disorganized retinal layers Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description derangement of the pattern of the sheets of cells comprising the optic part of the retina (Mammalian Phenotype Ontology, MP_0001328)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001328
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15 gene mutations causing the disorganized retinal layers phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AHR aryl hydrocarbon receptor
ALKBH1 alkB, alkylation repair homolog 1 (E. coli)
CCND1 cyclin D1
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
COL2A1 collagen, type II, alpha 1
HES1 hes family bHLH transcription factor 1
MCPH1 microcephalin 1
NDP Norrie disease (pseudoglioma)
RHO rhodopsin
RORB RAR-related orphan receptor B
RS1 retinoschisin 1
SOX2 SRY (sex determining region Y)-box 2
TP53BP2 tumor protein p53 binding protein 2
TTPA tocopherol (alpha) transfer protein
VSX2 visual system homeobox 2