abnormal axon fasciculation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the process by which axons form into nerve fiber bundles (Mammalian Phenotype Ontology, MP_0009450)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009450
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Genes

15 gene mutations causing the abnormal axon fasciculation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRG6 adhesion G protein-coupled receptor G6
CNR1 cannabinoid receptor 1 (brain)
CNTN1 contactin 1
CRTAC1 cartilage acidic protein 1
DSCAM Down syndrome cell adhesion molecule
ERBB3 erb-b2 receptor tyrosine kinase 3
FBXO45 F-box protein 45
HSPA5 heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa)
ISPD isoprenoid synthase domain containing
MEGF8 multiple EGF-like-domains 8
NR2E1 nuclear receptor subfamily 2, group E, member 1
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SEMA3F sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F
SOX10 SRY (sex determining region Y)-box 10