Panax japonicus (panax_japonicus)
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Imported from atlas release summary for Panax japonicus.
2933
Candidate Genes
105
Families
6
Pathways
Phylogenetic Position
The current species is positioned within the lineage framework used by this site. Its taxon group is highlighted below.
Species Metadata
Taxon group
Eudicots
Common name
/
Genome status
Genome-level resource available
Site Placement
- This page summarizes pathway coverage, family distributions, and the gene list for the species within the current public dataset.
- If you want to start from the public overview first, open the homepage and then return here for species-level drill-down.
- Family statistics correspond to enzyme families, while pathway statistics correspond to the real category-level pathways.
Pathway Coverage
6
Pathways
Family Distribution
2933
Candidate Genes
BAHD
5.92%
C4H
5.21%
C3'H/CYP98A
4.98%
4CL
4.61%
UGT
4.4%
POD
4.37%
7DLGT
3.53%
UFGT
3.34%
Other Families
63.65%
More Families (97)
IFS
224
3.19%
F3H
204
2.9%
NMT
192
2.73%
CYP76
190
2.7%
T3O
186
2.65%
DWF4/CYP90B1
148
2.11%
BBE
141
2.01%
STR
132
1.88%
CODM/T6ODM
123
1.75%
F3'H/CYP75B
116
1.65%
CAD
105
1.49%
TRI/TRII
100
1.42%
CYP71
97
1.38%
CAS
96
1.37%
H6H
89
1.27%
BR6OX2/CYP85A2
89
1.27%
SMT1/SMT2/SMT3
88
1.25%
LAC
80
1.14%
HCT
79
1.12%
IFR
77
1.1%
CYP90D1
77
1.1%
CSE
76
1.08%
GS
70
1.0%
TPS
67
0.95%
GES
65
0.92%
PYKS
60
0.85%
PAL
60
0.85%
RAS
60
0.85%
TAT
56
0.8%
G8O/G8H
52
0.74%
7DLH
50
0.71%
T16H
47
0.67%
SLS
45
0.64%
F5H/CYP84A
44
0.63%
COMT
44
0.63%
PMT
43
0.61%
SGD
42
0.6%
FNS
40
0.57%
F3'5'H/CYP75A
40
0.57%
NCS
38
0.54%
IO
38
0.54%
ANR
36
0.51%
COR
35
0.5%
CCR
34
0.48%
CYP51G1
30
0.43%
8HGO
29
0.41%
ANS/LDOX
28
0.4%
CPR
28
0.4%
CPD/CYP90A1
27
0.38%
GGPPS
27
0.38%
16OMT
26
0.37%
CCoAOMT
26
0.37%
BR6OX1/CYP85A1
26
0.37%
LAMT
24
0.34%
DFR
21
0.3%
DET2
21
0.3%
DXS
21
0.3%
CNMT
20
0.28%
AACT
20
0.28%
CYP719
19
0.27%
SQE
18
0.26%
MPO
17
0.24%
HPPR
16
0.23%
CHS
15
0.21%
HMGR
15
0.21%
CYP80B1
14
0.2%
ISY
14
0.2%
SQS/FDFT1
14
0.2%
TDC
13
0.18%
FPPS
13
0.18%
ROT3/CYP90C1
12
0.17%
SMO1/SMO2
11
0.16%
ADC
9
0.13%
CHI
9
0.13%
MCT/IspD
9
0.13%
TYDC_DDC
8
0.11%
PMK
8
0.11%
HDR/IspH
8
0.11%
HDS/IspG
8
0.11%
XMT_MXMT_DXMT
7
0.1%
MVK
7
0.1%
HYD1
6
0.09%
HMGS
6
0.09%
MDS/IspF
6
0.09%
DWF7
5
0.07%
IDI
5
0.07%
DXR
5
0.07%
CMK/IspE
4
0.06%
MVD
4
0.06%
6OMT_4OMT_SOMT
3
0.04%
FLS
3
0.04%
CPI1
3
0.04%
FK
3
0.04%
DWF5
3
0.04%
ODC
2
0.03%
DWF1
2
0.03%
CYP80F1
1
0.01%
Species Pathway Results
The links below show identification results for this species within each pathway, instead of opening the global pathway overview.
| Pathway | Candidate Genes | Families | Top family | Results |
|---|---|---|---|---|
| Terpenoid pathway | 891 | 19 | BAHD (343) | View species results |
| Alkaloid pathway | 619 | 23 | NMT (106) | View species results |
| Phenylpropanoid pathway | 617 | 12 | POD (272) | View species results |
| Flavonoid pathway | 356 | 12 | UFGT (209) | View species results |
| Rosmarinic acid pathway | 251 | 7 | C4H (63) | View species results |
| Steroid pathway | 199 | 14 | CAS (80) | View species results |
Broad Catalytic Groups
P450/oxygenase and BAHD/acyltransferase are counted separately as broad catalytic groups and are not mixed into the canonical enzyme-family count.
| Catalytic group | Families | Candidate genes | Included families |
|---|---|---|---|
| P450/oxygenase | 24 | 2288 | 7DLH, BR6OX1/CYP85A1, BR6OX2/CYP85A2, C3'H/CYP98A, C4H, CPD/CYP90A1, CYP51G1, CYP71, CYP719, CYP76, CYP80B1, CYP80F1, CYP90D1, DWF4/CYP90B1, F3'5'H/CYP75A, F3'H/CYP75B, F5H/CYP84A, G8O/G8H, IFS, IO, ROT3/CYP90C1, SLS, T16H, T3O |
| BAHD/acyltransferase | 3 | 555 | BAHD, HCT, RAS |
Identification Result List
Search the public identification results for this species; click pathway or family legends above to narrow within this species.
Current family filter: STR
| Gene | Pathway | Family | Confidence | Status | Best Target |
|---|---|---|---|---|---|
| panax_japonicus_GWHPBEIH032366.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH032649.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH033091.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH033097.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH033098.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH033099.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH033459.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH033535.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH033784.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH034514.1 | Alkaloid | STR | medium | pass | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH034833.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH035004.1 | Alkaloid | STR | medium | pass | STR__00003__sp_Q9M1B4_SSL13_ARATH |
| panax_japonicus_GWHPBEIH035311.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH036456.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH036706.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH037222.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH037283.1 | Alkaloid | STR | medium | pass | STR__00003__sp_Q9M1B4_SSL13_ARATH |
| panax_japonicus_GWHPBEIH038407.1 | Alkaloid | STR | medium | pass | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH039201.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH039203.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH039765.1 | Alkaloid | STR | medium | pass | STR__00003__sp_Q9M1B4_SSL13_ARATH |
| panax_japonicus_GWHPBEIH040687.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH040755.1 | Alkaloid | STR | medium | pass | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH040865.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH042553.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH042649.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH042848.1 | Alkaloid | STR | medium | pass | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH043262.1 | Alkaloid | STR | medium | pass | STR__00003__sp_Q9M1B4_SSL13_ARATH |
| panax_japonicus_GWHPBEIH045148.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH045220.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH045229.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH045417.1 | Alkaloid | STR | medium | pass | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH045778.1 | Alkaloid | STR | medium | pass | STR__00003__sp_Q9M1B4_SSL13_ARATH |
| panax_japonicus_GWHPBEIH046818.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH047462.1 | Alkaloid | STR | medium | pass | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH047762.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH047925.1 | Alkaloid | STR | medium | pass | STR__00003__sp_Q9M1B4_SSL13_ARATH |
| panax_japonicus_GWHPBEIH048252.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH048284.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH049648.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH049865.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH049943.1 | Alkaloid | STR | medium | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH050676.1 | Alkaloid | STR | medium | pass | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH052111.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH052315.1 | Alkaloid | STR | medium | pass | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH052684.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH052685.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH053165.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH053243.1 | Alkaloid | STR | low | borderline | STR__00001__sp_D3GE74_STR1_MEDTR |
| panax_japonicus_GWHPBEIH053970.1 | Alkaloid | STR | medium | pass | STR__00001__sp_D3GE74_STR1_MEDTR |