acute chest syndrome susceptibility ISO RGD:735618 9068941 associated with Anemia more ... RGD PMID:25263931 , REF_RGD_ID:11533931 acute chest syndrome susceptibility ISO RGD:735618 9068941 associated with Anemia more ... RGD PMID:14687036 , REF_RGD_ID:11533934 acute kidney failure ISO RGD:3186 9068941 in females, mRNA:increased expression:cortex of kidney (rat) RGD PMID:28947737 , REF_RGD_ID:13450947 Acute Liver Failure ISO RGD:3186 9068941 mRNA, protein:increased expression:liver RGD PMID:17276928 , REF_RGD_ID:2292148 acute lymphoblastic leukemia susceptibility ISO RGD:735618 9068941 DNA:SNP: :rs3918186(human) RGD PMID:23922896 , REF_RGD_ID:11533639 acute lymphoblastic leukemia disease_progression ISO RGD:735618 9068941 DNA:polymorphism more ... RGD PMID:20510681 , REF_RGD_ID:11533646 acute myeloid leukemia disease_progression ISO RGD:735618 9068941 DNA:polymorphgism: : 894 G>T(human) RGD PMID:24684492 , REF_RGD_ID:11533640 Alzheimer's disease onset ISO RGD:735618 9068941 DNA:snp:cds:p.E298D (human) RGD PMID:10514107 , REF_RGD_ID:1358752 angle-closure glaucoma susceptibility ISO RGD:735618 9068941 DNA:snps:introns:g.IVS5+1182G>A more ... RGD PMID:23422825 , REF_RGD_ID:7775046 angle-closure glaucoma ISO RGD:735618 9068941 DNA:duplication:intron:IVS4?-?+27 (human) RGD PMID:20069064 , REF_RGD_ID:7771573 anterior ischemic optic neuropathy susceptibility ISO RGD:735618 9068941 DNA:snp:promoter:g.-786T>C (human) RGD PMID:16633797 , REF_RGD_ID:7775040 Arteriovenous Fistula ISO RGD:3186 9068941 protein:increased expression:vena cava RGD PMID:17344190 , REF_RGD_ID:2292146 asthma susceptibility ISO RGD:735618 9068941 DNA:polymorphisms:promoter:c. -786C>T, -691C>T (human) RGD PMID:16837812 , REF_RGD_ID:4892058 asthma susceptibility ISO RGD:735618 9068941 DNA:repeats:intron RGD PMID:16081038 , REF_RGD_ID:4892062 asthma susceptibility ISO RGD:735618 9068941 DNA:snps more ... RGD PMID:18486767 , REF_RGD_ID:4892053 atherosclerosis ISO RGD:10997 9068941 RGD PMID:12163452 , REF_RGD_ID:7771607 atherosclerosis susceptibility ISO RGD:735618 9068941 DNA:snp:exon:c.894G>T (human) RGD PMID:21114134 , REF_RGD_ID:7771564 Behcet's disease susceptibility ISO RGD:735618 9068941 DNA:snp more ... RGD PMID:15705632 , REF_RGD_ID:7775048 Behcet's disease no_association ISO RGD:735618 9068941 DNA:snp:cds:p.E298D RGD PMID:16463158 , REF_RGD_ID:7771577 Behcet's disease no_association ISO RGD:735618 9068941 DNA:duplication:intron:g.IVS4?-?+27 (human) RGD PMID:21957880 , REF_RGD_ID:7775050 Behcet's disease susceptibility ISO RGD:735618 9068941 DNA:snp:cds:p.E298D (human) RGD PMID:11908569 , REF_RGD_ID:7771576 bladder neck obstruction ISO RGD:3186 9068941 mRNA:decreased expression:urinary bladder RGD PMID:21256554 , REF_RGD_ID:4891960 Brain Hypoxia ISO RGD:3186 9068941 protein:increased expression:caudate putamen (rat) RGD PMID:14980808 , REF_RGD_ID:7794714 brain ischemia ISO RGD:3186 9068941 RGD PMID:17600658 more ... breast cancer susceptibility ISO RGD:735618 9068941 DNA:polymorphism:promoter:-786T>C (human) RGD PMID:17063466 , REF_RGD_ID:2292074 breast cancer no_association ISO RGD:735618 9068941 DNA:polymorphism:exon:p.E298D (human) RGD PMID:16807677 , REF_RGD_ID:2292075 breast cancer disease_progression ISO RGD:735618 9068941 DNA:polymorphisms RGD PMID:17891484 , REF_RGD_ID:2292068 Bronchial Hyperreactivity ISO RGD:10997 9068941 protein:decreased expression:lung RGD PMID:19286931 , REF_RGD_ID:5132864 Bronchial Hyperreactivity ISO RGD:10997 9068941 RGD PMID:16714207 , REF_RGD_ID:4892061 bronchiolitis obliterans ISO RGD:3186 9068941 protein:increased expression:lung RGD PMID:15136885 , REF_RGD_ID:4892068 Cardiomegaly ISO RGD:3186 9068941 protein:increased expression:aorta RGD PMID:17487232 , REF_RGD_ID:2289120 Cardiomegaly treatment ISO RGD:3186 9068941 RGD PMID:29331788 , REF_RGD_ID:13504707 cardiomyopathy ISO RGD:3186 9068941 associated with Diabetes Mellitus more ... RGD PMID:17589825 , REF_RGD_ID:1642825 cardiomyopathy susceptibility ISO RGD:735618 9068941 associated with Beta-Thalassemia, DNA:repeats:intron: RGD PMID:25699607 , REF_RGD_ID:11533642 Cardiotoxicity treatment ISO RGD:735618 9068941 associated with Precursor Cell Lymphoblastic Leukemia-Lymphoma, DNA:polymorphism: :894G>T(human) RGD PMID:26345518 , REF_RGD_ID:11533645 Carotid Artery Injuries treatment ISO RGD:3186 9068941 RGD PMID:29207649 , REF_RGD_ID:13504723 central sleep apnea ISO RGD:735618 9068941 associated with heart failure, protein:decreased expression:serum RGD PMID:16806535 , REF_RGD_ID:4892059 Child Behavior Disorders susceptibility ISO RGD:735618 9068941 associated withPrecursor Cell Lymphoblastic Leukemia-Lymphoma more ... RGD PMID:23612386 , REF_RGD_ID:11533937 cholestasis ISO RGD:3186 9068941 protein:decreased activity:liver (rat) RGD PMID:11352814 , REF_RGD_ID:7775033 Chronic Cerebral Hypoperfusion ISO RGD:3186 9068941 RGD PMID:15703700 , REF_RGD_ID:13824977 chronic kidney disease treatment ISO RGD:3186 9068941 RGD PMID:29247650 , REF_RGD_ID:13504713 chronic kidney disease susceptibility ISO RGD:3186 9068941 mRNA:decreased expression:cortex of kidney (rat) RGD PMID:29018182 , REF_RGD_ID:13450920 colitis ISO RGD:3186 9068941 mRNA:increased expression:colon RGD PMID:17947450 , REF_RGD_ID:2292124 congenital diaphragmatic hernia ISO RGD:3186 9068941 protein:decreased expression:pulmonary artery (rat) RGD PMID:29216632 , REF_RGD_ID:13504720 congestive heart failure treatment ISO RGD:3186 9068941 RGD PMID:29351461 , REF_RGD_ID:13504746 coronary artery disease ISO RGD:735618 9068941 DNA:duplication:intron:IVS4?-?+27 (human) RGD PMID:8564837 , REF_RGD_ID:7421529 coronary artery disease susceptibility ISO RGD:735618 9068941 DNA:snp:promoter:g.-786T>C (human) RGD PMID:19761682 , REF_RGD_ID:7771578 coronary artery disease susceptibility ISO RGD:735618 9068941 DNA:snp:cds:c.894G>T (human) RGD PMID:16284093 , REF_RGD_ID:7771567 cystic fibrosis ISO RGD:735618 9068941 DNA:polymorphism:exon: c. 894G>T (human) RGD PMID:12406848 , REF_RGD_ID:4892049 diabetic angiopathy ISO RGD:3186 9068941 associated with Diabetes Mellitus more ... RGD PMID:19241604 , REF_RGD_ID:4891384 diabetic angiopathy treatment ISO RGD:3186 9068941 associated with Diabetes Mellitus, Experimental RGD PMID:29329611 , REF_RGD_ID:13504708 Diabetic Cardiomyopathies treatment ISO RGD:3186 9068941 associated with Diabetes Mellitus, Experimental RGD PMID:29274332 , REF_RGD_ID:13504685 Diabetic Gastroparesis ISO RGD:3186 9068941 mRNA:decreased expression:pyloric antrum (rat) RGD PMID:29071981 , REF_RGD_ID:13446417 Diabetic Nephropathies susceptibility ISO RGD:735618 9068941 associated with Diabetes Mellitus more ... RGD PMID:10868974 , REF_RGD_ID:7421530 Diabetic Nephropathies no_association ISO RGD:735618 9068941 associated with Diabetes Mellitus more ... RGD PMID:10741691 , REF_RGD_ID:7421534 Diabetic Nephropathies treatment ISO RGD:3186 9068941 associated with Diabetes Mellitus, Experimental RGD PMID:29336891 , REF_RGD_ID:13504726 diabetic retinopathy no_association ISO RGD:735618 9068941 associated with Diabetes Mellitus more ... RGD PMID:16581274 more ... diabetic retinopathy onset ISO RGD:735618 9068941 DNA:snps:promoter more ... RGD PMID:15890549 , REF_RGD_ID:7771565 diabetic retinopathy ISO RGD:735618 9068941 associated with Diabetes Mellitus more ... RGD PMID:17973941 , REF_RGD_ID:7421533 diabetic retinopathy no_association ISO RGD:735618 9068941 associated with Diabetes Mellitus more ... RGD PMID:22017289 , REF_RGD_ID:7777101 diabetic retinopathy ISO RGD:3186 9068941 associated with Diabetes Mellitus more ... RGD PMID:23059402 , REF_RGD_ID:7771569 diabetic retinopathy ISO RGD:735618 9068941 associated with Diabetes Mellitus more ... RGD PMID:11918626 , REF_RGD_ID:7421532 diabetic retinopathy treatment ISO RGD:3186 9068941 associated with Diabetes Mellitus, Experimental RGD PMID:18840783 , REF_RGD_ID:7771606 diabetic retinopathy severity ISO RGD:10997 9068941 associated with Diabetes Mellitus, Experimental RGD PMID:20435587 , REF_RGD_ID:7771568 diabetic retinopathy susceptibility ISO RGD:735618 9068941 associated with Diabetes Mellitus more ... RGD PMID:23776381 , REF_RGD_ID:7777103 Diaphragmatic Hernia ISO RGD:3186 9068941 mRNA, protein:decreased expression:lung RGD PMID:7576705 , REF_RGD_ID:5132862 Drug-Induced Enteropathy treatment ISO RGD:3186 9068941 RGD PMID:29064425 , REF_RGD_ID:13450913 end stage renal disease susceptibility ISO RGD:735618 9068941 DNA:duplication more ... RGD PMID:12701818 , REF_RGD_ID:7777097 end stage renal disease ISO RGD:3186 9068941 protein:decreased expression:glomerulus RGD PMID:18089446 , REF_RGD_ID:2292109 endometrial carcinoma disease_progression ISO RGD:735618 9068941 protein:increased expression:endometrium RGD PMID:9276029 , REF_RGD_ID:2292090 Endotoxemia ISO RGD:3186 9068941 protein:increased expression:aorta (rat) RGD PMID:10462376 , REF_RGD_ID:7794732 esophagus adenocarcinoma onset ISO RGD:735618 9068941 DNA:SNP:3'utr: (rs2070744) (human) RGD PMID:21472143 , REF_RGD_ID:126925218 Experimental Arthritis treatment ISO RGD:3186 9068941 RGD PMID:29337196 , REF_RGD_ID:13504725 Experimental Diabetes Mellitus ISO RGD:3186 9068941 RGD PMID:18825362 , REF_RGD_ID:4892007 Experimental Diabetes Mellitus ISO RGD:10997 9068941 protein:decreased expression:thoracic aorta (mouse) RGD PMID:21050844 , REF_RGD_ID:7777108 Experimental Diabetes Mellitus ISO RGD:3186 9068941 protein:increased expression:heart RGD PMID:18287592 , REF_RGD_ID:2292100 Experimental Diabetes Mellitus treatment ISO RGD:10997 9068941 RGD PMID:21050844 , REF_RGD_ID:7777108 Experimental Diabetes Mellitus treatment ISO RGD:3186 9068941 RGD PMID:28976888 , REF_RGD_ID:13450939 Experimental Liver Cirrhosis ISO RGD:3186 9068941 protein:decreased expression:liver RGD PMID:17918268 , REF_RGD_ID:2292126 Experimental Liver Cirrhosis ISO RGD:3186 9068941 protein:decreased expression:spleen RGD PMID:17481668 , REF_RGD_ID:2292140 familial hyperlipidemia ISO RGD:3186 9068941 protein:increased phosphorylation:aorta RGD PMID:17895290 , REF_RGD_ID:2292129 Fetal Growth Retardation ISO RGD:3186 9068941 associated with hyperinsulinemia, protein:decreased expression:placenta RGD PMID:19709742 , REF_RGD_ID:5132592 Fetal Growth Retardation ISO RGD:3186 9068941 RNA, protein:increased expression:thoracic aorta: RGD PMID:29741931 , REF_RGD_ID:13792602 gastric ulcer treatment ISO RGD:3186 9068941 RGD PMID:29095895 , REF_RGD_ID:13446410 Graft Occlusion, Vascular susceptibility ISO RGD:735618 9068941 DNA:repeats:intron RGD PMID:17365407 , REF_RGD_ID:11533930 Hemorrhagic Shock ISO RGD:3186 9068941 mRNA:increased expression: :multiple RGD PMID:15854664 , REF_RGD_ID:1580937 Hemorrhagic Shock treatment ISO RGD:3186 9068941 RGD PMID:29122552 , REF_RGD_ID:13450929 hepatopulmonary syndrome ISO RGD:3186 9068941 associated with Liver Cirrhosis, protein:increased expression:lung RGD PMID:18081228 , REF_RGD_ID:2292110 high grade glioma ISO RGD:735618 9068941 protein:increased expression:blood vessel endothelial cell RGD PMID:14672505 , REF_RGD_ID:2292080 Huntington's disease ISO RGD:3186 9068941 mRNA:increased expression:striatum (rat) RGD PMID:17850874 , REF_RGD_ID:2292130 Hyperemia ISO RGD:735618 9068941 DNA:SNP: :894G>T (human) RGD PMID:11668050 , REF_RGD_ID:7777102 Hyperoxia ISO RGD:3186 9068941 mRNA, protein:decreased expression:lung RGD PMID:17937862 , REF_RGD_ID:2292125 hypertension ISO RGD:735618 9068941 DNA:snp:cds:p.E298D (human) RGD PMID:9674630 , REF_RGD_ID:1580282 hypertension ISO RGD:3186 9068941 RGD PMID:11882615 , REF_RGD_ID:1580271 hypertension treatment ISO RGD:3186 9068941 RGD PMID:29084084 more ... hypertension no_association ISO RGD:735618 9068941 DNA:duplication more ... RGD PMID:10981549 , REF_RGD_ID:1580278 hypertension ISO RGD:3186 9068941 protein:decreased phosphorylation:brain RGD PMID:20813549 , REF_RGD_ID:4891993 hypertension ISO RGD:3186 9068941 associated with Pregnancy Complications RGD PMID:18047920 , REF_RGD_ID:2292113 Hypertriglyceridemia ISO RGD:3186 9068941 protein:decreased expression:aorta RGD PMID:17824809 , REF_RGD_ID:2292131 hypothyroidism ISO RGD:3186 9068941 protein:decreased activity:ovary (rat) RGD PMID:29214681 , REF_RGD_ID:13504721 ileus treatment ISO RGD:3186 9068941 RGD PMID:30852906 , REF_RGD_ID:151893492 impotence ISO RGD:3186 9068941 associated with Diabetes Mellitus more ... RGD PMID:20807325 , REF_RGD_ID:4891999 impotence ISO RGD:3186 9068941 associated with Cocaine-Related Disorders, protein:decreased expression:penis RGD PMID:17420087 , REF_RGD_ID:2292142 impotence treatment ISO RGD:3186 9068941 RGD PMID:29260891 , REF_RGD_ID:13504711 Insulin Resistance ISO RGD:3186 9068941 protein:decreased expression:serum RGD PMID:18298918 , REF_RGD_ID:2292098 Insulin Resistance treatment ISO RGD:3186 9068941 RGD PMID:28946194 , REF_RGD_ID:13450950 Intestinal Reperfusion Injury treatment ISO RGD:3186 9068941 RGD PMID:16610051 , REF_RGD_ID:7777112 Intimal Hyperplasia treatment ISO RGD:735618 9068941 RGD PMID:9576106 , REF_RGD_ID:11534002 intracranial aneurysm ISO RGD:3186 9068941 RGD PMID:21321533 , REF_RGD_ID:5131897 intracranial aneurysm ISO RGD:10997 9068941 RGD PMID:21321533 , REF_RGD_ID:5131897 Intracranial Hemorrhages treatment ISO RGD:3186 9068941 RGD PMID:29203281 , REF_RGD_ID:13504724 irritable bowel syndrome ISO RGD:3186 9068941 RGD PMID:23691109 , REF_RGD_ID:7771566 Kidney Reperfusion Injury treatment ISO RGD:3186 9068941 RGD PMID:29291552 , REF_RGD_ID:13504682 Kuhnt-Junius degeneration susceptibility ISO RGD:735618 9068941 DNA:snp:cds:c.894G>T (rs1799983) (human) RGD PMID:23276910 , REF_RGD_ID:7771558 Left Ventricular Hypertrophy ISO RGD:3186 9068941 mRNA, protein:altered expression:cardiac myocyte (rat) RGD PMID:9747440 , REF_RGD_ID:7794715 leiomyoma ISO RGD:735618 9068941 protein:increased expression:smooth muscle cell RGD PMID:10671823 , REF_RGD_ID:2292088 limb ischemia treatment ISO RGD:3186 9068941 RGD PMID:28979692 , REF_RGD_ID:13450931 limb ischemia treatment ISO RGD:3186 9068941 associated with Diabetes Mellitus, Experimental RGD PMID:19080171 , REF_RGD_ID:7794710 limb ischemia ISO RGD:735618 9068941 human gene in rat model RGD PMID:12171788 , REF_RGD_ID:7794776 liver cirrhosis treatment ISO RGD:3186 9068941 RGD PMID:12759254 , REF_RGD_ID:7794774 liver cirrhosis ISO RGD:3186 9068941 protein:decreased activity:liver (rat) RGD PMID:10535886 , REF_RGD_ID:7775034 Liver Reperfusion Injury treatment ISO RGD:3186 9068941 RGD PMID:28966130 , REF_RGD_ID:13450941 lung disease ISO RGD:10997 9068941 lung injury associated with hyperoxia RGD PMID:20497690 , REF_RGD_ID:4891426 lung disease ISO RGD:3186 9068941 lung injury associated with reperfusion injury, protein:decreased expression:lung RGD PMID:21056587 , REF_RGD_ID:4892011 lung disease ISO RGD:10997 9068941 ventilator-induced lung injury RGD PMID:20453164 , REF_RGD_ID:4892013 Lung Reperfusion Injury ISO RGD:3186 9068941 RGD PMID:20815765 , REF_RGD_ID:4892012 Lung Reperfusion Injury ISO RGD:10997 9068941 mRNA:increased expression:lung (mouse) RGD PMID:25382268 , REF_RGD_ID:11533932 lymphangioleiomyomatosis ISO RGD:735618 9068941 protein:increased expression:lung RGD PMID:11306434 , REF_RGD_ID:4892080 Lymphatic Metastasis susceptibility ISO RGD:735618 9068941 associated with Breast Neoplasms more ... RGD PMID:17262178 , REF_RGD_ID:2292070 macular retinal edema susceptibility ISO RGD:735618 9068941 associated with Diabetes Mellitus more ... RGD PMID:15333482 , REF_RGD_ID:7775044 Metabolic Syndrome treatment ISO RGD:3186 9068941 RGD PMID:28967023 , REF_RGD_ID:13461762 migraine ISO RGD:735618 9068941 associated with Glaucoma more ... RGD PMID:16123422 , REF_RGD_ID:7771539 myocardial infarction ISO RGD:735618 9068941 human gene in rat model RGD PMID:17637430 , REF_RGD_ID:7771561 myocardial infarction ISO RGD:3186 9068941 RGD PMID:22012955 , REF_RGD_ID:7771563 myocardial infarction susceptibility ISO RGD:735618 9068941 DNA:repeats:intron RGD PMID:10531147 , REF_RGD_ID:5128481 myocardial infarction treatment ISO RGD:10997 9068941 RGD PMID:29311930 , REF_RGD_ID:13503346 myocardial infarction ISO RGD:735618 9068941 RGD PMID:12362496 , REF_RGD_ID:1580283 myocardial infarction ISO RGD:3186 9068941 protein:decreased expression:aorta (rat) RGD PMID:28980197 , REF_RGD_ID:13450930 myocardial infarction ISO RGD:735618 9068941 DNA:duplication:intron:IVS4?-?+27 (human) RGD PMID:11903359 , REF_RGD_ID:1580284 Myocardial Ischemia susceptibility ISO RGD:735618 9068941 DNA:duplication more ... RGD PMID:15007011 , REF_RGD_ID:7777100 Myocardial Reperfusion Injury treatment ISO RGD:3186 9068941 RGD PMID:29274587 more ... Myocardial Reperfusion Injury ISO RGD:3186 9068941 RGD PMID:18390819 more ... Nasal Polyps ISO RGD:735618 9068941 protein:increased expression:nasal mucosa (human) RGD PMID:15942806 , REF_RGD_ID:7771559 Neoplasm Metastasis susceptibility ISO RGD:735618 9068941 associated with Prostatic Neoplasms, DNA:polymorphism RGD PMID:12445681 , REF_RGD_ID:2292087 Neoplasm Metastasis ISO RGD:735618 9068941 protein:increased expression:blood vessel endothelial cell RGD PMID:14672505 , REF_RGD_ID:2292080 Neoplasm Metastasis susceptibility ISO RGD:735618 9068941 associated with Breast Neoplasms, DNA:polymorphism:promoter:-786T>C (human) RGD PMID:14623178 , REF_RGD_ID:2292081 nephritis susceptibility ISO RGD:735618 9068941 associated with Purpura more ... RGD PMID:22895845 , REF_RGD_ID:11533935 obesity ISO RGD:3186 9068941 protein:decreased expression:artery RGD PMID:17623751 , REF_RGD_ID:2292133 obesity treatment ISO RGD:3186 9068941 RGD PMID:29180887 , REF_RGD_ID:13504728 obstructive sleep apnea severity ISO RGD:735618 9068941 protein:increased expression:endothelial cell RGD PMID:18413499 , REF_RGD_ID:4891909 obstructive sleep apnea ISO RGD:735618 9068941 protein:decreased expression, decreased phosphorylation:endothelial cells RGD PMID:20159829 , REF_RGD_ID:4892051 obstructive sleep apnea ISO RGD:735618 9068941 associated with heart failure, protein:decreased expression:serum RGD PMID:16806535 , REF_RGD_ID:4892059 obstructive sleep apnea ISO RGD:735618 9068941 DNA:polymorphism:exon: p. E298D (human) RGD PMID:18651156 , REF_RGD_ID:4892052 ovarian cancer disease_progression ISO RGD:735618 9068941 DNA:repeat:intron RGD PMID:12144818 , REF_RGD_ID:2298575 overnutrition ISO RGD:3186 9068941 mRNA:decreased expression:renal artery (rat) RGD PMID:28958692 , REF_RGD_ID:13450942 Pain ISO RGD:3186 9068941 RGD PMID:18079061 , REF_RGD_ID:2292111 Perennial Allergic Rhinitis ISO RGD:735618 9068941 DNA:snp:promoter:g.-786T>C (human) RGD PMID:18086269 , REF_RGD_ID:4892054 Phyllodes Tumor ISO RGD:735618 9068941 protein:increased expression:breast RGD PMID:15917410 , REF_RGD_ID:2292077 polycystic kidney disease ISO RGD:3186 9068941 protein:increased expression:kidney: RGD PMID:12675853 , REF_RGD_ID:11534000 portal hypertension ISO RGD:3186 9068941 mRNA:increased expression:aorta (rat) RGD PMID:10889169 , REF_RGD_ID:7794685 portal hypertension treatment ISO RGD:3186 9068941 associated with Liver Cirrhosis, Biliary RGD PMID:29263339 , REF_RGD_ID:13504710 portal hypertension ISO RGD:3186 9068941 RGD PMID:16142243 , REF_RGD_ID:1580269 pre-eclampsia treatment ISO RGD:3186 9068941 RGD PMID:29250138 , REF_RGD_ID:13504712 primary open angle glaucoma susceptibility ISO RGD:735618 9068941 DNA:snps more ... RGD PMID:22561696 , REF_RGD_ID:7775055 primary open angle glaucoma no_association ISO RGD:735618 9068941 DNA:snp:intron:g.IVS15+1759C>A (rs3918188) (human) RGD PMID:21245953 , REF_RGD_ID:7775039 primary open angle glaucoma susceptibility ISO RGD:735618 9068941 associated with Hypertension, DNA:snp:promoter:g.-786T>C (rs2070744) (human) RGD PMID:21670344 , REF_RGD_ID:7771542 primary open angle glaucoma ISO RGD:735618 9068941 DNA:snp:promoter:g.-690C>T (human) RGD PMID:9493554 , REF_RGD_ID:7771575 primary open angle glaucoma ISO RGD:735618 9068941 DNA:snps more ... RGD PMID:21245953 , REF_RGD_ID:7775039 primary open angle glaucoma susceptibility ISO RGD:735618 9068941 High Tension more ... RGD PMID:19815736 , REF_RGD_ID:7771543 primary open angle glaucoma ISO RGD:735618 9068941 DNA:duplication:intron:IVS4?-?+27 (human) RGD PMID:20069064 , REF_RGD_ID:7771573 prostate cancer disease_progression ISO RGD:735618 9068941 DNA:polymorphism:exon:p.E298D (human) RGD PMID:16458450 , REF_RGD_ID:2292076 pulmonary edema ISO RGD:3186 9068941 protein:increased expression:lung RGD PMID:14767587 , REF_RGD_ID:5132626 pulmonary embolism ISO RGD:3186 9068941 mRNA, protein:increased expression:lung RGD PMID:17219957 , REF_RGD_ID:2292151 pulmonary emphysema ISO RGD:10997 9068941 mRNA, protein:increased expression:lung RGD PMID:20956973 , REF_RGD_ID:4891415 pulmonary eosinophilia ISO RGD:10997 9068941 RGD PMID:16714207 , REF_RGD_ID:4892061 pulmonary hypertension ISO RGD:3186 9068941 RGD PMID:17065228 more ... pulmonary hypertension ISO RGD:10997 9068941 RNA:increased expression:lung RGD PMID:11686901 , REF_RGD_ID:5132631 pulmonary hypertension ISO RGD:10997 9068941 RGD PMID:19487814 , REF_RGD_ID:4892039 pulmonary hypertension ISO RGD:735618 9068941 associated with chronic obstructive pulmonary disease, DNA:polymorphism:cds:p.G894T (human) RGD PMID:18953956 , REF_RGD_ID:4892042 pulmonary hypertension ISO RGD:735618 9068941 associated with heart disease, protein:increased expression:endothelial cell RGD PMID:19912632 , REF_RGD_ID:5132602 pulmonary hypertension ISO RGD:735618 9068941 protein:increased expression:arteriole RGD PMID:21111729 , REF_RGD_ID:4892010 pulmonary hypertension ISO RGD:3186 9068941 mRNA, protein:increased expression:pulmonary endothelial cell RGD PMID:20724942 , REF_RGD_ID:4892004 pulmonary hypertension susceptibility ISO RGD:735618 9068941 associated with Beta-Thalassemia, DNA:repeats:intron: RGD PMID:25699607 , REF_RGD_ID:11533642 pulmonary hypertension ISO RGD:735618 9068941 DNA:polymorphism:cds:p.E298D (human) RGD PMID:21144100 , REF_RGD_ID:4892009 pulmonary hypertension treatment ISO RGD:3186 9068941 RGD PMID:29151278 , REF_RGD_ID:13504742 Pulmonary Hypertension, Hypoxia-Induced ISO RGD:3186 9068941 mRNA, protein:increased expression:pulmonary artery RGD PMID:9950873 , REF_RGD_ID:11533933 Radiation Pneumonitis susceptibility ISO RGD:735618 9068941 associated with carcinoma more ... RGD PMID:20811626 , REF_RGD_ID:5131286 renal hypertension ISO RGD:3186 9068941 RGD PMID:20938214 , REF_RGD_ID:4891989 respiratory allergy ISO RGD:735618 9068941 DNA:polymorphism: :c. -786C>T (human) RGD PMID:18086269 , REF_RGD_ID:4892054 Retina Reperfusion Injury ISO RGD:3186 9068941 protein:increased expression:retinal vasculature, retinal ganglion cell layer (rat) RGD PMID:12634478 , REF_RGD_ID:7775037 Retina Reperfusion Injury treatment ISO RGD:3186 9068941 RGD PMID:11496119 , REF_RGD_ID:7775036 Retina Reperfusion Injury ISO RGD:3186 9068941 mRNA:altered expression:retina (rat) RGD PMID:9950605 , REF_RGD_ID:7771570 retinal degeneration treatment ISO RGD:3186 9068941 RGD PMID:16209285 , REF_RGD_ID:7775035 retinal degeneration ISO RGD:3186 9068941 protein:increased expression:retina (rat) RGD PMID:16209285 , REF_RGD_ID:7775035 retinopathy of prematurity severity ISO RGD:735618 9068941 DNA:duplication:intron:IVS4?-?+27 (human) RGD PMID:18334945 , REF_RGD_ID:7771560 Right Ventricular Hypertrophy treatment ISO RGD:3186 9068941 associated with Hypertension, Pulmonary RGD PMID:22022327 , REF_RGD_ID:7794708 Sepsis ISO RGD:735618 9068941 protein:increased expression:heart RGD PMID:17999941 , REF_RGD_ID:2292119 sickle cell anemia severity ISO RGD:735618 9068941 DNA:polymorphisms more ... RGD PMID:24088668 , REF_RGD_ID:11533647 Spinal Cord Compression treatment ISO RGD:3186 9068941 RGD PMID:29323048 , REF_RGD_ID:13504709 Spinal Cord Injuries ISO RGD:3186 9068941 RGD PMID:17287083 , REF_RGD_ID:4891407 Stroke ISO RGD:3186 9068941 RGD PMID:18234158 , REF_RGD_ID:2292103 Stroke treatment ISO RGD:3186 9068941 RGD PMID:29152647 , REF_RGD_ID:13504814 Stroke susceptibility ISO RGD:735618 9068941 associated with Anemia more ... RGD PMID:25263931 , REF_RGD_ID:11533931 Subarachnoid Hemorrhage ISO RGD:3186 9068941 mRNA:increased expression:parietal cortex, arteriole (rat) RGD PMID:11273938 , REF_RGD_ID:7794687 Sudden Hearing Loss ISO RGD:735618 9068941 DNA:snp:cds:p.E298D (rs1799983) (human) RGD PMID:23560644 , REF_RGD_ID:7771541 telangiectasis susceptibility ISO RGD:735618 9068941 associated with radiation treatment of Breast Neoplasms, DNA:polymorphisms RGD PMID:18027873 , REF_RGD_ID:2292067 Testis Reperfusion Injury ISO RGD:3186 9068941 protein:increased expression:testis RGD PMID:18205898 , REF_RGD_ID:2292105 Thromboembolism susceptibility ISO RGD:735618 9068941 DNA:repeats:intron RGD PMID:10531147 , REF_RGD_ID:5128481 Thrombotic Microangiopathies ISO RGD:3186 9068941 protein:decreased expression:kidney: RGD PMID:10908153 , REF_RGD_ID:11533936 transient cerebral ischemia ISO RGD:3186 9068941 protein:increased expression:serum (rat) RGD PMID:29298658 , REF_RGD_ID:13503353 transient cerebral ischemia treatment ISO RGD:3186 9068941 RGD PMID:28944915 more ... Transplant Rejection treatment ISO RGD:3186 9068941 RGD PMID:29218089 , REF_RGD_ID:13504718 type 2 diabetes mellitus ISO RGD:3186 9068941 RGD PMID:18356581 , REF_RGD_ID:2292097 urinary bladder cancer ISO RGD:735618 9068941 protein:increased expression:urinary bladder RGD PMID:10475345 , REF_RGD_ID:2292089 vasculitis susceptibility ISO RGD:735618 9068941 DNA:polymorphism:exon:p.E298D (human) RGD PMID:14583572 , REF_RGD_ID:7775052 Vaso-occlusive Crisis susceptibility ISO RGD:735618 9068941 associated with Anemia more ... RGD PMID:25263931 , REF_RGD_ID:11533931 Venous Thrombosis susceptibility ISO RGD:735618 9068941 associated with orthopedic surgery, DNA:SNP::rs1799983(human) RGD PMID:23922896 , REF_RGD_ID:11533639 Ventricular Dysfunction, Right ISO RGD:3186 9068941 associated with Hypertension, Pulmonary RGD PMID:16820570 , REF_RGD_ID:4892044 vulva cancer disease_progression ISO RGD:735618 9068941 DNA:repeat:intron RGD PMID:15196865 , REF_RGD_ID:2292078