Selected-GenAtlas references SOURCE GeneCards NCBI Gene Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol ADGRG6 contributors: mct/npt/pgu - updated : 14-11-2023
HGNC name adhesion G protein-coupled receptor G6
HGNC id 13841
ASSOCIATED DISORDERS
corresponding disease(s) AMCN4
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional     --low  
in type 2 alveolar epithelial cells is decreased in chronic obstructive pulmonary disease (COPD)
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
SystemTypeDisorderPubmed
respiratorylungchr.Bronchopathy obstructive
as likely a novel therapeutic target for COPD
neurologyacquired 
represents an attractive potential target to stimulate repair in myelin disease or following nerve injury
ANIMAL & CELL MODELS
  • 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