retinal deposits Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormal accumulation of material on the retina (Mammalian Phenotype Ontology, MP_0006187)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006187
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Genes

7 gene mutations causing the retinal deposits phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6
CCL13 chemokine (C-C motif) ligand 13
CCR2 chemokine (C-C motif) receptor 2
CX3CR1 chemokine (C-X3-C motif) receptor 1
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
TUB tubby bipartite transcription factor
UBE3B ubiquitin protein ligase E3B