alcoholic hepatitis ISO RGD:731070 9068941 mRNA:decreased expression:liver RGD PMID:17258719 , REF_RGD_ID:1601135 allergic disease susceptibility ISO RGD:731070 9068941 DNA:polymorphism: :p.M235T human RGD PMID:10200023 , REF_RGD_ID:8142344 Alzheimer's disease ISO RGD:731070 9068941 protein:increased expression:cerebrospinal fluid RGD PMID:21297254 , REF_RGD_ID:5129180 Anaphylaxis ISO RGD:731070 9068941 RGD PMID:1422942 , REF_RGD_ID:8548893 anti-basement membrane glomerulonephritis ISO RGD:2069 9068941 mRNA more ... RGD PMID:7550093 , REF_RGD_ID:11039051 anti-basement membrane glomerulonephritis ISO RGD:2069 9068941 protein:increased expression:kidney, urine RGD PMID:21282555 , REF_RGD_ID:5129185 Aortic Calcification ISO RGD:2069 9068941 RGD PMID:23291307 , REF_RGD_ID:8549476 Aortic Coarctation treatment ISO RGD:731070 9068941 DNA:polymorphism: :c.704T>C human RGD PMID:21450583 , REF_RGD_ID:13432358 atherosclerosis treatment ISO RGD:2069 9068941 associated with Hypertension RGD PMID:22977667 , REF_RGD_ID:8549467 atrial fibrillation ISO RGD:731070 9068941 DNA:polymorphisms, haplotypes:promoter:multiple RGD PMID:18239384 , REF_RGD_ID:8548862 breast cancer susceptibility ISO RGD:731070 9068941 DNA:polymorphism: :p.M235T human RGD PMID:16823505 , REF_RGD_ID:8548861 breast cancer ISO RGD:731070 9068941 protein:increased expression:serum RGD PMID:23374911 , REF_RGD_ID:8548901 breast cancer ISO RGD:731070 9068941 DNA:polymorphisms more ... RGD PMID:23828384 , REF_RGD_ID:8548866 Cardiomegaly ISO RGD:2069 9068941 RGD PMID:21367774 more ... Cardiomegaly ISO RGD:10118 9068941 RGD PMID:19779471 , REF_RGD_ID:8548902 cardiovascular system disease no_association ISO RGD:731070 9068941 RGD PMID:8523390 , REF_RGD_ID:1566492 carotid artery disease susceptibility ISO RGD:731070 9068941 DNA:polymorphism: :p.M235T RGD PMID:17220293 , REF_RGD_ID:1601136 cerebrovascular disease susceptibility ISO RGD:731070 9068941 DNA:polymorphism: :p.M235T RGD PMID:17220293 , REF_RGD_ID:1601136 Chronic Intermittent Hypoxia ISO RGD:2069 9068941 mRNA, protein:increased expression:type I cell of carotid body RGD PMID:24036592 , REF_RGD_ID:11039031 chronic myeloid leukemia ISO RGD:731070 9068941 RGD PMID:19761684 , REF_RGD_ID:11039056 congestive heart failure onset ISO RGD:731070 9068941 DNA:polymorphisms: :p.M235T, p.T174M human RGD PMID:17145981 , REF_RGD_ID:1601140 congestive heart failure severity ISO RGD:731070 9068941 protein:increased expression:serum RGD PMID:24465706 , REF_RGD_ID:11039412 congestive heart failure treatment ISO RGD:2069 9068941 RGD PMID:21963897 , REF_RGD_ID:8549482 corneal neovascularization ISO RGD:10118 9068941 mRNA, protein:increased expression:cornea RGD PMID:18829859 , REF_RGD_ID:8548897 Diabetic Nephropathies no_association ISO RGD:731070 9068941 associated with Diabetes Mellitus more ... RGD PMID:11938025 , REF_RGD_ID:8548885 Diabetic Nephropathies ISO RGD:731070 9068941 associated with Diabetes Mellitus more ... RGD PMID:10862638 more ... Diabetic Nephropathies disease_progression ISO RGD:731070 9068941 associated with Diabetes Mellitus more ... RGD PMID:19014923 , REF_RGD_ID:11039058 diabetic retinopathy treatment ISO RGD:10118 9068941 associated with Diabetes Mellitus, Experimental RGD PMID:21792177 , REF_RGD_ID:8548900 diabetic retinopathy ISO RGD:731070 9068941 associated with Diabetes Mellitus more ... RGD PMID:10862638 , REF_RGD_ID:8548872 diabetic retinopathy treatment ISO RGD:2069 9068941 associated with Diabetes Mellitus, Experimental RGD PMID:21792177 , REF_RGD_ID:8548900 diffuse scleroderma ISO RGD:731070 9068941 protein:increased expression:serum RGD PMID:14730619 , REF_RGD_ID:8548886 dilated cardiomyopathy no_association ISO RGD:731070 9068941 DNA:polymorphisms: :p.T174M, p.M235T human RGD PMID:9270088 , REF_RGD_ID:1566491 dilated cardiomyopathy treatment ISO RGD:2069 9068941 RGD PMID:22120037 , REF_RGD_ID:8549486 Fabry disease severity ISO RGD:731070 9068941 DNA:polymorphism:promoter: RGD PMID:24020479 , REF_RGD_ID:13432161 Fetal Growth Retardation ISO RGD:731070 9068941 RGD PMID:20530295 , REF_RGD_ID:13432363 Fetal Growth Retardation ISO RGD:2069 9068941 mRNA more ... RGD PMID:26270574 , REF_RGD_ID:11538508 Fibrosis ISO RGD:2069 9068941 RGD PMID:21367774 , REF_RGD_ID:5129174 focal segmental glomerulosclerosis ISO RGD:2069 9068941 RGD PMID:21357516 , REF_RGD_ID:5129175 gastric ulcer treatment ISO RGD:2069 9068941 RGD PMID:24231511 , REF_RGD_ID:11039418 glomerulonephritis disease_progression ISO RGD:2069 9068941 RGD PMID:15888567 , REF_RGD_ID:13432360 Hemorrhage ISO RGD:731070 9068941 associated with Premature Birth, DNA:polymorphism:promoter:-6G>A human RGD PMID:19733287 , REF_RGD_ID:11039046 Henoch-Schoenlein purpura ISO RGD:731070 9068941 DNA:missense mutation:cds:p.M235T human RGD PMID:16521052 , REF_RGD_ID:11039045 Henoch-Schoenlein purpura severity ISO RGD:731070 9068941 DNA:missense mutation:cds:p.T174M human RGD PMID:20702504 , REF_RGD_ID:11039055 hydronephrosis ISO RGD:10118 9068941 RGD PMID:12399452 , REF_RGD_ID:1300273 hydronephrosis treatment ISO RGD:731070 9068941 RGD PMID:12399452 , REF_RGD_ID:1300273 hyperinsulinism ISO RGD:731070 9068941 associated with obesity, DNA:polymorphism: :p.M235T RGD PMID:16713443 , REF_RGD_ID:1601142 hypertension susceptibility ISO RGD:731070 9068941 DNA:polymorphism:promoter:-20C>A human RGD PMID:17161775 , REF_RGD_ID:1601139 hypertension treatment ISO RGD:2069 9068941 RGD PMID:19932924 , REF_RGD_ID:8549469 hypertension ISO RGD:731070 9068941 DNA:polymorphisms: :p.T174M, p.M235T human RGD PMID:1394429 , REF_RGD_ID:1300393 hypertension ISO RGD:2069 9068941 RGD PMID:12468106 more ... hypertension ISO RGD:10118 9068941 RGD PMID:19779471 , REF_RGD_ID:8548902 hypertension no_association ISO RGD:731070 9068941 DNA:polymorphisms: :-6G>A more ... RGD PMID:16514903 , REF_RGD_ID:1601143 hypertension susceptibility ISO RGD:731070 9068941 DNA:polymorphisms: :p.T174M, p.M235T human RGD PMID:16739866 , REF_RGD_ID:1601141 hypertension ISO RGD:2069 9068941 protein:increased expression:plasma, urine RGD PMID:21346625 , REF_RGD_ID:5129176 hypertension susceptibility ISO RGD:731070 9068941 DNA:polymorphism: :p.M235T RGD PMID:17334527 , REF_RGD_ID:1601130 hypertension ISO RGD:731070 9068941 DNA:polymorphism: :p.M268T human RGD PMID:21312059 , REF_RGD_ID:5129166 Hypertensive Nephropathy treatment ISO RGD:2069 9068941 RGD PMID:22089474 , REF_RGD_ID:8548895 hypertrophic cardiomyopathy susceptibility ISO RGD:731070 9068941 DNA:polymorphism:cds:p.M235Thuman RGD PMID:9023164 , REF_RGD_ID:13432163 hypertrophic cardiomyopathy no_association ISO RGD:731070 9068941 DNA:polymorphisms: :p.T174M, p.M235T human RGD PMID:9270088 , REF_RGD_ID:1566491 Hypotension ISO RGD:10118 9068941 RGD PMID:9466969 , REF_RGD_ID:737778 impotence treatment ISO RGD:2069 9068941 RGD PMID:17616753 , REF_RGD_ID:8548892 inflammatory bowel disease ISO RGD:731070 9068941 DNA:polymorphism: :p.M235T human RGD PMID:20717043 , REF_RGD_ID:11039049 intermediate coronary syndrome ISO RGD:731070 9068941 mRNA:increased expression:myocardium RGD PMID:11451295 , REF_RGD_ID:8548894 Intestinal Reperfusion Injury ISO RGD:2069 9068941 protein:increased expression:plasma RGD PMID:15001561 , REF_RGD_ID:13515113 liver cirrhosis ISO RGD:2069 9068941 RGD PMID:21873937 , REF_RGD_ID:8549465 Mammary Neoplasms, Experimental treatment ISO RGD:731070 9068941 RGD PMID:20837666 , REF_RGD_ID:5129167 Mammary Neoplasms, Experimental treatment ISO RGD:10118 9068941 RGD PMID:20837666 , REF_RGD_ID:5129167 Mammary Neoplasms, Experimental treatment ISO RGD:2069 9068941 RGD PMID:20837666 , REF_RGD_ID:5129167 meconium aspiration syndrome ISO RGD:2069 9068941 mRNA:increased expression:lung RGD PMID:14605247 , REF_RGD_ID:11039054 Metabolic Syndrome ISO RGD:2069 9068941 mRNA, protein:increased expression:adipose tissue RGD PMID:17260464 , REF_RGD_ID:1601134 middle cerebral artery infarction ISO RGD:2069 9068941 protein:increased expression:brain, serum RGD PMID:24090950 , REF_RGD_ID:9685436 mitral valve prolapse severity ISO RGD:731070 9068941 associated with Marfan Syndrome, DNA:haplotype:cds: p.M235Thuman RGD PMID:17379330 , REF_RGD_ID:13432357 multiple sclerosis ISO RGD:731070 9068941 protein:decreased expression:brain, astrocyte: RGD PMID:17715340 , REF_RGD_ID:13432361 myocardial infarction ISO RGD:2069 9068941 RGD PMID:21167013 , REF_RGD_ID:5129191 myocardial infarction ISO RGD:731070 9068941 associated with Coronary Artery Disease, DNA:polymorphism: :p.M235T human RGD PMID:11393670 , REF_RGD_ID:1566452 myocardial infarction susceptibility ISO RGD:731070 9068941 associated with hypertension, DNA:polymorphism: :p.M235T RGD PMID:17299437 , REF_RGD_ID:1601132 obesity ISO RGD:731070 9068941 DNA:polymorphism: :p.M235T RGD PMID:16713443 , REF_RGD_ID:1601142 obesity susceptibility ISO RGD:731070 9068941 DNA:polymorphism: :p.T174M RGD PMID:16514903 , REF_RGD_ID:1601143 otosclerosis ISO RGD:731070 9068941 DNA:missense mutation:cds:p.M235T human RGD PMID:18491423 , REF_RGD_ID:8548860 otosclerosis no_association ISO RGD:731070 9068941 DNA:missense mutation:cds:p.M235T rs699 human RGD PMID:19503013 , REF_RGD_ID:8548871 polycystic kidney disease ISO RGD:2069 9068941 RGD PMID:20798958 , REF_RGD_ID:12879406 pre-eclampsia ISO RGD:731070 9068941 DNA:polymorphism: :p.M235T human RGD PMID:8513325 , REF_RGD_ID:1300394 pre-eclampsia ISO RGD:731070 9068941 RGD PMID:20530295 , REF_RGD_ID:13432363 prediabetes syndrome ISO RGD:2069 9068941 associated with Diabetes Mellitus more ... RGD PMID:23322513 , REF_RGD_ID:8549461 Pregnancy-Induced Hypertension ISO RGD:2069 9068941 RGD PMID:17977916 , REF_RGD_ID:8548898 primary biliary cholangitis ISO RGD:2069 9068941 protein:increased expression:plasma RGD PMID:17532087 , REF_RGD_ID:9685452 pulmonary edema ISO RGD:731070 9068941 DNA:polymorphism: :p.M235T human RGD PMID:21393362 , REF_RGD_ID:5129160 pulmonary fibrosis treatment ISO RGD:2069 9068941 RGD PMID:24168260 , REF_RGD_ID:11039408 pulmonary hypertension ISO RGD:2069 9068941 RGD PMID:21381494 , REF_RGD_ID:5129162 Puromycin Aminonucleoside Nephrosis ISO RGD:2069 9068941 RGD PMID:8446257 , REF_RGD_ID:11039400 retinal vasculitis ISO RGD:10118 9068941 RGD PMID:19834028 , REF_RGD_ID:11039401 sciatic neuropathy ISO RGD:2069 9068941 RGD PMID:20886512 , REF_RGD_ID:5129198 sick sinus syndrome ISO RGD:731070 9068941 DNA:SNP:promoter:-6G>A human RGD PMID:22242192 , REF_RGD_ID:8548870 skin melanoma ISO RGD:731070 9068941 protein:increased expression:serum RGD PMID:19394758 , REF_RGD_ID:8548874 Stroke susceptibility ISO RGD:731070 9068941 associated with hypertension, DNA:polymorphism: :p.M235T RGD PMID:17299437 , REF_RGD_ID:1601132 Stroke susceptibility ISO RGD:731070 9068941 associated with sickle cell anemia, DNA:repeat:exon: RGD PMID:11754397 , REF_RGD_ID:11039048 systemic scleroderma ISO RGD:731070 9068941 protein:decreased expression:plasma RGD PMID:17360781 , REF_RGD_ID:8548889 temporal lobe epilepsy ISO RGD:2069 9068941 RGD PMID:22542773 , REF_RGD_ID:8549466 transient cerebral ischemia ISO RGD:2069 9068941 RGD PMID:21934531 , REF_RGD_ID:8549480 type 2 diabetes mellitus ISO RGD:731070 9068941 mRNA more ... RGD PMID:17170378 , REF_RGD_ID:1601138 type 2 diabetes mellitus no_association ISO RGD:731070 9068941 DNA:polymorphism: :p.T174M, p.M235T human RGD PMID:9258285 , REF_RGD_ID:8548863