absent hippocampal commissure Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence 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_0008223)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008223
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Genes

11 gene mutations causing the absent hippocampal commissure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARHGAP35 Rho GTPase activating protein 35
ARX aristaless related homeobox
BHLHE22 basic helix-loop-helix family, member e22
DCC DCC netrin 1 receptor
DCLK1 doublecortin-like kinase 1
DRAXIN dorsal inhibitory axon guidance protein
GLI3 GLI family zinc finger 3
LHX5 LIM homeobox 5
MAP1B microtubule-associated protein 1B
NTN1 netrin 1
PRDM8 PR domain containing 8