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Query

  for well, siRNA ID, RefSeq or HGNC symbol:     (ex: SON, COP, 30I23, 01202, negative controls: A04, B04)

Phenoprint

Well siRNA ID RefSeqHGNC symbol Phenoprint
42P11M-014656-00 NM_030797 FAM49A
nSETsirABCMLP

Similar phenoprints

Well siRNA ID RefSeqHGNC symbol Phenoprint
33L10M-007570-00 NM_014579 SLC39A2
nSETsirABCMLP
45M12M-024046-00 NM_138364
12D15M-012207-00 NM_006421 ARFGEF1
30J15M-016509-00 NM_007211 RASSF8
12A18M-010064-01 NM_001032288
NM_021988
NM_199144
NM_022442
NM_199203
NM_003349
XR_038933
XR_016054
XR_016022
XM_001716419
UBE2V1
TMEM189-UBE2V1
50A12M-018853-00 NM_144715 EFHB
15K21M-003845-01 NM_002336 LRP6
56K21M-031786-00 NM_198527 HDDC3
54G16M-031382-00 *XM_379011
10E20M-005804-00 NM_001748 CAPN2
35E23M-020255-00 NM_016056 TMBIM4
29B23M-019994-00 NM_005849 IGSF6
24J11M-006261-00 NM_001017424
NM_014217
NM_001017425
KCNK2
30D12M-019138-00 NM_016128 COPG
44K10M-010185-00 NM_032709 C10ORF33
40K19M-014097-00 NM_022489
NM_001031714
INF2
37N05M-010579-00 NM_018428 UTP6
67A09M-005415-01 NM_000674
NM_001048230
ADORA1
35C23M-021482-00 NM_198097
NM_015622
XM_001720226
C7ORF28B
C7ORF28A

Phenotype (primary screen)

Well siRNA ID RefSeq HGNC symbol Phenotype
42P11M-014656-00 NM_030797 FAM49A
Segmentation
Cell features
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