abnormal muller cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the elongated neuroglial cells that traverse all the layers of the retina and that act as supporting elements (Mammalian Phenotype Ontology, MP_0005547)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005547
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14 gene mutations causing the abnormal muller cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADRB2 adrenoceptor beta 2, surface
AIPL1 aryl hydrocarbon receptor interacting protein-like 1
ATOH7 atonal homolog 7 (Drosophila)
CBS cystathionine-beta-synthase
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CRB1 crumbs family member 1, photoreceptor morphogenesis associated
DMD dystrophin
GPR34 G protein-coupled receptor 34
HES5 hes family bHLH transcription factor 5
LAMA1 laminin, alpha 1
LAMB2 laminin, beta 2 (laminin S)
NEUROD1 neuronal differentiation 1
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta
PRPH2 peripherin 2 (retinal degeneration, slow)