| Description | mRNA expression profiles for cell lines or tissues following genetic perturbation (knockdown, knockout, over-expression, mutation) |
| Measurement | gene expression by microarray |
| Association | gene-gene associations by differential expression of gene A following perturbation of gene B |
| Category | transcriptomics |
| Resource | Gene Expression Omnibus |
| Citation(s) | |
| Last Updated |
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Attribute Similarity
Dataset
Gene Similarity
739 sets of genes differentially expressed following gene perturbations from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
| Gene Set | Description |
|---|---|
| A2BAR_Deficiency_GDS3662_520_mouse_Heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ABCA1_OE_GDS2303_189_mouse_LDL receptor-deficient livers | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ACADM_KO_GDS4546_512_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ACHE_OE_GDS891_241_mouse_Prefrontal cortex | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ADNP_Deficiency - NULL MUTATION_GDS2540_691_mouse_E9 embryos - Heterozygous mutant | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ADNP_Deficiency - NULL MUTATION_GDS2540_692_mouse_E9 embryos - Homozygous mutant | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| AICD_Induced expression / Over-expression_GDS1979_288_human_SHEP-SF neuroblastoma | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Aiolos_NULL MUTATION_GDS3473_572_mouse_Bone marrow pre-BII cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| AIRE_KO_GDS2015_33_mouse_thymic epithelial cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| AIRE_KO_GDS2274_245_mouse_Medullary thymic epithelial cells (with low CD80 expression) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| AIRE_KO_GDS2274_246_mouse_Medullary thymic epithelial cells (with high CD80 expression) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| AKT1_Activation - 2 week induction_GDS2308_717_mouse_Heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| AKT1_Activation - 6 week induction_GDS2308_718_mouse_Heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| AKT1_OE_GDS2308[_473_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| AKT1_OE_GDS2308_498_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| AKT1_OE_GDS2308_499_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| AKT1_OE_GDS2308_508_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ALAS2_OE_GDS2118_74_human_Blood | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ALDH1A2_KO_GDS4836_289_mouse_posterior embryonic brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ALDH1A2_KO_GDS4836_290_mouse_anterior embryonic brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ALK_KD_GDS2724_105_human_DAOY medulloblastoma cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| AMER1_OE_GDS4802_549_human_HEK293 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| AMPK gamma-3_KO_GDS1938_163_mouse_Skeletal muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| APLN_KO_GDS3228_601_mouse_Heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| APLP2_KO_GDS4414_371_mouse_prefrontal cortex | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| APLP2_KO_GDS4414_534_mouse_adult cortex | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| APLP2_KO_GDS4414_536_mouse_adult cortex | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| APOD_KO_GDS3913_487_mouse_Cerebellum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| APOD_OE_GDS3913_489_mouse_Cerebellum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| APP_KO_GDS4414_370_mouse_prefrontal cortex | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| AQP11_Deficiency_GDS3395_578_mouse_Kidney | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ARHGDIB_Transfection_GDS4455_551_human_UM-UC-3 bladder carcinoma cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ARX_KO_GSE12609_3_mouse_brain (subpallium, Pou3f-expressing cells) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ATM_Deficiency_GDS1544_769_mouse_Lymph nodes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ATM_KD_GSE54268_661_human_MCF-10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ATM_KD_GSE54268_662_human_MCF-10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ATM_KD_GSE54268_663_human_MCF-10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ATR_KD_GSE54268_664_human_MCF-10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| BCL11B_KO_GDS3178_296_mouse_striatum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| BCL11B_KO_GSE9330_4_mouse_brain (striatum) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| BHLHA15_KO_GDS4341_145_mouse_pancreas | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| BMI-1_DEPLETION_GDS2445_115_human_embryonic fibroblasts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Bmi-1_KD_GDS2724_102_human_DAOY medulloblastoma cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Bmi1_Deficiency_GDS4816_323_mouse_Primary lung cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| BNC1_KD_GDS1978_70_mouse_oocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| BNC1_KD_GDS1978_738_mouse_Oocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| BRAF_drug inhibition_GSE42872_368_human_A375 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| BRCA1_DEPLETION_GDS2189_121_human_MCF10A mammary epithelial cells (MECs) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| BRCA1_DEPLETION_GDS3791_38_human_Hela | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| BRCA1_DEPLETION_GDS3791_502_human_Hela cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| BRG1_DEPLETION_GDS2156_720_mouse_Embryos (maternally depleted) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Brn3a_KO_GDS1651_247_mouse_Embryonic (day 13.5) trigeminal ganglia - heterozygous | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Brn3a_KO_GDS1651_248_mouse_Embryonic (day 13.5) trigeminal ganglia - homozygous | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| BTK_KO_GDS1346_302_mouse_splenic B cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| c-MYC_KD_GDS2526_109_human_Hela cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| c-MYC_KD_GDS2526_110_human_BT-474 BREAST CANCER cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| c-MYC_KD_GDS2526_112_human_MCF-7 BREAST CANCER cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| c-MYC_KD_GDS2526_113_human_MDA-MB-231 BREAST CANCER cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| c-Myc_OE_GDS3321_157_mouse_lung adenocarcinomas alveolar epithelia | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CADM1_Deficiency_GDS2027_722_mouse_Testis | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CADM1_KO_GDS2026_301_mouse_testis | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CALR_KO_GDS3680_149_mouse_embryonic stem cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CAV1_Deficiency_GDS3551_559_mouse_Hearts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CAV1_KO_GDS3551_366_mouse_mouse heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CAV3_Deficiency_GDS3552_558_mouse_Hearts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CAV3_KO_GDS3533_17_mouse_mammary glands | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CAV3_KO_GDS3533_357_mouse_mammalian glands | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CBFA2T3_KD_GDS4045_458_human_Non-Hodgkin's lymphoma Reh cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CBFbeta_Deficiency_GDS3577_557_mouse_Regulatory T cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| cbp_cpb heterozygous mice_GSE30880_328_mouse_Hippocampus | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CBX2_KO_GDS4445_353_mouse_E11.5 XX embryonic gonads | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CBX2_KO_GDS4445_354_mouse_E11.5 XY embryonic gonads | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CD24_Reduced expression_GDS1392_93_human_Bone Marrow | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CFTR_Deficiency_GDS1843_191_mouse_Lungs - Animals examined at 3 weeks of age | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CFTR_Deficiency_GDS1843_192_mouse_Lungs - Animals examined at 6 weeks of age | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CHK1_KD_GSE54267_671_human_U2OS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CHK1_KD_GSE54267_672_human_U2OS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CHK1_KD_GSE54268_665_human_MCF-10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CHK1_KD_GSE54268_666_human_MCF-10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CHK2_KD_GSE54268_667_human_MCF-10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CHK2_KD_GSE54268_668_human_MCF-10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CHRNB4_Deficiency_GDS2309_714_mouse_Brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CIDEC_KO_GDS3776_552_mouse_Brown and white adipose tissues | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLDN18_KO_GDS4961_28_mouse_whole lung tissue | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLDN18_KO_GSE48443_44_mouse_lung | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLDN1_OE_GDS3510_31_human_CL1-5 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLDN1_OE_GDS3510_393_human_CL1-5 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GDS4791_104_mouse_testis | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GDS4791_106_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GDS4791_107_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GDS4791_108_mouse_brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GDS4791_374_mouse_Testies | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GDS4791_375_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GDS4791_376_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GDS4791_377_mouse_brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GDS4791_537_mouse_testis | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GDS4791_539_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GDS4791_541_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GDS4791_543_mouse_brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GSE40207_378_mouse_Testies | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GSE40207_379_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GSE40207_380_mouse_muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GSE40207_381_mouse_brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GSE40207_382_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GSE40207_388_mouse_testis | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GSE40207_392_mouse_Testis | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GSE40207_394_mouse_Liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GSE40207_396_mouse_Muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GSE40207_397_mouse_Brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CLPP_KO_GSE40207_399_mouse_Heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CMAH_KO_GDS4200_114_mouse_muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CMAH_KO_GDS4770_420_mouse_muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Cmah_KO_GDS4770_421_mouse_muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CNR_KO_GDS2820_636_mouse_Skin | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CREB_DEPLETION_GDS3487_41_human_K562 myeloid leukemia cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CSTB_KO_GDS5089_169_mouse_Cerebrellum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CSTB_KO_GDS5089_486_mouse_Cerebellum and granule neurons | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CSTB_KO_GDS5089_565_mouse_cerebellum and granule neurons | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CSTB_KO_GDS5090_198_mouse_Cerebellum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CSTB_KO_GDS5090_199_mouse_Cerebellum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CSTB_KO_GDS5090_200_mouse_Cerebellar granule cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CSTB_KO_GDS5090_398_mouse_cerebella | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CSTB_KO_GDS5091_23_mouse_cerebellar granule | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CSTB_KO_GSE47516_132_mouse_granule neurons | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CSTB_KO_GSE47516_18_mouse_brain (P7 cerebellum, P30 cerebellum, cerebellar granule cells) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CSTB_KO_GSE47516_677_mouse_mouse cerebellum P7 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CSTB_KO_GSE47516_678_mouse_mouse cerebellum at P30 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CTCF_DEPLETION_GDS3294_97_mouse_germinal vesicle (GV) oocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CtIP_DEPLETION_GDS2189_122_human_MCF10A mammary epithelial cells (MECs) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CTNNB1_Inactivation_GDS2984_628_mouse_Intestinal crypts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CTNNB1_OE_GDS4449_352_mouse_Embryonic kidney from E12.5 embryos (-catGOF-UB mutant) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CTNNB_Activation (deltaNB-cateninER transgenics)_GDS1560_766_mouse_Skin - 0 Day | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CTNNB_Activation (deltaNB-cateninER transgenics)_GDS1560_767_mouse_Skin - 1 Day | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CTNNB_Activation (deltaNB-cateninER transgenics)_GDS1560_768_mouse_Skin - 7 Day | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| CXCR7_Deficiency_GDS3183_604_mouse_Neonatal semilunar valves | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DBH_KO_GDS4324_362_mouse_Embryonic heart E10.5 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DBH_KO_GSE33906_53_mouse_heart (E10.5) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DES_KO_GDS4804_171_mouse_young skeletal muscles | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DICER1_Deficiency_GDS3685_518_mouse_Hepatocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DICER1_KO_GDS4504_582_mouse_bone marrow granulocyte-macrophage progenitors | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DICER1_KO_GDS4504_583_mouse_bone marrow granulocyte-macrophage progenitors | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DICER1_KO_GDS4504_584_mouse_bone marrow granulocyte-macrophage progenitors | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DICER1_KO_GDS4504_585_mouse_bone marrow granulocyte-macrophage progenitors | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DICER1_KO_GDS4504_586_mouse_bone marrow granulocyte-macrophage progenitors | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DJ-1_KD_GDS3750_373_human_SH-SY5Y | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DLX5_Deficiency_GDS4443_355_mouse_E10 embryos | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DLX5_Deficiency_GDS4443_356_mouse_E10.5 embryos otic vesicle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DLX5_KO_GSE22381_5_mouse_ear (otic vesicle) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DLX5_OE_GDS4577_345_mouse_Otic vesicle derived 2B1 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DMD_Deficiency_GDS2996_613_mouse_Cardiac muscles from 8-week (mdx animals) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DMD_Deficiency_GDS2996_614_mouse_Cardiac muscles from 10.5-month (mdx animals) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Dot1l_DELETION_GDS4295_426_mouse_AF9 - Mixed Lineage Leukemia (MLL) cells - 3 days | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DOT1L_DELETION_GDS4295_427_mouse_AF9 - Mixed Lineage Leukemia (MLL) cells - 5 days | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DOT1L_DELETION_GDS4295_428_mouse_AF9 - Mixed Lineage Leukemia (MLL) cells - 7 days | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DPP3_OE_GDS2653_650_human_IMR-32 neuroblastoma cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DUSP1_Deficiency_GDS1606_765_mouse_Spleen | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DUSP1_KO_GDS1606_772_mouse_spleens | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DUSP1_KO_GDS1606_773_mouse_spleens | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| DUSP1_KO_GDS1606_775_mouse_Spleens | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| E2A_Deficiency_GDS5084_271_mouse_DN2 thymocyte | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| E2A_KO_GDS5084_401_mouse_DN2 thymocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| E2A_KO_GSE43224_679_mouse_DN2 cells from WT and E2A-deficient murine fetal thymi | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| E2F1_KD_GDS4094_446_mouse_Mammary tumors | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| E2F2_KD_GDS4094_447_mouse_Mammary tumors (Myc-induced) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| E2F3_KD_GDS4094_448_mouse_Mammary tumors (Myc-induced) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EDD_DEPLETION_GDS2445_116_human_embryonic fibroblasts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EGFR_OE_GDS1925_167_human_Estrogen receptor (ER) alpha positive MCF-7 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EGR-1_KO_GDS3607_525_mouse_Retina - 30 Days (POST-NATAL) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EGR-1_KO_GDS3607_526_mouse_Retina - 42 Days (POST-NATAL) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EHMT2_KD_GDS4800_315_human_MDA-MB231 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EHMT2_KD_GSE34925_693_human_MDA-MB231 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EMX2_Deficiency_GDS3173_607_mouse_Embryonic urogenital epithelium - day 10.5 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EOMES_OE_GDS5077_65_human_RUES2 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EPCAM_OE_GDS4887_342_human_IL-28B | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EPCAM_OE_GDS4887_343_human_IL-28B | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| erbB-2_OE_GDS1925_164_human_Estrogen receptor (ER) alpha positive MCF-7 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ERRalpha_Deficiency_GDS2727_646_mouse_Heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ESET_KO_GDS4508_348_mouse_Dorsal telencephalon from E14.5 embryos | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ESR1_KD_GDS4061_453_human_MCF7 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ESR1_KD_GDS4065_452_human_MCF7 estrogen-sensitive breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ESRRG_Deficiency_GDS2811_637_mouse_Fetal heart - Heterozygous null mutant | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ESRRG_Deficiency_GDS2811_638_mouse_Fetal heart - Homozygous null mutant | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ETS2_KD_GDS5040_129_human_H441 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ETS2_KD_GDS5040_9_human_H441 lung cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ETS2_KD_GSE43459_687_human_H441 lung cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ETS2_KD_GSE62168_258_mouse_mouse trophoblast stem cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ETS2_KD_GSE62168_259_mouse_mouse trophoblast stem cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EWSR1_KD_GDS4962_465_human_Ewing sarcoma and prostate cancer | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EWSR1_KD_GDS4962_466_human_Ewing sarcoma and prostate cancer | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EWSR1_KD_GDS4962_467_human_not specified | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EWSR1_KD_GDS4962_468_human_Ewing sarcoma and prostate cancer | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EWSR1_KD_GDS4962_469_human_Ewing sarcoma and prostate cancer | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Ezh2_deficiency_GDS2717_141_mouse_lymph node T cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Ezh2_Deficiency_GDS4309_364_mouse_Hearts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| EZH2_DEPLETION_GDS2445_117_human_embryonic fibroblasts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Ezh2_KO_GDS3765_515_mouse_Primary preadipocyte cultures | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Fbxl10_OE_GDS4788_327_mouse_MEF fibroblast cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Fbxl10_OE_GDS4788_580_mouse_fibroblast cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Fbxl10_OE_GSE34691_579_mouse_fibroblast cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FFAR4_KO_GDS4811_507_mouse_adipose | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FGF23_OE_GDS3361_493_mouse_kidney | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FGFR3_KD_GDS4454_78_human_RT112 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FGFR3_KD_GDS4454_79_human_RT112 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FGFR3_KD_GSE41035_77_human_RT112 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FHL2_Deficiency_GDS3344_596_mouse_Spontaneously immortalized embryonic fibroblasts (EFs) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FIH_Deficiency_GDS3769_511_mouse_Immortalized embryonic fibroblasts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FIZZ2_KO_GDS4902_408_mouse_Lung | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FIZZ2_KO_GDS4902_409_mouse_Lung | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FMR1_KD_GDS4759_333_mouse_E16 primary cortical neuron cultures | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Fog2_KO_GDS3659_152_mouse_adult heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FOSL1_KO_GSE43695_680_mouse_lung, PBS treatment | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FOSL1_KO_GSE43695_681_mouse_lung, bleomycin treated | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FOXA1_OE_GDS4957_10_human_LNCaP prostate cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FOXA1_OE_GDS4957_144_human_LNCaP prostate cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FOXO1_KD_GDS2720_477_mouse_LSK | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FOXO1_KD_GDS2720_478_mouse_LSK | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FOXO1_KO_GSE40655_481_mouse_T reg | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FOXO1_KO_GSE46025_480_mouse_CD8 T cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FOXP3_ABLATION_GDS2525_64_mouse_mature regulatory T cells (Treg) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Fra-1_KO_GDS5078_402_mouse_Lung | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Fra-1_KO_GDS5078_403_mouse_Lung | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FSP27_KO_GDS3768_514_mouse_White adipose tissue (WAT) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| FURIN_Deficiency_GDS3512_568_mouse_T-cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GATA-1_KD_GDS1245_81_mouse_megakaryocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Gata-4_KO_GDS4782_329_mouse_Adult heart during pressure overload | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Gata-6_KO_GDS4782_330_mouse_Adult heart during pressure overload | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GATA3_Ectopic expression_GDS4080_622_human_Basal Breast Cancer Cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GATA4_Deletion - for the second exon_GDS2316_712_mouse_Heart ventricles (of GATA4 animals heterozygous) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GATA4_INACTIVATION_GDS3663_519_mouse_Endothelial-derived cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GATA4_KO_GDS3486_483_mouse_jejunum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GATA5_KO_GDS4809_170_mouse_Lung | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GATA5_KO_GSE47425_386_mouse_lung | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GATA5_KO_GSE47425_50_mouse_lung | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Get-1_Deficiency_GDS2629_161_mouse_embryonic skin | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GFAP_OE_GDS1488_254_mouse_Olfactory bulb of 23 day old | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GFAP_OE_GDS1488_255_mouse_Olfactory bulb of 4 month old | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Gfi1b_OE_GDS4302_425_mouse_AMuLV (pro-B Abelson leukemia virus transformed) cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GFI1_KO_GDS4204_147_mouse_HSC | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GK_KO_GDS1555_127_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GK_KO_GDS2610_162_mouse_Brown adipose tissue | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GLI3T_Lipofectamine transfection_GDS4346_616_human_Panc-1 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GLIS3_KO_GDS3812_500_mouse_Embryonic pancreas at E15.5 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GLO1_OE_GDS4991_546_mouse_anxiety disorders | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GPI-PLD_OE_GDS2049_176_human_Hepatoma HepG2 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GPR120_KO_GDS4830_413_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GPR120_KO_GDS4830_414_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GSK3A_KD_GDS4305_178_human_HL-60 acute myeloid leukemia cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GSK3A_KD_GDS4305_180_human_MOLM-14 myeloid leukemia cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GSK3A_KD_GDS4305_182_human_THP-1 acute myeloid leukemia cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GSK3A_KD_GDS4305_184_human_U937 acute myeloid leukemia cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GSK3B_KD_GDS4305_179_human_HL-60 acute myeloid leukemia cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GSK3B_KD_GDS4305_181_human_MOLM-14 myeloid leukemia cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GSK3B_KD_GDS4305_183_human_THP-1 acute myeloid leukemia cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GSK3B_KD_GDS4305_185_human_U937 acute myeloid leukemia cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| GSK3_INHIBITION_GDS4043_459_human_MLL leukemia cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| H19_DEPLETION_GDS4787_92_mouse_C2C12 myoblast cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| H6PD_KO_GDS3195_602_mouse_Skeletal muscle - Soleus | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| H6PD_KO_GDS3195_603_mouse_Skeletal muscle - Tibialis anterior | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HCaRG_OE_GDS1411_72_human_HEK293 embryonal kidney cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HCaRG_OE_GDS2426_711_human_HEK293 kidney cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HDAC1_KO_GDS2294_67_mouse_embryonic stem cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HDAC2_Deficiency_GDS2624_658_mouse_Embryonic heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HDAC3_KO_GDS4886_29_mouse_heart - 6 week old | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HDAC3_KO_GDS4886_66_mouse_Heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HDAC6_KO_GDS4375_372_mouse_CD4+CD25+ T-regulatory cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HDAC6_KO_GDS4375_532_mouse_Foxp3(+) Tregs | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HDAC6_KO_GSE27896_383_mouse_Foxp3+ T-regulatory cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HDAC_INHIBITION - trichostatin A_GDS2452_709_human_Endothelial cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HdhQ111/111_Knock-in_GDS4534_744_mouse_Striatum and cerebellum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HDH_CAG knock-in_GDS3935_569_mouse_Striatum and cerebellum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HER2_KO_GDS4056_567_human_breast biopsies | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HER2_OE_GDS4763_331_human_MCF10A - immortalized breast epithelial cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Her2_OE_GSE43730_683_human_MCF10A cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HES3_KD_GSE64449_187_mouse_Min6 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HES3_KO_GSE64449_186_mouse_Min6 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HIF-2alpha_DEPLETION_GDS2760_643_human_Hypoxic MCF-7 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HIF1A_DEPLETION_GDS2760_642_human_Hypoxic MCF-7 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HIF1A_NULL MUTATION_GDS1648_764_mouse_Hepatocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HMGA2_KO_GDS5048_26_mouse_embryonic lung | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HMGA2_KO_GSE55340_21_mouse_lung (E18.5) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Hmgn1_KO_GDS5010_405_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Hmgn1_KO_GDS5010_406_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Hmgn1_KO_GDS5010_407_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HMX1_Deficiency_GDS4810_324_mouse_Retinas of C57BL/6J | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HNF1A_OE_GDS1499_252_human_HEK293 embryonic kidney cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HNF1B_OE_GDS1499_253_human_HEK293 embryonic kidney cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HNF4alpha_DEPLETION_GDS4798_91_human_HepG2 hepatocellular carcinoma cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HNF4alpha_KO_GDS1915_173_mouse_Small intestine | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HNF4alpha_KO_GDS1916_168_mouse_Embryonic liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HNF4A_KD_GDS4798_550_human_HepG2 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HNF4A_KD_GSE29084_694_human_HepG2 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HOXB4_induction_GDS3036_138_mouse_ES cell-derived embryoid bodies (EBs) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Hoxc13_OE_GDS1890_174_mouse_Skin | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HSD17B4_KO_GDS3468_503_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HSF1_KD_GDS1733_750_human_HeLa cells - 0 Hour | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HSF1_KD_GDS1733_751_human_HeLa cells - 0.5 Hour by siHSF1_1 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HSF1_KD_GDS1733_752_human_HeLa cells - 2 Hour by siHSF1_1 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HSF1_KD_GDS1733_753_human_HeLa cells - 4 Hour by siHSF1_1 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HSF1_KD_GDS1733_754_human_HeLa cells - 0 Hour by siHSF1_2 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HSF1_KD_GDS1733_755_human_HeLa cells - 0.5 Hour by siHSF1_2 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HSF1_KD_GDS1733_756_human_HeLa cells - 2 Hour by siHSF1_2 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| HSF1_KD_GDS1733_757_human_HeLa cells - 4 Hour by siHSF1_2 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Hypb_Deficiency_GDS3641_522_mouse_Yolk sac from E9 embryos | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Hypb_Deficiency_GDS3641_523_mouse_Yolk sac from E10.5 embryos | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ID4_KO_GDS4178_620_mouse_Splenic B cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| IGF1_OE_GDS3484_538_human_MCF-7 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| IGF1_OE_GDS3484_540_human_MCF-7 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| IGF1_OE_GDS3484_542_human_MCF-7 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| IKBKB_Constitutional activation_GDS4119_621_mouse_Prostate epithelium | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| INSM1_Deficiency_GDS5066_272_mouse_Fetal pituitary glands from embryonic day 17.5 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| INSM1_KO_GDS5066_472_mouse_pituitary gland | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| INSM1_lack of the seven N-terminal amino acids_GDS5066_404_mouse_pituitary glands | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| IRAK4_Deficiency_GDS2641_653_mouse_Embryonic fibroblasts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| IRF6_KO_GDS2359_126_mouse_skin E17.5 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| IRS1_KO_GDS1219_303_mouse_brown preadipocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| IRS2_KO_GDS1219_304_mouse_brown preadipocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| IRS3P_KO_GDS1219_305_mouse_brown preadipocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| IRS4_KO_GDS1219_306_mouse_brown preadipocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ITGA7_OE_GDS3209_142_mouse_skeletal muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| JAG1_OE_GDS3571_40_human_endometrial stromal cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| JNK_KO_GDS3001_531_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| JUN_KO_GDS4205_294_mouse_B lymphoid cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Kdm1a_KD_GDS5055_274_mouse_3T3-L1 preadipocytes - 24h | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Kdm1a_KD_GDS5055_275_mouse_3T3-L1 preadipocytes - 48h | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KDM1A_KD_GDS5055_367_mouse_adipose tissue | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KDM1A_KD_GDS5055_457_mouse_adipose tissue | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KDM4C_natural variation_GSE41040_588_human_fibroblasts fron neonatal foreskin | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KDM4C_natural variation_GSE41040_589_human_fibroblasts fron neonatal foreskin | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KDM4C_natural variation_GSE41040_590_human_fibroblasts fron neonatal foreskin | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KLF15_Deficiency_GDS2687_648_mouse_Liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KLF15_Deficiency_GDS2687_649_mouse_Skeletal muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KLF15_KO_GDS4780_419_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KLF15_KO_GDS4780_509_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KLF5_KO_GDS3509_553_mouse_ES cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KLF7_KO_GDS2069_68_mouse_olfactory epithelia | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KLF9_Deficiency_GDS2703_647_mouse_Jejuna - intestine | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KRAP_Deficiency_GDS3527_566_mouse_Brown adipose tissues | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| KRAP_Deficiency_GDS3528_564_mouse_Liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LAMA2_Deficiency_GDS1778_747_mouse_Diaphragm (from dystrophia muscularis -dy/dy- mouse model) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LAMA2_Deficiency_GDS3371_595_mouse_Hind limb skeletal muscle (4-week old dy3K/dy3K animals) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LEDGF_KD_GDS1580_249_human_293T cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LHX1_KO_GDS2748_298_mouse_embryonic renal vesicles | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LHX1_NULL MUTATION - Ablation_GDS1748_748_mouse_Embryonic kidneys (from day E14.5) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LHX1_NULL MUTATION - Ablation_GDS1748_749_mouse_Embryonic kidneys (from day E18.5) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LHX8_Deficiency_GDS3254_600_mouse_Newborn ovaries | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LIPE_KO_GDS1318_501_mouse_muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LMNA_Lmna Gly609Gly knock-in_GDS4490_615_mouse_Liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LMX1B_KO_GDS3320_57_mouse_embryonic (e11.5) proximal hindlimb bud tissues | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LOX-1_OE_GDS4262_432_human_HAECT - aortic endothelial cell line - 2 Hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LOX-1_OE_GDS4262_433_human_HAECT - aortic endothelial cell line - 6 Hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LOX-1_OE_GDS4262_434_human_HAECT - aortic endothelial cell line - 12 Hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LOX-1_OE_GDS4262_435_human_HAECT - aortic endothelial cell line - 24 Hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LOXL2_DEPLETION_GDS4884_88_human_MDA-MB-231 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LOXL2_KD_GSE35600_688_human_MDA-MB-231 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LPIN1_OE_GDS2291_587_mouse_Liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LTBR_INHIBITION - 1 Day_GDS2004_733_mouse_Lymph nodes (MG-430A) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LTBR_INHIBITION - 1 Day_GDS2005_728_mouse_Lymph nodes (MG-430B) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LTBR_INHIBITION - 2 Days_GDS2004_734_mouse_Lymph nodes (MG-430A) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LTBR_INHIBITION - 2 Days_GDS2005_729_mouse_Lymph nodes (MG-430B) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LTBR_INHIBITION - 27 Day_GDS2004_736_mouse_Lymph nodes (MG-430A) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LTBR_INHIBITION - 27 Day_GDS2005_731_mouse_Lymph nodes (MG-430B) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LTBR_INHIBITION - 3 Days_GDS2005_730_mouse_Lymph nodes (MG-430B) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LTBR_INHIBITION - 3 Day_GDS2004_735_mouse_Lymph nodes (MG-430A) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LTBR_INHIBITION - 35 Day_GDS2004_737_mouse_Lymph nodes (MG-430A) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| LTBR_INHIBITION - 35 Day_GDS2005_732_mouse_Lymph nodes (MG-430B) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MAPK14_KD_GDS2693_533_mouse_A431 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MAPK14_KO_GDS2693_535_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MCAD_KO_GDS4546_422_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MCAD_KO_GDS4546_423_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Mdr2_KO_GDS1990_285_mouse_Livers of 3 month old | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Mdr2_KO_GDS1990_286_mouse_Livers of 12 month old | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MECOM_KO_GDS3343_554_mouse_Hematopoietic stem cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MECP2_KD_GDS4759_334_mouse_E16 primary cortical neuron cultures | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MED1_OE_GDS4846_11_human_LNCaP prostate cancer cell | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MEF2A_KD_GDS4759_340_mouse_E16 primary cortical neuron cultures | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MEF2D_KD_GDS4759_339_mouse_E16 primary cortical neuron cultures | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MEK_INHIBITION_GDS5029_278_human_SW480 KRAS-mutant colorectal cancer cell line - 4hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MEK_INHIBITION_GDS5029_279_human_SW480 KRAS-mutant colorectal cancer cell line - 16hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MEK_OE_GDS1925_165_human_Estrogen receptor (ER) alpha positive MCF-7 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Mel-18_KD_GDS2724_103_human_DAOY medulloblastoma cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MIF_DEPLETION_GDS3626_95_human_HEK293 kidney cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| miR-124_OE_GDS2657_770_human_HepG2 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| miR-124_OE_GDS2657_771_human_HepG2 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| miR-142-3p_OE_GSE28456_470_human_Raji cells (B lymphocytes) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MIR122_Antisense Inhibition_GDS1729_759_mouse_Livers (from C57BL/6 adult males) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MIR122_OE_GDS3470_573_human_Embryonic stem cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MIR140_OE_GDS3461_575_mouse_C3H10T1/2 fibroblast cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MIR140_Silencing_GDS3462_574_mouse_C3H10T1/2 fibroblast cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MIR221_KD_GDS4054_455_human_MCF7 breast cancer cells (fulvestrant-resistant) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MIR222_KD_GDS4054_456_human_MCF7 breast cancer cells (fulvestrant-resistant) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MIR34_OE_GDS2755_645_human_HCT116 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MIST1_KO_GDS1731_758_mouse_Pancreas | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MNAT1_Deficiency - Ablation_GDS2561_689_mouse_Heart - 2 week old | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MNAT1_Deficiency - Ablation_GDS2561_690_mouse_Heart - 4 week old | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MSTN_DEPLETION_GDS3637_94_mouse_mature skeletal muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MSTN_KO_GDS3637_439_mouse_muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MTDH_DEPLETION_GDS3179_98_human_LM2 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| mTert_OE_GDS1211_256_mouse_Embryonic fibroblasts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MYBL1_KO_GDS4485_349_mouse_Testis from 14 day old | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MYBL1_KO_GDS4485_350_mouse_Testis from 17 day old | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MYC_Activation - 2 hours_GDS2025_723_mouse_Pancreatic islet beta cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MYC_Activation - 21 days_GDS2025_727_mouse_Pancreatic islet beta cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MYC_Activation - 24 hours_GDS2025_726_mouse_Pancreatic islet beta cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MYC_Activation - 4 hours_GDS2025_724_mouse_Pancreatic islet beta cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MYC_Activation - 8 hours_GDS2025_725_mouse_Pancreatic islet beta cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MYC_KD_GSE22139_685_human_medulloblastoma | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MYC_OE_GDS4763_332_human_MCF10A - immortalized breast epithelial cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MYC_OE_GSE43730_684_human_MCF10A cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MYD88_Deficiency_GDS2650_652_mouse_LUNG | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| MYOC_OE_GDS1640_269_mouse_retina | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Nanog_KD_GDS1824_134_mouse_embryonic stem cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NCOA2_KO_GDS4785_172_mouse_Liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NCOA2_KO_GDS5087_24_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NCOA2_KO_GSE41558_19_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NET1_KD_GDS4196_436_human_AGS - gastric adenocarcinoma cells - (63 shRNA Knock-Down) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NET1_KD_GDS4196_437_human_AGS - gastric adenocarcinoma cells - (65 shRNA Knock-Down) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NEUROD1_Deficiency_GDS3000_612_mouse_Pineal glands of neonates | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NFE2L2_KO_GDS514_699_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NFE2L2_Mutation_GDS4498_597_mouse_Skin | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NFIA_Deficiency_GDS2775_639_mouse_Embryonic brains (at E18) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NFIA_Deficiency_GDS2775_640_mouse_Postnatal brains (at P16) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NHE3_Deficiency_GDS3323_599_mouse_Colon | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NIX_Deficiency_GDS2630_160_mouse_spleen | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NIX_Deficiency_GDS2630_655_mouse_Spleen | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NLGN1_KD_GDS4759_335_mouse_E16 primary cortical neuron cultures | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NLGN3_KD_GDS4759_336_mouse_E16 primary cortical neuron cultures | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Nmyc_OE_GDS2406_14_mouse_LUNG | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| not applicable_asthma_GSE43696_369_mouse_bronchial epithelial cell | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| not applicable_cell type comparison_GSE49439_365_human_podocytes and progenitors | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| not applicable_Hypothermia_GSE54229_131_mouse_Embryonic fibroblas | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NOTCH1_Deficiency_GDS2848_635_mouse_Hair follicles | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NOTCH_INHIBITION_GDS2794_61_human_MOLT4 (T-cell acute lymphoblast leukemia) cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Nrf2_deficiency_GDS3406_156_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NRL_Deficiency_GDS1693_235_mouse_Photoreceptors cells of retinas at E16 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NRL_Deficiency_GDS1693_236_mouse_Photoreceptors cells of retinas at P2 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NRL_Deficiency_GDS1693_237_mouse_Photoreceptors cells of retinas at P6 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NRL_Deficiency_GDS1693_238_mouse_Photoreceptors cells of retinas at P10 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NRL_Deficiency_GDS1693_239_mouse_Photoreceptors cells of retinas at 4 weeks | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NRL_Deficiency_GDS2936_629_mouse_Retinas - 2 days | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NRL_Deficiency_GDS2936_630_mouse_Retinas - 10 days | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| NRL_Deficiency_GDS2936_631_mouse_Retinas - 2 months | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| OBF-1_NULL MUTATION_GDS3473_571_mouse_Bone marrow pre-BII cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| OCT4_KD_GDS1824_135_mouse_embryonic stem (ES) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| OPTN_KD_GDS2892_268_human_HeLa | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| OTT1_KO_GDS4315_146_mouse_HSC | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Otx2_KO_GDS4440_143_mouse_fourth ventricular choroid plexus tissue | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| OTX2_KO_GDS4440_424_mouse_brain (fourth ventricular choroid plexus) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| OTX2_KO_GSE27630_51_mouse_brain (fourth ventricular choroid plexus, E13) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| OTX2_silencing_GDS4472_136_human_D425 medulloblastoma (MB) cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| p107_Deficiency_GDS3176_606_mouse_Skin | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| P63_DEPLETION_GDS2534_63_human_ME180 cervical carcinoma cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PARK7_KD_GDS3750_2_human_SH-SY5Y | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Parkin_OE_GDS4476_55_human_U87MG | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PARP2_KD_GSE43981_676_human_HepG2 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PAX3_Knock-in_GDS3331_598_mouse_Palatal shelves (E14.5 embryos - palate) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PAX5_OE_GDS4978_547_human_L428 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PAX5_OE_GDS4978_548_human_L428-PAX5 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PCDH12_Deficiency_GDS3415_577_mouse_Embryonic placentas (12.5 day) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PDE10A_KO_GDS4542_291_mouse_striatum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PDE10A_KO_GDS4542_292_mouse_hippocampus | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PDE10A_KO_GSE40377_581_mouse_Striatum and hippocampus | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PDSS2_KO_GDS3454_120_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PDX1_KO_GDS4348_360_mouse_Proximal small intestine | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PEBP1_KO_GDS4334_617_mouse_Pancreatic beta cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PEBP1_KO_GSE31150_52_mouse_pancreas | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PFKL_OE_GDS1079_201_mouse_myoblasts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PFKL_OE_GDS1980_203_mouse_dermal fibroblasts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PFKL_OE_GDS3353_76_human_B cells in blood | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PFKL_OE_GDS4410_202_human_biceps | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PFKL_OE_GDS4410_75_human_Biceps muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PGC-1alpha_Deficiency_GDS4904_310_mouse_Aged gastrocnemius muscle - 10 weeks | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PGC-1alpha_Deficiency_GDS4904_311_mouse_Aged gastrocnemius muscle - 24 months | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PGC1alpha_DEPLETION_GDS4989_283_human_A375P melanoma cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PHGDH_KO_GDS2874_125_mouse_embryonic head tissue | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PIAS1_Depletion_GDS5076_12_human_MDA-MB 231 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PIAS1_KD_GSE44024_133_human_breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PIN1_DEPLETION_GDS4070_450_human_MDA-MB-231 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PKBalpha_KO_GDS1784_193_mouse_Embryonic fibroblasts (MEFs) - 0 hour | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PKBalpha_KO_GDS1784_194_mouse_Embryonic fibroblasts (MEFs) - 2h | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PKBalpha_KO_GDS1784_195_mouse_Embryonic fibroblasts (MEFs) - 6h | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PKBalpha_KO_GDS1784_196_mouse_Embryonic fibroblasts (MEFs) - 24h | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PKBalpha_KO_GDS1784_197_mouse_Embryonic fibroblasts (MEFs) - 48h | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PLAGL2_deficiency_GDS3010_139_mouse_embryonic small intestine | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PLIN5_OE_GSE44192_482_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| POR_DELETION_GDS1093_240_mouse_Liver from male 3 month old | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| POR_KO_GDS1349_497_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| POR_KO_GDS1678_760_mouse_Colon | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| POR_KO_GDS1678_761_mouse_ILEUM | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| POR_KO_GDS1678_762_mouse_Jejunum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| POR_KO_GDS1678_763_mouse_Liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPAR-Beta_DELETION_GDS4320_363_mouse_Pancreatic beta-cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPARalpha_OE_GDS2289_244_mouse_Skeletal muscles | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPARA_agonist activation_GSE17250_475_mouse_Isolated hepatocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPARA_agonist activation_GSE17251_474_human_Isolated hepatocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPARA_Deficiency_GDS2934_632_mouse_Small intestine | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPARA_KO_GDS2886_484_mouse_small intestine | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPARA_KO_GDS3748_516_mouse_Livers | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPARD_KO_GDS4320_619_mouse_Pancreas | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPARD_KO_GSE16048_54_mouse_pancreas (islets, PDX1-expressing cells) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPARGC1A_KO_GDS2391_299_mouse_brain striatum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPARGC1A_NULL MUTATION_GDS2149_721_mouse_Brown adipocyte | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPARGC1B_Hypomorphic Mutation_GDS2515_695_mouse_Skeletal muscle - (quadriceps muscles) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPIF_KO_GSE23028_45_mouse_heart (8 wk) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PPP1R1A_KO_GDS1920_708_mouse_hippocampus | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| pRb_Deficiency_GDS3176_605_mouse_Skin | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PRC_DEPLETION_GDS3532_96_human_U2OS cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PRC_Partial Depletion_GDS3531_563_human_U2OS cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PRDM16_DEPLETION_GDS4021_460_mouse_WAT - white adipose tissue (stromal-vascular cells) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PRKAG3_KO_GDS1398_703_mouse_gastrocnemicus muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PRKAG3_KO_GSE4063_389_mouse_Skeletal muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PRKAG3_Mutation (R225Q)_GSE4067_390_mouse_Skeletal muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PRKCA_KO_GDS2141_300_mouse_small intestine | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PRKCZ_KO_GDS4310_293_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PrPC_KO_GDS4352_358_mouse_Developing hippocampus from FVB newborns (4.5-day-old) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PrPC_KO_GDS4352_359_mouse_Developing hippocampus from adults (3-mo-old) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PSIP1_Deficiency_GDS2883_633_human_T-cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PTEN_DELETION_GDS2446_59_human_HCT116 colon cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PTEN_DELETION_GDS2446_710_human_HCT116 colon cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PTEN_KD_GDS2958_100_human_HCC827 - NON-SMALL CELL LUNG carcinoma cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PTEN_KD_GDS2958_101_human_SKBR-3 MAMMARY ADENOCARCINOMA cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PTEN_KD_GDS2958_99_human_A431 - EPIDERMOID carcinoma cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PTEN_KD_GDS4759_337_mouse_E16 primary cortical neuron cultures | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PTHrP_KD_GDS1664_438_human_MDA-MB-231 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PTHrP_KD_GDS1664_71_human_MDA-MB-231 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PTK7_KD_GSE50138_674_human_H1299 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PTK7_KD_GSE50138_675_human_H2009 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PTPN1_KD_GSE54157_673_human_KM-H2 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| PU.1_KD_GDS2411_175_mouse_Preleukemic hematopoietic stem cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RAB3A_KO_GDS2482_705_mouse_Cortex | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RAB3A_KO_GDS2482_706_mouse_Hippocampus | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RAB3A_KO_GDS2483_700_mouse_Cortex | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RAB3A_KO_GDS2483_701_mouse_Hippocampus | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RAB3A_Mutation - D77G point mutation_GDS2482_702_mouse_Cortex | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RAB3A_Mutation - D77G point mutation_GDS2482_704_mouse_Hippocampus | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RAB3A_Mutation - D77G point mutation_GDS2483_697_mouse_Cortex | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RAB3A_Mutation - D77G point mutation_GDS2483_698_mouse_Hippocampus | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Raf-1_OE_GDS1925_166_human_Estrogen receptor (ER) alpha positive MCF-7 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RALDH2_KO_GSE43578_6_mouse_head (rostral or posterior) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RARA_KD_GDS4065_42_human_MCF-7 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RARRES1_KD_GDS4818_314_human_SUM149 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RASGRF1_KD_GDS2816_287_human_Hippocampus | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RB1_KD_GSE50532_591_human_OSTEOBLASTS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RB1_KD_GSE50532_592_human_OSTEOBLASTS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RB1_KD_GSE50532_593_human_OSTEOBLASTS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RB1_KD_GSE50532_623_human_OSTEOBLASTS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RB1_KD_GSE50532_624_human_OSTEOBLASTS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RB1_KD_GSE50532_627_human_OSTEOBLASTS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RB1_KD_GSE50532_641_human_OSTEOBLASTS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RB1_KD_GSE50532_654_human_OSTEOBLASTS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RB1_KD_GSE50532_656_human_OSTEOBLASTS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RB1_KD_GSE50532_657_human_OSTEOBLASTS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RB1_KD_GSE50532_659_human_OSTEOBLASTS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RB1_KD_GSE50532_660_human_OSTEOBLASTS | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RBL1_KO_GDS1931_740_mouse_Neurospheres (MG-430A) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RBL1_KO_GDS1932_739_mouse_Neurospheres | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RBP2_deficiency_GDS2731_62_mouse_embryonic fibroblasts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RB_Deficiency_GDS2757_644_mouse_Embryonic livers (day 12.5) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| REDD1_Repression_GDS3558_73_human_Blood Myeloid Cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RhoGDIbeta_KD_GDS2864_634_human_MDA-MB-231 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RIF1_KD_GDS4943_13_mouse_J1 ESC | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Rif1_KD_GDS4943_242_mouse_J1 embryonic stem cell (ESCs) line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Rif1_KD_GDS4943_243_mouse_F1 embryonic stem cell (ESCs) line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Rkip1_KO_GDS4331_15_mouse_C57BL/C pancreas | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RNA helicase p68_KD_GDS2152_625_mouse_skeletal muscle cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RNA helicase p68_KD_GDS2152_626_mouse_skeletal muscle cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ROCK_INHIBITION_GDS3944_461_mouse_Forebrain astrocytes - 2 Hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ROCK_INHIBITION_GDS3944_462_mouse_Forebrain astrocytes - 6 Hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ROCK_INHIBITION_GDS3944_463_mouse_Forebrain astrocytes - 12 Hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ROCK_INHIBITION_GDS3944_464_mouse_Forebrain astrocytes - 24 Hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RP1_KO_GDS1845_190_mouse_Retinas | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RUNX1_KO_GDS1511_250_mouse_Embryos at E8.5 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RUNX1_KO_GDS1511_251_mouse_Embryos at E12 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| RUNX2_NULL MUTATION_GDS2184_719_mouse_Embryonal bone (MG-U74A) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| S1P_Deficiency_GDS3654_521_mouse_Liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SARM_KO_GDS4842_411_mouse_brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SARM_KO_GDS4842_412_mouse_brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SCA1_Knock-in_GDS1756_231_mouse_Cerebellum tissue - 4 weeks of age | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SCA1_Knock-in_GDS1756_232_mouse_Cerebellum tissue - 12 weeks of age | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SCA1_Knock-in_GDS1756_233_mouse_Forebrain tissue - 4 weeks of age | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SCA1_Knock-in_GDS1756_234_mouse_Forebrain tissue - 12 weeks of age | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SCA1_Knock-in_GDS3544_561_mouse_Cerebellum - 4 Weeks | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SCA1_Knock-in_GDS3544_562_mouse_Cerebellum - 12 Weeks | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SCA7_Knock-in_GDS3545_560_mouse_Cerebellum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SCARA5_Down Expression_GSE32323_611_human_Colorectal Cancer Cell lines | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Scd1_DELETION_GDS4910_309_mouse_Skin | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SCD_KO_GSE24243_46_mouse_Skin (8-9 wk) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SETDB1_KO_GSE40296_7_mouse_brain (telencephalon) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SFRP5_KO_GDS4988_27_mouse_gonadal white adipose tissue HFD | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SFTPC_KO_GDS4876_476_mouse_Lung Type II cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SFTPC_KO_GSE35989_48_mouse_lung (type II cells) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SHANK3_KD_GDS4759_338_mouse_E16 primary cortical neuron cultures | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SIRT1_Deficiency_GDS4895_316_mouse_Brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SIRT1_KO_GDS3666_295_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SIRT1_KO_GDS4895_410_mouse_brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SIRT1_KO_GDS4895_43_mouse_brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SIRT1_KO_GSE28790_47_mouse_brain (3 mo) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Sirt1_OE_GDS2658_140_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SIRT3_KO_GDS4058_16_mouse_BROWN ADIPOSE TISSUE | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SIRT3_KO_GDS4058_454_mouse_BROWN ADIPOSE TISSUE | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SIRT3_KO_GDS4817_416_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SIRT3_KO_GDS4817_417_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SIRT4_KO_GDS4823_22_mouse_Liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SIRT4_KO_GDS4823_30_mouse_hepatocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SIRT4_KO_GDS4823_505_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SIRT4_KO_GSE56321_391_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SLC18A3_KD_GDS4325_618_mouse_Heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SLC39A13_Deficiency_GDS3485_570_mouse_Chondrocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SLC9A3_KO_GDS3323_495_mouse_colon | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SNAI1_OE_GDS4596_344_human_SW480 - Colorectal cancer cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SNCA_KO_GDS4153_442_mouse_Cerebellum - 6 month | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SNCA_KO_GDS4153_443_mouse_Striatum - 6 months | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SNCA_KO_GDS4153_444_mouse_Cerebellum - 21 month | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SNCA_KO_GDS4153_445_mouse_Striatum - 21 month | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SNCA_KO_GDS4153_527_mouse_striatum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SNCA_KO_GDS4153_528_mouse_cerebellum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SNCA_KO_GDS4153_529_mouse_cerebellum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SNCA_KO_GDS4153_530_mouse_striatum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SOCS3_DELETION_GDS1254_80_mouse_ES (embryonic stems cells) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SOCS3_KO_GDS3149_297_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SOCS3_KO_GDS3149_8_mouse_multiple cell types | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SOD2_KO_GDS1080_128_mouse_heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SON_KD_GDS4448_35_human_HeLa | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SOX10_KO_GDS3480_257_rat_Schwannoma cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SOX11_DEPLETION_GDS4801_326_human_Z138 mantle cell lymphoma (MCL) cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SOX17_OE_GDS3300_124_human_HESC (CA1 and CA2) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SOX2_Deficiency_GDS4853_319_human_AZ-521 gastric cancer (GC) cell line - 8 Hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SOX2_Deficiency_GDS4853_320_human_AZ-521 gastric cancer (GC) cell line - 12 Hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SOX2_Deficiency_GDS4853_321_human_AZ-521 gastric cancer (GC) cell line - 18 Hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SOX2_Deficiency_GDS4853_322_human_AZ-521 gastric cancer (GC) cell line - 24 Hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SOX4_KD_GDS2193_37_human_adenoid cystic carcinoma derived cells ACC3 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SOX7_OE_GDS3300_123_human_HESC (CA1 and CA2) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SP3_Deficiency_GDS3058_610_mouse_Embryonic heart (day 12.5 C57Bl/6) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SPARC_Deficiency_GDS3636_524_mouse_Lens epithelium | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SQSTM1_OE_GDS2653_651_human_IMR-32 neuroblastoma cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SRC-2_Deficiency_GDS5087_270_mouse_Heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SRC-2_KO_GDS5087_485_mouse_Heart | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SRF_KO_GDS3732_148_mouse_HSC | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ST6GAL1_Deficiency_GDS3151_608_mouse_Mammary tumors | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| STAT1_KD_GDS4754_159_human_JURKAT | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| STAT3_deficiency_GDS3106_58_mouse_type II alveolar cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| STAT3_OE_GDS3444_576_mouse_Cultured embryonic stem (ES) cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| STAU1_DELETION_GDS3370_56_human_HeLa | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SUZ12_DEPLETION_GDS2445_119_human_embryonic fibroblasts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SYK_DEPLETION_GDS3609_36_human_MCF10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SYK_KD_GDS3609_440_human_MCF10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SYK_KD_GDS3609_441_human_MCF10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SYNCRIP_KD_GDS3578_86_human_MM1S | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SYNCRIP_OE_GDS1806_82_human_T-lymphocytes from normal donors were activated with anti-CD3 and IL2 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SYNCRIP_OE_GDS1886_83_human_THP-1 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SYNCRIP_OE_GDS3186_84_mouse_wild type 129 mouse retina | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SYNCRIP_OE_GDS3575_87_mouse_C57BL/6 mice | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| SYNCRIP_OE_GDS4596_85_human_SW480 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TAF7L_KO_GDS2857_556_mouse_ES cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TARDBP_KD_GDS3730_118_human_HEK293E | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Tcf1_KO_GDS1473_307_mouse_Pancreatic islets | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Tcof1_KD_GDS998_155_mouse_neuroblastoma N1E-115 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Tcof1_OE_GDS998_154_mouse_neuroblastoma N1E-115 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TDP43_KD_GSE18632_1_human_HEK293E | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TET2_KO_GDS4287_429_mouse_LSK - bone marrow progenitor population | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TET2_KO_GDS4287_430_mouse_CMP - bone marrow progenitor population | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TET2_KO_GDS4287_431_mouse_GMP - bone marrow progenitor population | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TGF-beta_OE_GDS2974_137_mouse_corneas | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TGFB2_KD_GDS4483_351_mouse_Embryonic palatal tissue | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TGFBR2_KO_GDS5008_282_mouse_Embryonic palatal mesenchymal cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TGM2_KD_GSE23702_713_human_NB4 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TGM2_KD_GSE23702_715_human_NB4 cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TGM2_KD_GSE23702_716_human_NB4 cells, 72h ATRA-induced differentiation | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TIA1_KO_GSE54418_260_mouse_cerebellum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TIA1_KO_GSE54418_261_mouse_midbrain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TIA1_KO_GSE54418_262_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TIA1_KO_GSE54418_263_mouse_spinal cord | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TIA1_KO_GSE54418_264_mouse_cerebellum | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TIA1_KO_GSE54418_265_mouse_midbrain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TIA1_KO_GSE54418_266_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TIA1_KO_GSE54418_267_mouse_spinal cord | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TMEM88B_KD_GPL10558_471_human_cardiovascular progenitors cells differentiated from hES cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TMEM88_KD_GSE43805_682_human_hES cells differentiated along the cardiac lineage | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TMOD3_KO_GDS4827_313_mouse_Liver erythroblast | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TMOD3_KO_GDS4827_39_mouse_fetal liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TMOD3_KO_GDS4827_415_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TMOD3_KO_GDS4827_418_mouse_liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TNKS_INHIBITION_GDS5029_280_human_SW480 KRAS-mutant colorectal cancer cell line - 4hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TNKS_INHIBITION_GDS5029_281_human_SW480 KRAS-mutant colorectal cancer cell line - 16hours | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TOP2B_drug inhibition_GSE1417_341_human_HeLa | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TP53BP1_KD_GSE54268_669_human_MCF-10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TP53BP1_KD_GSE54268_670_human_MCF-10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TP53INP2_KO_GDS5053_277_mouse_Skeletal muscle - SKM-KO | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TP53INP2_KO_GDS5053_544_mouse_skeletal muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TP53INP2_KO_GSE54917_384_mouse_Quadriceps muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TP53INP2_OE_GDS5053_312_mouse_Skeletal muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TP53INP2_OE_GDS5054_276_mouse_SKM-Tg - Skeletal muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TP53INP2_OE_GDS5054_385_mouse_Muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TP53INP2_OE_GDS5054_387_mouse_muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TP53INP2_OE_GDS5054_545_mouse_skeletal muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TP53_DEPLETION_GDS4070_451_human_MDA-MB-231 breast cancer cells (depleted of MUTANT-p53) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TP63_NULL MUTATION_GDS1434_308_mouse_Skin at embryonic age E18.5 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TRIB1_KO_GDS2944_555_mouse_Macrophages | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TRIM24_Deficiency_GDS3087_609_mouse_Hepatocellular carcinoma (HCC) tumors | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TRIM33_KD_GDS4071_449_human_HMEC-TR mammary epithelial cell line | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TRPS1_Mutation_GDS4493_594_mouse_Whisker pads | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TRPV4_DEPLETION_GDS4851_89_mouse_3T3-F442A adipocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TSC1_Deficiency_GDS4572_346_mouse_Naive CD4 T cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TSC1_Deficiency_GDS4572_347_mouse_Naive CD8 T cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| TYK2_KD_GDS4754_158_human_JURKAT | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| UBB_KO_GDS3906_491_mouse_Testis - 7 Days | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| UBB_KO_GDS3906_492_mouse_Testis - 14 Days | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| UBB_KO_GDS3906_494_mouse_Testis - 21 Days | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| UBB_KO_GDS3906_496_mouse_Testis - 28 Days | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| UPF1_Deficiency_GDS2781_188_human_HeLa cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Usp22_DEPLETION_GDS4973_284_mouse_E14 embryonic stem cells (ESCs) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| USP2_KO_GDS5079_25_mouse_kidney | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| USP2_KO_GSE43517_20_mouse_kidney | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| VAChT_KD_GDS4325_361_mouse_Heart from C57BL/6 males | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| VHL_Deficiency_GDS3769_513_mouse_Immortalized embryonic fibroblasts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| VPRBP_KD_GDS4829_90_human_DU145 prostate cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| WFS1_KO_GDS4526_111_mouse_brain | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| WFS1_KO_GSE33372_395_mouse_hypothalamus | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| WTAP_KD_GDS2010_69_human_HUVEC (umbilical vein endothelial cells) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| WTX_OE_GDS4802_325_human_HEK293 embryonic kidney cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| WTX_OE_GDS4802_34_human_HEK293 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| XBP1_OE_GDS2861_60_human_MCF7 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| XBP1_OE_GDS5065_273_mouse_F424a adipocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| YAP_OE_GDS3220_32_human_MCF10A | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| YY1_Deficiency_GDS4856_318_mouse_Soleus skeletal muscle | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| YY1_KD_GDS3788_488_human_HeLa | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| YY1_KO_GSE39009_49_mouse_skeletal muscle (6 mo) | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| YY2_KD_GDS3788_490_human_HeLa | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ZBTB20_Deficiency_GDS3718_517_mouse_Developing hippocampus | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| Zfp36l2_deficiency_GDS3574_153_mouse_E14.5 fetal liver | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ZFP36_Deficiency_GDS2456_707_mouse_Fibroblasts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ZFX_KD_GSE43021_130_human_NOMO1 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ZFX_KO_GDS2718_150_mouse_embryonic stem cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ZFX_KO_GDS2718_151_mouse_hematopoietic stem cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ZMPSTE24_Deficiency_GDS3775_506_mouse_Embryonic fibroblasts | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ZNF217_OE_GDS4885_317_human_MDA-MB-231 breast cancer cells | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ZNF750_KD_GDS4599_177_human_HaCaT keratinocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ZNF750_KD_GSE38039_696_human_HaCaT keratinocytes | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ZXDC1_KD_GSE45417_686_human_U937 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
| ZXDC_KD_GDS5070_504_human_U937 | gene perturbation identified as [gene symbol]_[perturbation]_[GEO accession]_[perturbation ID]_[organism]_[cell or tissue] |
