202176_AT |
ERCC3 |
excision repair cross-complementing rodent repair deficiency, complementation group 3 (xeroderma pigmentosum group B complementing) |
202545_AT |
PRKCD |
protein kinase C, delta |
202618_S_AT |
MECP2 |
methyl CpG binding protein 2 (Rett syndrome) |
202856_S_AT |
SLC16A3 |
solute carrier family 16, member 3 (monocarboxylic acid transporter 4) |
203976_S_AT |
CHAF1A |
chromatin assembly factor 1, subunit A (p150) |
204067_AT |
SUOX |
sulfite oxidase |
204709_S_AT |
KIF23 |
kinesin family member 23 |
204729_S_AT |
STX1A |
syntaxin 1A (brain) |
204785_X_AT |
IFNAR2 |
interferon (alpha, beta and omega) receptor 2 |
206542_S_AT |
SMARCA2 |
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 |
207239_S_AT |
PCTK1 |
PCTAIRE protein kinase 1 |
207598_X_AT |
XRCC2 |
X-ray repair complementing defective repair in Chinese hamster cells 2 |
209041_S_AT |
UBE2G2 |
ubiquitin-conjugating enzyme E2G 2 (UBC7 homolog, yeast) |
209282_AT |
PRKD2 |
protein kinase D2 |
209575_AT |
IL10RB |
interleukin 10 receptor, beta |
209731_AT |
NTHL1 |
nth endonuclease III-like 1 (E. coli) |
210514_X_AT |
HLA-G |
HLA-G histocompatibility antigen, class I, G |
210567_S_AT |
SKP2 |
S-phase kinase-associated protein 2 (p45) |
210734_X_AT |
MAX |
MYC associated factor X |
212593_S_AT |
PDCD4 |
programmed cell death 4 (neoplastic transformation inhibitor) |
212669_AT |
CAMK2G |
calcium/calmodulin-dependent protein kinase (CaM kinase) II gamma |
214483_S_AT |
ARFIP1 |
ADP-ribosylation factor interacting protein 1 (arfaptin 1) |
215383_X_AT |
SPG21 |
spastic paraplegia 21 (autosomal recessive, Mast syndrome) |
218411_S_AT |
MBIP |
MAP3K12 binding inhibitory protein 1 |
218476_AT |
POMT1 |
protein-O-mannosyltransferase 1 |
218921_AT |
SIGIRR |
single immunoglobulin and toll-interleukin 1 receptor (TIR) domain |
221760_AT |
MAN1A1 |
mannosidase, alpha, class 1A, member 1 |
221920_S_AT |
SLC25A37 |
solute carrier family 25, member 37 |
222164_AT |
FGFR1 |
fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome) |
37577_AT |
ARHGAP19 |
Rho GTPase activating protein 19 |