abnormal retina inner limiting membrane morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the row of fused Muller cell processes and astrocytes that separates the retinal nerve fiber layer from the vitreous (Mammalian Phenotype Ontology, MP_0010235)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010235
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7 gene mutations causing the abnormal retina inner limiting membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
COL4A1 collagen, type IV, alpha 1
FKRP fukutin related protein
LAMA1 laminin, alpha 1
LAMB2 laminin, beta 2 (laminin S)
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
PXDN peroxidasin
TCF7L1 transcription factor 7-like 1 (T-cell specific, HMG-box)