abnormal rib development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomalous formation of the bones forming the bony wall of the chest (Mammalian Phenotype Ontology, MP_0002823)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002823
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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