abnormal spinal cord interneuron morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of neurons that exclusively interact with other neurons in the spinal cord (Mammalian Phenotype Ontology, MP_0004100)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004100
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23 gene mutations causing the abnormal spinal cord interneuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASCL1 achaete-scute family bHLH transcription factor 1
CHN1 chimerin 1
CUX2 cut-like homeobox 2
DBX1 developing brain homeobox 1
DRAXIN dorsal inhibitory axon guidance protein
EVX1 even-skipped homeobox 1
FUZ fuzzy planar cell polarity protein
GDF7 growth differentiation factor 7
GLI2 GLI family zinc finger 2
HHAT hedgehog acyltransferase
IFT122 intraflagellar transport 122
INTU inturned planar cell polarity protein
ISL1 ISL LIM homeobox 1
MBD4 methyl-CpG binding domain protein 4
NEUROG2 neurogenin 2
NKX6-1 NK6 homeobox 1
OLIG2 oligodendrocyte lineage transcription factor 2
PAK4 p21 protein (Cdc42/Rac)-activated kinase 4
PAX6 paired box 6
SHH sonic hedgehog
TK2 thymidine kinase 2, mitochondrial
TLX3 T-cell leukemia homeobox 3
VSX2 visual system homeobox 2