 in total
Gene ID Gene Symbol Description Source
2876 GPX1 glutathione peroxidase 1
2923 PDIA3 protein disulfide isomerase family A member 3
3037 HAS2 hyaluronan synthase 2
3073 HEXA hexosaminidase subunit alpha
3098 HK1 hexokinase 1
3099 HK2 hexokinase 2
3383 ICAM1 intercellular adhesion molecule 1
3425 IDUA alpha-L-iduronidase
3482 IGF2R insulin like growth factor 2 receptor
3897 L1CAM L1 cell adhesion molecule
Related Glycoprotein
Displaying entries 131 - 132 of 132 in total
UniProt ID Protein Name Source
Q9Y286 Sialic acid-binding Ig-like lectin 7
Q9Y2H2 Phosphatidylinositide phosphatase SAC2
The Human Phenotype Ontology
Displaying entries 21 - 30 of 31 in total
HPO ID HPO Term
HP:0002172 Postural instability
HP:0002578 Gastroparesis
HP:0003394 Muscle spasm
HP:0004409 Hyposmia
HP:0012332 Abnormal autonomic nervous system physiology
HP:0012452 Restless legs
HP:0012760 Reduced social reciprocity
HP:0100543 Cognitive impairment
HP:0100660 Dyskinesia
HP:0100710 Impulsivity
Displaying 1 entry
Gene ID Gene Symbol Description
8867 SYNJ1 synaptojanin 1

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Acknowledgements

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Partly supported by NIH Common Fund Grant #1U01GM125267-01


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