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FLASH GENE
Symbol NR0B2 contributors: mct - updated : 09-10-2018
HGNC name nuclear receptor subfamily 0, group B, member 2
HGNC id 7961
ASSOCIATED DISORDERS
corresponding disease(s)
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional germinal mutation     loss of function
loss of function and mutation leading to in maturity onset diabetes of the young (MODY) mild obesity in Japenese subjects
constitutional     --over  
of NR1H4, NR0B2, SLC10A1 and ABCB11 was significantly up-regulated in the non-alcoholic steatohepatitis (NASH) in comparison with simple steatosis (SS) patients
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS