MYL9, myosin light chain 9, 10398

N. diseases: 52; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
0.010 Biomarker disease BEFREE Expression pattern and prognostic significance of myosin light chain 9 (MYL9): a novel biomarker in glioblastoma. 31270134 2019
CUI: C0280099
Disease: Adult Solid Neoplasm
Adult Solid Neoplasm
0.010 Biomarker group BEFREE MYL9 protein in 136 primary ESCC tissues and other types of solid tumor was detected using immunohistochemistry. 28388691 2017
CUI: C0750927
Disease: Apraxia, Developmental Verbal
Apraxia, Developmental Verbal
0.010 Biomarker disease BEFREE After inhibiting MLCK activity by using its specific inhibitor ML-7, the ER stress activator Tm failed to activate the MLCK/MLC2 pathway and could neither trigger CAS in mice nor induce VSMCs contraction in vitro. 29378169 2018
CUI: C1527311
Disease: Brain Edema
Brain Edema
0.300 Biomarker phenotype CTD_human Inhibition of the myosin light chain kinase prevents hypoxia-induced blood-brain barrier disruption. 17419808 2007
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 AlteredExpression disease BEFREE Second, using the total RNA and protein extracted from lung cancer tissues (n = 240), adjacent non-cancer tissues (n = 240), and normal lung tissues (n = 300), we examined the MYLK and MYL9 expression levels by quantitative real-time PCR and Western blot. 25179839 2014
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.010 GeneticVariation group BEFREE Pseudo-phosphorylation of cardiac myosin regulatory light chain (RLC) has never been examined as a rescue method to alleviate a cardiomyopathy phenotype brought about by a disease causing mutation in the myosin RLC. 24374283 2014
Cardiomyopathy, Hypertrophic, Familial
0.030 GeneticVariation disease BEFREE This study focuses on the aspartic acid to valine substitution (D166V) in the myosin RLC shown to be associated with a malignant phenotype of familial hypertrophic cardiomyopathy (FHC). 24374283 2014
Cardiomyopathy, Hypertrophic, Familial
0.030 PosttranslationalModification disease BEFREE Our data suggest that myosin RLC phosphorylation may have important translational implications for the treatment of RLC mutations-induced HCM and possibly play a role in other disease settings accompanied by depressed Ser15-RLC phosphorylation. 31101927 2019
Cardiomyopathy, Hypertrophic, Familial
0.030 GeneticVariation disease BEFREE The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice. 16076902 2005
CUI: C0006114
Disease: Cerebral Edema
Cerebral Edema
0.300 Biomarker phenotype CTD_human Inhibition of the myosin light chain kinase prevents hypoxia-induced blood-brain barrier disruption. 17419808 2007
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma
0.010 Biomarker disease BEFREE Expression pattern and prognostic significance of myosin light chain 9 (MYL9): a novel biomarker in glioblastoma. 31270134 2019
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma
0.010 AlteredExpression disease BEFREE In this report, we show that when human osteosarcoma derived clonal cells (TE 85 clone F-5) (HOS), which are immortalized and nontumorigenic, undergo transformation following infection by Kirsten murine sarcoma virus (K-HOS) or by a chemical carcinogen [N-methyl-N-nitro-N-nitrosoguanidine (MNNG-HOS)], the smooth muscle MLC-2 mRNA is repressed. 1599878 1992
CUI: C0279068
Disease: Childhood Solid Neoplasm
Childhood Solid Neoplasm
0.010 Biomarker phenotype BEFREE MYL9 protein in 136 primary ESCC tissues and other types of solid tumor was detected using immunohistochemistry. 28388691 2017
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.030 AlteredExpression disease BEFREE MBNL1-AS1 and MYL9 were poorly expressed in colon cancer. 31255531 2020
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.030 GeneticVariation disease BEFREE As an example, IG-SVM achieved a classification accuracy of 90.32% for colon cancer, which is difficult to be accurately classified, only based on three genes including CSRP1, MYL9, and GUCA2B. 29246519 2017
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.030 Biomarker disease BEFREE Colon cancer cell-derived 12(S)-HETE induces the retraction of cancer-associated fibroblast via MLC2, RHO/ROCK and Ca<sup>2+</sup> signalling. 28013338 2017
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 Biomarker disease BEFREE The significance for pVHL function of two further genes upregulated by wild-type pVHL was initially unclear, but re-expression of GNG4 (G protein gamma-4 subunit/guanine nucleotide-binding protein-4) and MLC2 (myosin light chain) in a RCC cell line suppressed tumour cell growth. pVHL regulation of CDKN1C, SPARC and GNG4 was not mimicked by hypoxia, whereas for six of 11 novel targets analysed (including DOC-2/DAB2 and MLC2) the effects of pVHL inactivation and hypoxia were similar. 15824735 2005
CUI: C0750970
Disease: Cytotoxic Brain Edema
Cytotoxic Brain Edema
0.300 Biomarker phenotype CTD_human Inhibition of the myosin light chain kinase prevents hypoxia-induced blood-brain barrier disruption. 17419808 2007
CUI: C0472388
Disease: Cytotoxic Cerebral Edema
Cytotoxic Cerebral Edema
0.300 Biomarker phenotype CTD_human Inhibition of the myosin light chain kinase prevents hypoxia-induced blood-brain barrier disruption. 17419808 2007
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.010 GeneticVariation disease BEFREE Three proteins, collapsin response mediator protein 2 (CRMP2), ubiquitin carboxyl-terminal hydrolase isozyme L1 (UCH-L1) and myosin regulatory light polypeptide 9 (MYL9), were simultaneously identified from the two sets of samples from females with or without endometriosis by two-dimensional electrophoresis (2-DE). 23670619 2013
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.010 Biomarker disease BEFREE Therefore, we aimed to study the expression pattern and clinical significance of MYL9 in GBM. 31270134 2019
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.010 Biomarker disease BEFREE Therefore, we aimed to study the expression pattern and clinical significance of MYL9 in GBM. 31270134 2019
CUI: C0017658
Disease: Glomerulonephritis
Glomerulonephritis
0.010 Biomarker disease BEFREE In the kidney and immune organs, only Ifi202 expression increased with the development of GN in B6.MRLc1(82-100), and significant differences from C57BL/6 were observed even before disease onset. 20167632 2010
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma
0.010 Biomarker disease BEFREE Automatic replanning was performed for 16 PC cases, initially planned for MLC1 (4 mm MLC) and reoptimized for MLC2 (5 mm) and MLC3 (10 mm) and for 19 HNC cases, replanned from MLC2 to MLC3. 29846751 2018
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
Hyperlipoproteinemia Type IIa
0.020 GeneticVariation disease BEFREE This study focuses on the aspartic acid to valine substitution (D166V) in the myosin RLC shown to be associated with a malignant phenotype of familial hypertrophic cardiomyopathy (FHC). 24374283 2014