exotropia Gene Set
Genes
18 genes associated with the exotropia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACADSB
|
acyl-CoA dehydrogenase, short/branched chain
|
|
ADGRG1
|
adhesion G protein-coupled receptor G1
|
|
ATRX
|
alpha thalassemia/mental retardation syndrome X-linked
|
|
BCOR
|
BCL6 corepressor
|
|
CDKL5
|
cyclin-dependent kinase-like 5
|
|
COL4A1
|
collagen, type IV, alpha 1
|
|
DPAGT1
|
dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase)
|
|
EFNB1
|
ephrin-B1
|
|
KIF21A
|
kinesin family member 21A
|
|
MECP2
|
methyl CpG binding protein 2
|
|
PHOX2A
|
paired-like homeobox 2a
|
|
SLC17A5
|
solute carrier family 17 (acidic sugar transporter), member 5
|
|
SLC6A8
|
solute carrier family 6 (neurotransmitter transporter), member 8
|
|
TBX1
|
T-box 1
|
|
TGFBR1
|
transforming growth factor, beta receptor 1
|
|
TGFBR2
|
transforming growth factor, beta receptor II (70/80kDa)
|
|
TUBB3
|
tubulin, beta 3 class III
|
|
UBE3A
|
ubiquitin protein ligase E3A
|
