abnormal fourth ventricle morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the irregularly shaped cavity in the rhombencephalon, between the medulla oblongata, the pons, and the isthmus in front, and the cerebellum behind; it is continuous with the central canal of the cord below and with the cerebral aqueduct above, and through its lateral and median apertures it communicates with the subarachnoid space (Mammalian Phenotype Ontology, MP_0000828)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000828
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Genes

21 gene mutations causing the abnormal fourth ventricle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
COL18A1 collagen, type XVIII, alpha 1
CP ceruloplasmin (ferroxidase)
FGFR2 fibroblast growth factor receptor 2
FOXC1 forkhead box C1
GDF7 growth differentiation factor 7
GSX2 GS homeobox 2
KDM2B lysine (K)-specific demethylase 2B
L1CAM L1 cell adhesion molecule
LATS2 large tumor suppressor kinase 2
MKS1 Meckel syndrome, type 1
MSX1 msh homeobox 1
MYH10 myosin, heavy chain 10, non-muscle
NEK1 NIMA-related kinase 1
NPAS3 neuronal PAS domain protein 3
PHOX2B paired-like homeobox 2b
RB1 retinoblastoma 1
TEAD1 TEA domain family member 1 (SV40 transcriptional enhancer factor)
TMEM67 transmembrane protein 67
UCHL5 ubiquitin carboxyl-terminal hydrolase L5
ZNF423 zinc finger protein 423