abnormal horizontal cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the laterally interconnecting neurons in the outer plexiform layer of the retina that connect rods of one part of the retina with cones in another part of the retina (Mammalian Phenotype Ontology, MP_0006068)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006068
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12 gene mutations causing the abnormal horizontal cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
CNGB1 cyclic nucleotide gated channel beta 1
CRX cone-rod homeobox
ERC2 ELKS/RAB6-interacting/CAST family member 2
FOXN4 forkhead box N4
GJA10 gap junction protein, alpha 10, 62kDa
MEGF10 multiple EGF-like-domains 10
MEGF11 multiple EGF-like-domains 11
OTX2 orthodenticle homeobox 2
PROX1 prospero homeobox 1
PTF1A pancreas specific transcription factor, 1a
RORB RAR-related orphan receptor B