LGALS14, galectin 14, 56891

N. diseases: 35; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.020 Biomarker disease BEFREE The ClC-2 Cl- channel is thus a potential target for therapy in cystic fibrosis. 11401826 2001
CUI: C0017638
Disease: Glioma
Glioma
0.010 Biomarker disease BEFREE Transcripts for ClC-2 thru ClC-7 were detected in a human glioma cell line by PCR, whereas only ClC-2, ClC-3, and ClC-5 protein could be identified by Western blot. 12843258 2003
CUI: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy
0.030 Biomarker disease BEFREE Three different mutations in the CLCN2 gene, encoding the voltage-dependent homodimeric ClC-2 channel, have been associated with idiopathic generalized epilepsy (IGE). 15252188 2004
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.020 Biomarker disease BEFREE Further studies evaluating other phenotypes associated with CF may be useful in the future to assess the ability of CLC-2 to modify CF disease severity. 15507145 2004
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized
0.010 GeneticVariation disease BEFREE Functional evaluation of human ClC-2 chloride channel mutations associated with idiopathic generalized epilepsies. 15252188 2004
CUI: C0024115
Disease: Lung diseases
Lung diseases
0.010 Biomarker group BEFREE Fisher's analysis within this data set, did not demonstrate a significant relationship between the severity of lung disease and SNPs in the CLC-2 gene. 15507145 2004
CUI: C4552766
Disease: Miscarriage
Miscarriage
0.310 Biomarker disease CTD_human Gene expression in cultured endometrium from women with different outcomes following IVF. 18539642 2008
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion
0.300 Biomarker phenotype CTD_human Gene expression in cultured endometrium from women with different outcomes following IVF. 18539642 2008
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal
0.300 Biomarker phenotype CTD_human Gene expression in cultured endometrium from women with different outcomes following IVF. 18539642 2008
CUI: C3830362
Disease: Early Pregnancy Loss
Early Pregnancy Loss
0.300 Biomarker phenotype CTD_human Gene expression in cultured endometrium from women with different outcomes following IVF. 18539642 2008
CUI: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy
0.030 Biomarker disease BEFREE Heterozygous mutations in the CLCN2 gene encoding the voltage-gated chloride channel CLC2 have been identified in patients with idiopathic generalized epilepsy (IGE). 19191339 2009
CUI: C0009806
Disease: Constipation
Constipation
0.010 Biomarker phenotype BEFREE Lubiprostone, used clinically (b.i.d.) to treat constipation, has been reported to increase transepithelial Cl(-) transport in T84 cells by activating ClC-2 channels. 21140215 2011
CUI: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy
0.030 GeneticVariation disease BEFREE To test for a potential pathophysiological impact of ClC-2 regulation by ATP, we studied ClC-2 channels carrying naturally occurring sequence variants found in patients with idiopathic generalized epilepsy, G715E, R577Q, and R653T. 23632988 2013
MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS
0.030 Biomarker disease BEFREE GlialCAM brings MLC1 and the ClC-2 Cl(-) channel to cell-cell junctions, even though the role of ClC-2 in MLC disease remains incompletely understood. 23793458 2013
CUI: C0009319
Disease: Colitis
Colitis
0.010 Biomarker disease BEFREE The role of ClC-2 was investigated in TJ barrier function in dextran sodium sulfate (DSS)-induced colitis in ClC-2 knockout mice and ClC-2 knockdown intestinal Caco-2 cells. 24030525 2013
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.010 AlteredExpression disease BEFREE Furthermore, ClC-2 expression is markedly reduced in the colon of human patients with ulcerative colitis. 24030525 2013
CUI: C0027765
Disease: nervous system disorder
nervous system disorder
0.010 Biomarker group BEFREE We assessed the localisation of ClC-2 with immunohistochemistry and electron microscopy in post-mortem human brains of individuals without neurological disorders. 23707145 2013
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle
0.010 Biomarker disease BEFREE Thus, CLC‑2 may be a promising and potential novel therapeutic strategy for combating primary open‑angle glaucoma. 23934342 2013
CUI: C1720983
Disease: Channelopathies
Channelopathies
0.010 Biomarker disease BEFREE Nearly every aspect of ClC-2 is discussed in the review: molecular features, biophysical characteristics, pharmacological properties, cellular function, regulation of expression and function, and channelopathies. 24378849 2013
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
0.030 Biomarker disease BEFREE Disrupting MLC1 and GlialCAM and ClC-2 interactions in leukodystrophy entails glial chloride channel dysfunction. 24647135 2014
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.030 Biomarker group BEFREE Defects in the astrocytic membrane protein MLC1, the adhesion molecule GlialCAM or the chloride channel ClC-2 underlie human leukoencephalopathies. 24647135 2014
MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS
0.030 Biomarker disease BEFREE Our data unmask an unforeseen functional relationship between MLC1 and ClC-2 in vivo, which is probably mediated by GlialCAM, and suggest that ClC-2 participates in the pathogenesis of megalencephalic leukoencephalopathy with subcortical cysts. 24647135 2014
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
0.030 Biomarker disease BEFREE Mutations in the genes encoding the astrocytic protein MLC1, the cell adhesion molecule GlialCAM or the Cl(-) channel ClC-2 underlie human leukodystrophies. 26033718 2015
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 AlteredExpression disease BEFREE Modified AS1411-aptamer suppressed HCC cell growth in vitro and in vivo by up-regulating galectin-14 expressions. 27494117 2016
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
0.030 Biomarker disease BEFREE GlialCAM, a regulatory subunit of ClC-2 in glial cells and involved in the leukodystrophy megalencephalic leukoencephalopathy with subcortical cysts (MLC), increases the activity of a ClC-2 mutant by affecting ClC-2 gating and by stabilising the mutant at the plasma membrane. 28905383 2017