decreased amacrine cell number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction in the number of one of the three types of interneurons found in the inner nuclear layer of the mature retina (Mammalian Phenotype Ontology, MP_0008106)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008106
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Genes

9 gene mutations causing the decreased amacrine cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTPBP1 ATP/GTP binding protein 1
BARHL2 BarH-like homeobox 2
BHLHE22 basic helix-loop-helix family, member e22
FOXN4 forkhead box N4
GDF11 growth differentiation factor 11
LAMB2 laminin, beta 2 (laminin S)
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
PTF1A pancreas specific transcription factor, 1a
RORB RAR-related orphan receptor B