abnormal hippocampal mossy fiber morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence or misprojection of axons of neuronal cells in the dentate gyrus (Mammalian Phenotype Ontology, MP_0002761)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002761
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25 gene mutations causing the abnormal hippocampal mossy fiber morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNG2 calcium channel, voltage-dependent, gamma subunit 2
CHL1 cell adhesion molecule L1-like
CKB creatine kinase, brain
DCX doublecortin
FMR1 fragile X mental retardation 1
GDI1 GDP dissociation inhibitor 1
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6
LGI1 leucine-rich, glioma inactivated 1
LRRK2 leucine-rich repeat kinase 2
LYST lysosomal trafficking regulator
MT3 metallothionein 3
NR2E1 nuclear receptor subfamily 2, group E, member 1
NRP2 neuropilin 2
OLIG3 oligodendrocyte transcription factor 3
PLXNA2 plexin A2
PLXNA3 plexin A3
PLXNA4 plexin A4
PPP3CA protein phosphatase 3, catalytic subunit, alpha isozyme
SEMA6A sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A
SEMA6B sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6B
SLC30A3 solute carrier family 30 (zinc transporter), member 3
ST8SIA2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2
STON2 stonin 2
TP73 tumor protein p73
TUBA1A tubulin, alpha 1a