abnormal rib development Gene Set
Genes
17 gene mutations causing the abnormal rib development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Symbol |
Name |
BMP5
|
bone morphogenetic protein 5
|
FOXC1
|
forkhead box C1
|
FST
|
follistatin
|
HOXB8
|
homeobox B8
|
HOXC4
|
homeobox C4
|
KMT2A
|
lysine (K)-specific methyltransferase 2A
|
LFNG
|
LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
|
MEOX1
|
mesenchyme homeobox 1
|
MYF5
|
myogenic factor 5
|
MYF6
|
myogenic factor 6 (herculin)
|
NABP2
|
nucleic acid binding protein 2
|
PAX3
|
paired box 3
|
PITX2
|
paired-like homeodomain 2
|
PSEN1
|
presenilin 1
|
PSIP1
|
PC4 and SFRS1 interacting protein 1
|
RAI1
|
retinoic acid induced 1
|
VANGL2
|
VANGL planar cell polarity protein 2
|