- Concept UI
- M000762845
- Registry Numbers
- 0
- 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).
- Terms
-
Gap Junction beta-1 Protein
Preferred Term
Term UI
T001135651
Date03/30/2023
LexicalTag
NON
ThesaurusID
NLM (2024)
-
Gap Junction B1
Term UI
T001133105
Date02/22/2023
LexicalTag
NON
ThesaurusID
NLM (2024)
-
Cx32 Protein
Term UI
T001133106
Date02/22/2023
LexicalTag
ABX
ThesaurusID
NLM (2024)
-
GJB1 Protein
Term UI
T001133107
Date02/22/2023
LexicalTag
ABX
ThesaurusID
NLM (2024)
-
Connexin 32 Protein
Term UI
T001135653
Date03/30/2023
LexicalTag
NON
ThesaurusID
NLM (2024)
-
Gap Junction beta1 Protein
Term UI
T001135654
Date03/30/2023
LexicalTag
NON
ThesaurusID
NLM (2024)
-
Connexin 32
Term UI
T001135652
Date03/30/2023
LexicalTag
NON
ThesaurusID
NLM (2024)