abnormal skeletal muscle regeneration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the ability to repair skeletal muscle after injury or disease (Mammalian Phenotype Ontology, MP_0013237)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013237
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Genes

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

Symbol Name
BEX1 brain expressed, X-linked 1
BVES blood vessel epicardial substance
CAPN6 calpain 6
CCL13 chemokine (C-C motif) ligand 13
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
COL6A3 collagen, type VI, alpha 3
FOXJ3 forkhead box J3
IFNG interferon, gamma
LAMA2 laminin, alpha 2
MAMSTR MEF2 activating motif and SAP domain containing transcriptional regulator
MYOD1 myogenic differentiation 1
NACA nascent polypeptide-associated complex alpha subunit
PLAU plasminogen activator, urokinase
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
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