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| Gene ID | Contig24884_at |
| Gene name | |
| Functional description | Similar to At5g10140: FLC (FLOWERING LOCUS C) (Ev=1e-1) |
| HF | Ev | BS | Gene ID | Repr. ID | Gene Name | Functional Description | Ev | AGI code | Arabidopsis gene name | O.I. | C.G. | S.X. | Other DB |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0.08 | 7e-8 | 57 | Contig12483_at | Contig12483 | - | - | 2e-3 | At3g57390 | AGL18 | O.I. | C.G. | S.X. | |
| 0.08 | 4e-6 | 52 | Contig16350_at | Contig16350 | - | - | 9e-3 | At3g57390 | AGL18 | O.I. | C.G. | S.X. | |
| 0.05 | 2e-5 | 50 | Contig10383_at | Contig10383 | - | - | 6e-4 | At2g22540 | SVP (SHORT VEGETATIVE PHASE) | O.I. | C.G. | S.X. | |
| 0.07 | 7e-5 | 48 | Contig2200_s_at | Contig2200 | - | - | 2e-3 | At2g45650 | AGL6 (AGAMOUS-LIKE 6) | O.I. | C.G. | S.X. | |
| 0.04 | 3e-4 | 46 | Contig14348_at | Contig14348 | - | - | 3e-3 | At1g71692 | AGL12 (AGAMOUS-LIKE 12) | O.I. | C.G. | S.X. | |
| 0.03 | 3e-4 | 46 | Contig3831_at | Contig3831 | - | - | 3e-15 | At4g18960 | AG (AGAMOUS) | O.I. | C.G. | S.X. | |
| 0.06 | 1e-3 | 44 | Contig2198_at | Contig2198 | - | - | 3e-6 | At1g24260 | SEP3 (SEPALLATA3) | O.I. | C.G. | S.X. | |
| 0.07 | 7e-2 | 38 | Contig7416_at | Contig7416 | - | - | 2e-4 | At5g60910 | AGL8 (agamous-like 8) | O.I. | C.G. | S.X. | |
| 0.01 | 7e-2 | 38 | Contig4208_at | Contig4208 | - | - | 6e-6 | At2g36580 | pyruvate kinase, putative | O.I. | C.G. | S.X. |
| HF | Ev | BS | Gene ID | Organism | Repr. ID | Gene Name | Functional Description | Ev | AGI code | Arabidopsis gene name | O.I. | C.G. | S.X. | Other DB |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0.03 | 1e-1 | 38 | At5g10140 | Arabidopsis thaliana | 830878 | FLC (FLOWERING LOCUS C) | MADS-box protein encoded by FLOWERING LOCUS C - transcription factor that functions as a repressor of floral transition and contributes to temperature compensation of the circadian clock. Expression is downregulated during cold treatment. Vernalization, FRI and the autonomous pathway all influence the state of FLC chromatin. Both maternal and paternal alleles are reset by vernalization, but their earliest activation differs in timing and location. Histone H3 trimethylation at lysine 4 and histone acetylation are associated with active FLC expression, whereas histone deacetylation and histone H3 dimethylation at lysines 9 and 27 are involved in FLC repression. Expression is also repressed by two small RNAs (30- and 24-nt) complementary to the FLC sense strand 3’ to the polyA site. The small RNAs are most likely derived from an antisense transcript of FLC. Interacts with SOC1 and FT chromatin in vivo. Member of a protein complex. | - | - | - | O.I. | C.G. | S.X. | |
| 0.03 | 2e-1 | 38 | PsAffx.C78000026_at | Glycine max | PsAffx.C78000026 | - | - | 1e+0 | At2g18680 | unknown protein | O.I. | C.G. | S.X. | |
| 0.47 | 3e-115 | 416 | Os04g0614100 | Oryza sativa | AY177698.1 | - | Transcription factor, MADS-box domain containingprotein | 4e+0 | At5g23260 | TT16 (TRANSPARENT TESTA16) | O.I. | C.G. | S.X. | |
| 0.05 | 1e-2 | 42 | PtpAffx.201225.1.S1_s_at | Populus trichocarpa | pmrna2438 | hypothetical protein | - | 6e-24 | At2g14210 | AGL44 (AGAMOUS-LIKE 44) | O.I. | C.G. | S.X. | |
| 0.19 | 7e-13 | 75 | Ta.27569.1.S1_at | Triticum aestivum | CD888059 | MADS-box transcription factor TaAGL35 | - | 8e-2 | At5g51870 | AGL71 (AGAMOUS-LIKE 71) | O.I. | C.G. | S.X. | |
| 0.05 | 3e-3 | 42 | 1609046_at | Vitis vinifera | CB971729 | hypothetical protein LOC100256085 | - | 1e-13 | At2g45650 | AGL6 (AGAMOUS-LIKE 6) | O.I. | C.G. | S.X. | |
| 0.15 | 3e-19 | 95 | Zm.9560.1.A1_at | Zea mays | BM382073 | m17 protein | - | 3e-2 | At1g77080 | - | O.I. | C.G. | S.X. |
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