| Yeast Systematic Name | Yeast Symbol | SGDID | Analog Name | Analog Description | EC | Organism | Disease | Structure | Uniprot | Human ID | Human Symbol | HHsearch Probability | HHsearch E_value | HHsearch P_value | HHsearch Score | Flag Disease related | Flag Homo sapiens | Flag Mus musculus | Flag Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YJL093C | TOK1 | SGDID:S000003629 | IRK10 |
Inward rectifier potassium channel Kirbac3.1 |
Magnetospirillum magnetotacticum | 1xl6_b | D9N164 | 98.50 | 2.40E-11 | 2.40E-15 | 122.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YJL093C | TOK1 | SGDID:S000003629 | KCNJ12 |
ATP-sensitive inward rectifier potassium channel 12 (Inward rectifier K(+) channel Kir2.2) (Potassium channel, inwardly rectifying subfamily J member 12) |
Gallus gallus | 3sph_a | F1NHE9 | 98.60 | 1.00E-11 | 1.00E-15 | 126.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YJL093C | TOK1 | SGDID:S000003629 | KCNK1 HOHO1 KCNO1 TWIK1 |
Potassium channel subfamily K member 1 (Inward rectifying potassium channel protein TWIK-1) (Potassium channel K2P1) (Potassium channel KCNO1) |
Homo sapiens | Hypokalemia,Myasthenic Syndrome, Congenital, 8,Birk-Barel Syndrome,Long Qt Syndrome 1,Autonomic Peripheral Neuropathy |
3ukm_c | O00180 | ENSG00000135750 | KCNK1 | 99.20 | 5.50E-16 | 5.80E-20 | 152.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YJL093C | TOK1 | SGDID:S000003629 | KCNK2 TREK TREK1 |
Potassium channel subfamily K member 2 (Outward rectifying potassium channel protein TREK-1) (TREK-1 K(+) channel subunit) (Two pore domain potassium channel TREK-1) (Two pore potassium channel TPKC1) |
Homo sapiens | Migraine With Or Without Aura 1,Dentin Sensitivity,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2x,Disease Of Mental Health,Birk-Barel Syndrome |
4twk_a | O95069 | ENSG00000082482 | KCNK2 | 99.40 | 5.20E-17 | 5.30E-21 | 161.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YJL093C | TOK1 | SGDID:S000003629 | Kcnj6 Girk2 Kcnj7 W |
G protein-activated inward rectifier potassium channel 2 (GIRK-2) (Inward rectifier K(+) channel Kir3.2) (Potassium channel, inwardly rectifying subfamily J member 6) |
Mus musculus | 3sya_a | P48542 | 98.50 | 2.30E-11 | 2.20E-15 | 124.50 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YJL093C | TOK1 | SGDID:S000003629 | KCNK10 TREK2 |
Potassium channel subfamily K member 10 (Outward rectifying potassium channel protein TREK-2) (TREK-2 K(+) channel subunit) |
Homo sapiens | Migraine With Or Without Aura 1,Birk-Barel Syndrome |
4bw5_d | P57789 | ENSG00000100433 | KCNK10 | 99.30 | 7.60E-17 | 8.00E-21 | 158.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YJL093C | TOK1 | SGDID:S000003629 | Kcnj3 Girk1 |
G protein-activated inward rectifier potassium channel 1 (GIRK-1) (Inward rectifier K(+) channel Kir3.1) (Potassium channel, inwardly rectifying subfamily J member 3) |
Mus musculus | 2qks_a | P63250 | 98.50 | 2.50E-11 | 2.50E-15 | 122.70 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YJL093C | TOK1 | SGDID:S000003629 | DF122_01560 |
DF122_01560 |
Burkholderia pseudomallei | 1p7b_a | P83698 | 98.60 | 1.00E-11 | 1.00E-15 | 126.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YJL093C | TOK1 | SGDID:S000003629 | Kcnk2 |
Potassium channel subfamily K member 2 (Outward rectifying potassium channel protein TREK-1) (TREK-1 K(+) channel subunit) (Two pore potassium channel TPKC1) |
Mus musculus | 6cq9_b | P97438 | 99.30 | 4.80E-16 | 5.00E-20 | 155.80 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YJL093C | TOK1 | SGDID:S000003629 | KCNK4 TRAAK |
Potassium channel subfamily K member 4 (TWIK-related arachidonic acid-stimulated potassium channel protein) (TRAAK) (Two pore potassium channel KT4.1) (Two pore K(+) channel KT4.1) |
Homo sapiens | Erythrasma,Primary Syphilis,Hypertrichosis,Migraine With Or Without Aura 1,Seizure Disorder,Epilepsy,Overgrowth Syndrome,Gingival Hypertrophy,Paroxysmal Extreme Pain Disorder,Gingival Overgrowth,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, And Gingival Overgrowth Syndrome,Birk-Barel Syndrome,Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema |
4wfe_b | Q9NYG8 | ENSG00000182450 | KCNK4 | 99.30 | 6.40E-17 | 6.60E-21 | 161.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |