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search submit
ND00191
DNA
from
LCL
Description:
POPULATION/CONVENIENCE CONTROL
Affected:
No
Gender:
Female
Age:
80
YR
(At Sampling)
Sample Description
Overview
Characterizations
Phenotypic Data
Publications
External Links
Images
Overview
Repository
NINDS Repository
Subcollection
Control
Parkinsonism
Quantity
20 µg
Quantitation Method
Please see our
FAQ
Biopsy Source
Peripheral vein
Cell Type
B-Lymphocyte
Tissue Type
Blood
Transformant
Epstein-Barr Virus
Sample Source
DNA from LCL
Race
White
Subject Type
case-spouse
Family Type
NUCLEAR FAMILIES - ONE AFFECTED
Country of Origin
USA
Family Member
2
Family History
N
Relation to Proband
spouse
Species
Homo
sapiens
Common Name
Human
Characterizations
Gene
LRRK2
Chromosomal Location
12q12
Allelic Variant 1
; WILDTYPE
Identified Mutation
WILDTYPE for GLY2019
Gene
LRRK2
Chromosomal Location
12q12
Allelic Variant 2
; WILDTYPE
Identified Mutation
WILDTYPE for GLY2019
Phenotypic Data
Demographic Data
Relation to Proband
spouse
Age at Sampling
80 YR
Gender
Female
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 yet reported
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
Unaffected spouse
Medical History
Amyotrophic lateral sclerosis
present
absent
Ataxia
No Data
Autism
No Data
Bipolar (manic-depressive)
No Data
Brain aneurysm
No Data
Cancer
No Data
Dementia
Alzheimer's
Dementia
absent
Depression
No Data
Diabetes
No Data
Dystonia
No Data
Epilepsy
No Data
Heart disease
No Data
Hypertension
No Data
Memory loss
No Data
Migraine
No Data
Multiple sclerosis
No Data
Muscle disease
No Data
Obsessive Compulsive
No Data
Parkinson's
No Data
Schizophrenia
No Data
Stroke
No Data
Suicide/Attempt
No Data
Tourettes
No Data
Other
No Data
Family History
Amyotrophic lateral sclerosis
present
absent
Ataxia
present
absent
Autism
present
absent
Bipolar (manic-depressive)
No Data
Brain aneurysm
present
absent
Cancer
present
absent
Dementia
Alzheimer's
Dementia
absent
Depression
present
absent
Diabetes
present
absent
Dystonia
No Data
Epilepsy
No Data
Heart disease
No Data
Hypertension
No Data
memory loss
No Data
Migraine
No Data
Multiple sclerosis
No Data
Muscle disease
No Data
Obsessive Compulsive
No Data
Parkinson's
No Data
Schizophrenia
No Data
Stroke
No Data
Suicide/Attempt
No Data
Tourettes
No Data
Other
No Data
Optional data
smoking history
No Data
years smoking
No Data
Neurological examination
yes
no
State Examination (MMSE) score
No Data
Handedness
No Data
Publications
Li Y, Rowland C, Schrodi S, Laird W, Tacey K, Ross D, Leong D, Catanese J, Sninsky J, Grupe A
, A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan American journal of human genetics78:1090-2; author reply 1092-4 2006
PubMed ID:
16685663
External Links
dbSNP
dbSNP ID: 18359
dbGaP Link
phs000126
Images
View
pedigree
Culture Protocols
Temperature
37 C
Percent CO2
5%
Percent O2
AMBIENT
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.:
$0.00
USD
U.S. Academic or
Non-profit:
$0.00
USD
NINDS Repository Submitter (past or current) and/or Current NINDS Grantee
$0.00
USD
Add to Cart
How to Order
Ordering Instructions
MTA / Assurance Form
Statement of Research Intent Form
Related Products
Same Subject
ND00191 - B-Lymphocyte
Same Family
NINDS0016