abdominal aortic aneurysm ISO RGD:3732 9068941 mRNA, protein:increased expression:aorta RGD PMID:17196988 , REF_RGD_ID:1625699 acute myeloid leukemia disease_progression ISO RGD:730872 9068941 RGD PMID:16769586 , REF_RGD_ID:11035289 acute myeloid leukemia ISO RGD:730872 9068941 protein:increased expression:serum RGD PMID:1596865 , REF_RGD_ID:11035286 adult respiratory distress syndrome ISO RGD:3732 9068941 mRNA:increased expression:lung RGD PMID:25070658 , REF_RGD_ID:11035305 Alcoholic Fatty Liver ISO RGD:3732 9068941 RGD PMID:11477087 , REF_RGD_ID:1625694 alcoholic liver cirrhosis susceptibility ISO RGD:730872 9068941 DNA:SNP: : 47T>Chuman RGD PMID:26873981 , REF_RGD_ID:11060603 Alcoholic Liver Diseases treatment ISO RGD:11330 9068941 RGD PMID:32236798 , REF_RGD_ID:27095880 Alzheimer's disease ISO RGD:730872 9068941 RGD PMID:16369462 , REF_RGD_ID:1579972 anemia ISO RGD:11330 9068941 RGD PMID:8790408 , REF_RGD_ID:1581262 Aortic Calcification ISO RGD:3732 9068941 associated with Renal Insufficiency more ... RGD PMID:25430697 , REF_RGD_ID:11038653 asthma ISO RGD:730872 9068941 RGD PMID:15743779 , REF_RGD_ID:1581231 Bacteremia ISO RGD:11330 9068941 mRNA:increased expression:liver: RGD PMID:24253037 , REF_RGD_ID:26923958 bilirubin metabolic disorder treatment ISO RGD:730872 9068941 associated with acute lymphoblastic leukemia, DNA:SNP: :rs4880human RGD PMID:27019981 , REF_RGD_ID:11060605 bladder neck obstruction ISO RGD:3732 9068941 RGD PMID:21060756 , REF_RGD_ID:7175518 Brain Injuries ISO RGD:11330 9068941 RGD PMID:16248885 , REF_RGD_ID:1581214 brain ischemia ISO RGD:11330 9068941 RGD PMID:10212301 , REF_RGD_ID:1625695 breast cancer ISO RGD:730872 9068941 RGD PMID:15883815 , REF_RGD_ID:1581240 Breast Neoplasms ISO RGD:730872 9068941 RGD PMID:15168344 , REF_RGD_ID:1581248 Cardiac Arrhythmias ISO RGD:3732 9068941 RGD PMID:15454275 , REF_RGD_ID:1581234 cardiomyopathy ISO RGD:730872 9068941 associated with hemochromatosis, DNA:polymorphism: :p.A16V human RGD PMID:15591282 , REF_RGD_ID:1580836 cardiomyopathy ISO RGD:11330 9068941 RGD PMID:15890620 , REF_RGD_ID:1581220 carotid artery disease ISO RGD:730872 9068941 RGD PMID:12732398 , REF_RGD_ID:1580838 Central Nervous System Infections ISO RGD:730872 9068941 RGD PMID:15337840 , REF_RGD_ID:1581246 Chemical and Drug Induced Liver Injury severity ISO RGD:3732 9068941 RGD PMID:19647030 , REF_RGD_ID:26923961 Chemical and Drug Induced Liver Injury susceptibility ISO RGD:730872 9068941 DNA:SNP:cds:p.Val16Alahuman RGD PMID:20578157 , REF_RGD_ID:26923957 Chemical and Drug Induced Liver Injury susceptibility ISO RGD:11330 9068941 RGD PMID:19332662 , REF_RGD_ID:26923959 Chemical and Drug Induced Liver Injury treatment ISO RGD:730872 9068941 associated with acute lymphoblastic leukemia, DNA:SNP: :rs4880human RGD PMID:27019981 , REF_RGD_ID:11060605 Colorectal Neoplasms onset ISO RGD:730872 9068941 RGD PMID:11836586 , REF_RGD_ID:1581258 congenital diaphragmatic hernia ISO RGD:3732 9068941 mRNA:decreased expression:lung RGD PMID:26534761 , REF_RGD_ID:11035301 cystitis ISO RGD:3732 9068941 mRNA:decreased expression:urinary bladder RGD PMID:26109091 , REF_RGD_ID:11035303 Diabetic Nephropathies ISO RGD:730872 9068941 RGD PMID:17192491 , REF_RGD_ID:7175540 dilated cardiomyopathy ISO RGD:730872 9068941 RGD PMID:10425186 , REF_RGD_ID:1580837 dilated cardiomyopathy ISO RGD:11330 9068941 RGD PMID:11677043 , REF_RGD_ID:1581260 disease of cellular proliferation ISO RGD:11330 9068941 RGD PMID:14679299 , REF_RGD_ID:8158045 Drug-induced Neutropenia susceptibility ISO RGD:730872 9068941 associated with female breast cancer, DNA:missense mutation:cds:p.V16A rs4880 human RGD PMID:20309628 , REF_RGD_ID:11035278 esophagus adenocarcinoma ISO RGD:3732 9068941 RGD PMID:17785574 , REF_RGD_ID:2317403 exfoliation syndrome ISO RGD:730872 9068941 associated with glaucoma more ... RGD PMID:18055805 , REF_RGD_ID:7794853 exfoliation syndrome ISO RGD:730872 9068941 associated with cataract, mRNA:increased expression:lens epithelium: RGD PMID:23805041 , REF_RGD_ID:8158048 Experimental Diabetes Mellitus ISO RGD:3732 9068941 protein:increased activity:testes RGD PMID:19891634 , REF_RGD_ID:2317382 Hearing Loss, Noise-Induced susceptibility ISO RGD:730872 9068941 DNA:SNP:cds:p.V16Ars4880human RGD PMID:20534900 , REF_RGD_ID:8158046 Hearing Loss, Noise-Induced susceptibility ISO RGD:730872 9068941 DNA:polymorphisms:intron:IVS3-23T>G, IVS3-60T>G human RGD PMID:15345661 , REF_RGD_ID:8158044 hemolytic anemia ISO RGD:11330 9068941 RGD PMID:11304553 , REF_RGD_ID:11035277 Hemorrhagic Shock treatment ISO RGD:3732 9068941 RGD PMID:26073907 , REF_RGD_ID:26923954 hepatocellular carcinoma susceptibility ISO RGD:730872 9068941 associated with liver cirrhosis, DNA:SNP:cds:p.Ala16Valrs1799725human RGD PMID:19731237 , REF_RGD_ID:26923907 hepatocellular carcinoma ISO RGD:730872 9068941 protein:increased expression:saliva RGD PMID:31041878 , REF_RGD_ID:27095881 hepatocellular carcinoma disease_progression ISO RGD:730872 9068941 RGD PMID:27221200 , REF_RGD_ID:26923955 hepatocellular carcinoma ISO RGD:730872 9068941 RGD PMID:15869407 , REF_RGD_ID:1581242 Huntington's disease susceptibility ISO RGD:11330 9068941 RGD PMID:11161607 , REF_RGD_ID:13464352 hyperhomocysteinemia treatment ISO RGD:3732 9068941 RGD PMID:24563435 , REF_RGD_ID:11035307 Hyperoxia ISO RGD:3732 9068941 RGD PMID:2001291 , REF_RGD_ID:729952 hypertension ISO RGD:3732 9068941 RGD PMID:16716903 , REF_RGD_ID:1580833 hypertension ISO RGD:730872 9068941 RGD PMID:16716903 , REF_RGD_ID:1580833 Hypopharyngeal Neoplasms susceptibility ISO RGD:730872 9068941 DNA:polymorphism: :rs5746134human RGD PMID:21940907 , REF_RGD_ID:8158078 hypothyroidism treatment ISO RGD:3732 9068941 RGD PMID:29896255 , REF_RGD_ID:38549578 inclusion body myositis ISO RGD:730872 9068941 RGD PMID:11837748 , REF_RGD_ID:1581257 infectious mononucleosis ISO RGD:730872 9068941 RGD PMID:7964476 , REF_RGD_ID:11035288 intestinal disease treatment ISO RGD:3732 9068941 associated with Shock, Hemorrhagic RGD PMID:26301045 , REF_RGD_ID:11035302 Kuhnt-Junius degeneration susceptibility ISO RGD:730872 9068941 DNA:polymorphism:cds:p.V16Ars4880human RGD PMID:18573360 , REF_RGD_ID:8158102 Leber hereditary optic neuropathy ISO RGD:11330 9068941 RGD PMID:12601034 , REF_RGD_ID:8158104 Leber hereditary optic neuropathy treatment ISO RGD:730872 9068941 RGD PMID:15293270 , REF_RGD_ID:8158101 liver cirrhosis disease_progression ISO RGD:730872 9068941 DNA:SNP:cds:p.Ala16Valrs1799725human RGD PMID:19731237 , REF_RGD_ID:26923907 lung cancer ISO RGD:730872 9068941 RGD PMID:15213518 , REF_RGD_ID:1581247 Lymphatic Metastasis disease_progression ISO RGD:730872 9068941 associated with tongue neoplasms RGD PMID:20618948 , REF_RGD_ID:8547519 macular degeneration ISO RGD:11330 9068941 RGD PMID:17898259 , REF_RGD_ID:8158047 melanoma ISO RGD:730872 9068941 protein:increased expression:serum: RGD PMID:8541726 , REF_RGD_ID:8547533 Metabolic Syndrome treatment ISO RGD:11330 9068941 RGD PMID:28875871 , REF_RGD_ID:26923956 Mouth Neoplasms susceptibility ISO RGD:730872 9068941 DNA:polymorphism: :rs4342445human RGD PMID:21940907 , REF_RGD_ID:8158078 multiple myeloma ISO RGD:730872 9068941 RGD PMID:15908783 , REF_RGD_ID:1581238 mycosis fungoides ISO RGD:730872 9068941 protein:increased expression:skin: RGD PMID:20833513 , REF_RGD_ID:8547521 myocardial infarction ISO RGD:730872 9068941 RGD PMID:2313102 , REF_RGD_ID:1580840 myocardial infarction ISO RGD:3732 9068941 RGD PMID:14575298 more ... Myocardial Ischemia ISO RGD:11330 9068941 RGD PMID:15681709 , REF_RGD_ID:1581233 Myocardial Reperfusion Injury ISO RGD:11330 9068941 RGD PMID:11864929 , REF_RGD_ID:1581222 Myocardial Reperfusion Injury treatment ISO RGD:730872 9068941 RGD PMID:12668130 , REF_RGD_ID:11035287 Nasal Polyps ISO RGD:730872 9068941 associated with Rhinosinusitis more ... RGD PMID:23921602 , REF_RGD_ID:8547534 nephrotic syndrome ISO RGD:730872 9068941 RGD PMID:9152291 , REF_RGD_ID:11035285 neuronal ceroid lipofuscinosis ISO RGD:730872 9068941 RGD PMID:12946273 , REF_RGD_ID:1581253 non-alcoholic fatty liver disease ISO RGD:730872 9068941 RGD PMID:15094225 , REF_RGD_ID:1581245 non-alcoholic fatty liver disease treatment ISO RGD:11330 9068941 RGD PMID:24597775 , REF_RGD_ID:11352823 non-alcoholic steatohepatitis susceptibility ISO RGD:3732 9068941 mRNA:decreased expression:liver rat RGD PMID:20606728 , REF_RGD_ID:21076282 non-alcoholic steatohepatitis susceptibility ISO RGD:730872 9068941 RGD PMID:24649902 , REF_RGD_ID:26923960 optic neuritis ISO RGD:730872 9068941 associated with Encephalomyelitis more ... RGD PMID:17251466 , REF_RGD_ID:8158052 optic neuritis ISO RGD:11330 9068941 associated with Encephalomyelitis more ... RGD PMID:17251466 , REF_RGD_ID:8158052 osteoporosis susceptibility ISO RGD:730872 9068941 DNA:SNPs:intron more ... RGD PMID:26336112 , REF_RGD_ID:11035299 osteoporosis no_association ISO RGD:730872 9068941 DNA:SNPs:5' utr more ... RGD PMID:26336112 , REF_RGD_ID:11035299 ovarian cancer ISO RGD:730872 9068941 RGD PMID:16179351 , REF_RGD_ID:1581239 pancreatic cancer ISO RGD:730872 9068941 RGD PMID:12700280 , REF_RGD_ID:1581235 pancreatic cancer disease_progression ISO RGD:730872 9068941 protein:decreased expression:pancreas RGD PMID:12499913 , REF_RGD_ID:2317410 pancreatic cancer susceptibility ISO RGD:730872 9068941 DNA:polymorphism:cds:p.A16V human RGD PMID:18205184 , REF_RGD_ID:2317406 Parkinson's disease susceptibility ISO RGD:11330 9068941 RGD PMID:11161607 , REF_RGD_ID:13464352 polyneuropathy ISO RGD:730872 9068941 associated with Diabetes Mellitus more ... RGD PMID:12815947 , REF_RGD_ID:1581254 Presbycusis ISO RGD:3732 9068941 protein:decreased expression, decreased activity:auditory cortex: RGD PMID:24505357 , REF_RGD_ID:8158103 primary biliary cholangitis ISO RGD:730872 9068941 protein:increased expression:serum RGD PMID:1682406 , REF_RGD_ID:2317411 primary open angle glaucoma susceptibility ISO RGD:730872 9068941 DNA:polymorphism: :rs2842980human RGD PMID:23638916 , REF_RGD_ID:8158079 Prostatic Neoplasms ISO RGD:730872 9068941 RGD PMID:15512801 , REF_RGD_ID:1581244 pseudoxanthoma elasticum onset ISO RGD:730872 9068941 DNA:polymorphism:cds:c.47C>Trs4880human RGD PMID:17693525 , REF_RGD_ID:8547520 psoriasis ISO RGD:730872 9068941 mRNA:increased expression:skin: RGD PMID:7744320 , REF_RGD_ID:8547526 Pulmonary Arterial Hypertension ISO RGD:730872 9068941 protein:decreased expression:small pulmonary artery RGD PMID:20529999 , REF_RGD_ID:27095884 Pulmonary Arterial Hypertension ISO RGD:3732 9068941 protein:decreased expression:pulmonary artery RGD PMID:20529999 , REF_RGD_ID:27095884 reactive arthritis ISO RGD:730872 9068941 RGD PMID:14687717 , REF_RGD_ID:1581251 renal fibrosis ISO RGD:11330 9068941 RGD PMID:19458120 , REF_RGD_ID:7175536 Reperfusion Injury ISO RGD:730872 9068941 RGD PMID:15087276 , REF_RGD_ID:1581259 Reperfusion Injury ISO RGD:3732 9068941 protein:increased expression:liver RGD PMID:15612529 , REF_RGD_ID:1582141 Retina Reperfusion Injury treatment ISO RGD:730872 9068941 RGD PMID:22240151 , REF_RGD_ID:8158043 Retina Reperfusion Injury ISO RGD:3732 9068941 protein:decreased activity:retina: RGD PMID:22240151 , REF_RGD_ID:8158043 retinitis pigmentosa ISO RGD:11330 9068941 RGD PMID:19293779 , REF_RGD_ID:8158049 sensorineural hearing loss ISO RGD:3732 9068941 protein:increased activity:cochlea: RGD PMID:15109710 , REF_RGD_ID:8547516 Sepsis ISO RGD:3732 9068941 mRNA, protein:increased expression:lung RGD PMID:26266917 , REF_RGD_ID:11035300 Skin Neoplasms disease_progression ISO RGD:11330 9068941 RGD PMID:22009531 , REF_RGD_ID:8547525 Skin Neoplasms ISO RGD:730872 9068941 RGD PMID:15130280 , REF_RGD_ID:8547532 Skin Neoplasms ISO RGD:11330 9068941 RGD PMID:12032821 , REF_RGD_ID:8547517 status epilepticus ISO RGD:3732 9068941 mRNA, protein:increased expression:hippocampus RGD PMID:25333348 , REF_RGD_ID:11035304 stomach cancer ISO RGD:730872 9068941 RGD PMID:12469139 , REF_RGD_ID:1581255 systemic lupus erythematosus ISO RGD:730872 9068941 DNA:SNP, haplotype: :1183C>T human RGD PMID:14611903 , REF_RGD_ID:1581249 Tardive Dyskinesia ISO RGD:730872 9068941 associated with schizophrenia RGD PMID:12960753 , REF_RGD_ID:1581250 Thyroid Neoplasms ISO RGD:730872 9068941 RGD PMID:15887859 , REF_RGD_ID:1581241 Tongue Neoplasms ISO RGD:730872 9068941 mRNA, protein:increased expression:tongue: RGD PMID:20618948 , REF_RGD_ID:8547519 transient cerebral ischemia treatment ISO RGD:3732 9068941 RGD PMID:30716316 , REF_RGD_ID:27095883 type 1 diabetes mellitus ISO RGD:730872 9068941 DNA:polymorphism: :p.A16V human RGD PMID:18423055 , REF_RGD_ID:2312364 type 2 diabetes mellitus ISO RGD:730872 9068941 DNA:polymorphism: :p.A16V human RGD PMID:18423055 , REF_RGD_ID:2312364 urinary bladder cancer ISO RGD:730872 9068941 RGD PMID:17974967 , REF_RGD_ID:7175539 urticaria ISO RGD:730872 9068941 protein:increased expression:skin RGD PMID:12780723 , REF_RGD_ID:8547524 vitiligo disease_progression ISO RGD:730872 9068941 DNA more ... RGD PMID:24036105 , REF_RGD_ID:8547522