skeletal muscle fiber atrophy Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description acquired diminution of the size of skeletal muscle fibers associated with wasting as from death and reabsorbtion of cells, diminished cellular proliferation, decreased cellular volume, pressure, ischemia, malnutrition, reduced function or malfunction, or hormonal changes; occurs with age, immobilization, weightlessness, malnutrition or denervation (Mammalian Phenotype Ontology, MP_0009413)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009413
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Genes

16 gene mutations causing the skeletal muscle fiber atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
AR androgen receptor
BARX2 BARX homeobox 2
CHAT choline O-acetyltransferase
DES desmin
IGHMBP2 immunoglobulin mu binding protein 2
ITGA7 integrin, alpha 7
LAMC1 laminin, gamma 1 (formerly LAMB2)
LDB3 LIM domain binding 3
MYH4 myosin, heavy chain 4, skeletal muscle
SLC18A3 solute carrier family 18 (vesicular acetylcholine transporter), member 3
TCAP titin-cap
TTN titin
TTPA tocopherol (alpha) transfer protein
VEGFA vascular endothelial growth factor A
WASF1 WAS protein family, member 1