Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "I"
221 to 230 of 359 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

221
Insulin receptor substrate 1
HIRS-1
Alzheimer disease, Hepatocellular carcinoma, Ischemic heart disease, Coronary artery disease, Diabetes mellitus, Experimental diabetes, Diabetes mellitus type 2, Hyperinsulinism, Hyperlipidemia, Diabetes mellitus, type 2, Myocardial ischemia, Nasopharyngeal carcinoma, Obesity, Oligodendroglioma, Prostatic neoplasm
View all (2 more)

222
Interferon stimulated exonuclease gene 20
CD25, HEM45
Aortic stenosis, Aortic valve disease, Color vision deficiency, Complex regional pain syndrome, Hearing loss, Liver cirrhosis, Obesity

223
ISL LIM homeobox 1
ISLET1, Isl-1
Atrial fibrillation, Atrial septal defect, Bladder exstrophy, Bladder exstrophy and epispadias complex, Cardiomyopathy, Congenital heart defects, Congenital heart disease, Diabetes mellitus type 1, Diabetes mellitus type 2, Myocardial infarction, Neuroblastoma, Psychiatric disorders, Urogenital abnormalities, Ventricular septal defect

224
Immunoglobulin superfamily containing leucine rich repeat
HsT17563, Meflin
Gout, Hodgkin lymphoma, Squamous cell carcinoma

225
Integrin subunit alpha 1
CD49a, VLA1
Attention deficit hyperactivity disorder, Obstructive pulmonary disease, Coronary artery disease, Diabetes mellitus type 2, Hearing loss, Myocardial infarction, Diabetes mellitus, type 2

226
Integrin subunit alpha 2
BR, CD49B, FMAIT3, GPIa, HPA-5, VLA-2, VLAA2
Angina pectoris, Arteriosclerosis, Behcet disease, Bone fracture, Central nervous system cancer, Combined molybdoflavoprotein enzyme deficiency, Diabetes mellitus, Diabetes mellitus type 2, Diabetic retinopathy, Endometriosis, Glioblastoma, Glioma, Glycoprotein ia deficiency, Hyperalgesia, Myocardial infarction
View all (6 more)

227
Integrin subunit alpha 2b
BDPLT16, BDPLT2, CD41, CD41B, FMAIT2, GP2B, GPIIb, GT, GT1, GTA, HPA3, PPP1R93
Juvenile arthritis, Macrothrombocytopenia, Platelet-type bleeding disorder, Carotid artery thrombosis, Cerebral hemorrhage, Cerebrovascular disorder, Glanzmann thrombasthenia, Juvenile idiopathic arthritis, Liver cirrhosis, Parkinson disease, Oligoarticular juvenile idiopathic arthritis, Stroke, Von willebrand disorder

228
Integrin subunit alpha 3
CD49C, FRP-2, GAP-B3, GAPB3, ILNEB, JEB7, MSK18, VCA-2, VL3A, VLA3a
Anemia, Bronchopulmonary dysplasia, Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome, Eczema, Junctional epidermolysis bullosa, Nephrotic syndrome, Pancreatic cancer, Diabetes mellitus, type 2

229
Integrin subunit alpha 4
CD49D, IA4
Autism, Cone-rod dystrophy, Crohn disease, Inflammatory bowel disease, Lymphocytic b-cell leukemia, Periodontal disease, Periodontitis, Retinitis pigmentosa, Schizophrenia, Ulcerative colitis

230
Integrin subunit alpha 5
CD49e, FNRA, VLA-5, VLA5A
Squamous cell carcinoma, Stomach neoplasms