Description:
TUBEROUS SCLEROSIS 2; TSC2
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Heritable Diseases |
| Class |
Other Disorders of Known Biochemistry |
| Alternate IDs |
GM18032 [TUBEROUS SCLEROSIS 2; TSC2] |
| Quantity |
25 µg |
| Quantitation Method |
Please see our FAQ |
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Biopsy Source
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Peripheral vein
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Cell Type
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B-Lymphocyte
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Tissue Type
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Blood
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Transformant
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Epstein-Barr Virus
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Sample Source
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DNA from LCL
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Race
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White
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Family Member
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4
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Relation to Proband
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half-brother
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Confirmation
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Clinical summary/Case history
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Species
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Homo sapiens
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Common Name
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Human
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Remarks
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis |
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| Remarks |
Clinically not affected; height, 173 cm; weight; 68 kg; CT scan of brain was normal; ultrasound of kidneys normal; family history of tuberous sclerosis; brother of GM08296 (affected); half-brother of GM08299 (affected); son of GM08584 (unaffected); mutation not found in TSC2 gene |
| Smith M, Smalley S, Cantor R, Pandolfo M, Gomez MI, Baumann R, Flodman P, Yoshiyama K, Nakamura Y, Julier C, et al, Mapping of a gene determining tuberous sclerosis to human chromosome 11q14-11q23. Genomics6(1):105-14 1990 |
| PubMed ID: 2303253 |
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| Wendt, Genetic counseling for the offspring of a clinically asymptomatic obligate carrier of the tuberous sclerosis gene. Am J Hum Genet37:A138 (1985):105-14 1985 |
| PubMed ID: 2303253 |
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