abnormal superior colliculus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the paired superior eminence of the mesencephalic tectum that is involved in auditory processing (Mammalian Phenotype Ontology, MP_0000904)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000904
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Genes

15 gene mutations causing the abnormal superior colliculus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AP3B1 adaptor-related protein complex 3, beta 1 subunit
CD247 CD247 molecule
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal)
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
EN1 engrailed homeobox 1
GLI3 GLI family zinc finger 3
LMX1B LIM homeobox transcription factor 1, beta
NGFR nerve growth factor receptor
OTX1 orthodenticle homeobox 1
POU4F2 POU class 4 homeobox 2
STRBP spermatid perinuclear RNA binding protein
SUZ12 SUZ12 polycomb repressive complex 2 subunit
TAL2 T-cell acute lymphocytic leukemia 2
TENM2 teneurin transmembrane protein 2
VAC14 Vac14 homolog (S. cerevisiae)