Data table |
ID |
Row |
Col |
GB_LIST |
SPOT_ID |
Accessions |
SEQUENCE |
ProbeUID |
ControlType |
ProbeName |
GeneName |
SystematicName |
Description |
1 |
1 |
1 |
|
--HsCGHBrightCorner |
|
|
0 |
1 |
HsCGHBrightCorner |
HsCGHBrightCorner |
HsCGHBrightCorner |
|
2 |
1 |
2 |
|
--NegativeControl |
|
|
1 |
-1 |
(-)3xSLv1 |
NegativeControl |
NegativeControl |
|
3 |
1 |
3 |
|
A_14_P115839 |
|
GTTGGAATATTAAAACAGTATAGCAGTGGCACTGGAAAGGCACACTGATTATCATCATTT |
2 |
0 |
A_14_P115839 |
chr3:018780643-018780702 |
chr3:018780643-018780702 |
Unknown |
4 |
1 |
4 |
NM_004646 |
|
ref|NM_004646|gb|AF035835 |
CATTTCATTTTTGAGACGACGTTTACAATCTGCCCTGTCCTTTTGGAGAAGTTTAGTT |
4 |
0 |
A_14_P138950 |
NPHS1 |
chr19:041008990-041009047 |
Homo sapiens nephrosis 1, congenital, Finnish type (nephrin) (NPHS1), mRNA [NM_004646] |
5 |
1 |
5 |
NM_017859 |
|
ref|NM_017859|gb|AK000524 |
ACACAGCAAGGACAGAGGAACAGCAAACAAGGACAAGGGAAGGAG |
6 |
0 |
A_16_P03549975 |
UCKL1 |
chr20:062048974-062049018 |
Homo sapiens uridine-cytidine kinase 1-like 1 (UCKL1), mRNA [NM_017859] |
6 |
1 |
6 |
NM_015047 |
|
ref|NM_015047|gb|BX648708 |
ACCCATTAAATGAAAAAAAGCAAATTTCATAAGAATAAATATAGGTCAATTGCATGTGAA |
8 |
0 |
A_16_P00024200 |
KIAA0090 |
chr1:019300490-019300549 |
Homo sapiens KIAA0090 protein (KIAA0090), mRNA [NM_015047] |
7 |
1 |
7 |
NM_018962 |
|
ref|NM_018962|gb|AB037158 |
TACTGCCACTCTGAATTTGATGCTCTCCTCTGCCAAAATAGTCTTAGAATTGCAAAC |
10 |
0 |
A_16_P03584307 |
DSCR6 |
chr21:037307276-037307332 |
Homo sapiens Down syndrome critical region gene 6 (DSCR6), mRNA [NM_018962] |
8 |
1 |
8 |
|
A_14_P138260 |
|
AAGTTTGACCAACAGGATGTGAATAAAATCCAATCCTAAATCTCTGACTGTTTCACATCA |
12 |
0 |
A_14_P138260 |
chr3:036246365-036246424 |
chr3:036246365-036246424 |
Unknown |
9 |
1 |
9 |
|
A_14_P131265 |
|
AGTTCAATTCCAATCATGACTCATTGGCTTAGCCATCAAAGTTTATCTTTCCTTTTGAAC |
14 |
0 |
A_14_P131265 |
chr3:118756165-118756224 |
chr3:118756165-118756224 |
Unknown |
10 |
1 |
10 |
NM_004504 |
|
ref|NM_004504|gb|BC030592 |
TGAAATCTATCTCCATGACAACATTCACACAACAGGAAATTGAATTCTTACAAAAACATG |
16 |
0 |
A_14_P135304 |
HRB |
chr2:228181794-228181853 |
Homo sapiens HIV-1 Rev binding protein (HRB), mRNA [NM_004504] |
11 |
1 |
11 |
|
A_16_P02079559 |
|
ACAGGTGCAATGAAGTCATAATTATTCTTAAACTAATATTTTGACTATTCCATGTCTGGA |
18 |
0 |
A_16_P02079559 |
chr9:024277463-024277522 |
chr9:024277463-024277522 |
Unknown |
12 |
1 |
12 |
NM_003982 |
|
ref|NM_003982|gb|BX248291 |
TATAAAAAGAAATTATGGAGGCAAATTGTGAAATTTAACATCTTCAGAGAATAAGATAGG |
20 |
0 |
A_16_P02874260 |
SLC7A7 |
chr14:022316369-022316428 |
Homo sapiens solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 (SLC7A7), mRNA [NM_003982] |
13 |
1 |
13 |
NM_173653 |
|
ref|NM_173653|gb|BC035779 |
GCACTAACATATAACATAGTTCACATACCTGAAAACATCATCATGTGCTGAAAGTTCCAG |
22 |
0 |
A_14_P135194 |
SLC9A9 |
chr3:144695165-144695224 |
Homo sapiens solute carrier family 9 (sodium/hydrogen exchanger), isoform 9 (SLC9A9), mRNA [NM_173653] |
14 |
1 |
14 |
NM_000034 |
|
ref|NM_000034|gb|BC062756 |
GGATTGTTACTAAGTGAACTAAGTGAAAATATTTTAATTTAATTGTAACTAAGTATTTGA |
24 |
0 |
A_16_P03134367 |
ALDOA |
chr16:029986803-029986862 |
Homo sapiens aldolase A, fructose-bisphosphate (ALDOA), transcript variant 1, mRNA [NM_000034] |
15 |
1 |
15 |
NM_032030 |
|
ref|NM_032030|gb|AF352327 |
CTCCATGTATGAGAACAGCCTAATCCTGGAGAACATTACTAGTTTTGTTTCATCTTCCTA |
26 |
0 |
A_14_P111497 |
FKSG83 |
chr6:027401385-027401444 |
Homo sapiens FKSG83 (FKSG83), mRNA [NM_032030] |
16 |
1 |
16 |
NM_020137 |
|
ref|NM_020137|gb|AB032993 |
TGCCATGGAAGCACTGCTCACTTCCAGGTGCTTCACCTGCAAGAT |
28 |
0 |
A_16_P03702938 |
GRIPAP1 |
chrX:048588736-048588780 |
Homo sapiens GRIP1 associated protein 1 (GRIPAP1), transcript variant 1, mRNA [NM_020137] |
17 |
1 |
17 |
|
A_14_P105275 |
|
ATTAATTTTACGTTTGTGCGATATACAAATAAGTGAGAGCCCTTCAGTGTTCAGTGCTCA |
30 |
0 |
A_14_P105275 |
chr4:112074591-112074650 |
chr4:112074591-112074650 |
Unknown |
18 |
1 |
18 |
NM_001427 |
|
ref|NM_001427|ens|ENST00000297375 |
GAGGGTGAACTTCGCTCTTTGCCTTAAACCTCTTTATTTCATTGCAGTAATAGTTTTACG |
32 |
0 |
A_14_P128961 |
EN2 |
chr7:154756593-154756652 |
Homo sapiens engrailed homolog 2 (EN2), mRNA [NM_001427] |
19 |
1 |
19 |
NM_032866 |
|
ref|NM_032866|gb|AY274808 |
CCAGGAATACACGCATCTGCACAAATATATGAATGTCTAGCACAAAAGATTTGCAAATCA |
34 |
0 |
A_16_P03037034 |
CGNL1 |
chr15:055607783-055607842 |
Homo sapiens cingulin-like 1 (CGNL1), mRNA [NM_032866] |
20 |
1 |
20 |
NM_000158 |
|
ref|NM_000158|gb|L07956 |
AATCCATCAAAGCGATATTCTTCCAACCACCATCTTATGTTTGACAGAAGGAATCTTAAA |
36 |
0 |
A_14_P108066 |
GBE1 |
chr3:081725796-081725855 |
Homo sapiens glucan (1,4-alpha-), branching enzyme 1 (glycogen branching enzyme, Andersen disease, glycogen storage disease type IV) (GBE1), mRNA [NM_000158] |