Chromosome | Gene | Transcript | Category | ID | Start | End |
---|---|---|---|---|---|---|
chr_1 | g10326 | g10326.t2 | TTS | g10326.t2 | 8922253 | 8922253 |
chr_1 | g10326 | g10326.t2 | isoform | g10326.t2 | 8922274 | 8922812 |
chr_1 | g10326 | g10326.t2 | exon | g10326.t2.exon1 | 8922274 | 8922812 |
chr_1 | g10326 | g10326.t2 | cds | g10326.t2.CDS1 | 8922274 | 8922510 |
chr_1 | g10326 | g10326.t2 | TSS | g10326.t2 | 8923070 | 8923070 |
>g10326.t2 Gene=g10326 Length=539
GGACTAAAAATTATACTATAGAAGATGAAAATAAGTTGAGAAACTTAGGTGCAGAGTTTA
TCAAGACAAATAGAGGAGGTCTTATTACATTTCATGGACCTGGACAGCTTGTTGCATATC
CAATTATCAATTTAAAAAATTTCAAGCAAGGTGTTCGTTGGTACGTGAATAGTATTGAAA
GAACGATAATAAATTTATGCCATAAATATGAATTAAACGCAACCACTACAACTGATACGG
GTGTATGGATTAATGATAGAAAGATTTGTGCTATTGGCATTCATGTTAGTCGATATGTGA
CAATGCATGGACTTGCATTGAATTGTAACACTGATTTAAGTTGGTTCAATCATATTGTAC
CTTGTGGAATCGAAGACAAAGAAGTTACATCTCTTTCTAAAGAATGCAAAAGAGACATTC
AAATAAATGATGTTATTCCAGAATTAATTGCAAGCTTCAGCACAATTTTTGAAAGCAAAA
CTATTTTAGTTAATCAAGAACAAGTTGATGAGATTAAAAAAAATTCTTTAGAGAAATAA
>g10326.t2 Gene=g10326 Length=78
MHGLALNCNTDLSWFNHIVPCGIEDKEVTSLSKECKRDIQINDVIPELIASFSTIFESKT
ILVNQEQVDEIKKNSLEK
Transcript | Database | ID | Name | Start | End | E.value | |
---|---|---|---|---|---|---|---|
4 | g10326.t2 | Gene3D | G3DSA:3.30.930.10 | Bira Bifunctional Protein; Domain 2 | 1 | 57 | 0.000 |
1 | g10326.t2 | PANTHER | PTHR10993:SF7 | LIPOYLTRANSFERASE 2, MITOCHONDRIAL-RELATED | 1 | 66 | 0.000 |
2 | g10326.t2 | PANTHER | PTHR10993 | OCTANOYLTRANSFERASE | 1 | 66 | 0.000 |
5 | g10326.t2 | ProSiteProfiles | PS51733 | Biotinyl protein ligase (BPL) and lipoyl protein ligase (LPL) catalytic domain profile. | 1 | 60 | 21.806 |
3 | g10326.t2 | SUPERFAMILY | SSF55681 | Class II aaRS and biotin synthetases | 1 | 57 | 0.000 |
IUPRED3 score over 0.5 is predictive of a disordered region.
GOID | TERM | ONTOLOGY |
---|---|---|
GO:0006464 | cellular protein modification process | BP |
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.