impaired skeletal muscle regeneration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced ability to repair skeletal muscle after injury or disease (Mammalian Phenotype Ontology, MP_0013239)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013239
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Genes

10 gene mutations causing the impaired skeletal muscle regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BVES blood vessel epicardial substance
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
FOXJ3 forkhead box J3
IFNG interferon, gamma
MAMSTR MEF2 activating motif and SAP domain containing transcriptional regulator
NACA nascent polypeptide-associated complex alpha subunit
PLAU plasminogen activator, urokinase
TRIM32 tripartite motif containing 32
WFIKKN1 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1
WFIKKN2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2