Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3094
Gene Symbol: HINT1
HINT1
0.800 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 3094
Gene Symbol: HINT1
HINT1
0.800 Biomarker disease CTD_human
Entrez Id: 3094
Gene Symbol: HINT1
HINT1
0.800 GeneticVariation disease CLINVAR
Entrez Id: 5286
Gene Symbol: PIK3C2A
PIK3C2A
0.010 AlteredExpression disease BEFREE Isaacs's syndrome (IS), is a rare neurological disorder, characterized by sustained muscular activity, fasciculations, cramps, myokymia, excessive sweating, and occasional elevation of creatine phosphokinase (CPK) enzyme. 28660750 2018
Entrez Id: 3736
Gene Symbol: KCNA1
KCNA1
0.220 Biomarker disease RGD Kcna1-mutant rats dominantly display myokymia, neuromyotonia and spontaneous epileptic seizures. 22206926 2012
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2
0.100 Biomarker disease BEFREE Contactin-associated protein-2 antibodies occur with neuromyotonia and thymoma with the Morvan's syndrome in addition to Netrin 1 receptor antibodies but may not be responsible for peripheral nerve hyperexcitability. 28682959 2017
Entrez Id: 7063
Gene Symbol: THM
THM
0.010 Biomarker disease BEFREE Thymoma recurrence was more frequent in those with (4/5, 80%) than in those without (28/263, 10%, P < 0.001) neuromyotonia. 30714278 2019
Entrez Id: 3094
Gene Symbol: HINT1
HINT1
0.800 GeneticVariation disease BEFREE A case of neuromyotonia and axonal motor neuropathy: A report of a HINT1 mutation in the United States. 26182879 2015
Entrez Id: 3094
Gene Symbol: HINT1
HINT1
0.800 CausalMutation disease CLINVAR A case of neuromyotonia and axonal motor neuropathy: A report of a HINT1 mutation in the United States. 26182879 2015
Entrez Id: 3736
Gene Symbol: KCNA1
KCNA1
0.220 Biomarker disease MGD A mouse model of episodic ataxia type-1. 12612586 2003
Entrez Id: 3094
Gene Symbol: HINT1
HINT1
0.800 GeneticVariation disease BEFREE A Novel Variant in the HINT1 Gene in a Girl with Autosomal Recessive Axonal Neuropathy with Neuromyotonia: Thorough Neurological Examination Gives the Clue. 26760849 2016
Entrez Id: 9211
Gene Symbol: LGI1
LGI1
0.030 Biomarker disease BEFREE Although acquired autoimmune neuromyotonia (NMT) is associated with voltage-gated potassium channel (VGKC)-complex antibodies, to date there has been no systematic study of autoantibodies to the specific antigens leucine-rich glioma inactivated protein 1 (LGI1), contactin-associated protein 2 (CASPR2), and contactin 2 together with the full clinical syndrome, particularly pain and autonomic and central nervous system involvement. 30242309 2018
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2
0.100 Biomarker disease BEFREE Although acquired autoimmune neuromyotonia (NMT) is associated with voltage-gated potassium channel (VGKC)-complex antibodies, to date there has been no systematic study of autoantibodies to the specific antigens leucine-rich glioma inactivated protein 1 (LGI1), contactin-associated protein 2 (CASPR2), and contactin 2 together with the full clinical syndrome, particularly pain and autonomic and central nervous system involvement. 30242309 2018
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
0.010 Biomarker disease BEFREE Although acquired autoimmune neuromyotonia (NMT) is associated with voltage-gated potassium channel (VGKC)-complex antibodies, to date there has been no systematic study of autoantibodies to the specific antigens leucine-rich glioma inactivated protein 1 (LGI1), contactin-associated protein 2 (CASPR2), and contactin 2 together with the full clinical syndrome, particularly pain and autonomic and central nervous system involvement. 30242309 2018
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2
0.100 Biomarker disease BEFREE Anti-CASPR2 antibodies have been associated not only with limbic encephalitis but also with neuromyotonia and Morvan syndrome. 27432809 2017
Entrez Id: 1630
Gene Symbol: DCC
DCC
0.010 Biomarker disease BEFREE Antibodies against Netrin-1 receptors (DCC and UNC5a) and Caspr2 often coexist and associate with thymoma in patients with neuromyotonia and myasthenia gravis. 28251919 2017
Entrez Id: 90249
Gene Symbol: UNC5A
UNC5A
0.010 Biomarker disease BEFREE Antibodies against Netrin-1 receptors (DCC and UNC5a) and Caspr2 often coexist and associate with thymoma in patients with neuromyotonia and myasthenia gravis. 28251919 2017
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2
0.100 Biomarker disease BEFREE Antibodies against Netrin-1 receptors (DCC and UNC5a) and Caspr2 often coexist and associate with thymoma in patients with neuromyotonia and myasthenia gravis. 28251919 2017
Entrez Id: 9211
Gene Symbol: LGI1
LGI1
0.030 Biomarker disease BEFREE Autoantibodies against the extracellular domains of the voltage-gated potassium channel (VGKC) complex proteins, leucine-rich glioma-inactivated 1 (LGI1) and contactin-associated protein-2 (CASPR2), are found in patients with limbic encephalitis, faciobrachial dystonic seizures, Morvan's syndrome and neuromyotonia. 28115470 2017
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2
0.100 Biomarker disease BEFREE Autoantibodies against the extracellular domains of the voltage-gated potassium channel (VGKC) complex proteins, leucine-rich glioma-inactivated 1 (LGI1) and contactin-associated protein-2 (CASPR2), are found in patients with limbic encephalitis, faciobrachial dystonic seizures, Morvan's syndrome and neuromyotonia. 28115470 2017
Entrez Id: 3094
Gene Symbol: HINT1
HINT1
0.800 Biomarker disease BEFREE Axonal neuropathy with neuromyotonia: there is a HINT. 28007994 2017
Entrez Id: 3094
Gene Symbol: HINT1
HINT1
0.800 GeneticVariation disease BEFREE Based on the clinical presentation and molecular genetic analyses, ARAN-NM was diagnosed in both patients and NM_005340.6: c.112T > C; p.(Cys38Arg) and NM_005340.6: c.289G > A; p.(Val97Met) in HINT1 gene were believe to be causative for the disorder. 30006059 2019
Entrez Id: 3094
Gene Symbol: HINT1
HINT1
0.800 GeneticVariation disease BEFREE Biallelic mutations in the HINT1 gene were recently identified as the cause of axonal neuropathy with neuromyotonia. 26194197 2015
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
0.010 Biomarker disease BEFREE By EMG, we found the clinical and electrophysiological signs of neuromyotonia, that is, continuous spontaneous motor unit discharges, often in rhythmic patterns (myokymia), in P0 -/-, Pmp22 -/-, Trembler, Trembler-J, and Pmp22-overexpressing mice. 10586256 1999
Entrez Id: 9423
Gene Symbol: NTN1
NTN1
0.030 Biomarker disease BEFREE Coexisting Caspr2 and Netrin-1 receptor antibodies were associated with concurrent thymoma, myasthenia gravis, and neuromyotonia, often with Morvan syndrome (<i>p</i> = 0.009). 28251919 2017