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GM07415 LCL from B-Lymphocyte

Description:

TUBEROUS SCLEROSIS 1; TSC1
TSC1 GENE; TSC1

Affected:

Yes

Sex:

Male

Age:

37 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Hereditary Cancers
Class Other Disorders of Known Biochemistry
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race White
Family Member 3
Relation to Proband father
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Seizures since age 4; white spots; periungual fibromas of toes; pits in tooth enamel; receives Dilantin; 5 affected sibs, father & daughter; 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

Characterizations

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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
 
GENE MAPPING & DOSAGE STUDIES - Y CHROMOSOME PCR analysis of DNA from this cell culture gave a positive result with a primer for Yq11, DYS227.
 
Gene TSC1
Chromosomal Location 9q34
Allelic Variant 1 ; TUBEROUS SCLEROSIS, TYPE I
Identified Mutation c.994_995insA

Phenotypic Data

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Remarks Seizures since age 4; white spots; periungual fibromas of toes; pits in tooth enamel; receives Dilantin; 5 affected sibs, father & daughter; 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

Publications

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Xia Y, Katz M, Chandramohan D, Bechor E, Podgursky B, Hoxie M, Zhang Q, Chertman W, Kang J, Blue E, Chen J, Schleede J, Slotnick NR, Du X, Boostanfar R, Urcia E, Behr B, Cohen J, Siddiqui N, The first clinical validation of whole-genome screening on standard trophectoderm biopsies of preimplantation embryos F&S reports5:63-71 2023
PubMed ID: 38524212
 
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
 
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

External Links

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dbSNP dbSNP ID: 10978
Gene Cards TSC1
Gene Ontology GO:0007155 cell adhesion
GO:0007266 Rho protein signal transduction
GO:0045786 negative regulation of cell cycle
NCBI Gene Gene ID:7248
NCBI GTR 191100 TUBEROUS SCLEROSIS 1; TSC1
605284 TSC COMPLEX SUBUNIT 1; TSC1
OMIM 191100 TUBEROUS SCLEROSIS 1; TSC1
605284 TSC COMPLEX SUBUNIT 1; TSC1
Omim Description EPILOIAADENOMA SEBACEUM, INCLUDED
  HAMARTIN, INCLUDED
  TS
  TUBEROSE SCLEROSIS; TSC
  TUBEROUS SCLEROSIS 1; TSC1

Culture Protocols

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Split Ratio 1:3
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
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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How to Order
  • Ordering Instructions
  • MTA / Assurance Form
  • Statement of Research Intent Form
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