Search
Descriptor English: Connexin 30
Descriptor Spanish: Conexina 30
Descriptor conexina 30
Entry term(s) canales CX30
proteína GJB6
proteína beta-6 de la unión en hendidura
Scope note: Subunidad beta de las uniones comunicantes que forma hemicanales heteroméricos al aparearse con subunidades alfa como la conexina 40 o la CONEXINA 43. Las mutaciones en el gen de la conexina 30 (GJ6B) se asocian al SÍNDROME DE CLOUSTON y a algunas formas hereditarias de sordera.
Descriptor Portuguese: Conexina 30
Descriptor French: Connexine 30
Entry term(s): CX30 Channels
Channels, CX30
GJB6 Protein
Gap Junction beta 6 Protein
Gap Junction beta-6 Protein
Tree number(s): D12.776.543.585.250.150
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D000075302
Scope note: A gap junction beta subunit that forms heteromeric hemichannels when paired with alpha subunits such as connexin-40 or CONNEXIN 43. Mutations in the connexin 30 gene (GJ6B) are associated with CLOUSTON'S SYNDROME and some hereditary forms of deafness.
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
Previous Indexing: Connexins (1996-2017)
Public MeSH Note: 2018
History Note: 2018
DeCS ID: 57131
Unique ID: D000075302
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2018/01/01
Date of Entry: 2017/07/11
Revision Date: 2017/05/24
Connexin 30 - Preferred
Concept UI M000630161
Scope note A gap junction beta subunit that forms heteromeric hemichannels when paired with alpha subunits such as connexin-40 or CONNEXIN 43. Mutations in the connexin 30 gene (GJ6B) are associated with CLOUSTON'S SYNDROME and some hereditary forms of deafness.
Preferred term Connexin 30
Entry term(s) CX30 Channels
Channels, CX30
GJB6 Protein
Gap Junction beta 6 Protein
Gap Junction beta-6 Protein



We want your feedback on the new DeCS / MeSH website

We invite you to complete a survey that will take no more than 3 minutes.


Go to survey