L2L L2L Microarray Analysis Tool

Gene in N07CA.profile.d50

Results summary View all lists in GO:BiolProc View all genes in N07CA.profile.d50
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