decreased cns synapse formation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a reduction in the frequency of the process of generating the initial connections between an axon and effector tissue or neuron (Mammalian Phenotype Ontology, MP_0004998)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004998
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Genes

12 gene mutations causing the decreased cns synapse formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACTL6B actin-like 6B
AGRN agrin
CACNG2 calcium channel, voltage-dependent, gamma subunit 2
CAV1 caveolin 1, caveolae protein, 22kDa
CC2D1A coiled-coil and C2 domain containing 1A
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal)
KALRN kalirin, RhoGEF kinase
KLK8 kallikrein-related peptidase 8
LRRTM4 leucine rich repeat transmembrane neuronal 4
MECP2 methyl CpG binding protein 2
PURA purine-rich element binding protein A
STAU1 staufen double-stranded RNA binding protein 1