herniated diaphragm Gene Set
Genes
22 gene mutations causing the herniated diaphragm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
CHAT
|
choline O-acetyltransferase
|
|
DNASE2
|
deoxyribonuclease II, lysosomal
|
|
EFEMP2
|
EGF containing fibulin-like extracellular matrix protein 2
|
|
FBN1
|
fibrillin 1
|
|
FGF10
|
fibroblast growth factor 10
|
|
FGFRL1
|
fibroblast growth factor receptor-like 1
|
|
FREM1
|
FRAS1 related extracellular matrix 1
|
|
FUZ
|
fuzzy planar cell polarity protein
|
|
GATA4
|
GATA binding protein 4
|
|
HLX
|
H2.0-like homeobox
|
|
HOXB4
|
homeobox B4
|
|
KIF7
|
kinesin family member 7
|
|
KL
|
klotho
|
|
LOX
|
lysyl oxidase
|
|
LRP1
|
low density lipoprotein receptor-related protein 1
|
|
MET
|
MET proto-oncogene, receptor tyrosine kinase
|
|
PBX1
|
pre-B-cell leukemia homeobox 1
|
|
PDGFRA
|
platelet-derived growth factor receptor, alpha polypeptide
|
|
SLIT3
|
slit homolog 3 (Drosophila)
|
|
SOX7
|
SRY (sex determining region Y)-box 7
|
|
WDR35
|
WD repeat domain 35
|
|
WT1
|
Wilms tumor 1
|
