Parkinson's disease 19A

Summary
Synonym
  • juvenile onset Parkinson disease 19A
  • juvenile onset Parkinson's disease 19A
Definition
An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31.
Super Class
autosomal recessive disease early-onset Parkinson's disease
External Links
Disease Ontology
DOID:0060891
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying entries 11 - 20 of 164 in total
Gene ID Gene Symbol Description Source
308 ANXA5 annexin A5
353 APRT adenine phosphoribosyltransferase
410 ARSA arylsulfatase A
427 ASAH1 N-acylsphingosine amidohydrolase 1
683 BST1 bone marrow stromal cell antigen 1
811 CALR calreticulin
847 CAT catalase
929 CD14 CD14 molecule
952 CD38 CD38 molecule
960 CD44 CD44 molecule (IN blood group)
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 54 in total
HPO ID HPO Term
HP:0001761 Pes cavus
HP:0002014 Diarrhea
HP:0002018 Nausea
HP:0002019 Constipation
HP:0002063 Rigidity
HP:0002066 Gait ataxia
HP:0002067 Bradykinesia
HP:0002141 Gait imbalance
HP:0002172 Postural instability
HP:0002304 Akinesia
Displaying 1 entry
Gene ID Gene Symbol Description
8867 SYNJ1 synaptojanin 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024