myotonic dystrophy type 2 Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A myotonic disease that is characterized by myotonia and progressive, proximal muscle wasting and weakness affecting the skeletal and smooth muscles of the neck, shoulders, elbows and hips and has_physical_basis_in the autosomal dominant inheritance of the CNBP (ZNF9) gene containing an expansion of a CCTG repeat in intron one. (Human Disease Ontology, DOID_0050759)
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Genes

28 genes co-occuring with the disease myotonic dystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CNBP CCHC-type zinc finger, nucleic acid binding protein 3.37274
MBNL1 muscleblind-like splicing regulator 1 1.92482
DMPK dystrophia myotonica-protein kinase 1.78985
YIPF7 Yip1 domain family, member 7 1.35289
CELF1 CUGBP, Elav-like family member 1 1.27257
CLCN1 chloride channel, voltage-sensitive 1 1.24732
MTMR1 myotubularin related protein 1 1.18066
C10ORF2 chromosome 10 open reading frame 2 1.03872
SCN4A sodium channel, voltage gated, type IV alpha subunit 1.02988
SMARCA5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5 0.932898
PCBP2 poly(rC) binding protein 2 0.911022
WNT5B wingless-type MMTV integration site family, member 5B 0.832329
INSR insulin receptor 0.828229
BEAN1 brain expressed, associated with NEDD4, 1 0.751271
RAD23B RAD23 homolog B (S. cerevisiae) 0.689893
COCH cochlin 0.665166
NEDD4 neural precursor cell expressed, developmentally down-regulated 4, E3 ubiquitin protein ligase 0.643404
HNRNPK heterogeneous nuclear ribonucleoprotein K 0.571884
SRSF2 serine/arginine-rich splicing factor 2 0.542767
MN1 meningioma (disrupted in balanced translocation) 1 0.43753
MIR221 microRNA 221 0.42664
SCN3A sodium channel, voltage gated, type III alpha subunit 0.400826
MTM1 myotubularin 1 0.392629
PML promyelocytic leukemia 0.380739
SCN8A sodium channel, voltage gated, type VIII alpha subunit 0.347511
TNS1 tensin 1 0.269398
TTN titin 0.253831
ODC1 ornithine decarboxylase 1 0.162306