malocclusion Gene Set
Genes
37 gene mutations causing the malocclusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ANTXR1
|
anthrax toxin receptor 1
|
|
ATR
|
ATR serine/threonine kinase
|
|
BAZ1B
|
bromodomain adjacent to zinc finger domain, 1B
|
|
CBX2
|
chromobox homolog 2
|
|
CCND1
|
cyclin D1
|
|
CDO1
|
cysteine dioxygenase type 1
|
|
CTSK
|
cathepsin K
|
|
DIAPH1
|
diaphanous-related formin 1
|
|
DMRT3
|
doublesex and mab-3 related transcription factor 3
|
|
DNM3OS
|
DNM3 opposite strand/antisense RNA
|
|
DYM
|
dymeclin
|
|
EHD1
|
EH-domain containing 1
|
|
FGFR2
|
fibroblast growth factor receptor 2
|
|
FGFR3
|
fibroblast growth factor receptor 3
|
|
FOXA2
|
forkhead box A2
|
|
GTF2IRD1
|
GTF2I repeat domain containing 1
|
|
HFM
|
Hemifacial microsomia
|
|
LMNA
|
lamin A/C
|
|
LTBP1
|
latent transforming growth factor beta binding protein 1
|
|
LTBP3
|
latent transforming growth factor beta binding protein 3
|
|
MAST4
|
microtubule associated serine/threonine kinase family member 4
|
|
MECOM
|
MDS1 and EVI1 complex locus
|
|
MECP2
|
methyl CpG binding protein 2
|
|
MMP14
|
matrix metallopeptidase 14 (membrane-inserted)
|
|
MSX2
|
msh homeobox 2
|
|
NPHP3
|
nephronophthisis 3 (adolescent)
|
|
NPR2
|
natriuretic peptide receptor 2
|
|
PAPSS2
|
3'-phosphoadenosine 5'-phosphosulfate synthase 2
|
|
PITX2
|
paired-like homeodomain 2
|
|
RAI1
|
retinoic acid induced 1
|
|
SIRT6
|
sirtuin 6
|
|
SLC39A13
|
solute carrier family 39 (zinc transporter), member 13
|
|
SPRY4
|
sprouty homolog 4 (Drosophila)
|
|
TGFB1
|
transforming growth factor, beta 1
|
|
TOM1L2
|
target of myb1-like 2 (chicken)
|
|
WHSC1
|
Wolf-Hirschhorn syndrome candidate 1
|
|
ZIC3
|
Zic family member 3
|
