abnormal presphenoid bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the anterior part of the body of the sphenoid bone in front of the basisphenoid; it is usually a separate bone in the young or fetus, but becomes a part of the sphenoid in the adult (Mammalian Phenotype Ontology, MP_0004448)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004448
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Genes

28 gene mutations causing the abnormal presphenoid bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALX1 ALX homeobox 1
APAF1 apoptotic peptidase activating factor 1
ARID5B AT rich interactive domain 5B (MRF1-like)
CHRD chordin
CHUK conserved helix-loop-helix ubiquitous kinase
CSRNP1 cysteine-serine-rich nuclear protein 1
DLX5 distal-less homeobox 5
DLX6 distal-less homeobox 6
FGFR2 fibroblast growth factor receptor 2
FOXC2 forkhead box C2
FOXF2 forkhead box F2
GLI2 GLI family zinc finger 2
GSC goosecoid homeobox
HAND2 heart and neural crest derivatives expressed 2
IRF6 interferon regulatory factor 6
LMO4 LIM domain only 4
MKS1 Meckel syndrome, type 1
MN1 meningioma (disrupted in balanced translocation) 1
OTX2 orthodenticle homeobox 2
PHC1 polyhomeotic homolog 1 (Drosophila)
PKD1 polycystic kidney disease 1 (autosomal dominant)
PTCH1 patched 1
SCHIP1 schwannomin interacting protein 1
SGPL1 sphingosine-1-phosphate lyase 1
SKI SKI proto-oncogene
SP3 Sp3 transcription factor
TIPARP TCDD-inducible poly(ADP-ribose) polymerase
TMEM107 transmembrane protein 107