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: 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: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.010 Biomarker disease BEFREE Our aim was to investigate the potential role of a ClC-2 chloride channel activator, lubiprostone, which is reported to have beneficial effects on LGS, in the development of atherosclerosis in apolipoprotein E-deficient (ApoE-/-) mice. 31206525 2019
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.010 Biomarker disease BEFREE Our aim was to investigate the potential role of a ClC-2 chloride channel activator, lubiprostone, which is reported to have beneficial effects on LGS, in the development of atherosclerosis in apolipoprotein E-deficient (ApoE-/-) mice. 31206525 2019
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: C0267509
Disease: Chronic idiopathic constipation
Chronic idiopathic constipation
0.010 Biomarker phenotype BEFREE Lubiprostone is a ClC-2 chloride channel activator approved for the treatment of chronic idiopathic constipation (CIC) and opioid-induced constipation (OIC) in adults and irritable bowel syndrome with constipation (IBS-C) in women. 28849329 2017
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: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.010 Biomarker disease BEFREE Paraffin-embedded tissues from CHMs and control placentas were used for tissue microarray (TMA) construction, immunohistochemistry, and immunoscoring for galectin-14. 31658584 2019
CUI: C1384514
Disease: Conn Syndrome
Conn Syndrome
0.010 Biomarker disease BEFREE We now show that almost all known PA-associated CLCN2 mutations markedly increase ClC-2 chloride currents and generate knock-in mice expressing a constitutively open ClC-2 Cl<sup>-</sup> channel as mouse model for PA. 31615979 2019
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: 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: 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: C0747845
Disease: early pregnancy
early pregnancy
0.010 AlteredExpression phenotype BEFREE In conclusion, these results show that Gal-13 and Gal-14 already provide an immunoprivileged environment at the maternal-fetal interface during early pregnancy, and their reduced expression is related to miscarriages. 31275299 2019
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: 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: C3713420
Disease: Familial Hyperaldosteronism
Familial Hyperaldosteronism
0.010 GeneticVariation disease BEFREE Elevated aldosterone and blood pressure in a mouse model of familial hyperaldosteronism with ClC-2 mutation. 31727896 2019
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.010 AlteredExpression phenotype BEFREE Our results showed that ClC-2 mRNA and protein expressions in GDM group were significantly increased in white matter of fetal rats after E18 stage, and elevated the level of TNF-α and iNOS in white matter at P0 and P3 stage of newborn rats. 28255270 2017
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: 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: C0020428
Disease: Hyperaldosteronism
Hyperaldosteronism
0.010 GeneticVariation disease BEFREE In the adrenal, ClC-2 has been demonstrated to localize predominantly to the zona glomerulosa (ZG), and functional analysis suggests that mutations in ClC-2 predispose ZG cells to depolarization, thus leading to calcium influx via activation of voltage-gated calcium channels and increased aldosterone production. 30949771 2019
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
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: 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
Irritable bowel syndrome with constipation
0.010 Biomarker disease BEFREE Lubiprostone is a ClC-2 chloride channel activator approved for the treatment of chronic idiopathic constipation (CIC) and opioid-induced constipation (OIC) in adults and irritable bowel syndrome with constipation (IBS-C) in women. 28849329 2017
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
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