skeletal muscle fibrosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description formation of fibrous tissue within skeletal muscle as a result of repair or a reactive process (Mammalian Phenotype Ontology, MP_0009419)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009419
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Genes

19 gene mutations causing the skeletal muscle fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BARX2 BARX homeobox 2
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
COL6A3 collagen, type VI, alpha 3
CRYAB crystallin, alpha B
DMD dystrophin
DYSF dysferlin
FKRP fukutin related protein
IFNG interferon, gamma
IGHMBP2 immunoglobulin mu binding protein 2
LAMA2 laminin, alpha 2
LARGE like-glycosyltransferase
LMNA lamin A/C
MBNL2 muscleblind-like splicing regulator 2
MMP14 matrix metallopeptidase 14 (membrane-inserted)
MYF5 myogenic factor 5
PAX7 paired box 7
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
SYT7 synaptotagmin VII
VCP valosin containing protein