Description:
THANATOPHORIC DYSPLASIA; TD
FIBROBLAST GROWTH FACTOR RECEPTOR 3; FGFR3
Repository
|
NIGMS Human Genetic Cell Repository
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Subcollection |
Heritable Diseases |
Class |
Disorders of Connective Tissue, Muscle, and Bone |
Cell Type
|
Fibroblast
|
Transformant
|
Untransformed
|
Race
|
Black/African American
|
Relation to Proband
|
proband
|
Confirmation
|
Clinical summary/Case history
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Species
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Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
Passage Frozen |
2 |
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis |
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MUTATION VERIFICATION |
The gene mutation for this cell line was detected by sequencing only. |
|
Gene |
FGFR3 |
Chromosomal Location |
4p16.3 |
Allelic Variant 1 |
134934.0006; THANATOPHORIC DYSPLASIA, TYPE I; TD1 |
Identified Mutation |
SER371CYS; In 1 out of 39 individuals with type I TD (187600), Tavormina et al. (1995) found an A-to-T transversion at nucleotide 1111 that caused a ser371-to-cys substitution in the extracellular region of the FGFR3 protein.
|
Remarks |
Severely dwarfed; extremely short extremities; small hands and feet; large head; distended abdomen; normal fibroblast alkaline phosphatase activity; negative family history; donor subject has an A>T transversion at nucleotide 1111 in exon 9 of the FGFR3 gene (1111A>T) resulting in a substitution of cysteine for serine at codon 371 [Ser371Cys (S371C)] |
Tavormina PL, Shiang R, Thompson LM, Zhu YZ, Wilkin DJ, Lachman RS, Wilcox WR, Rimoin DL, Cohn DH, Wasmuth JJ, Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3. Nat Genet9:321-8 1995 |
PubMed ID: 7773297 |
Passage Frozen |
2 |
Split Ratio |
1:3 |
Temperature |
37 C |
Percent CO2 |
5% |
Medium |
Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent |
Serum |
15% fetal bovine serum Not inactivated |
Substrate |
None specified |
Subcultivation Method |
trypsin-EDTA |
Supplement |
- |
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