Gene ID | Contig4541_at |
Gene name | |
Functional description | Similar to At5g63980: SAL1 (Ev=1e-4) |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
0.52 | 0 | 714 | Contig4542_at | Contig4542 | - | - | 5e-5 | At5g63980 | SAL1 | O.I. | C.G. | S.X. | |
0.47 | 6e-116 | 416 | Contig4543_at | Contig4543 | - | - | 2e-5 | At5g63980 | SAL1 | O.I. | C.G. | S.X. | |
0.13 | 8e-29 | 127 | Contig19538_at | Contig19538 | - | - | 2e+0 | At3g51140 | - | O.I. | C.G. | S.X. | |
0.04 | 1e-2 | 40 | Contig13707_at | Contig13707 | - | - | 3e-5 | At4g05090 | inositol monophosphatase family protein | O.I. | C.G. | S.X. | |
0.02 | 2e-1 | 36 | Contig17672_at | Contig17672 | - | - | 2e-16 | At5g23300 | PYRD (pyrimidine d) | O.I. | C.G. | S.X. | |
0.01 | 2e-1 | 36 | Contig4737_s_at | Contig4737 | - | - | 3e-29 | At2g35040 | AICARFT/IMPCHase bienzyme family protein | O.I. | C.G. | S.X. | |
0.01 | 2e-1 | 36 | Contig4612_at | Contig4612 | - | - | 4e+0 | At5g43610 | ATSUC6 (Sucrose-proton symporter 6) | O.I. | C.G. | S.X. | |
0.01 | 9e-1 | 34 | Contig3100_at | Contig3100 | - | - | 1e-5 | At4g16830 | nuclear RNA-binding protein (RGGA) | O.I. | C.G. | S.X. | |
0.03 | 9e-1 | 34 | HVSMEn0015O03r2_at | HVSMEn0015O03r2 | - | - | 5e-2 | At4g35030 | protein kinase family protein | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
0.04 | 1e-4 | 48 | At5g63980 | Arabidopsis thaliana | 836519 | SAL1 | Encodes a bifunctional protein that has 3'(2'),5'-bisphosphate nucleotidase and inositol polyphosphate 1-phosphatase activities and rescues sulfur assimilation mutants in yeast. It is involved in the response to cold, drought (negative regulator of drought tolerance), and ABA. Mutants in this gene exhibit enhanced induction of stress genes in response to cold, ABA, salt and dehydration due to higher accumulation of the second messenger, inositol (1,4,5)- triphosphate (IP(3)). Involved in degradation of small mRNAs. Mutants also affect the accumulation of miRNA target cleavage products. Regulates light-dependent repression of hypocotyl elongation and flowering time via its 3'(2'),5'-bisphosphate nucleotidase activity. | - | - | - | O.I. | C.G. | S.X. | |
0.04 | 6e-1 | 36 | Gma.1478.1.S1_at | Glycine max | AI442810 | - | - | 2e-31 | At5g63980 | SAL1 | O.I. | C.G. | S.X. | |
0.43 | 3e-59 | 230 | Os12g0183300 | Oryza sativa | U33283.1 | - | 3'(2'),5'-bisphosphate nucleotidase (EC 3.1.3.7)(3'(2'),5- bisphosphonucleoside 3'(2')-phosphohydrolase)(DPNPase) | 5e-5 | At5g63980 | SAL1 | O.I. | C.G. | S.X. | |
0.02 | 6e-1 | 36 | PtpAffx.202661.1.S1_at | Populus trichocarpa | pmrna5312 | kip-related cyclin-dependent kinase inhibitor 3 | - | 1e-6 | At5g48820 | ICK6 (INHIBITOR/INTERACTOR WITH CYCLIN-DEPENDENT KINASE) | O.I. | C.G. | S.X. | |
0.72 | 0 | 928 | TaAffx.113407.1.S1_at | Triticum aestivum | CA613327 | - | - | 2e-3 | At5g63980 | SAL1 | O.I. | C.G. | S.X. | |
0.03 | 8e+0 | 30 | 1622334_at | Vitis vinifera | CD713078 | - | - | 3e-1 | At1g27360 | squamosa promoter-binding protein-like 11 (SPL11) | O.I. | C.G. | S.X. | |
0.41 | 4e-64 | 244 | Zm.676.1.S1_a_at | Zea mays | AF288075.1 | diphosphonucleotide phosphatase1 | - | 8e-4 | At5g63980 | SAL1 | O.I. | C.G. | S.X. |
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