Genomic Location: QPEY01000048.1:221591...221824
NR annotation: MCL4121906.1, hypothetical protein [Idotea baltica]
Species Hydra viridissima · all data for this species · gene families
| UniProt accession | Description |
|---|
| A8E4L1 | Cytochrome c oxidase assembly protein COX19 OS=Bos taurus OX=9913 GN=COX19 PE=3 SV=1 |
| Q49B96 | Cytochrome c oxidase assembly protein COX19 OS=Homo sapiens OX=9606 GN=COX19 PE=1 SV=1 |
| Q8K0C8 | Cytochrome c oxidase assembly protein COX19 OS=Mus musculus OX=10090 GN=Cox19 PE=1 SV=1 |
No Pfam domain signature was recorded for BRAKERKREP00000010583.1 in Hydra viridissima.
Search by domain instead of by gene. Any accession above (InterPro, Pfam, PANTHER, GO, KEGG) can be used as a query on the
Functional Domain Search page, which searches all 148 annotated genomes at once.
| KO | Enzyme | Enzyme ID | Pathway | Map ID | Source |
|---|
| K18183 | COX19; cytochrome c oxidase assembly protein subunit 19 | - | Mitochondrial biogenesis | ko03029 | deepkoala |
Searching by KO or pathway ID across
all species is available on the
KEGG Pathway page.
Expression pattern (RNA-seq)
Transcript abundance of BRAKERKREP00000010583.1 across
29 RNA-seq samples of Hydra viridissima.
Values are TPM (transcripts per million) from the StringTie quantification; one bar is one
sample, grouped and coloured by condition, sorted by expression within each group.
29Samples
11TPM > 0
7Conditions
26.9Max TPM
6.1Mean TPM
By condition
| Condition | Samples | TPM > 0 |
Mean TPM | Max TPM | Mean, relative to max |
| whole body |
18 |
3 |
2.72 |
19.90 |
|
| Whole |
6 |
5 |
15.57 |
26.95 |
|
| aposymbioic hydra M9 strain · aposymbioic hydra rep1 |
1 |
1 |
16.21 |
16.21 |
|
| aposymbioic hydra M9 strain · aposymbioic hydra rep2 |
1 |
1 |
12.93 |
12.93 |
|
| symbioic hydra M9 strain · symbioic hydra rep1 |
1 |
1 |
5.27 |
5.27 |
|
| symbioic hydra M9 strain · symbioic hydra rep2 |
1 |
0 |
0.00 |
0.00 |
|
| unannotated |
1 |
0 |
0.00 |
0.00 |
|
Source: CnidoSite RNA-seq expression matrices (HVIRI_TPM,
StringTie quantification over 29 runs), joined to SRA sample
metadata. Samples whose tissue/treatment is not recorded in the source metadata are grouped
by the descriptor carried in the expression matrix itself.