ullrich congenital muscular dystrophy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050558)
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Genes

29 genes co-occuring with the disease ullrich congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
COL6A2 collagen, type VI, alpha 2 2.8551
COL6A3 collagen, type VI, alpha 3 2.7917
COL6A1 collagen, type VI, alpha 1 2.62496
COL6A5 collagen, type VI, alpha 5 1.53921
SMG1 SMG1 phosphatidylinositol 3-kinase-related kinase 1.48077
SMG8 SMG8 nonsense mediated mRNA decay factor 1.38996
UPF1 UPF1 regulator of nonsense transcripts homolog (yeast) 1.37207
PPIF peptidylprolyl isomerase F 1.3027
FKBP14 FK506 binding protein 14, 22 kDa 1.16821
PLOD3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 1.1312
LAMA2 laminin, alpha 2 1.02861
CAPN3 calpain 3, (p94) 0.774523
MIR133B microRNA 133b 0.70434
SEPN1 selenoprotein N, 1 0.699919
CSPG4 chondroitin sulfate proteoglycan 4 0.696306
MIR31 microRNA 31 0.514956
BNIP3 BCL2/adenovirus E1B 19kDa interacting protein 3 0.42814
LMNA lamin A/C 0.423265
FBXO32 F-box protein 32 0.416896
BGN biglycan 0.348981
HTRA1 HtrA serine peptidase 1 0.300173
DYSF dysferlin 0.287235
TGFBR1 transforming growth factor, beta receptor 1 0.268332
SERPINH1 serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1) 0.243295
FBN1 fibrillin 1 0.224196
MYOG myogenin (myogenic factor 4) 0.221108
DMD dystrophin 0.199033
BECN1 beclin 1, autophagy related 0.18591
DAG1 dystroglycan 1 (dystrophin-associated glycoprotein 1) 0.183248