Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0522254
Disease: Analgesic Overuse Headache
Analgesic Overuse Headache
0.010 GeneticVariation disease BEFREE When genotype distribution for RAMP1 rs7590387 was compared between healthy controls (n = 209) and MOH patients, carriers of rs7590387GG were found at lower risk of developing MOH (OR: 0.43, 95%CI: 0.22-0.85, P = 0.011). 25881990 2015
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.040 AlteredExpression group BEFREE We hypothesized that upregulation of RAMP1 would favorably enhance autonomic regulation and attenuate hypertension. 20100989 2010
CUI: C0338480
Disease: Common Migraine
Common Migraine
0.010 GeneticVariation disease BEFREE We herein investigated the role of polymorphisms in calcitonin gene-related peptide (CGRP)-related genes looking at the association of rs3781719 (T > C) in the calcitonin gene-related polypeptide-alpha (CALCA) gene and of rs3754701 (T > A) and rs7590387 (C > G) at the receptor activity modifying 1 (RAMP1) locus with triptan response in patients with migraine without aura (MwoA). 25881990 2015
CUI: C0334606
Disease: Fibrous Meningioma
Fibrous Meningioma
0.010 AlteredExpression disease BEFREE We have identified several genes (BMPR1B, DMD, RAMP1) with expression signatures specific for fibrous meningiomas. 18365142 2008
CUI: C0036690
Disease: Septicemia
Septicemia
0.010 AlteredExpression disease BEFREE We examined the expression of CRLR and RAMP1, 2, and 3 in several tissues from mice in a sepsis model induced by lipopolysaccharide (LPS). 10777702 2000
CUI: C0243026
Disease: Sepsis
Sepsis
0.010 AlteredExpression disease BEFREE We examined the expression of CRLR and RAMP1, 2, and 3 in several tissues from mice in a sepsis model induced by lipopolysaccharide (LPS). 10777702 2000
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
0.010 Biomarker disease BEFREE Using a RAMP1 knockout-mouse (RAMP1<sup>-/-</sup>) we examined the role of the CGRP-receptor in the acute-phase of cerulein-induced pancreatitis. 31109903 2019
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.010 AlteredExpression disease LHGDN Unaltered mRNA expression of calcitonin-like receptor and receptor activity modifying proteins in human arteries in stroke and myocardial infarction. 18198792 2007
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 AlteredExpression disease LHGDN Unaltered mRNA expression of calcitonin-like receptor and receptor activity modifying proteins in human arteries in stroke and myocardial infarction. 18198792 2007
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 AlteredExpression group LHGDN Unaltered mRNA expression of calcitonin-like receptor and receptor activity modifying proteins in human arteries in stroke and myocardial infarction. 18198792 2007
CUI: C0004096
Disease: Asthma
Asthma
0.020 AlteredExpression disease BEFREE To determine whether functional RAMP1 is expressed by airway epithelial cells and whether there are alterations in asthma. 20933260 2010
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.060 PosttranslationalModification group BEFREE This study provides the first evidence that DNA methylation at RAMP1 promoter might play a role in migraine. 26501962 2015
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.010 Biomarker disease BEFREE These results suggested that this T-A-T RAMP1 gene haplotype might have utility as a genetic marker for EH and that the RAMP1 gene or a neighbouring gene may be associated with increased susceptibility to EH. 28181496 2017
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.060 Biomarker group BEFREE These results demonstrate that RAMP1 is functionally rate limiting for CGRP receptor activity in the trigeminal ganglion, which raises the possibility that elevated RAMP1 might sensitize some individuals to CGRP actions in migraine. 17344407 2007
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 Biomarker phenotype BEFREE These data provide novel insights into the role of RAMP1 in promoting prostate tumorigenesis and support the potential of RAMP1 as a novel biomarker and possible therapeutic target in prostate cancer. 23867798 2013
CUI: C0009319
Disease: Colitis
Colitis
0.010 Biomarker disease BEFREE The study compared the severity of colitis in wild-type (WT) mice, mice treated with a CGRP receptor antagonist (CGRP<sub>8-37</sub> ), and RAMP1 knockout (<sup>-/-</sup> ) mice. 27513455 2017
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.010 GeneticVariation disease BEFREE The results suggest that the T-A-C haplotype is a genetic marker for CI, and that RAMP1 or neighbouring genes are associated with increased susceptibility to CI. 19710695 2010
CUI: C0747845
Disease: early pregnancy
early pregnancy
0.010 Biomarker phenotype BEFREE The present study was designed to determine the cellular localization of CALCA and its receptor components, CALCRL and receptor activity modifying protein 1 (RAMP1), at the human implantation site during early pregnancy; to assess whether CALCA regulates in vitro angiogenesis of human endothelial cells; and to examine whether CALCA can improve angiogenic imbalance in preeclamptic placental explants. 17267696 2007
CUI: C0265191
Disease: Chronic acquired lymphedema
Chronic acquired lymphedema
0.010 Biomarker disease BEFREE The present study examined whether RAMP1 plays a role in increased lymphangiogenesis during secondary lymphedema. 29078910 2017
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.060 AlteredExpression group BEFREE The neuropeptide CGRP, acting through the G-protein coupled receptor CALCRL and its coreceptor RAMP1, plays a key role in migraines, which has led to the clinical development of several inhibitory compounds. 31756985 2019
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.010 AlteredExpression phenotype BEFREE The findings for this study are: 1) relaxation responses of OA were higher for bradykinin (78.55 ± 3.91 vs 52.67 ± 2.19; P < .05) in pregnancy with FGR compared to the normal, 2) relaxation response of OA segments to CGRP was similar with no change in the expression of G-protein couple receptor-calcitonin receptor-like receptor complex in normal healthy pregnancy and pregnancy complicated by FGR, 3) maximal relaxation response of OA were significantly (P < .05) lower for both ADM (18.2 ± 6.7 vs 38 ± 2.5) and ADM2 (26.9 ± 6.7 vs 48 ± 2.6) along with decreases in their respective ligand-receptor complex in FGR compared to the normal pregnancies, 4) expression of calcitonin receptor-like receptor mRNA was higher but its immunoreactivity was lower in OA from FGR pregnancy compared to the normal, and 5) mRNA and protein levels of RAMP1, RAMP2, and RAMP3 were lower in OA isolated from FGR pregnancies compared to the normal. 27258937 2016
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.100 GeneticVariation disease GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.100 GeneticVariation disease GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
CUI: C0023893
Disease: Liver Cirrhosis, Experimental
Liver Cirrhosis, Experimental
0.300 Biomarker disease CTD_human Systems level analysis and identification of pathways and networks associated with liver fibrosis. 25380136 2014
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.010 Biomarker disease BEFREE Role of receptor activity modifying protein 1 in function of the calcium sensing receptor in the human TT thyroid carcinoma cell line. 24454825 2014