muscle hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the musculature. (Human Phenotype Ontology, HP_0009004)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000734
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Genes

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

Symbol Name
FGFRL1 fibroblast growth factor receptor-like 1
GAB1 GRB2-associated binding protein 1
IGF1 insulin-like growth factor 1 (somatomedin C)
IGF1R insulin-like growth factor 1 receptor
MET MET proto-oncogene, receptor tyrosine kinase
MYOG myogenin (myogenic factor 4)
PITX1 paired-like homeodomain 1
SAMD4A sterile alpha motif domain containing 4A
SIX1 SIX homeobox 1
SKI SKI proto-oncogene
Funding