abnormal optic disc morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the area in the retina where all of the axons of the ganglion cells exit the retina to form the optic nerve (Mammalian Phenotype Ontology, MP_0008259)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008259
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10 gene mutations causing the abnormal optic disc morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DNASE1L2 deoxyribonuclease I-like 2
FGF10 fibroblast growth factor 10
FKRP fukutin related protein
GDF6 growth differentiation factor 6
MTERF4 mitochondrial transcription termination factor 4
PAX2 paired box 2
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta
RXRA retinoid X receptor, alpha
SIRT1 sirtuin 1
TFB1M transcription factor B1, mitochondrial