| Descriptor English: | Gap Junction beta-1 Protein | ||||||
| Descriptor Spanish: |
Proteína beta1 de Unión Comunicante
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| Descriptor Portuguese: | Proteína beta-1 de Junções Comunicantes | ||||||
| Descriptor French: | Without translation | ||||||
| Entry term(s): |
Connexin 32 Connexin 32 Protein Cx32 Protein GJB1 Protein Gap Junction B1 Gap Junction beta 1 Protein Gap Junction beta1 Protein Protein, Connexin 32 Protein, Cx32 Protein, GJB1 |
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| Tree number(s): |
D12.776.543.585.250.600 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000097002 | ||||||
| Scope note: | A GAP JUNCTION beta subunit containing four transmembrane domains expressed in myelinating SCHWANN CELLS and is localized to peripheral MYELIN (e.g., noncompact myelin in the paranode and Schmitt-Lanterman incisures). Mutations in the human gene GJB1 are associated with X-linked CHARCOT-MARIE-TOOTH DISEASE type 1 (CMT1X). |
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| Allowable Qualifiers: |
AD administration & dosage AE adverse effects AG agonists AI antagonists & inhibitors AN analysis BI biosynthesis BL blood CF cerebrospinal fluid CH chemistry CL classification CS chemical synthesis DE drug effects DF deficiency EC economics GE genetics HI history IM immunology IP isolation & purification ME metabolism PD pharmacology PH physiology PK pharmacokinetics PO poisoning RE radiation effects SD supply & distribution ST standards TO toxicity TU therapeutic use UL ultrastructure UR urine |
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| Public MeSH Note: | 2024; see under CONNEXINS 1993-2023 |
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| History Note: | 2024(1993) |
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| DeCS ID: | 60543 | ||||||
| Unique ID: | D000097002 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2024/01/01 | ||||||
| Date of Entry: | 2023/07/26 | ||||||
| Revision Date: | 2023/05/31 |
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CHEMICALS AND DRUGS
Amino Acids, Peptides, and Proteins [D12]Amino Acids, Peptides, and Proteins
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Gap Junction beta-1 Protein
- Preferred
| Concept UI |
M000762845 |
| Scope note | A GAP JUNCTION beta subunit containing four transmembrane domains expressed in myelinating SCHWANN CELLS and is localized to peripheral MYELIN (e.g., noncompact myelin in the paranode and Schmitt-Lanterman incisures). Mutations in the human gene GJB1 are associated with X-linked CHARCOT-MARIE-TOOTH DISEASE type 1 (CMT1X). |
| Preferred term | Gap Junction beta-1 Protein |
| Entry term(s) |
Connexin 32 Connexin 32 Protein Cx32 Protein GJB1 Protein Gap Junction B1 Gap Junction beta 1 Protein Gap Junction beta1 Protein Protein, Connexin 32 Protein, Cx32 Protein, GJB1 |
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