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| Gene ID | Os09g0363900 |
| Gene name | |
| Functional description | Similar to At1g72970: HTH (HOTHEAD) (Ev=1e-3) |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0.34 | 5e-32 | 141 | Os08g0401500 | AK068301.1 | - | Mandelonitrile lyase-like protein | 1e-12 | At1g72970 | HTH (HOTHEAD) | O.I. | C.G. | S.X. | |
| 0.04 | 3e-2 | 42 | Os04g0573100 | AK106787.1 | - | Glucose-methanol-choline oxidoreductase domaincontaining protein | 1e+0 | At5g51950 | glucose-methanol-choline (GMC) oxidoreductase family protein | O.I. | C.G. | S.X. | |
| 0.03 | 3e-2 | 42 | Os02g0678300 | 9630.m04415 | - | Glucose-methanol-choline oxidoreductase domaincontaining protein | 7e-2 | At1g12570 | glucose-methanol-choline (GMC) oxidoreductase family protein | O.I. | C.G. | S.X. | |
| 0.03 | 3e-2 | 42 | Os10g0524500 | AF251031.1 | - | Mandelonitrile lyase-like protein | 7e-5 | At5g51950 | glucose-methanol-choline (GMC) oxidoreductase family protein | O.I. | C.G. | S.X. | |
| 0.01 | 3e-2 | 42 | Os10g0524400 | AK108768.1 | - | Phospholipase D (EC 3.1.4.4) | 2e-19 | At4g11840 | PLDGAMMA3 | 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-3 | 46 | At1g72970 | Arabidopsis thaliana | 843628 | HTH (HOTHEAD) | Originally identified as a mutation that causes floral organs to fuse together. About 10-20% of mutants also have defects in ovules. Mutants have reduced fertility most likely as because of fusions that pistil emergence. The protein has similarity to the mandelonitrile lyase family of FAD containing oxidoreductases and is predicted to be secreted (SignalP).It is expressed in all tissue layers of roots, inflorescences, stems, leaves, and flowers and is also expressed in siliques. Expression is highest in inflorescence and flower tissue.Transmission of mutant alleles to the progeny shows non mendelian segregation- a percentage of mutant alleles revert back to a previous parental (e.g. grandparental) wild type allele. It has been suggested that an RNA template driven or other extra-DNA genomic mechanism may be responsible for the non-mendelian inheritance of HTH. Reversion events in alleles at other loci have also been observed to occur in plants with an hth mutant background indicating a genome wide effect. | - | - | - | O.I. | C.G. | S.X. | |
| 0.16 | 6e-9 | 63 | Gma.10072.1.S1_at | Glycine max | CD399353 | - | - | 1e-11 | At1g72970 | HTH (HOTHEAD) | O.I. | C.G. | S.X. | |
| 0.77 | 0 | 1596 | Contig2265_at | Hordeum vulgare | Contig2265 | - | - | 4e-3 | At1g72970 | HTH (HOTHEAD) | O.I. | C.G. | S.X. | |
| 0.10 | 6e-6 | 54 | PtpAffx.58803.1.S1_at | Populus trichocarpa | CK090504 | hypothetical protein | - | 4e-7 | At1g72970 | HTH (HOTHEAD) | O.I. | C.G. | S.X. | |
| 0.69 | 0 | 700 | Ta.3651.1.S1_at | Triticum aestivum | CK152094 | - | - | 1e-3 | At1g12570 | glucose-methanol-choline (GMC) oxidoreductase family protein | O.I. | C.G. | S.X. | |
| 0.01 | 1e+0 | 34 | 1614959_at | Vitis vinifera | BQ799150 | hypothetical protein LOC100257499 | - | 1e-10 | At5g47060 | senescence-associated protein-related | O.I. | C.G. | S.X. | |
| 0.35 | 1e-109 | 397 | Zm.1657.1.A1_at | Zea mays | BG842419 | hypothetical protein LOC100192014 | - | 7e-2 | At5g51950 | glucose-methanol-choline (GMC) oxidoreductase family protein | O.I. | C.G. | S.X. |
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