GlyCosmos Portal

Parkinson's disease 19A

Synonym

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

Disease Ontology

DOID:0060891

Mondo Disease Ontology

ORDO

OMIM

Related Genes

Displaying entries **161 - 164** of **164** in total

« First

‹ Prev

…

13

14

15

16

17
Gene ID	Gene Symbol	Description	Source
161357	MDGA2	MAM domain containing glycosylphosphatidylinositol anchor 2	DisGeNET
165679	SPTSSB	serine palmitoyltransferase small subunit B	DisGeNET
283871	PGP	phosphoglycolate phosphatase	DisGeNET
284348	LYPD5	LY6/PLAUR domain containing 5	DisGeNET

Related Glycoprotein

Displaying entries **111 - 120** of **132** in total

« First

‹ Prev

…

8

9

10

11

12

13

14

Next ›

Last »
UniProt ID	Protein Name	Source
Q7Z553	MAM domain-containing glycosylphosphatidylinositol anchor protein 2	DisGeNET
Q8IVS2	Malonyl-CoA-acyl carrier protein transacylase, mitochondrial	DisGeNET
Q8IY17	Patatin-like phospholipase domain-containing protein 6	DisGeNET
Q8TDQ7	Glucosamine-6-phosphate isomerase 2	DisGeNET
Q92187	CMP-N-acetylneuraminate-poly-alpha-2,8-sialyltransferase	DisGeNET
Q92819	Hyaluronan synthase 2	DisGeNET
Q96B86	Repulsive guidance molecule A	DisGeNET
Q99685	Monoglyceride lipase	DisGeNET
Q99798	Aconitate hydratase, mitochondrial	DisGeNET
Q9BVK6	Transmembrane emp24 domain-containing protein 9	DisGeNET

Displaying entries **41 - 50** of 54 in total

« First

‹ Prev

1

2

3

4

5

6

Next ›

Last »
HPO ID	HPO Term
HP:0007256	Abnormal pyramidal sign
HP:0007311	Short stepped shuffling gait
HP:0008969	Leg muscle stiffness
HP:0012332	Abnormal autonomic nervous system physiology
HP:0012378	Fatigue
HP:0012444	Brain atrophy
HP:0012452	Restless legs
HP:0012638	Abnormal nervous system physiology
HP:0012760	Reduced social reciprocity
HP:0100022	Abnormality of movement