abnormal inferior colliculus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the paired inferior eminence of the mesencephalic tectum that is involved in preliminary visual processing, and control of eye movements (Mammalian Phenotype Ontology, MP_0000776)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000776
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19 gene mutations causing the abnormal inferior colliculus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EN1 engrailed homeobox 1
EN2 engrailed homeobox 2
FGF17 fibroblast growth factor 17
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FOXB1 forkhead box B1
GBX2 gastrulation brain homeobox 2
GLI3 GLI family zinc finger 3
KAT6B K(lysine) acetyltransferase 6B
LRP6 low density lipoprotein receptor-related protein 6
MID1 midline 1
OTX1 orthodenticle homeobox 1
OTX2 orthodenticle homeobox 2
PAX5 paired box 5
SUZ12 SUZ12 polycomb repressive complex 2 subunit
TAL2 T-cell acute lymphocytic leukemia 2
TFAP2D transcription factor AP-2 delta (activating enhancer binding protein 2 delta)
UNC5C unc-5 homolog C (C. elegans)
WNT1 wingless-type MMTV integration site family, member 1