thin diaphragm muscle Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced thickness of the diaphragm muscle (Mammalian Phenotype Ontology, MP_0000761)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000761
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Genes

25 gene mutations causing the thin diaphragm muscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM19 ADAM metallopeptidase domain 19
BARX2 BARX homeobox 2
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CHAT choline O-acetyltransferase
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
DES desmin
DNASE2 deoxyribonuclease II, lysosomal
DOCK1 dedicator of cytokinesis 1
ECEL1 endothelin converting enzyme-like 1
FGFRL1 fibroblast growth factor receptor-like 1
ILF3 interleukin enhancer binding factor 3, 90kDa
LMNB1 lamin B1
LOX lysyl oxidase
MET MET proto-oncogene, receptor tyrosine kinase
MNX1 motor neuron and pancreas homeobox 1
MUSK muscle, skeletal, receptor tyrosine kinase
MYOG myogenin (myogenic factor 4)
NRG1 neuregulin 1
PAX3 paired box 3
PAX7 paired box 7
SIX1 SIX homeobox 1
SLIT3 slit homolog 3 (Drosophila)
SNAP25 synaptosomal-associated protein, 25kDa
STAC3 SH3 and cysteine rich domain 3
TNNT3 troponin T type 3 (skeletal, fast)