GM22565
Fibroblast from Skin, Arm
Description:
EHLERS-DANLOS SYNDROME: TYPE IV; ARTERIAL, ECCHYMOTIC TYPE
COLLAGEN, TYPE III, ALPHA-1; COL3A1
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Heritable Diseases |
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Biopsy Source
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Arm
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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, Arm
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Family Member
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1
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Family History
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N
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Relation to Proband
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proband
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Confirmation
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Molecular characterization before cell line submission to CCR
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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 |
5.26 |
| Passage Frozen |
3 |
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin confirmed by LINE assay |
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| Gene |
COL3A1 |
| Chromosomal Location |
2q31 |
| Allelic Variant 1 |
G334R; EHLERS-DANLOS SYNDROME, TYPE IV |
| Identified Mutation |
GLY334ARG |
| Remarks |
Clinically affected; abnormal procollagen III motility by protein electrophoresis; lipomas on forehead; hypoplastic auricles; thin lips; small dentition; overbite; gingivitis; micrognathia; high palate; wide pharynx; blue sclerae; vental hernias; palpable mass in abdomen; severe scoliosis; kyphosis; limitation in elbows and hips; hyperextension in knees; pes planus; sacral dimple; neck mobility limited to the left; Beighton score 2/9; legs hurt when lying in bed; lump on side of neck; occasional lump in throat when swallowing; occasional orthopnea; slight beading on both middle cerebral arteries mostly on left side; mild disc disease in midthoracic spine; mild type 2 endplate changes at level C4-C5 along with disc osteophyte causing high grade stenosis with associate mild cord compression; disc osteophy complex with mild ligamentum flavum hypertrophy causing moderate to severe stenosis; mild disc disease in midthoracic; see GM22564 Lymphoid; donor subject is heterozygous for a missense mutation in exon 22 of the COL3A1 gene resulting in the substitution of arginine for glycine at codon 334 [Gly334Arg (G334R)] |
| Gene Cards |
COL3A1 |
| Gene Ontology |
GO:0005201 extracellular matrix structural constituent |
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GO:0005581 collagen |
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GO:0005586 collagen type III |
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GO:0005737 cytoplasm |
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GO:0006817 phosphate transport |
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GO:0008015 circulation |
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GO:0009887 organogenesis |
| NCBI Gene |
Gene ID:1281 |
| NCBI GTR |
120180 COLLAGEN, TYPE III, ALPHA-1; COL3A1 |
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130050 EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC |
| OMIM |
120180 COLLAGEN, TYPE III, ALPHA-1; COL3A1 |
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130050 EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC |
| Omim Description |
EDS IV |
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EDS4 |
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EHLERS-DANLOS SYNDROME, ARTERIAL TYPE |
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EHLERS-DANLOS SYNDROME, ECCHYMOTIC TYPE |
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EHLERS-DANLOS SYNDROME, SACK-BARABAS TYPE |
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EHLERS-DANLOS SYNDROME, TYPE IV, AUTOSOMAL DOMINANT |
| Cumulative PDL at Freeze |
5.3 |
| Passage Frozen |
3 |
| Split Ratio |
1:3 |
| Temperature |
37 C |
| Percent CO2 |
5% |
| Percent O2 |
AMBIENT |
| 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 |
| Supplement |
- |
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