GM28306
Fibroblast from Skin, Skin
Description:
BLAU SYNDROME; BLAUS
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Heritable Diseases PIGI Consented Sample |
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Biopsy Source
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Skin
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Cell Type
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Fibroblast
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Tissue Type
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Skin
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Transformant
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Untransformed
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Sample Source
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Fibroblast from Skin, Skin
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Race
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White
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Subject Type
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trio
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Ethnicity
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Not Hispanic/Latino
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Ethnicity
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Netherlands
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Country of Origin
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NETHERLANDS
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Family Member
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2
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Family History
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N
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Relation to Proband
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mother
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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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| PDL at Freeze |
7.94 |
| Passage Frozen |
3 |
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| 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 |
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BLAU SYNDROME |
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GRANULOMATOSIS, FAMILIAL, BLAU TYPE |
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GRANULOMATOUS INFLAMMATORY ARTHRITIS, DERMATITIS, AND UVEITIS, FAMILIAL |
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JABS SYNDROME |
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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 |
- |
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