Chromosome | Gene | Transcript | Category | ID | Start | End |
---|---|---|---|---|---|---|
chr_3 | g1385 | g1385.t4 | TSS | g1385.t4 | 10436828 | 10436828 |
chr_3 | g1385 | g1385.t4 | isoform | g1385.t4 | 10436930 | 10437572 |
chr_3 | g1385 | g1385.t4 | exon | g1385.t4.exon1 | 10436930 | 10436970 |
chr_3 | g1385 | g1385.t4 | exon | g1385.t4.exon2 | 10437032 | 10437174 |
chr_3 | g1385 | g1385.t4 | cds | g1385.t4.CDS1 | 10437079 | 10437174 |
chr_3 | g1385 | g1385.t4 | exon | g1385.t4.exon3 | 10437246 | 10437572 |
chr_3 | g1385 | g1385.t4 | cds | g1385.t4.CDS2 | 10437246 | 10437572 |
chr_3 | g1385 | g1385.t4 | TTS | g1385.t4 | 10437590 | 10437590 |
>g1385.t4 Gene=g1385 Length=511
ATGGCAAAACCTAATATACTTGTTACGGGGACTCCAGGTATGTGCAGGCAAGTCTCATTT
TGCAAAACAAATTGCCGAAGAAAATGGAATGAGATTTCTTGAAATAAGCAAAATTGTACA
GGACAATGGCTTTACAGACGGTTTCGATGAAACACTCAATTGTCCAATATTGGATGAAGA
TAAGTTGCTTGACTATCTTGAACCACTTATGAACGAGGGAAATAATGTAGCAGAATATCA
TTCCTCTGAGTTCTTTCCTGAACGTTGGTTTCAAGCTGTTTATGTGGTGAGATGCAATAC
TGATGTTTTATTCAAGAGACTCGAAGAGAGAGGATACAATGCAAAAAAGATTCAGAACAA
TGTTGAATATGAAATATTTCAAATGGCACTGGATGAAGCAAAGAGCAGCTATAAGCCGGA
AATAGTATTTGAAGTACGTGGTGAAAATGAAAAAGACCTCGAAGATAATTTAAAGAAGGT
TGGTGAATTTATAAACAATTATGAAGAATGA
>g1385.t4 Gene=g1385 Length=140
MRFLEISKIVQDNGFTDGFDETLNCPILDEDKLLDYLEPLMNEGNNVAEYHSSEFFPERW
FQAVYVVRCNTDVLFKRLEERGYNAKKIQNNVEYEIFQMALDEAKSSYKPEIVFEVRGEN
EKDLEDNLKKVGEFINNYEE
Transcript | Database | ID | Name | Start | End | E.value | |
---|---|---|---|---|---|---|---|
4 | g1385.t4 | Gene3D | G3DSA:3.40.50.300 | - | 1 | 140 | 0e+00 |
2 | g1385.t4 | PANTHER | PTHR12595 | POS9-ACTIVATING FACTOR FAP7-RELATED | 2 | 139 | 0e+00 |
1 | g1385.t4 | Pfam | PF13238 | AAA domain | 6 | 97 | 0e+00 |
3 | g1385.t4 | SUPERFAMILY | SSF52540 | P-loop containing nucleoside triphosphate hydrolases | 3 | 131 | 2e-07 |
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