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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YBR024W | SCO2 | SGDID:S000000228 | SCO1 SCOD1 |
Protein SCO1 homolog, mitochondrial |
Homo sapiens | Cardioencephalomyopathy,Mitochondrial Complex Iv Deficiency, Nuclear Type 4,Hypertrophic Cardiomyopathy,Alzheimer Disease,Mitochondrial Complex Iv Deficiency, Nuclear Type 1,Mitochondrial Disorders,Gracile Syndrome,Fatal Infantile Cardioencephalomyopathy Due To Cytochrome C Oxidase Deficiency,Mitochondrial Dna Depletion Syndrome 9,Leigh Syndrome |
2ggt_b | O75880 | ENSG00000133028 | SCO1 | 98.20 | 4.80E-10 | 6.10E-14 | 82.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR024W | SCO2 | SGDID:S000000228 | mpt53 mpb53 Rv2878c MTCY274.09c |
Soluble secreted antigen MPT53 |
Mycobacterium tuberculosis | 1lu4_a | P9WG65 | 98.30 | 2.30E-10 | 2.40E-14 | 89.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR024W | SCO2 | SGDID:S000000228 | SCO1 YBR037C YBR0406 |
Protein SCO1, mitochondrial |
Saccharomyces cerevisiae | 2b7j_d | P23833 | 99.00 | 5.50E-14 | 6.80E-18 | 110.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YBR024W | SCO2 | SGDID:S000000228 | SCO2 |
Protein SCO2 homolog, mitochondrial |
Homo sapiens | Cardioencephalomyopathy,Mitochondrial Dna Depletion Syndrome,Seizure Disorder,Degenerative Myopia,Myopia,Hypertrophic Cardiomyopathy,Complement Component 2 Deficiency,Mitochondrial Metabolism Disease,Anisometropia,Mitochondrial Neurogastrointestinal Encephalomyopathy,Refractive Error,Spinal Muscular Atrophy,Muscular Atrophy,Mitochondrial Complex Iv Deficiency, Nuclear Type 1,Rare Isolated Myopia,Leigh Syndrome With Cardiomyopathy,Dilated Cardiomyopathy,Myopia 6,Cycloplegia,Mitochondrial Disorders,Charcot-Marie-Tooth Disease,Juvenile Glaucoma,Autosomal Recessive Axonal Charcot-Marie-Tooth Disease Due To Copper Metabolism Defect,Mitochondrial Dna Depletion Syndrome 2,Mitochondrial Dna Depletion Syndrome 1,Mitochondrial Dna Depletion Syndrome 4b,Lactic Acidosis,Mitochondrial Complex Iv Deficiency, Nuclear Type 2,Fatal Infantile Cardioencephalomyopathy Due To Cytochrome C Oxidase Deficiency,Leber Hereditary Optic Neuropathy, Modifier Of,Mitochondrial Dna Depletion Syndrome 3,Spinal Muscular Atrophy, Type I,Cardiomyopathy, Infantile Hypertrophic,Kearns-Sayre Syndrome,Leigh Syndrome,Myoclonic Epilepsy Associated With Ragged-Red Fibers,Neuropathy, Ataxia, And Retinitis Pigmentosa,3-Methylglutaconic Aciduria, Type Iii |
2rli_a | O43819 | ENSG00000284194 | SCO2 | 98.20 | 2.60E-10 | 3.40E-14 | 83.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YBR024W | SCO2 | SGDID:S000000228 | SCO3966 |
SCO3966 |
Streptomyces coelicolor | 4bpy_a | Q93J40 | 98.40 | 7.90E-11 | 1.00E-14 | 86.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |