Ullrich Congenital Muscular Dystrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050558)
External Link https://www.disgenet.org/browser/0/1/0/C4225314
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Genes

17 genes associated with the disease Ullrich Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BGN biglycan
COL12A1 collagen, type XII, alpha 1
COL6A1 collagen, type VI, alpha 1
COL6A2 collagen, type VI, alpha 2
COL6A3 collagen, type VI, alpha 3
COL6A5 collagen, type VI, alpha 5
CSPG4 chondroitin sulfate proteoglycan 4
DMD dystrophin
FN1 fibronectin 1
GPX4 glutathione peroxidase 4
LAMA2 laminin, alpha 2
SEMA6A sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A
SMCP sperm mitochondria-associated cysteine-rich protein
SMG1 SMG1 phosphatidylinositol 3-kinase-related kinase
TNC tenascin C
UPF1 UPF1 regulator of nonsense transcripts homolog (yeast)
VWF von Willebrand factor