Diseases caused by mutations in ORAI1 and STIM1

Medicine & Life Sciences

• ORAI1 Protein 99%
• Gain of Function Mutation 97%
• Stromal Interaction Molecule 1 79%
• Loss of Function Mutation 55%
• Mutation 55%
• Muscular Diseases 53%
• Stormorken Syndrome 52%
• Congenital Structural Myopathies 38%
• Ectodermal Dysplasia 34%
• Channelopathies 34%
• Sweat Glands 31%
• Severe Combined Immunodeficiency 31%
• Disease Susceptibility 27%
• Dental Enamel 26%
• Autoimmunity 24%
• Endoplasmic Reticulum 23%
• Thrombocytopenia 23%
• Ions 20%
• Skeletal Muscle 19%
• Blood Platelets 19%
• Homeostasis 18%
• Cell Membrane 18%
• Tooth 17%
• Hemorrhage 15%
• Genes 9%

Arts & Humanities

• Mutation 100%
• Syndrome 65%
• Protein 59%
• Defects 48%
• Homeostasis 37%
• Autoimmunity 36%
• Diathesis 35%
• Plasma 33%
• Enamel 31%
• Activation 26%
• Teeth 25%
• Conducting 24%
• Molecules 23%
• Physiology 22%
• Membrane 22%
• Gene 21%
• Cells 17%
• Causes 14%
• Interaction 13%

Chemical Compounds

• Mutation 83%
• Protein 20%
• Pore 16%
• Plasma 15%