Chromosome | Gene | Transcript | Category | ID | Start | End |
---|---|---|---|---|---|---|
chr_2 | g4851 | g4851.t2 | TSS | g4851.t2 | 5411953 | 5411953 |
chr_2 | g4851 | g4851.t2 | isoform | g4851.t2 | 5412088 | 5412703 |
chr_2 | g4851 | g4851.t2 | exon | g4851.t2.exon1 | 5412088 | 5412703 |
chr_2 | g4851 | g4851.t2 | cds | g4851.t2.CDS1 | 5412088 | 5412648 |
chr_2 | g4851 | g4851.t2 | TTS | g4851.t2 | 5412662 | 5412662 |
>g4851.t2 Gene=g4851 Length=616
ATGCAAGTATTAGCAAAAGCATTGGCAAAGCGTGGTCATGAAATTACTTTTATATCTGGA
TTTCCATTTGATAAACCAATTGAAAATTATCGTGACATAAAAATAAAATTGAGTGATGAA
GACTCAAGAGAAATGGAAGAAATGACAAAATCTATGGGAGGAAATCCAGGTTCAAAATCA
TTCTTTCAACTTTTGGGTTTCTTTTCACGAATGTTTTATAAAATTGGCAATGATACTCTT
CAATCAGCTGATGTTAAAAAGTTGATGGCTGAAGAACAATTTGACCTTGTTATTGCTGGC
TATTTTATGACTGAGTATTTACTTGGTCTTGCTACTCATTTCAATTGTCCATCGATAGTC
TTCTTCTCTGGAAATTTAGTTTCTTCACTCCATAAAATGGTAGGCAATCCATTATCGCCG
GCTGGTGCGCCCCATGGAATGTTGAAGAGTAAAGAAATCAACACTTTTAAACTGAGACTT
CAAAACTTTTTACTTCATGGACTTGATTTACTAATTTTTAGACCATATTTTAATTATCGT
GCACGACAAATCTACAAGTGAGTTACATAAGCTACAAAAAAGATTACAATAATAAACAAT
GTTTATATTTTTCAGT
>g4851.t2 Gene=g4851 Length=186
MQVLAKALAKRGHEITFISGFPFDKPIENYRDIKIKLSDEDSREMEEMTKSMGGNPGSKS
FFQLLGFFSRMFYKIGNDTLQSADVKKLMAEEQFDLVIAGYFMTEYLLGLATHFNCPSIV
FFSGNLVSSLHKMVGNPLSPAGAPHGMLKSKEINTFKLRLQNFLLHGLDLLIFRPYFNYR
ARQIYK
Transcript | Database | ID | Name | Start | End | E.value | |
---|---|---|---|---|---|---|---|
4 | g4851.t2 | Gene3D | G3DSA:3.40.50.2000 | Glycogen Phosphorylase B; | 1 | 181 | 0 |
1 | g4851.t2 | PANTHER | PTHR48043 | EG:EG0003.4 PROTEIN-RELATED | 2 | 181 | 0 |
2 | g4851.t2 | PANTHER | PTHR48043:SF114 | DOROTHY, ISOFORM A-RELATED | 2 | 181 | 0 |
3 | g4851.t2 | SUPERFAMILY | SSF53756 | UDP-Glycosyltransferase/glycogen phosphorylase | 1 | 176 | 0 |
IUPRED3 score over 0.5 is predictive of a disordered region.
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