Symbol
| ADGRG6
| contributors: mct/npt/pgu - updated : 14-11-2023
|
HGNC name
| adhesion G protein-coupled receptor G6
|
HGNC id
| 13841
|
corresponding disease(s)
|
AMCN4
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
|  
|  
| --low
|  
|
in type 2 alveolar epithelial cells is decreased in chronic obstructive pulmonary disease (COPD) | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
|
System | Type | Disorder | Pubmed |
respiratory | lung | chr.Bronchopathy obstructive | |
as likely a novel therapeutic target for COPD | neurology | acquired | | |
represents an attractive potential target to stimulate repair in myelin disease or following nerve injury |
| | | |
| Gpr126 deletion causes heart phenotypes in mice causing embryonic lethality | |
a mutation in Gpr126 causes a severe congenital hypomyelinating peripheral neuropathy in mice |
|
Gpr126-/- mice have a lethal arthrogryposis phenotype |
|
Gpr126-null mice with a heterozygous placenta survive but exhibit GPR126-defective peripheral nervous system (PNS) phenotype |