abnormal amacrine cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of one of the three types of interneurons found in the inner nuclear layer of the mature retina; they integrate, modulate, and interpose a temporal domain in the visual message presented to the retinal ganglion cells, with which they synapse in the inner plexiform layer (Mammalian Phenotype Ontology, MP_0005240)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005240
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24 gene mutations causing the abnormal amacrine cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTPBP1 ATP/GTP binding protein 1
AIFM1 apoptosis-inducing factor, mitochondrion-associated, 1
ASIC3 acid sensing (proton gated) ion channel 3
ATOH7 atonal homolog 7 (Drosophila)
BARHL2 BarH-like homeobox 2
BHLHE22 basic helix-loop-helix family, member e22
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
DSCAM Down syndrome cell adhesion molecule
DSCAML1 Down syndrome cell adhesion molecule like 1
FAT3 FAT atypical cadherin 3
FOXN4 forkhead box N4
GDF11 growth differentiation factor 11
LAMB2 laminin, beta 2 (laminin S)
LAMC3 laminin, gamma 3
MEGF10 multiple EGF-like-domains 10
NEUROD1 neuronal differentiation 1
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
PLXNA2 plexin A2
PLXNA4 plexin A4
POU4F2 POU class 4 homeobox 2
PTF1A pancreas specific transcription factor, 1a
RORB RAR-related orphan receptor B
RS1 retinoschisin 1
SEMA6A sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A