HCRTR1, hypocretin receptor 1, 3061

N. diseases: 71; N. variants: 6
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma
0.010 Biomarker disease BEFREE Here we demonstrated by RT-PCR the expression of the OX2-R, but not the OX1-R, gene in 10 benign secreting pheochromocytomas. 11600547 2001
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
Adrenal Gland Pheochromocytoma
0.010 Biomarker disease BEFREE Here we demonstrated by RT-PCR the expression of the OX2-R, but not the OX1-R, gene in 10 benign secreting pheochromocytomas. 11600547 2001
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.020 GeneticVariation disease BEFREE In this study of American and Icelandic patients with narcolepsy, the authors found no significant association between narcolepsy and single-nucleotide polymorphisms in the genes for hypocretin or its two known receptors, hypocretin receptor-1 and hypocretin receptor-2. 11723285 2001
CUI: C0851578
Disease: Sleep Disorders
Sleep Disorders
0.010 Biomarker group BEFREE This evidence suggests that the structure of the OX2R gene, and its homologue, the OX1R gene, both members of the G protein-coupled receptor (GPCR) family, and the gene encoding the peptide ligands, the prepro-orexin/hypocretin gene, may be variables in the etiology of sleep disorders. 15274044 2004
CUI: C0001430
Disease: Adenoma
Adenoma
0.010 AlteredExpression group LHGDN All adenomas expressed OX1-R and OX2-R mRNAs, and real-time PCR showed that the expression of both receptors was up-regulated in adenomas, compared with normal adrenal cortex. 15797953 2005
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.320 GeneticVariation disease BEFREE Screening of the orexin signaling system detected a 408 isoleucine to valine mutation in HCRTR1 that showed significant genotypic association with polydipsic-hyponatremic schizophrenia (p = .012). 15978554 2005
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.320 Biomarker disease PSYGENET Screening of the orexin signaling system detected a 408 isoleucine to valine mutation in HCRTR1 that showed significant genotypic association with polydipsic-hyponatremic schizophrenia (p = .012). 15978554 2005
CUI: C0600427
Disease: Cocaine Dependence
Cocaine Dependence
0.310 Biomarker disease CTD_human Role for hypocretin in mediating stress-induced reinstatement of cocaine-seeking behavior. 16357203 2005
CUI: C0009171
Disease: Cocaine Abuse
Cocaine Abuse
0.300 Biomarker disease CTD_human Role for hypocretin in mediating stress-induced reinstatement of cocaine-seeking behavior. 16357203 2005
CUI: C0236736
Disease: Cocaine-Related Disorders
Cocaine-Related Disorders
0.300 Biomarker group CTD_human Role for hypocretin in mediating stress-induced reinstatement of cocaine-seeking behavior. 16357203 2005
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.320 GeneticVariation disease BEFREE [2005 Biol Psychiatry 58 401-407] reported an association between the 408Val allele of the orexin 1 receptor (HCRTR1) gene and polydipsia-hyponatremia in a sample of Japanese patients with SCZ. 17999203 2007
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.320 GeneticVariation disease LHGDN [2005 Biol Psychiatry 58 401-407] reported an association between the 408Val allele of the orexin 1 receptor (HCRTR1) gene and polydipsia-hyponatremia in a sample of Japanese patients with SCZ. 17999203 2007
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.320 Biomarker disease PSYGENET [2005 Biol Psychiatry 58 401-407] reported an association between the 408Val allele of the orexin 1 receptor (HCRTR1) gene and polydipsia-hyponatremia in a sample of Japanese patients with SCZ. 17999203 2007
CUI: C0020625
Disease: Hyponatremia
Hyponatremia
0.010 GeneticVariation phenotype BEFREE [2005 Biol Psychiatry 58 401-407] reported an association between the 408Val allele of the orexin 1 receptor (HCRTR1) gene and polydipsia-hyponatremia in a sample of Japanese patients with SCZ. 17999203 2007
CUI: C0085602
Disease: Polydipsia
Polydipsia
0.010 GeneticVariation phenotype BEFREE (2005) previously demonstrated an association between the 408Val allele of the HCRTR1 gene and polydipsia.In contrast with Meerabux et al. study, we found that the 408Ile allele was associated with polydipsia in our sample (chi2 = 8.00, df = 1, P = 0.0047; OR = 0.53; 95%CI = 0.34-0.83). 17999203 2007
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.020 AlteredExpression disease BEFREE To determine whether hypocretin receptor gene (hcrtR1 and hcrtR2) expression is affected after long-term hypocretin ligand loss in humans and animal models of narcolepsy. 18714784 2008
CUI: C0751362
Disease: Narcolepsy-Cataplexy Syndrome
Narcolepsy-Cataplexy Syndrome
0.010 AlteredExpression disease BEFREE Both sporadic narcoleptic dogs and human narcolepsy-cataplexy subjects showed a significant decrease in hcrtR1 expression, while declines in hcrtR2 expression were not significant in these cases. 18714784 2008
CUI: C0600427
Disease: Cocaine Dependence
Cocaine Dependence
0.310 Biomarker disease CTD_human Orexin/hypocretin is necessary for context-driven cocaine-seeking. 19591850 2010
CUI: C0009171
Disease: Cocaine Abuse
Cocaine Abuse
0.300 Biomarker disease CTD_human Orexin/hypocretin is necessary for context-driven cocaine-seeking. 19591850 2010
CUI: C0236736
Disease: Cocaine-Related Disorders
Cocaine-Related Disorders
0.300 Biomarker group CTD_human Orexin/hypocretin is necessary for context-driven cocaine-seeking. 19591850 2010
CUI: C0600427
Disease: Cocaine Dependence
Cocaine Dependence
0.310 Biomarker disease CTD_human Orexin A/hypocretin-1 selectively promotes motivation for positive reinforcers. 19741128 2009
CUI: C0009171
Disease: Cocaine Abuse
Cocaine Abuse
0.300 Biomarker disease CTD_human Orexin A/hypocretin-1 selectively promotes motivation for positive reinforcers. 19741128 2009
CUI: C0236736
Disease: Cocaine-Related Disorders
Cocaine-Related Disorders
0.300 Biomarker group CTD_human Orexin A/hypocretin-1 selectively promotes motivation for positive reinforcers. 19741128 2009
CUI: C0038587
Disease: Substance Withdrawal Syndrome
Substance Withdrawal Syndrome
0.310 Biomarker disease CTD_human Antagonism of orexin type 1 receptors in the locus coeruleus attenuates signs of naloxone-precipitated morphine withdrawal in rats. 20667500 2010
CUI: C0086189
Disease: Drug Withdrawal Symptoms
Drug Withdrawal Symptoms
0.300 Biomarker phenotype CTD_human Antagonism of orexin type 1 receptors in the locus coeruleus attenuates signs of naloxone-precipitated morphine withdrawal in rats. 20667500 2010