thin retinal ganglion layer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced thickness of the innermost nuclear layer of the retina, which contains neurons that project axons through the optic nerve to the brain (Mammalian Phenotype Ontology, MP_0008507)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008507
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Genes

10 gene mutations causing the thin retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BARHL2 BarH-like homeobox 2
BMP4 bone morphogenetic protein 4
CCND1 cyclin D1
FST follistatin
HR hair growth associated
LAMA1 laminin, alpha 1
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
PAX2 paired box 2
POU4F2 POU class 4 homeobox 2
RPL24 ribosomal protein L24