CALB1, calbindin 1, 793

N. diseases: 68; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0036572
Disease: Seizures
Seizures
0.020 Biomarker phenotype BEFREE We propose that chronic suppression of calbindin by ΔFosB is one mechanism through which intermittent seizures drive persistent cognitive deficits in conditions accompanied by recurrent seizures. 29035369 2017
CUI: C0036572
Disease: Seizures
Seizures
0.020 GeneticVariation phenotype BEFREE In a subset of APdE9 mice, seizure phenotype was associated with a loss of calbindin-D28k immunoreactivity in dentate granular cells and ectopic expression of neuropeptide Y in mossy fibers. 19295151 2009