gingivitis Gene Set
Genes
22 genes associated with the gingivitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ALMS1
|
Alstrom syndrome protein 1
|
|
B3GALT6
|
UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
|
|
B4GALT7
|
xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7
|
|
CD40LG
|
CD40 ligand
|
|
COL3A1
|
collagen, type III, alpha 1
|
|
CTSC
|
cathepsin C
|
|
CYBA
|
cytochrome b-245, alpha polypeptide
|
|
CYBB
|
cytochrome b-245, beta polypeptide
|
|
FERMT1
|
fermitin family member 1
|
|
ITGB2
|
integrin, beta 2 (complement component 3 receptor 3 and 4 subunit)
|
|
LYST
|
lysosomal trafficking regulator
|
|
NCF1
|
neutrophil cytosolic factor 1
|
|
NCF2
|
neutrophil cytosolic factor 2
|
|
NCF4
|
neutrophil cytosolic factor 4, 40kDa
|
|
OCRL
|
oculocerebrorenal syndrome of Lowe
|
|
PLG
|
plasminogen
|
|
SAMD9
|
sterile alpha motif domain containing 9
|
|
SLC6A19
|
solute carrier family 6 (neutral amino acid transporter), member 19
|
|
STAT3
|
signal transducer and activator of transcription 3 (acute-phase response factor)
|
|
TNXB
|
tenascin XB
|
|
TSC1
|
tuberous sclerosis 1
|
|
TSC2
|
tuberous sclerosis 2
|
