narrow eye opening Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005287
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Genes

29 gene mutations causing the narrow eye opening phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDO1 cysteine dioxygenase type 1
CLEC16A C-type lectin domain family 16, member A
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
DLK1 delta-like 1 homolog (Drosophila)
EDA ectodysplasin A
EDARADD EDAR-associated death domain
FGF10 fibroblast growth factor 10
FOXP3 forkhead box P3
FRAS1 Fraser extracellular matrix complex subunit 1
GAS1 growth arrest-specific 1
GRM1 glutamate receptor, metabotropic 1
IKZF2 IKAROS family zinc finger 2 (Helios)
IRX5 iroquois homeobox 5
KDM4B lysine (K)-specific demethylase 4B
KLHDC2 kelch domain containing 2
MSX2 msh homeobox 2
MYSM1 Myb-like, SWIRM and MPN domains 1
PRMT3 protein arginine methyltransferase 3
PTPN2 protein tyrosine phosphatase, non-receptor type 2
RARA retinoic acid receptor, alpha
RARB retinoic acid receptor, beta
RARG retinoic acid receptor, gamma
SCD stearoyl-CoA desaturase (delta-9-desaturase)
SIRT1 sirtuin 1
SIRT6 sirtuin 6
SOAT1 sterol O-acyltransferase 1
SPNS2 spinster homolog 2 (Drosophila)
THBS1 thrombospondin 1
TMC8 transmembrane channel-like 8