Description:
TUBEROUS SCLEROSIS 1; TSC1
TSC1 GENE; TSC1
Repository
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NIGMS Human Genetic Cell Repository
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Subcollection |
Heritable Diseases Hereditary Cancers |
Class |
Other Disorders of Known Biochemistry |
Quantity |
25 µg |
Quantitation Method |
Please see our FAQ |
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
|
White
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Family Member
|
1
|
Relation to Proband
|
proband
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Confirmation
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Clinical summary/Case history
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ISCN
|
46,XX
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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 and by Chromosome Analysis |
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GENE MAPPING & DOSAGE STUDIES - Y CHROMOSOME |
PCR analysis of DNA from this cell culture gave a negative result with a primer for Yq11, DYS227. |
|
Gene |
TSC1 |
Chromosomal Location |
9q34 |
Allelic Variant 1 |
; TUBEROUS SCLEROSIS, TYPE I |
Identified Mutation |
c.994_995insA |
Remarks |
Seizures since age 2; white spots; shagreen patch; CT scan showed brain calcifications; receives Tegretol; 46,XX; donor subject is heterozygous for a 1bp insertion at nucleotide 994 in exon 10 of the TSC1 gene (c.994_995insA) resulting in a protein truncation |
Au KS, Williams AT, Roach ES, Batchelor L, Sparagana SP, Delgado MR, Wheless JW, Baumgartner JE, Roa BB, Wilson CM, Smith-Knuppel TK, Cheung MY, Whittemore VH, King TM, Northrup H, Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States Genetics in medicine : official journal of the American College of Medical Genetics9:88-100 2007 |
PubMed ID: 17304050 |
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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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