Chromosome | Gene | Transcript | Category | ID | Start | End |
---|---|---|---|---|---|---|
chr_4 | g14398 | g14398.t2 | TTS | g14398.t2 | 266020 | 266020 |
chr_4 | g14398 | g14398.t2 | isoform | g14398.t2 | 266046 | 266487 |
chr_4 | g14398 | g14398.t2 | exon | g14398.t2.exon1 | 266046 | 266487 |
chr_4 | g14398 | g14398.t2 | cds | g14398.t2.CDS1 | 266046 | 266477 |
chr_4 | g14398 | g14398.t2 | TSS | g14398.t2 | NA | NA |
>g14398.t2 Gene=g14398 Length=442
GCATGATCCAATGGCAATGCGTCCTTTTCTAGGTTATAATTTTGGAAAATATTTACAACA
TTGGTTAAATATGGAAGTTGCTGGTTGTAAAATGCCTAAAATTTTTCATGTGAATTGGTT
CCTTAAAGGAAATGATGGAAAGTTTTTATGGCCAGGATATGGTGAAAATTCACGAGTTCT
TGATTGGATTTTAAAGCGAATTGAAGGTGAAGAGTGTTTTGATGAAACTTCAATTGGAAA
AGTTCCATGCAGTAATTCAATTCGATTAGATGGATTAAAACAAGAAGTTGACATGAAAAA
ATTATTTAAAATTGATAAGGAGTTTTGGTTAAAAGAAGTGAAAGAAATTCAAAAGTTTTA
TGAAGAACAAGTTGGAAATGATTTGCCAGAGGCAGTGAAAAATGAATTGAATGGATTGAA
GGAAAGAGTCGAACAAATGTAA
>g14398.t2 Gene=g14398 Length=143
MAMRPFLGYNFGKYLQHWLNMEVAGCKMPKIFHVNWFLKGNDGKFLWPGYGENSRVLDWI
LKRIEGEECFDETSIGKVPCSNSIRLDGLKQEVDMKKLFKIDKEFWLKEVKEIQKFYEEQ
VGNDLPEAVKNELNGLKERVEQM
Transcript | Database | ID | Name | Start | End | E.value | |
---|---|---|---|---|---|---|---|
5 | g14398.t2 | Gene3D | G3DSA:3.90.228.20 | - | 1 | 141 | 0 |
2 | g14398.t2 | PANTHER | PTHR11561 | PHOSPHOENOLPYRUVATE CARBOXYKINASE | 1 | 143 | 0 |
3 | g14398.t2 | PANTHER | PTHR11561:SF1 | PHOSPHOENOLPYRUVATE CARBOXYKINASE, CYTOSOLIC [GTP] | 1 | 143 | 0 |
1 | g14398.t2 | Pfam | PF00821 | Phosphoenolpyruvate carboxykinase C-terminal P-loop domain | 1 | 140 | 0 |
4 | g14398.t2 | SUPERFAMILY | SSF53795 | PEP carboxykinase-like | 1 | 142 | 0 |
IUPRED3 score over 0.5 is predictive of a disordered region.
GOID | TERM | ONTOLOGY |
---|---|---|
GO:0006094 | gluconeogenesis | BP |
GO:0005525 | GTP binding | MF |
GO:0004611 | phosphoenolpyruvate carboxykinase activity | MF |
GO:0017076 | purine nucleotide binding | 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.