Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 84876
Gene Symbol: ORAI1
ORAI1 		0.700 Biomarker disease GENOMICS_ENGLAND ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia. 20004786 2009
Entrez Id: 84876
Gene Symbol: ORAI1
ORAI1 		0.700 Biomarker disease GENOMICS_ENGLAND A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function. 16582901 2006
Entrez Id: 84876
Gene Symbol: ORAI1
ORAI1 		0.700 GeneticVariation disease UNIPROT A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function. 16582901 2006
Entrez Id: 84876
Gene Symbol: ORAI1
ORAI1 		0.700 GeneticVariation disease UNIPROT A severe defect in CRAC Ca2+ channel activation and altered K+ channel gating in T cells from immunodeficient patients. 16147976 2005
Entrez Id: 84876
Gene Symbol: ORAI1
ORAI1 		0.700 CausalMutation disease CLINVAR
Entrez Id: 84876
Gene Symbol: ORAI1
ORAI1 		0.700 GermlineCausalMutation disease ORPHANET
Entrez Id: 84876
Gene Symbol: ORAI1
ORAI1 		0.700 Biomarker disease CTD_human
Entrez Id: 10743
Gene Symbol: RAI1
RAI1 		0.300 Biomarker disease GENOMICS_ENGLAND