microretrognathia Gene Set
Genes
12 genes associated with the microretrognathia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
B3GAT3
|
beta-1,3-glucuronyltransferase 3
|
|
CANT1
|
calcium activated nucleotidase 1
|
|
CHST14
|
carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
|
|
EIF4A3
|
eukaryotic translation initiation factor 4A3
|
|
KIF7
|
kinesin family member 7
|
|
NAA10
|
N(alpha)-acetyltransferase 10, NatA catalytic subunit
|
|
OCLN
|
occludin
|
|
OFD1
|
oral-facial-digital syndrome 1
|
|
ORC6
|
origin recognition complex, subunit 6
|
|
PAX1
|
paired box 1
|
|
SLC35A3
|
solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member A3
|
|
TMEM70
|
transmembrane protein 70
|
