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ND01039 DNA from LCL

Description:

ESSENTIAL TREMOR-MOVEMENT DISORDER
PARKIN; PARK2

Affected:

Yes

Sex:

Male

Age:

72 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Images

Overview

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Repository NINDS Repository
Subcollection Parkinsonism
Quantity 3 µg
Quantitation Method Please see our FAQ
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race White
Subject Type family with at least 3 members, including 1 proband, not a trio
Family Type NUCLEAR FAMILIES - ONE AFFECTED
Ethnicity Not Hispanic/Latino
Ethnicity TURKISH
Country of Origin USA
Family Member 3
Family History Y
Relation to Proband father
Species Homo sapiens
Common Name Human

Characterizations

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Gene PARK2
Chromosomal Location 6q25.2-q27
Allelic Variant 1 602544.0002; PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE
Identified Mutation EX4DEL; In 4 patients with autosomal recessive juvenile parkinsonism (600116) from 3 unrelated families, Kitada et al. [Nature 392: 605-608 (1998)] demonstrated a deletion affecting only exon 4 of the parkin gene.

Phenotypic Data

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Demographic Data
Relation to Proband father
Age at Sampling 72 YR
Sex Male
Age of Onset(If not a control) No Data
Age at Diagnosis(If not a control) No Data
Hispanic or Latino/Not Hispanic or Latino Not Hispanic/Latino
Racial Category White
Country USA
Diagnosed By No Data
 
Data Elements
Clinical Element Type: Control
  (Baseline)
Data collected by
This data was collected by  No Data
Longitudinal Data
Is this data Longitudinal (Follow-Up) Data? yes  no  
Type of Control
Type of Control  Related to an affected individual (REQUIRES SPECIAL APPROVAL)
Medical History
Amyotrophic lateral sclerosis present  absent  
Ataxia present  absent  
Autism present  absent  
Bipolar (manic-depressive) present  absent  
Brain aneurysm present  absent  
Cancer present  absent  
Dementia Alzheimer's
Dementia
absent
Depression present  absent  
Diabetes present  absent  
Dystonia present  absent  
Epilepsy present  absent  
Heart disease present  absent  
Hypertension  No Data
Memory loss present  absent  
Migraine present  absent  
Multiple sclerosis present  absent  
Muscle disease present  absent  
Obsessive Compulsive  No Data
Parkinson's present  absent  
Schizophrenia present  absent  
Stroke present  absent  
Suicide/Attempt present  absent  
Tourettes  No Data
Other present   absent 
Notes: ESSENTIAL TREMOR; OBLIGATE CARRIER OF EXON 4 DELETION IN PARKIN
Family History
Amyotrophic lateral sclerosis present  absent  
Ataxia present  absent  
Autism present  absent  
Bipolar (manic-depressive) present  absent  
Brain aneurysm present  absent  
Cancer present  absent  
Dementia Alzheimer's
Dementia
absent
Depression present  absent  
Diabetes present  absent  
Dystonia present  absent  
Epilepsy present  absent  
Heart disease present  absent  
Hypertension  No Data
memory loss present  absent  
Migraine present  absent  
Multiple sclerosis present  absent  
Muscle disease present  absent  
Obsessive Compulsive  No Data
Parkinson's present   absent 
Notes: DAUGHTERS-2 AND SON
Schizophrenia present  absent  
Stroke present  absent  
Suicide/Attempt present  absent  
Tourettes  No Data
Other present  absent  
Optional data
smoking history never  former smoker  current smoker  
years smoking  1 PACK PER DAY
Neurological examination yes  no  
State Examination (MMSE) score  No Data
Handedness  No Data

Publications

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Dogu O, Johnson J, Hernandez D, Hanson M, Hardy J, Apaydin H, Ozekmekci S, Sevim S, Gwinn-Hardy k, Singleton A., A consanguineous Turkish family with early-onset Parkinson's disease an exon 4 parkin deletion Mov Disord19(7):812-6 2004
PubMed ID: 15254940

External Links

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dbSNP dbSNP ID: 20053
Gene Cards PARK2
PRKN
Gene Ontology GO:0004197 cysteine-type endopeptidase activity
GO:0004842 ubiquitin-protein ligase activity
GO:0006508 proteolysis and peptidolysis
GO:0006511 ubiquitin-dependent protein catabolism
GO:0006512 ubiquitin cycle
GO:0007417 central nervous system development
NCBI Gene Gene ID:2111
Gene ID:5071
NCBI GTR 190300 TREMOR, HEREDITARY ESSENTIAL, 1; ETM1
602544 PARKIN; PARK2
OMIM 190300 TREMOR, HEREDITARY ESSENTIAL, 1; ETM1
602544 PARKIN; PARK2
Omim Description TREMOR, FAMILIAL ESSENTIAL, 1; FET1
  TREMOR, HEREDITARY ESSENTIAL, 1; ETM1

Images

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View pedigree 

Culture Protocols

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Temperature 37 C
Percent CO2 5%
Medium Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not Inactivated
Substrate None specified
Subcultivation Method dilution - add fresh medium
Supplement -
Pricing
Commercial and Non-U.S.:
$0.00USD
U.S. Academic or
Non-profit:
$0.00USD
NINDS Repository Submitter (past or current) and/or Current NINDS Grantee
$0.00USD
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How to Order
  • Ordering Instructions
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  • ND01039 - B-Lymphocyte
Same Family
  • NINDS0104

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