spacer

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
26M16M-019708-00 NM_003007
NM_198139
SEMG1
nSETsirABCMLP

Similar phenoprints

Well siRNA ID RefSeqHGNC symbol Phenoprint
60F11M-028071-00 *XM_374033
nSETsirABCMLP
40E22M-016323-00 NM_022760 FAM113A
10H21M-008265-00 NM_006088 TUBB2C
29M06M-012128-00 NM_005791 MPHOSPH10
26C08M-011159-00 NM_000990
NM_001089587
RPL27A
05E16M-008837-00 NM_032456
NM_032457
NM_002589
PCDH7
18G10M-010989-00 NM_000477 ALB
04E11M-017611-00 NM_006051
NM_133174
NM_133173
NM_133172
APBB3
24J16M-009294-00 NM_023033
NM_005371
XR_037151
XR_019542
XR_017097
METTL1
60I13M-027763-00 XM_001722545 FLJ41481
04K18M-008805-00 NM_004381 CREBL1
54D22M-006320-00 NM_001105558 WEE2
37G07M-007449-00 NM_018420 SLC22A15
25C18M-019642-00 XR_041459
XR_041457
XR_041458
SLC22A18AS
32D11M-013946-00 NM_015481 ZNF385A
45N09M-008374-01 NM_052998 ADC
08J05M-011631-00 NM_001014444
NM_001888
CRYM
60C05M-027646-00 NM_001099790
NM_001099850
XM_001713666
PRAMEF19
PRAMEF18
PRAMEF3
50M11M-007336-00 NM_173512 SLC38A11

Phenotype (primary screen)

Well siRNA ID RefSeq HGNC symbol Phenotype
26M16M-019708-00 NM_003007
NM_198139
SEMG1
Segmentation
Cell features
spacer
spacer