| Chromosome | Gene | Transcript | Category | ID | Start | End |
|---|---|---|---|---|---|---|
| chr_2 | g6786 | g6786.t5 | TSS | g6786.t5 | 18601649 | 18601649 |
| chr_2 | g6786 | g6786.t5 | isoform | g6786.t5 | 18602514 | 18603033 |
| chr_2 | g6786 | g6786.t5 | exon | g6786.t5.exon1 | 18602514 | 18603033 |
| chr_2 | g6786 | g6786.t5 | cds | g6786.t5.CDS1 | 18602589 | 18603032 |
| chr_2 | g6786 | g6786.t5 | TTS | g6786.t5 | NA | NA |
>g6786.t5 Gene=g6786 Length=520
TGTCTTCAAAATATCTATTCATGTCATGGTCTTGATATCATAACTGTTGAAGGAATTGGT
AGCAAAAAGGATGGCATGCATAAAATTCAAAAACGATTGGCTGATTTTAATGGAACTCAA
TGTGGATTTTGTACTCCTGGGATGGTCATGAATATGTTTTCATTGATGGAAGCGAAAAAT
GGAAAAGTGACAATGGAAGAAGTTGAGAATTCGTTTGGTGGAAATATATGCAGATGCACT
GGTTATCGACCAATTTTAGATGCATTCAAATCACTTGCAATTGATGCTGATAAGAATCTT
TTGGATGCATGCAAGGACATTGAAGATTTGAGTGATATTAAAATGTGTCCAAAATCAGGA
AATCCTTGTTCTGGCAAATGCAGTTCATTGTTGAATATTGAAAAAAATCCAATGAGCTTC
ACTTTTGATGATGAACGCGAGTTTCACAAAGTTTATAATTTAGAACAACTTTTTAAGATA
ATGGGAACAATAAAATATCGTCCATACATTTTGATTGGAG
>g6786.t5 Gene=g6786 Length=148
MHKIQKRLADFNGTQCGFCTPGMVMNMFSLMEAKNGKVTMEEVENSFGGNICRCTGYRPI
LDAFKSLAIDADKNLLDACKDIEDLSDIKMCPKSGNPCSGKCSSLLNIEKNPMSFTFDDE
REFHKVYNLEQLFKIMGTIKYRPYILIG
| Transcript | Database | ID | Name | Start | End | E.value | |
|---|---|---|---|---|---|---|---|
| 5 | g6786.t5 | Gene3D | G3DSA:3.30.365.10 | Aldehyde Oxidoreductase; domain 4 | 1 | 147 | 0 |
| 2 | g6786.t5 | PANTHER | PTHR11908:SF132 | ALDEHYDE OXIDASE 1-RELATED | 1 | 139 | 0 |
| 3 | g6786.t5 | PANTHER | PTHR11908 | XANTHINE DEHYDROGENASE | 1 | 139 | 0 |
| 1 | g6786.t5 | Pfam | PF01799 | [2Fe-2S] binding domain | 2 | 64 | 0 |
| 4 | g6786.t5 | SUPERFAMILY | SSF47741 | CO dehydrogenase ISP C-domain like | 2 | 89 | 0 |
IUPRED3 score over 0.5 is predictive of a disordered region.
| GOID | TERM | ONTOLOGY |
|---|---|---|
| GO:0046872 | metal ion binding | MF |
| GO:0055114 | NA | NA |
| GO:0016491 | oxidoreductase activity | MF |
This gene did not have any KEGG ortholog annotations (KAAS, GHOSTZ).
TPM values are indicated as average +/- STDEV.
Differentially expressed genes were identified with DESeq2 using the ‘run_DE_analysis.pl’ script from Trinity. Transcripts were determined as differentially expressed when (1) FDR < 0.05 (2) fold change > 2 (TPM calculated by RSEM). DE information and fold change between conditions are indicated in the plot below. There were no conditions that were differentially expressed