Description:
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED; CMTX1
GAP JUNCTION PROTEIN, BETA-1, 32-KD; GJB1
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Heritable Diseases |
| Class |
Disorders of the Nervous System |
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Cell Type
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Fibroblast
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Transformant
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Untransformed
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Race
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White
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Family Member
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4
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Relation to Proband
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brother-in-law
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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 |
8 |
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis |
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| Remarks |
Clinically unaffected; affected daughter is GM04595; affected spouse is GM04594. |
| Bone LJ, Dahl N, Lensch MW, Chance PF, Kelly T, Le Guern E, Magi S, Parry G, Shapiro H, Wang S, et al, New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease. Neurology45:1863-6 1995 |
| PubMed ID: 7477983 |
| Gene Cards |
GJB1 |
| Gene Ontology |
GO:0005922 connexon complex |
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GO:0006810 transport |
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GO:0007267 cell-cell signaling |
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GO:0007399 neurogenesis |
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GO:0015285 connexon channel activity |
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GO:0016021 integral to membrane |
| NCBI Gene |
Gene ID:2705 |
| NCBI GTR |
302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1 |
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304040 GAP JUNCTION PROTEIN, BETA-1; GJB1 |
| OMIM |
302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1 |
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304040 GAP JUNCTION PROTEIN, BETA-1; GJB1 |
| Omim Description |
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED; CMTX1 |
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CMT2, FORMERLY |
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CMTX |
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HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED |
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HMSN, X-LINKED |
| Passage Frozen |
8 |
| 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 |
15% fetal bovine serum Not inactivated |
| Substrate |
None specified |
| Subcultivation Method |
trypsin-EDTA |
| Supplement |
- |
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