GM28306
Fibroblast from Skin, Skin
Description:
BLAU SYNDROME; BLAUS
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Heritable Diseases PIGI Consented Sample |
Biopsy Source
|
Skin
|
Cell Type
|
Fibroblast
|
Tissue Type
|
Skin
|
Transformant
|
Untransformed
|
Sample Source
|
Fibroblast from Skin, Skin
|
Race
|
White
|
Subject Type
|
trio
|
Ethnicity
|
Not Hispanic/Latino
|
Ethnicity
|
Netherlands
|
Country of Origin
|
NETHERLANDS
|
Family Member
|
2
|
Family History
|
N
|
Relation to Proband
|
mother
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
PDL at Freeze |
7.94 |
Passage Frozen |
3 |
|
Remarks |
Unaffected mother of affected son GM28303 (LCL) and GM28304 (fibro); LCL is GM28305. |
NCBI GTR |
186580 BLAU SYNDROME; BLAUS |
OMIM |
186580 BLAU SYNDROME; BLAUS |
Omim Description |
ARTHROCUTANEOUVEAL GRANULOMATOSIS; ACUG |
|
BLAU SYNDROME |
|
GRANULOMATOSIS, FAMILIAL, BLAU TYPE |
|
GRANULOMATOUS INFLAMMATORY ARTHRITIS, DERMATITIS, AND UVEITIS, FAMILIAL |
|
JABS SYNDROME |
|
SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES |
Cumulative PDL at Freeze |
7.94 |
Passage Frozen |
3 |
Split Ratio |
1:3 |
Temperature |
37 C |
Percent CO2 |
5% |
Percent O2 |
3% |
Medium |
Eagles Minimum Essential Medium with Earle's salts:Dulbecco's modified MEM with 2mM L-glutamine or equivalent |
Serum |
15% fetal bovine serum Not inactivated |
Supplement |
- |
|
|