| Chromosome | Gene | Transcript | Category | ID | Start | End |
|---|---|---|---|---|---|---|
| chr_2 | g5241 | g5241.t1 | TSS | g5241.t1 | 8076484 | 8076484 |
| chr_2 | g5241 | g5241.t1 | isoform | g5241.t1 | 8076538 | 8077004 |
| chr_2 | g5241 | g5241.t1 | exon | g5241.t1.exon1 | 8076538 | 8076764 |
| chr_2 | g5241 | g5241.t1 | cds | g5241.t1.CDS1 | 8076538 | 8076764 |
| chr_2 | g5241 | g5241.t1 | exon | g5241.t1.exon2 | 8076851 | 8077004 |
| chr_2 | g5241 | g5241.t1 | cds | g5241.t1.CDS2 | 8076851 | 8077004 |
| chr_2 | g5241 | g5241.t1 | TTS | g5241.t1 | NA | NA |
>g5241.t1 Gene=g5241 Length=381
ATGGAAACTGATCAGCAATTATTAGAGAAAAATGTTAGTCCATCAGAAATCAAACAATAT
TCGCCAATGGCTAAAGAATGGTGGAATACAAAAGATGGTCCAATGTATATCTTGCACGAC
ATGAATAAAATGAGGCTTGATCTCGTTTTTGATGGTTTGATATCAAACTGGTGTTTAAAA
TCATGGCAAGAAAGAGCCAAATGCATTTCAAGGATTAAAAATTTTAGACCTTGGCTGTGT
GGAGGAATTTTAGTTGAGGCTCTAGCAAAGCTCAAAGCAGAAGTTACTGGCTTAGATCCT
AATGAAGCCCTTCTAGAAGTTGCAAAAGAGCACATTGAAACACAAGAAGACATTCGTGGC
AAATGTTCGTTATTTACTTGA
>g5241.t1 Gene=g5241 Length=126
METDQQLLEKNVSPSEIKQYSPMAKEWWNTKDGPMYILHDMNKMRLDLVFDGLISNWCLK
SWQERAKCISRIKNFRPWLCGGILVEALAKLKAEVTGLDPNEALLEVAKEHIETQEDIRG
KCSLFT
| Transcript | Database | ID | Name | Start | End | E.value | |
|---|---|---|---|---|---|---|---|
| 4 | g5241.t1 | Gene3D | G3DSA:3.40.50.150 | Vaccinia Virus protein VP39 | 1 | 124 | 0e+00 |
| 1 | g5241.t1 | PANTHER | PTHR43464 | METHYLTRANSFERASE | 6 | 121 | 0e+00 |
| 2 | g5241.t1 | PANTHER | PTHR43464:SF25 | UBIQUINONE BIOSYNTHESIS O-METHYLTRANSFERASE, MITOCHONDRIAL | 6 | 121 | 0e+00 |
| 3 | g5241.t1 | SUPERFAMILY | SSF53335 | S-adenosyl-L-methionine-dependent methyltransferases | 6 | 117 | 1e-07 |
IUPRED3 score over 0.5 is predictive of a disordered region.
Data is missing for g5241/g5241.t1; file /home/yuki.yoshida/nias/analysis/reanalysis/18_revice/midgebase/iupred3/g5241.t1.fa.iupred3.txt does not exist
There are no GO annotations for this transcript.
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