abnormal spinal cord white matter morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the regions of the spinal cord that are largely or entirely composed of myelinated nerve cell axons and contain few or no neural cell bodies or dendrites (Mammalian Phenotype Ontology, MP_0008027)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008027
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23 gene mutations causing the abnormal spinal cord white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AFG3L2 AFG3-like AAA ATPase 2
ATRN attractin
CACNA2D2 calcium channel, voltage-dependent, alpha 2/delta subunit 2
CHN1 chimerin 1
DCC DCC netrin 1 receptor
EPHA4 EPH receptor A4
GALC galactosylceramidase
ISPD isoprenoid synthase domain containing
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KCNN2 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 2
KLC1 kinesin light chain 1
NPR2 natriuretic peptide receptor 2
NRP2 neuropilin 2
NTN1 netrin 1
PITPNA phosphatidylinositol transfer protein, alpha
ROBO1 roundabout, axon guidance receptor, homolog 1 (Drosophila)
ROBO2 roundabout, axon guidance receptor, homolog 2 (Drosophila)
RUNX3 runt-related transcription factor 3
TENM4 teneurin transmembrane protein 4
UCHL1 ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
UNC5C unc-5 homolog C (C. elegans)
USP14 ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase)
ZNF24 zinc finger protein 24