Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 767
Gene Symbol: CA8
CA8
0.170 Biomarker phenotype BEFREE Patients with unknown cerebellar ataxia were screened for autoimmune cerebellar ataxia (ACA)-related antibodies, including glutamic acid decarboxylase 65 (GAD65), delta/notch-like epidermal growth factor-related receptor (Tr/DNER), zinc finger protein 4 (ZIC4), inositol 1,4,5-triphosphate receptor 1 (ITPR1), Homer protein homologue 3 (Homer-3), neurochondrin (NCDN), Purkinje cell antibody 2 (PCA-2) and carbonic anhydrase-related protein VII (CARPVII). 31179511 2019
Entrez Id: 767
Gene Symbol: CA8
CA8
0.170 Biomarker phenotype BEFREE Carbonic anhydrase-related protein VIII (CA8) is an IP<sub>3</sub>R1-regulating protein abundantly expressed in cerebellar Purkinje cells and is a causative gene of congenital ataxia. 30429331 2018
Entrez Id: 767
Gene Symbol: CA8
CA8
0.170 GeneticVariation phenotype BEFREE In addition, homozygous missense mutations in carbonic anhydrase-related protein VIII (CARP), which suppresses the ability of IP3 to bind to IP3R1, cause a recessively inherited ataxia with mild cognitive impairment with/without quadrupedal gait. 26827887 2016
Entrez Id: 767
Gene Symbol: CA8
CA8
0.170 GeneticVariation phenotype BEFREE Single mutations in CA8 were reported to cause novel syndromes like ataxia, mild mental retardation or the predisposition to quadrupedal gait. 24794067 2014
Entrez Id: 767
Gene Symbol: CA8
CA8
0.170 GeneticVariation phenotype BEFREE Recent reports have shown that mutations in the CA8 gene are associated with mental retardation and ataxia in humans and ataxia in mice. 23087022 2013
Entrez Id: 767
Gene Symbol: CA8
CA8
0.170 GeneticVariation phenotype BEFREE Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII. 21812104 2011
Entrez Id: 767
Gene Symbol: CA8
CA8
0.170 GeneticVariation phenotype BEFREE A mutation in the CA8 gene has been associated with ataxia, mild mental retardation and quadrupedal gait in humans and with lifelong gait disorder in mice, suggesting an important role for CARP VIII in the brain. 20819067 2010
Entrez Id: 767
Gene Symbol: CA8
CA8
0.170 GeneticVariation phenotype CLINVAR