쿠도아 셉템푼타타(학명: Kudoa Septempunctata)는 점액포자충강 다각목(Multivalvulida)에 속하는 기생충이다. 7개의 극낭을 가지고 있어 칠성쿠도아충이라고도 불린다. 2010년 대한민국에서 일본으로 수입된 양식 넙치에서 처음 발견 및 분리되었다. 쿠도아속에 속한 다른 종과 달리 감염어에서 사후 근육 융해를 일으키지 않는다. 쿠도아 셉템푼타타에 감염된 넙치를 회로 먹은 후 급성 식중독이 발병한 사례가 보고되었다.
No narrative description available for this taxon yet.
A DNA barcode is a short, standardised stretch of genes that works like a fingerprint — enough to tell one species from another. Below is the molecular trace Kudoa septempunctata has left across the world's sequence archives.
At a glance
DNA specimens34
BINs1
Marker genes10
eDNA detections28
Countries2
The DNA barcodethe species' typical barcode, built from every sequenced specimen
COI-5P1 362 bp consensus3 specimens
ACGT
▸ drag or hover over the strip to read any position — letter and how much it varies
Violet ticks below the strip = positions where individuals differ; flat = the species' unchanging signature. 99% of positions are identical in every specimen.
Diversity (π)0.59%
Haplotypes2
BIN1
Most divergent pair0.88%
Where individuals differ — all 12 variable positions, in barcode order
★ the standard DNA barcode for this group — the short region actually read to tell this species apart. The rest are extra genes sequenced along the way.
★COI-3P★COI-5P18S-3P18S-5PCOIIND1ND3ND4LND5-0ND6
animal barcoderibosomalmitochondrial
Organelle genome
Besides the big genome in the nucleus, cells carry a small, circular loop of DNA inside the cell's energy factories — the mitochondria. It is inherited almost only from the mother and is a leftover from ancient bacteria that moved into the cell. The mitochondrial markers above (ND*, COX, CYTB…) are read from exactly this loop. Outer ring = one strand, inner ring = the other.
▸ Tap any coloured segment — or a gene chip — to see what it is
Pick a coloured segment on the ring — or a gene chip — to read what that gene does.
protein-codingrRNAtRNA
09Environmental DNA28 detections
Where the DNA of Kudoa septempunctata was picked up in samples of water, soil or air — nobody saw the organism, only its DNA left behind. A trace is a clue that the species was near, not a confirmed sighting.
Signal
Detections DNA found28
Studies independent surveys1
Countries1
Signal confidence: weakweighed across independent studies, places & mapped detections
Where its DNA was found
0 of 28 detections have coordinates
Open the map1 country0
How strong is each trace?
DNA read depthRead counts were not reported for this species — the map shows presence only, not how strong each trace was.
Modelled climatemodelled
−15°Ctemperature across detection sites+40°C
Temperature median7.40 °C 7.40–7.40
Seasonal swing summer↔winter25.4 °C
Max temp (day)9.60 °C
Min temp (night)3.00 °C
Precipitation344 mm/mo
Air humidity64.9 %
Moisture balance263 mm/mo
Vapour deficit428 Pa
Wind speed2.90 m/s
Cloud cover44.6 %
CHELSA 1981–2010, ~9 km grid, at location & month of 2 detection points · median with p10–p90 · reflects where sampling happened, not only the true niche
How to read this: each dot is one detection of this species' DNA in an environmental sample. The confidence meter weighs how many independent studies and places back up the signal — one detection in one study is a hint; many across several studies is solid. Records dated before 2008 (when eDNA methods began) are treated as likely mislabeled and left off the map.
