| Gene ID | At1g12320 |
| Gene name | unknown protein |
| Functional description | F:molecular_function unknown;P:biological_process unknown;C:cellular_component unknown;P |
| Std2 GX | %ile | GSM ID | Assay name | GSE ID | Experiment title | Link to GEO |
|---|---|---|---|---|---|---|
| 334.2 | 100.0 | GSM142625 | MC002_ATH1_A1.3-dubos-wtx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 270.4 | 100.0 | GSM142623 | MC002_ATH1_A1.1-dubos-wtx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 223.9 | 100.0 | GSM142624 | MC002_ATH1_A1.2-dubos-wtx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 205.3 | 100.0 | GSM142631 | MC002_ATH1_A3.3-dubos-6kx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 175.8 | 100.0 | GSM142629 | MC002_ATH1_A3.1-dubos-6kx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 151.6 | 99.9 | GSM142630 | MC002_ATH1_A3.2-dubos-6kx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 139.4 | 99.9 | GSM142642 | MC002_ATH1_A7.2-dubos-wLh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 139.3 | 99.9 | GSM142646 | MC002_ATH1_A8.3-dubos-aih | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 130.6 | 99.9 | GSM142644 | MC002_ATH1_A8.1-dubos-aih | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 122.0 | 99.9 | GSM142641 | MC002_ATH1_A7.1-dubos-wLh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 116.7 | 99.9 | GSM142643 | MC002_ATH1_A7.3-dubos-wLh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 98.5 | 99.9 | ArrayExpress | E-MEXP-509-raw-cel-829148420 | - | - | - |
| 96.6 | 99.9 | ArrayExpress | E-MEXP-509-raw-cel-829148561 | - | - | - |
| 72.1 | 99.9 | GSM142645 | MC002_ATH1_A8.2-dubos-aih | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 60.5 | 99.8 | GSM142647 | MC002_ATH1_A9.1-dubos-aah | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 60.4 | 99.8 | ArrayExpress | E-MEXP-509-raw-cel-829148877 | - | - | - |
| 57.8 | 99.8 | ArrayExpress | E-ATMX-31-raw-cel-1516947984 | - | - | - |
| 56.5 | 99.8 | ArrayExpress | E-MEXP-509-raw-cel-829148129 | - | - | - |
| 55.4 | 99.8 | ArrayExpress | E-ATMX-31-raw-cel-1516948018 | - | - | - |
| 54.4 | 99.8 | ArrayExpress | E-MEXP-509-raw-cel-829148525 | - | - | - |
| 54.2 | 99.8 | ArrayExpress | E-MEXP-509-raw-cel-829148808 | - | - | - |
| 52.6 | 99.8 | ArrayExpress | E-MEXP-509-raw-cel-829148492 | - | - | - |
| 52.5 | 99.8 | ArrayExpress | E-MEXP-509-raw-cel-829148456 | - | - | - |
| 50.6 | 99.8 | GSM253651 | Ler 1 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 50.6 | 99.8 | GSM142648 | MC002_ATH1_A9.2-dubos-aah | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 49.3 | 99.8 | ArrayExpress | E-MEXP-509-raw-cel-829148090 | - | - | - |
| 48.5 | 99.8 | ArrayExpress | E-ATMX-31-raw-cel-1516948001 | - | - | - |
| 48.5 | 99.8 | ArrayExpress | E-MEXP-509-raw-cel-829148842 | - | - | - |
| 46.0 | 99.8 | GSM142636 | MC002_ATH1_A5.2-dubos-5kx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 45.4 | 99.8 | ArrayExpress | E-MEXP-509-raw-cel-829148201 | - | - | - |
| 42.3 | 99.8 | ArrayExpress | E-MEXP-509-raw-cel-829148913 | - | - | - |
| 40.7 | 99.8 | GSM142649 | MC002_ATH1_A9.3-dubos-aah | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 40.3 | 99.8 | GSM253645 | High_Mo_seg_pool_Ler_col_F2 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 38.9 | 99.8 | ArrayExpress | E-MEXP-509-raw-cel-829148385 | - | - | - |
| 35.8 | 99.7 | ArrayExpress | E-MEXP-509-raw-cel-829148772 | - | - | - |
| 34.6 | 99.7 | GSM253650 | Ler 3 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 34.4 | 99.7 | GSM253652 | Ler 2 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 33.4 | 99.7 | ArrayExpress | E-MEXP-509-raw-cel-829148703 | - | - | - |
| 33.1 | 99.7 | ArrayExpress | E-MEXP-509-raw-cel-829148597 | - | - | - |
| 30.5 | 99.7 | ArrayExpress | E-MEXP-509-raw-cel-829148632 | - | - | - |
| 30.0 | 99.7 | ArrayExpress | E-MEXP-509-raw-cel-829148165 | - | - | - |
| 29.4 | 99.7 | GSM133749 | Turner_A-3-Turne-Mut-Base1_SLD | GSE5729 | Role of COV in vascular patterning | |
| 28.8 | 99.7 | GSM133750 | Turner_A-4-Turne-Mut-Base2_SLD | GSE5729 | Role of COV in vascular patterning | |
| 27.4 | 99.7 | ArrayExpress | E-MEXP-509-raw-cel-829148348 | - | - | - |
| 27.4 | 99.7 | GSM142637 | MC002_ATH1_A5.3-dubos-5kx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 24.4 | 99.6 | GSM253646 | Low_Mo_seg_pool_Ler_col_F2 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 23.2 | 99.6 | ArrayExpress | E-MEXP-509-raw-cel-829148313 | - | - | - |
| 23.0 | 99.6 | GSM204069 | protoplast_hypoxia_rep1 | GSE8248 | Identification of hypoxia-inducible genes in Arabidopsis mesophyll cells | |
| 22.8 | 99.6 | ArrayExpress | E-MEXP-509-raw-cel-829148240 | - | - | - |
| 22.7 | 99.6 | GSM128661 | Underwood_1-14_Cor-5x10e7-10h_Rep2_ATH1 | GSE5520 | Genome-wide transcriptional analysis of the compatible A. thaliana-P. syringae pv. tomato DC3000 interaction | |
| 22.4 | 99.6 | ArrayExpress | E-MEXP-509-raw-cel-829148738 | - | - | - |
| 21.4 | 99.6 | GSM142635 | MC002_ATH1_A5.1-dubos-5kx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 20.8 | 99.6 | GSM205428 | met1-3_leaf_fourth-selfed generation_rep01 | GSE8279 | Transgenerational Stability of the Arabidopsis Epigenome Is Coordinated by CG Methylation | |
| 20.7 | 99.6 | ArrayExpress | E-MEXP-509-raw-cel-829148276 | - | - | - |
| 20.6 | 99.6 | GSM205430 | met1-3_leaf_fourth-selfed generation_rep02 | GSE8279 | Transgenerational Stability of the Arabidopsis Epigenome Is Coordinated by CG Methylation | |
| 19.4 | 99.6 | ArrayExpress | E-MEXP-509-raw-cel-829148666 | - | - | - |
| 18.2 | 99.5 | GSM133753 | Turner_A-7-Turne-WT-Base1_SLD | GSE5729 | Role of COV in vascular patterning | |
| 16.9 | 99.5 | GSM143298 | Low_Na_seg_pool_ts_col_F2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 16.7 | 99.5 | GSM143300 | Ts_genomic_hyb_3 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 16.6 | 99.5 | GSM142656 | MC002_ATH1_A12.1-dubos-arh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 15.8 | 99.5 | GSM143301 | Ts_genomic_hyb_2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 15.5 | 99.5 | GSM253649 | Col-0-2 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 14.4 | 99.4 | GSM133748 | Turner_A-2-Turne-Mut-Top2_SLD | GSE5729 | Role of COV in vascular patterning | |
| 14.4 | 99.4 | ArrayExpress | E-MEXP-265-raw-cel-414619106 | - | - | - |
| 13.7 | 99.4 | GSM142657 | MC002_ATH1_A12.2-dubos-arh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 13.2 | 99.4 | GSM253648 | Col-0-1 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 13.2 | 99.4 | GSM142653 | MC002_ATH1_A11.1-dubos-mxh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 12.3 | 99.3 | GSM143302 | Ts_genomic_hyb_1 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 12.1 | 99.3 | GSM142655 | MC002_ATH1_A11.3-dubos-mxh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 11.7 | 99.3 | GSM143306 | High_Na_seg_pool_tsu_col_F2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 11.5 | 99.3 | GSM253647 | Col-0 3 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | |
| 11.5 | 99.3 | GSM253200 | Nontransgenic(ga1-3rgargl2)-DEX-REP2 | GSE10019 | Identification of RGA downstream genes by using steroid-inducible system | |
| 11.1 | 99.2 | ArrayExpress | E-ATMX-33-raw-cel-1562596197 | - | - | - |
| 11.1 | 99.2 | GSM142658 | MC002_ATH1_A12.3-dubos-arh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 10.9 | 99.2 | GSM189112 | HSP90_Reduced_RNAi-A3_Biological_Replicate_2_Technical_Replicate_1 | GSE7796 | Phenotypic Diversity and Altered Environmental Plasticity in Arabidopsis thaliana with Reduced HSP90 Levels | |
| 10.7 | 99.2 | GSM142654 | MC002_ATH1_A11.2-dubos-mxh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | |
| 10.5 | 99.2 | GSM133752 | Turner_A-6-Turne-WT-Top2_SLD | GSE5729 | Role of COV in vascular patterning | |
| 10.3 | 99.2 | ArrayExpress | E-MEXP-265-raw-cel-414619001 | - | - | - |
| 10.3 | 99.2 | ArrayExpress | E-MEXP-1443-raw-cel-1581869921 | - | - | - |
| 9.7 | 99.1 | GSM143309 | Tsu_genomic_hyb_2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 9.5 | 99.1 | ArrayExpress | E-ATMX-33-raw-cel-1562596241 | - | - | - |
| 9.4 | 99.1 | GSM133751 | Turner_A-5-Turne-WT-Top1_SLD | GSE5729 | Role of COV in vascular patterning | |
| 9.0 | 99.1 | ArrayExpress | E-MEXP-265-raw-cel-414619213 | - | - | - |
| 8.9 | 99.0 | GSM143299 | High_Na_seg_pool_ts_col_F2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | |
| 8.8 | 99.0 | GSM205426 | met1-3_leaf_second-selfed generation_rep02 | GSE8279 | Transgenerational Stability of the Arabidopsis Epigenome Is Coordinated by CG Methylation | |
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