Microdeletion Syndromes Gene Set
Genes
17 genes associated with the disease Microdeletion Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ANK3
|
ankyrin 3, node of Ranvier (ankyrin G)
|
|
ANKRD11
|
ankyrin repeat domain 11
|
|
CDKL5
|
cyclin-dependent kinase-like 5
|
|
DNASE1L3
|
deoxyribonuclease I-like 3
|
|
EHMT1
|
euchromatic histone-lysine N-methyltransferase 1
|
|
FOXP1
|
forkhead box P1
|
|
KMT2B
|
lysine (K)-specific methyltransferase 2B
|
|
MAN2C1
|
mannosidase, alpha, class 2C, member 1
|
|
MBD5
|
methyl-CpG binding domain protein 5
|
|
NSD2
|
nuclear receptor binding SET domain protein 2
|
|
PRDM9
|
PR domain containing 9
|
|
SETD5
|
SET domain containing 5
|
|
SLC25A1
|
solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1
|
|
SNRPN
|
small nuclear ribonucleoprotein polypeptide N
|
|
SNURF
|
SNRPN upstream reading frame
|
|
TBX1
|
T-box 1
|
|
ZNF507
|
zinc finger protein 507
|
