abnormal hippocampal commissure morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the triangular subcallosal plate of commissural fibers resulting from the converging of the right and left fornix bundles which exchange numerous fibers and which curve back in the contralateral fornix to end in the hippocampus of the opposite side (Mammalian Phenotype Ontology, MP_0008221)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008221
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24 gene mutations causing the abnormal hippocampal commissure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APP amyloid beta (A4) precursor protein
ARHGAP35 Rho GTPase activating protein 35
ARX aristaless related homeobox
BHLHE22 basic helix-loop-helix family, member e22
CABLES1 Cdk5 and Abl enzyme substrate 1
DCC DCC netrin 1 receptor
DCLK1 doublecortin-like kinase 1
DRAXIN dorsal inhibitory axon guidance protein
ENAH enabled homolog (Drosophila)
FGF2 fibroblast growth factor 2 (basic)
GLI3 GLI family zinc finger 3
HESX1 HESX homeobox 1
LHX5 LIM homeobox 5
MAP1B microtubule-associated protein 1B
MARCKS myristoylated alanine-rich protein kinase C substrate
NDST1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
NFIA nuclear factor I/A
NR2F1 nuclear receptor subfamily 2, group F, member 1
NTN1 netrin 1
PRDM8 PR domain containing 8
ROBO1 roundabout, axon guidance receptor, homolog 1 (Drosophila)
SOX3 SRY (sex determining region Y)-box 3
USP14 ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase)
ZNF423 zinc finger protein 423