abnormal neuron specification Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description defects in the developmental patterning of neurons resulting in ectopic placement, decreased numbers or absence of mature neurons (Mammalian Phenotype Ontology, MP_0002948)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002948
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10 gene mutations causing the abnormal neuron specification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CADPS2 Ca++-dependent secretion activator 2
DISP1 dispatched homolog 1 (Drosophila)
GLI2 GLI family zinc finger 2
GPSM2 G-protein signaling modulator 2
ISL2 ISL LIM homeobox 2
NAPA N-ethylmaleimide-sensitive factor attachment protein, alpha
NKX2-2 NK2 homeobox 2
NKX6-1 NK6 homeobox 1
OLIG3 oligodendrocyte transcription factor 3
TULP3 tubby like protein 3