abnormal retinal progenitor cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the cells that give rise to the various cells of the retina (Mammalian Phenotype Ontology, MP_0006071)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006071
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Genes

9 gene mutations causing the abnormal retinal progenitor cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
E2F1 E2F transcription factor 1
FIGN fidgetin
MAB21L2 mab-21-like 2 (C. elegans)
MYD88 myeloid differentiation primary response 88
RPL24 ribosomal protein L24
TICAM1 toll-like receptor adaptor molecule 1
TLR4 toll-like receptor 4
TP53BP2 tumor protein p53 binding protein 2
VSX2 visual system homeobox 2