Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders
0.210 Biomarker group BEFREE The hyperpolarization-activated cyclic nucleotide-gated channel 1(HCN1) could be inhibited by the ketamine, a drug to alleviate depression and anxiety, and regulated the BDNF expression, however, the effects of ketamine in alleviating PTSD symptoms by regulating the HCN1-related BDNF have been poorly perceived. 29596995 2018
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders
0.210 Biomarker group RGD Our results suggest that HCN1 protein could be a potential target for treatment of anxiety and depression disorders. 22884333 2012
CUI: C0525045
Disease: Mood Disorders
Mood Disorders
0.200 Biomarker group RGD Enhancement of dorsal hippocampal activity by knockdown of HCN1 channels leads to anxiolytic- and antidepressant-like behaviors. 22884333 2012
Child Development Disorders, Pervasive
0.100 GeneticVariation group GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
CUI: C0085584
Disease: Encephalopathies
Encephalopathies
0.100 Biomarker group HPO
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
0.100 Biomarker group HPO
CUI: C0442874
Disease: Neuropathy
Neuropathy
0.020 Biomarker group BEFREE Selective HCN1 block as a strategy to control oxaliplatin-induced neuropathy. 29339292 2018
CUI: C0442874
Disease: Neuropathy
Neuropathy
0.020 AlteredExpression group BEFREE In the current study, we used a neuropathy rat model induced by chronic constriction injury (CCI) of sciatic nerve to evaluate the change of expression of HCN1/HCN2 mRNA in peripheral nerve and spinal cord. 27901476 2017
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm
0.010 Biomarker group BEFREE In this study, we investigated whether single nucleotide polymorphisms (SNPs) identified by genome-wide association study (GWAS) (MAP3K1, FGFR2, TNRC9, HCN1, and 5p12), and SNPs involved in the metabolism of estrogen (CYP19, COMT, ESR1, and UGT1A1), tamoxifen (CYP2C9, CYP2C19, CYP3A5, and CYP2D6), and chemotherapeutic agents (ABCB1, ALDH3A1, and CYP2B6) are associated with the prognoses of 414 hormone receptor (HR)-positive early breast cancers with negative or 1 to 3 nodal metastases. 28178648 2017
CUI: C0036572
Disease: Seizures
Seizures
0.440 Biomarker phenotype HPO
CUI: C0036572
Disease: Seizures
Seizures
0.440 AlteredExpression phenotype BEFREE Aberrant SUMOylation has been linked to neurological diseases that also display alterations in HCN1 and HCN2 channel expression, such as seizures and Parkinson's disease. 28127275 2016
CUI: C0036572
Disease: Seizures
Seizures
0.440 Biomarker phenotype BEFREE The Hcn1-knockout rats were also more vulnerable to pentylenetetrazol-induced acute convulsions. 30408474 2019
CUI: C0036572
Disease: Seizures
Seizures
0.440 Biomarker phenotype BEFREE Two experiments were performed: (1) cortical expression of ion channels Nav1.1, Nav1.6, and HCN1 (previously shown to be dysregulated in WAG/Rij) measured by immunocytochemistry in adult treated rats; and (2) electroencephalogram (EEG) recordings to measure seizure severity at serial time points after stopping the treatment. 18070091 2008
CUI: C0036572
Disease: Seizures
Seizures
0.440 GeneticVariation phenotype BEFREE In contrast, no change in HCN1 transcript was noted at an age prior to seizure expression or in a SWD-free model in which the R43Q mutation has been crossed into a seizure-resistant genetic background. 24368169 2014
CUI: C0036572
Disease: Seizures
Seizures
0.440 Biomarker phenotype CTD_human Therefore, down-regulation of HCN1 associated with human epilepsy and rodent models may be a contributing factor in seizure behavior. 20384728 2010
CUI: C0004134
Disease: Ataxia
Ataxia
0.400 Biomarker phenotype HPO
CUI: C0004134
Disease: Ataxia
Ataxia
0.400 Biomarker phenotype CTD_human In this study we showed that the motor coordination impairment observed in HCN1-/- mice is paralleled by a decline of GABA content in the cerebellum. 19747469 2009
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
0.400 Biomarker phenotype CTD_human Gabapentin treatment improves motor coordination in a mice model of progressive ataxia. 19747469 2009
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
0.400 Biomarker phenotype HPO
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
0.400 Biomarker phenotype CTD_human Increased seizure severity and seizure-related death in mice lacking HCN1 channels. 20384728 2010
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
0.400 Biomarker phenotype HPO
CUI: C4048158
Disease: Convulsions
Convulsions
0.310 Biomarker phenotype CTD_human Increased seizure severity and seizure-related death in mice lacking HCN1 channels. 20384728 2010
CUI: C4048158
Disease: Convulsions
Convulsions
0.310 Biomarker phenotype BEFREE The Hcn1-knockout rats were also more vulnerable to pentylenetetrazol-induced acute convulsions. 30408474 2019
CUI: C4317109
Disease: Epileptic Seizures
Epileptic Seizures
0.310 Biomarker phenotype CTD_human Increased seizure severity and seizure-related death in mice lacking HCN1 channels. 20384728 2010
CUI: C4317109
Disease: Epileptic Seizures
Epileptic Seizures
0.310 Biomarker phenotype BEFREE Taken together, HCN1 is proposed to play an important role in the molecular linkage between epileptic seizures and Aβ generation, and in the aggravation of sporadic AD. 23034178 2012