abnormal ciliary body morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the thickened portion of the vascular tunic, which lies between the choroid and the iris (Mammalian Phenotype Ontology, MP_0005099)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005099
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Genes

17 gene mutations causing the abnormal ciliary body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATF4 activating transcription factor 4
CENPJ centromere protein J
FBXO47 F-box protein 47
FOXC1 forkhead box C1
FOXE3 forkhead box E3
FOXF2 forkhead box F2
GAS1 growth arrest-specific 1
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LMX1B LIM homeobox transcription factor 1, beta
MAB21L1 mab-21-like 1 (C. elegans)
MITF microphthalmia-associated transcription factor
PVRL1 poliovirus receptor-related 1 (herpesvirus entry mediator C)
PVRL3 poliovirus receptor-related 3
PXDN peroxidasin
SPARC secreted protein, acidic, cysteine-rich (osteonectin)
SPNS2 spinster homolog 2 (Drosophila)
TCF7L1 transcription factor 7-like 1 (T-cell specific, HMG-box)