Select | Gene | Cds | Cds_length | GC_content | Pep | Pep_length |
---|---|---|---|---|---|---|
Acco08g0489 | ATGGCCTGCCGGACACTGAAAGCCGGAAACTTGGATCCAGAGAGAAAGAGAAGTGGCGGACTGAGGACAAAACAGGCGGGAAGAGGATCGTGCCGTGTTCGGGAGAAAAGACTTTTTCGCGCTTTTTTTAATCCCGTCGTTGAAACGATGGGTTTATTGTTGAAAGAAGCCTTGAAGACTCTGTGCGGTCGGAATCAATGGTCTTATGCTGTGTTCTGGAAGATCGGCTGCCACAATCCTAAGCTTTTAATATGGGAGGAATGCTATTATGAACCCTTGCCCTTCGGAGGTGTGGAAGGCGACAGAGTATGTTCTTTGATTAACAGAATGGTGGTGAATAATTCAGTCAATATTGCTGGAGAAGGGATAATTGGACGGGCAGCATTCACGGGAAACCATCAATGGATTCTCTTGAATAATTTTACTAGACCTGCATATCCCCCCGAGGTATACAATGAAGTGCATCATCAATTTTTGGCTGGAATGCAGACCATAGTTATTATTCCTGTGCTTCCTCATGGGGTTGTTCAACTTGGTTCTTTTTTGGCAGACATACGTTATTGA | 564 | 0.4486 | MACRTLKAGNLDPERKRSGGLRTKQAGRGSCRVREKRLFRAFFNPVVETMGLLLKEALKTLCGRNQWSYAVFWKIGCHNPKLLIWEECYYEPLPFGGVEGDRVCSLINRMVVNNSVNIAGEGIIGRAAFTGNHQWILLNNFTRPAYPPEVYNEVHHQFLAGMQTIVIIPVLPHGVVQLGSFLADIRY | 187 |
Select | Seq ID | Length | Analysis | Description | Start | End | IPR | GO |
---|---|---|---|---|---|---|---|---|
Acco08g0489 | 187 | PANTHER | TRANSCRIPTION FACTOR BHLH155-LIKE ISOFORM X1-RELATED | 50 | 181 | IPR043561 | GO:0003700|GO:0006355 | |
Acco08g0489 | 187 | MobiDBLite | consensus disorder prediction | 1 | 28 | - | - | |
Acco08g0489 | 187 | Pfam | bHLH-MYC and R2R3-MYB transcription factors N-terminal | 107 | 181 | IPR025610 | - | |
Acco08g0489 | 187 | Pfam | bHLH-MYC and R2R3-MYB transcription factors N-terminal | 54 | 91 | IPR025610 | - |
Select | Gene | Chromosome | Start | End | Duplicated_type |
---|---|---|---|---|---|
Acco08g0489 | Acco-ChrAcco08 | 3854901 | 3857196 | Transposed |
Select | Gene | Gene_start | Gene_end | Function | Ath_gene | Identity(%) | E-value | Score |
---|---|---|---|---|---|---|---|---|
Acco08g0489 | 50 | 182 | Basic Helix-Loop-Helix Transcription Factor Gene Family | AT2G27230 | 56.944 | 6.00e-51 | 171 |
Select | Gene_1 | Chr_1 | Start_1 | End_1 | Gene_2 | Chr_2 | Start_2 | End_2 | Event_name |
---|---|---|---|---|---|---|---|---|---|
Acco01g3625 | 01 | 52656223 | 52661581 | Acco08g0489 | 08 | 3854901 | 3857196 | CCT |