abnormal embryonic/fetal subventricular zone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the transient proliferative population of neurons that expands exponentially during late prenatal development; it is a continuous germinal zone distinct from the ventricular zone that surrounds the brain ventricles (Mammalian Phenotype Ontology, MP_0004274)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004274
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Genes

29 gene mutations causing the abnormal embryonic/fetal subventricular zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRA2 adhesion G protein-coupled receptor A2
APAF1 apoptotic peptidase activating factor 1
CDK5RAP2 CDK5 regulatory subunit associated protein 2
CELSR3 cadherin, EGF LAG seven-pass G-type receptor 3
CUX2 cut-like homeobox 2
EBF1 early B-cell factor 1
FEZF1 FEZ family zinc finger 1
FKBP8 FK506 binding protein 8, 38kDa
FOXG1 forkhead box G1
FRS2 fibroblast growth factor receptor substrate 2
GSX2 GS homeobox 2
HHEX hematopoietically expressed homeobox
HTT huntingtin
ID4 inhibitor of DNA binding 4, dominant negative helix-loop-helix protein
IFT88 intraflagellar transport 88
ITGB8 integrin, beta 8
NR2E1 nuclear receptor subfamily 2, group E, member 1
PATZ1 POZ (BTB) and AT hook containing zinc finger 1
PAX6 paired box 6
PHGDH phosphoglycerate dehydrogenase
PIKFYVE phosphoinositide kinase, FYVE finger containing
PSEN1 presenilin 1
ROBO1 roundabout, axon guidance receptor, homolog 1 (Drosophila)
SHH sonic hedgehog
SOX11 SRY (sex determining region Y)-box 11
SPTAN1 spectrin, alpha, non-erythrocytic 1
TOP2B topoisomerase (DNA) II beta 180kDa
TP53BP2 tumor protein p53 binding protein 2
VAX1 ventral anterior homeobox 1