Top 105 probe sets selected for genes overexpressed in DS AMkL compared with non-DS AMkL
Gene name . | Fold change . | Gene symbol . | GenBank no. . | Chromosomal location . | Description . |
---|---|---|---|---|---|
219870_at | 0.5 | ATF71P2 | NM_024997 | 16p13.2 | Activating transcription factor 7 interacting protein 2 |
203377_s_at | 0.498 | CDC40 | NM_015891 | 6q22.1 | Cell division cycle 40 homolog (yeast) |
217793_at | 0.494 | RAB11B | AL575337 | 19p13.3 | RAB11B, member RAS oncogene family |
206875_s_at | 0.491 | SLK | NM_014720 | 10q25.1 | SNF1 sucrose nonfermenting like kinase (yeast) |
203910_at | 0.491 | PARG1 | NM_004815 | 1p22.1 | PTPL1-associated RhoGAP1 |
221832_s_at | 0.491 | AOF2 | AV741657 | 1p36.11 | Amine oxidase (flavin containing) domain 2 |
210718_s_at | 0.49 | LOC51326 | AF119889 | 17q21.32 | ARF protein |
218712_at | 0.489 | FLJ20508 | NM_017850 | 1p34.2 | Hypothetical protein FLJ20508 |
214801_at | 0.485 | — | W88821 | — | CDNA FLJ11392 fis, clone HEMBA1000575 |
212246_at | 0.482 | MCFD2 | BE880828 | 2p21 | Multiple coagulation factor deficiency 2 |
202008_s_at | 0.48 | NID | NM_002508 | 1q43 | Nidogen (enactin) |
202421_at | 0.476 | IGSF3 | AB007935 | 1p13 | Immunoglobulin superfamily, member 3 |
222329_x_at | 0.463 | — | AW974816 | — | Transcribed sequence with weak similarity to protein sp:P39188 (Homo sapiens) ALU1_HUMAN Alu subfamily J sequence contamination warning entry |
202557_at | 0.46 | STCH | AI718418 | 21q11.1 | Stress 70 protein chaperone, microsome-associated, 60 kDa |
209045_at | 0.459 | XPNPEP1 | AF195530 | 10q25.3 | X-prolyl aminopeptidase (aminopeptidase P) 1, soluble |
218344_s_at | 0.457 | FLJ10876 | NM_018254 | 1q32.3 | Hypothetical protein FLJ10876 |
202468_s_at | 0.451 | CTNNAL1 | NM_003798 | 9q31.2 | Catenin (cadherin-associated protein), α-like 1 |
203015_s_at | 0.451 | SSX2IP | AW136988 | — | Synovial sarcoma, X breakpoint 2 interacting protein |
203224_at | 0.447 | FLJ11149 | BF340123 | 9q21.31 | Riboflavin kinase |
203225_s_at | 0.443 | FLJ11149 | NM_018339 | 9q21.31 | Riboflavin kinase |
202932_at | 0.442 | YES1 | NM_005433 | 18p11.31–p11.21 | v-yes-1 Yamaguchi sarcoma viral oncogene homolog 1 |
214205_x_at | 0.44 | TXNL2 | AK022131 | 6p25.3 | Thioredoxin-like 2 |
204417_at | 0.439 | GALC | NM_000153 | 14q31 | Galactosylceramidase (Krabbe disease) |
210818_s_at | 0.437 | BACH1 | AF026199 | 21q22.11 | BTB and CNC homology 1, basic leucine zipper transcription factor 1 |
207332_s_at | 0.433 | TFRC | NM_003234 | 3q26.2-qter | Transferrin receptor (p90, CD71) |
202949_s_at | 0.432 | FHL2 | NM_001450 | 2q12-q14 | Four and a half LIM domains 2 |
221580_s_at | 0.425 | MGC5306 | BC001972 | 11q21 | Hypothetical protein MGC5306 |
207386_at | 0.42 | CYP7B1 | NM_004820 | 8q21.3 | Cytochrome P450, family 7, subfamily B, polypeptide 1 |
207845_s_at | 0.42 | APC10 | NM_014885 | 4q31 | Anaphase-promoting complex subunit 10 |
212884_x_at | 0.414 | APOE | AI358867 | 19q13.2 | Apolipoprotein E |
212978_at | 0.413 | TA-LRRP | AU146004 | 1p22.2 | T-cell activation leucine repeat-rich protein |
211810_s_at | 0.405 | GALC | D25284 | 14q31 | Galactosylceramidase (Krabbe disease) |
202506_at | 0.405 | SSFA2 | NM_006751 | 2q32.1 | Sperm-specific antigen 2 |
206693_at | 0.403 | IL7 | NM_000880 | 8q12-q13 | Interleukin-7 |
203640_at | 0.401 | — | BE328496 | 13q32.2 | hs98f09.x1 NCI_CGAP_Kid13 Homo sapiens cDNA clone IMAGE:3145289 3′, mRNA sequence |
208398_s_at | 0.392 | TBPL1 | NM_004865 | 6q22.1–q22.3 | TBP-like 1 |
214252_s_at | 0.388 | — | AV700514 | 13q21.1–q32 | AV700514 GKC Homo sapiens cDNA clone GKCDQC04 3′, mRNA sequence |
204624_at | 0.387 | ATP7B | NM_000053 | 13q14.2–q21 | ATPase, Cu++ transporting, β polypeptide (Wilson disease) |
213757_at | 0.386 | EIF5A | AA393940 | 17p13-p12 | Eukaryotic translation initiation factor 5A |
203789_s_at | 0.382 | SEMA3C | NM_006379 | 7q21-q31 | Sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C |
209267_s_at | 0.373 | SLC39A8 | AB040120 | 4q22-q24 | Solute carrier family 39 (zinc transporter), member 8 |
216063_at | 0.369 | HBBP1 | N55205 | — | Transcribed sequence with moderate similarity to protein sp:P02096 (Homo sapiens) HBG_HUMAN hemoglobin γ-A and γ-G chains |
208691_at | 0.367 | TFRC | BC001188 | 3q26.2-qter | Transferrin receptor (p90, CD71) |
212990_at | 0.366 | SYNJ1 | AB020717 | 21q22.2 | Synaptojanin 1 |
213358_at | 0.365 | KIAA0802 | AB018345 | 18p11.22 | KIAA0802 protein |
202558_s_at | 0.361 | STCH | NM_006948 | 21q11.1 | Stress 70 protein chaperone, microsome-associated, 60 kDa |
203019_x_at | 0.36 | SSX2IP | NM_014021 | — | Synovial sarcoma, X breakpoint 2 interacting protein |
205667_at | 0.358 | WRN | NM_000553 | 8p12-p11.2 | Werner syndrome |
219177_at | 0.355 | BRIX | NM_018321 | 5p13.3 | BRIX |
209676_at | 0.354 | TFPI | J03225 | 2q31-q32.1 | Tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor) |
212558_at | 0.351 | GDAP1L1 | BF508662 | 20q12 | Ganglioside-induced differentiation-associated protein 1-like 1 |
203017_s_at | 0.346 | SSX21P | R52678 | — | Synovial sarcoma, X breakpoint 2 interacting protein |
204976_s_at | 0.338 | AMMECR1 | AK023637 | Xq22.3 | Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis chromosomal region, gene 1 |
216398_at | 0.338 | GYPE | U05255 | 4q31.1 | Glycophorin E |
219795_at | 0.334 | SLC6A14 | NM_007231 | Xq23-q24 | Solute carrier family 6 (neurotransmitter transporter), member 14 |
203544_s_at | 0.329 | STAM | NM_003473 | 10p14-p13 | Signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 |
210664_s_at | 0.318 | TFPI | AF021834 | 2q31-q32.1 | Tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor) |
202479_s_at | 0.316 | TRB2 | BC002637 | 2p25.1 | Tribbles homolog 2 |
202481_at | 0.31 | DHRS3 | NM_004753 | 1p36.1 | Dehydrogenase/reductase (SDR family) member 3 |
217388_s_at | 0.31 | KYNU | D55639 | 2q22.3 | Kynureninase (L-kynurenine hydrolase) |
Gene name . | Fold change . | Gene symbol . | GenBank no. . | Chromosomal location . | Description . |
---|---|---|---|---|---|
219870_at | 0.5 | ATF71P2 | NM_024997 | 16p13.2 | Activating transcription factor 7 interacting protein 2 |
203377_s_at | 0.498 | CDC40 | NM_015891 | 6q22.1 | Cell division cycle 40 homolog (yeast) |
217793_at | 0.494 | RAB11B | AL575337 | 19p13.3 | RAB11B, member RAS oncogene family |
206875_s_at | 0.491 | SLK | NM_014720 | 10q25.1 | SNF1 sucrose nonfermenting like kinase (yeast) |
203910_at | 0.491 | PARG1 | NM_004815 | 1p22.1 | PTPL1-associated RhoGAP1 |
221832_s_at | 0.491 | AOF2 | AV741657 | 1p36.11 | Amine oxidase (flavin containing) domain 2 |
210718_s_at | 0.49 | LOC51326 | AF119889 | 17q21.32 | ARF protein |
218712_at | 0.489 | FLJ20508 | NM_017850 | 1p34.2 | Hypothetical protein FLJ20508 |
214801_at | 0.485 | — | W88821 | — | CDNA FLJ11392 fis, clone HEMBA1000575 |
212246_at | 0.482 | MCFD2 | BE880828 | 2p21 | Multiple coagulation factor deficiency 2 |
202008_s_at | 0.48 | NID | NM_002508 | 1q43 | Nidogen (enactin) |
202421_at | 0.476 | IGSF3 | AB007935 | 1p13 | Immunoglobulin superfamily, member 3 |
222329_x_at | 0.463 | — | AW974816 | — | Transcribed sequence with weak similarity to protein sp:P39188 (Homo sapiens) ALU1_HUMAN Alu subfamily J sequence contamination warning entry |
202557_at | 0.46 | STCH | AI718418 | 21q11.1 | Stress 70 protein chaperone, microsome-associated, 60 kDa |
209045_at | 0.459 | XPNPEP1 | AF195530 | 10q25.3 | X-prolyl aminopeptidase (aminopeptidase P) 1, soluble |
218344_s_at | 0.457 | FLJ10876 | NM_018254 | 1q32.3 | Hypothetical protein FLJ10876 |
202468_s_at | 0.451 | CTNNAL1 | NM_003798 | 9q31.2 | Catenin (cadherin-associated protein), α-like 1 |
203015_s_at | 0.451 | SSX2IP | AW136988 | — | Synovial sarcoma, X breakpoint 2 interacting protein |
203224_at | 0.447 | FLJ11149 | BF340123 | 9q21.31 | Riboflavin kinase |
203225_s_at | 0.443 | FLJ11149 | NM_018339 | 9q21.31 | Riboflavin kinase |
202932_at | 0.442 | YES1 | NM_005433 | 18p11.31–p11.21 | v-yes-1 Yamaguchi sarcoma viral oncogene homolog 1 |
214205_x_at | 0.44 | TXNL2 | AK022131 | 6p25.3 | Thioredoxin-like 2 |
204417_at | 0.439 | GALC | NM_000153 | 14q31 | Galactosylceramidase (Krabbe disease) |
210818_s_at | 0.437 | BACH1 | AF026199 | 21q22.11 | BTB and CNC homology 1, basic leucine zipper transcription factor 1 |
207332_s_at | 0.433 | TFRC | NM_003234 | 3q26.2-qter | Transferrin receptor (p90, CD71) |
202949_s_at | 0.432 | FHL2 | NM_001450 | 2q12-q14 | Four and a half LIM domains 2 |
221580_s_at | 0.425 | MGC5306 | BC001972 | 11q21 | Hypothetical protein MGC5306 |
207386_at | 0.42 | CYP7B1 | NM_004820 | 8q21.3 | Cytochrome P450, family 7, subfamily B, polypeptide 1 |
207845_s_at | 0.42 | APC10 | NM_014885 | 4q31 | Anaphase-promoting complex subunit 10 |
212884_x_at | 0.414 | APOE | AI358867 | 19q13.2 | Apolipoprotein E |
212978_at | 0.413 | TA-LRRP | AU146004 | 1p22.2 | T-cell activation leucine repeat-rich protein |
211810_s_at | 0.405 | GALC | D25284 | 14q31 | Galactosylceramidase (Krabbe disease) |
202506_at | 0.405 | SSFA2 | NM_006751 | 2q32.1 | Sperm-specific antigen 2 |
206693_at | 0.403 | IL7 | NM_000880 | 8q12-q13 | Interleukin-7 |
203640_at | 0.401 | — | BE328496 | 13q32.2 | hs98f09.x1 NCI_CGAP_Kid13 Homo sapiens cDNA clone IMAGE:3145289 3′, mRNA sequence |
208398_s_at | 0.392 | TBPL1 | NM_004865 | 6q22.1–q22.3 | TBP-like 1 |
214252_s_at | 0.388 | — | AV700514 | 13q21.1–q32 | AV700514 GKC Homo sapiens cDNA clone GKCDQC04 3′, mRNA sequence |
204624_at | 0.387 | ATP7B | NM_000053 | 13q14.2–q21 | ATPase, Cu++ transporting, β polypeptide (Wilson disease) |
213757_at | 0.386 | EIF5A | AA393940 | 17p13-p12 | Eukaryotic translation initiation factor 5A |
203789_s_at | 0.382 | SEMA3C | NM_006379 | 7q21-q31 | Sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C |
209267_s_at | 0.373 | SLC39A8 | AB040120 | 4q22-q24 | Solute carrier family 39 (zinc transporter), member 8 |
216063_at | 0.369 | HBBP1 | N55205 | — | Transcribed sequence with moderate similarity to protein sp:P02096 (Homo sapiens) HBG_HUMAN hemoglobin γ-A and γ-G chains |
208691_at | 0.367 | TFRC | BC001188 | 3q26.2-qter | Transferrin receptor (p90, CD71) |
212990_at | 0.366 | SYNJ1 | AB020717 | 21q22.2 | Synaptojanin 1 |
213358_at | 0.365 | KIAA0802 | AB018345 | 18p11.22 | KIAA0802 protein |
202558_s_at | 0.361 | STCH | NM_006948 | 21q11.1 | Stress 70 protein chaperone, microsome-associated, 60 kDa |
203019_x_at | 0.36 | SSX2IP | NM_014021 | — | Synovial sarcoma, X breakpoint 2 interacting protein |
205667_at | 0.358 | WRN | NM_000553 | 8p12-p11.2 | Werner syndrome |
219177_at | 0.355 | BRIX | NM_018321 | 5p13.3 | BRIX |
209676_at | 0.354 | TFPI | J03225 | 2q31-q32.1 | Tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor) |
212558_at | 0.351 | GDAP1L1 | BF508662 | 20q12 | Ganglioside-induced differentiation-associated protein 1-like 1 |
203017_s_at | 0.346 | SSX21P | R52678 | — | Synovial sarcoma, X breakpoint 2 interacting protein |
204976_s_at | 0.338 | AMMECR1 | AK023637 | Xq22.3 | Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis chromosomal region, gene 1 |
216398_at | 0.338 | GYPE | U05255 | 4q31.1 | Glycophorin E |
219795_at | 0.334 | SLC6A14 | NM_007231 | Xq23-q24 | Solute carrier family 6 (neurotransmitter transporter), member 14 |
203544_s_at | 0.329 | STAM | NM_003473 | 10p14-p13 | Signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 |
210664_s_at | 0.318 | TFPI | AF021834 | 2q31-q32.1 | Tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor) |
202479_s_at | 0.316 | TRB2 | BC002637 | 2p25.1 | Tribbles homolog 2 |
202481_at | 0.31 | DHRS3 | NM_004753 | 1p36.1 | Dehydrogenase/reductase (SDR family) member 3 |
217388_s_at | 0.31 | KYNU | D55639 | 2q22.3 | Kynureninase (L-kynurenine hydrolase) |