GM19693
Fibroblast from Skin, Thigh
Description:
GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED)
EHLERS-DANLOS SYNDROME, TYPE III
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Heritable Diseases |
| Class |
Disorders of Carbohydrate Metabolism |
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Biopsy Source
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Thigh
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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, Thigh
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Race
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White
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Ethnicity
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SCOTTISH/IRISH/ENGLISH
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Family Member
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3
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Relation to Proband
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son
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Confirmation
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Clinical summary/Case history
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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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| Passage Frozen |
2 |
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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 |
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| Remarks |
Clinically affected with GSD IX; at 9 months had cessation of growth, excess weight gain (75th percentile) and enlarged liver; treated with high protein diet and Viokase; weight was over 95% by 18 months and off the charts by age 30 months; weight gain began to drop at age 4; at age 6 years height and weight were normal; learning disability associated with spatial sequential issues; symptoms of Ehlers-Danlos syndrome hypermobility type include chronic joint pain in shoulders and knees, pes planus, and bilateral hiatal hernias; diagnosis of EDS has not been confirmed clinically; mother (GM19647) is clinically affected with EDS hypermobility type; clinically affected father is GM19688; 2 brothers clinically affected with GSD IX, including GM 19695; brother not clinically affected with GSD IX is GM19698; same donor as GM19694 Lymphoid |
| dbSNP |
dbSNP ID: 21052 |
| Gene Ontology |
GO:0004689 phosphorylase kinase activity |
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GO:0005516 calmodulin binding |
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GO:0005964 phosphorylase kinase complex |
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GO:0005975 carbohydrate metabolism |
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GO:0005977 glycogen metabolism |
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GO:0006091 energy pathways |
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GO:0006464 protein modification |
| NCBI Gene |
Gene ID:5256 |
| NCBI GTR |
130020 EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE; EDSHMB |
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306000 GLYCOGEN STORAGE DISEASE IXa1; GSD9A1 |
| OMIM |
130020 EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE; EDSHMB |
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306000 GLYCOGEN STORAGE DISEASE IXa1; GSD9A1 |
| Omim Description |
GLYCOGEN STORAGE DISEASE IX, INCLUDED |
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GLYCOGEN STORAGE DISEASE VIII |
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GLYCOGENOSIS VIIIA |
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HEPATIC PHOSPHORYLASE KINASE DEFICIENCY; PHK |
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LIVER GLYCOGENOSIS, X-LINKED, TYPE I |
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LIVER GLYCOGENOSIS, X-LINKED, TYPE II, INCLUDED; XLG2, INCLUDED |
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PHKA, INCLUDED |
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PHOSPHORYLASE KINASE DEFICIENCY OF LIVER; PYK; PYKL |
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X-LINKED LIVER GLYCOGENOSIS; XLGPHOSPHORYLASE KINASE, LIVER, ALPHA-2 SUBUNIT, INCLUDED; PHKA2, INCLUDED |
| Passage Frozen |
2 |
| Split Ratio |
1:4 |
| 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 |
10% fetal bovine serum Not inactivated |
| Substrate |
None specified |
| Subcultivation Method |
trypsin-EDTA |
| Supplement |
- |
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