Description:
METACHROMATIC LEUKODYSTROPHY
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Heritable Diseases Lysosomal Storage Diseases |
Class |
Disorders of Lipid Metabolism |
Quantity |
25 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
|
Family Member
|
1
|
Relation to Proband
|
proband
|
Confirmation
|
Biochemical characterization after cell line submission to CCR
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis |
|
GENE MAPPING & DOSAGE STUDIES - Y CHROMOSOME |
PCR analysis of DNA from this cell culture gave a negative result with a primer for Yq11, DYS227. |
|
cerebroside-sulfatase |
According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number: 3.1.6.8 |
|
Remarks |
Juvenile type; HLA type A2,A29,B12,B16; same patient as GM01785; deficient arylsulfatase A in lymphoblast culture |
Tempesta MC, Levade T, Salvayre R, Arylsulfatases A and B in EBV-transformed lymphoid cell lines: studies on their molecular forms in cells from patients with inborn sulfatase deficiencies. Comparative diagnostic value of enzymatic assays. Clin Chim Acta202:149-65 1991 |
PubMed ID: 1687673 |
dbSNP |
dbSNP ID: 10375 |
NCBI GTR |
250100 METACHROMATIC LEUKODYSTROPHY; MLD |
OMIM |
250100 METACHROMATIC LEUKODYSTROPHY; MLD |
Omim Description |
ARYLSULFATASE A DEFICIENCY; ARSA DEFICIENCY |
|
CEREBRAL SCLEROSIS, DIFFUSE, METACHROMATIC FORM |
|
CEREBROSIDE SULFATASE DEFICIENCYARYLSULFATASE A, INCLUDED; ARSA, INCLUDED |
|
METACHROMATIC LEUKODYSTROPHY, ADULT, INCLUDED |
|
METACHROMATIC LEUKODYSTROPHY, JUVENILE, INCLUDED |
|
METACHROMATIC LEUKODYSTROPHY, LATE-INFANTILE |
|
METACHROMATIC LEUKOENCEPHALOPATHY |
|
MLD |
|
PSEUDOARYLSULFATASE A DEFICIENCY, INCLUDED |
|
SULFATIDE LIPIDOSIS |
|
|