Irido-Corneo-Trabecular Dysgenesis (Disorder) Gene Set
Genes
35 genes associated with the disease Irido-Corneo-Trabecular Dysgenesis (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
B3GLCT
|
beta 3-glucosyltransferase
|
|
CDH2
|
cadherin 2, type 1, N-cadherin (neuronal)
|
|
CENPF
|
centromere protein F, 350/400kDa
|
|
CYP1B1
|
cytochrome P450, family 1, subfamily B, polypeptide 1
|
|
DNAJB1
|
DnaJ (Hsp40) homolog, subfamily B, member 1
|
|
FKRP
|
fukutin related protein
|
|
FKTN
|
fukutin
|
|
FLNA
|
filamin A, alpha
|
|
FOXC1
|
forkhead box C1
|
|
FOXD3
|
forkhead box D3
|
|
FOXE3
|
forkhead box E3
|
|
HDAC9
|
histone deacetylase 9
|
|
ISPD
|
isoprenoid synthase domain containing
|
|
KERA
|
keratocan
|
|
LARGE
|
like-glycosyltransferase
|
|
NCAPG2
|
non-SMC condensin II complex, subunit G2
|
|
NDP
|
Norrie disease (pseudoglioma)
|
|
NECTIN1
|
nectin cell adhesion molecule 1
|
|
OAF
|
OAF homolog (Drosophila)
|
|
PAX1
|
paired box 1
|
|
PAX3
|
paired box 3
|
|
PAX6
|
paired box 6
|
|
PITX2
|
paired-like homeodomain 2
|
|
PITX3
|
paired-like homeodomain 3
|
|
POMT1
|
protein-O-mannosyltransferase 1
|
|
POMT2
|
protein-O-mannosyltransferase 2
|
|
RB1
|
retinoblastoma 1
|
|
RBL2
|
retinoblastoma-like 2
|
|
SHOX
|
short stature homeobox
|
|
SLC4A11
|
solute carrier family 4, sodium borate transporter, member 11
|
|
SOSTDC1
|
sclerostin domain containing 1
|
|
SOX3
|
SRY (sex determining region Y)-box 3
|
|
TFAP2A
|
transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
|
|
TRIM44
|
tripartite motif containing 44
|
|
WDR37
|
WD repeat domain 37
|
