| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YDR379C-A | SDH6 | SGDID:S000007605 | Complex1_LYR_1 |
Complex1_LYR-like |
pfam Domain | PF13232 | 99.00 | 7.30E-14 | 5.30E-18 | 67.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
| YDR379C-A | SDH6 | SGDID:S000007605 | MIEF1 |
MIEF1 upstream open reading frame protein (Alternative MIEF1 protein) (AltMIEF1) (MIEF1 microprotein) (MIEF1-MP) |
Homo sapiens | Optic Nerve Disease,Optic Atrophy 1,Cranial Nerve Disease,Smith-Magenis Syndrome,Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 1,3-Methylglutaconic Aciduria, Type Iii |
5oom_v | L0R8F8 | ENSG00000143314 | MRPL24 | 99.20 | 1.70E-15 | 1.20E-19 | 75.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YDR379C-A | SDH6 | SGDID:S000007605 | NDUFB9 UQOR22 |
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9 (Complex I-B22) (CI-B22) (NADH-ubiquinone oxidoreductase B22 subunit) |
Bos taurus | 5ldw_n | Q02369 | 99.20 | 8.20E-16 | 5.70E-20 | 89.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YDR379C-A | SDH6 | SGDID:S000007605 | YALI0_D07216g |
YALI0_D07216g |
Yarrowia lipolytica | 6gcs_r | Q6C9Z1 | 99.30 | 5.60E-16 | 4.00E-20 | 84.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YDR379C-A | SDH6 | SGDID:S000007605 | YALI0_A01419g |
YALI0_A01419g |
Yarrowia lipolytica | 6gcs_p | Q6CI60 | 99.10 | 8.30E-15 | 5.90E-19 | 81.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YDR379C-A | SDH6 | SGDID:S000007605 | Ndufb9 |
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9 (Complex I-B22) (CI-B22) (NADH-ubiquinone oxidoreductase B22 subunit) |
Mus musculus | 6g2j_n | Q9CQJ8 | 99.30 | 2.10E-16 | 1.40E-20 | 92.50 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YDR379C-A | SDH6 | SGDID:S000007605 | Ndufa6 |
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 6 (Complex I-B14) (CI-B14) (NADH-ubiquinone oxidoreductase B14 subunit) |
Mus musculus | 6g2j_w | Q9CQZ5 | 99.10 | 2.00E-14 | 1.40E-18 | 80.30 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YDR379C-A | SDH6 | SGDID:S000007605 | LYRM4 C6orf149 ISD11 CGI-203 |
LYR motif-containing protein 4 |
Homo sapiens | Chromosome 6pter-P24 Deletion Syndrome,Cerebellar Disease,Friedreich Ataxia,Combined Oxidative Phosphorylation Deficiency 19,Hypercholesterolemia, Familial, 4,Lactic Acidosis,Anemia, Sideroblastic, 1,Autosomal Recessive Cerebellar Ataxia,Combined Oxidative Phosphorylation Deficiency,3-Methylglutaconic Aciduria, Type Iii |
5wgb_b | Q9HD34 | ENSG00000214113 | LYRM4 | 99.20 | 4.90E-15 | 3.50E-19 | 77.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YDR379C-A | SDH6 | SGDID:S000007605 | NDUFB11 UNQ111/PRO1064 |
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial (Complex I-ESSS) (CI-ESSS) (NADH-ubiquinone oxidoreductase ESSS subunit) (Neuronal protein 17.3) (Np17.3) (p17.3) |
Homo sapiens | Sideroblastic Anemia,Neuropathy,Microphthalmia,Endocardial Fibroelastosis,Anemia, Sideroblastic, 1,Strabismus,Linear Skin Defects With Multiple Congenital Anomalies 3,Mitochondrial Complex I Deficiency, Nuclear Type 30,Mitochondrial Complex I Deficiency, Nuclear Type 1,Linear Skin Defects With Multiple Congenital Anomalies 1,Optic Atrophy 2,Cardiomyopathy, Infantile Histiocytoid,Leigh Syndrome |
5xtd_e | Q9NX14 | ENSG00000147123 | NDUFB11 | 99.10 | 5.90E-15 | 4.20E-19 | 80.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YDR379C-A | SDH6 | SGDID:S000007605 | NDUFB9 LYRM3 UQOR22 |
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9 (Complex I-B22) (CI-B22) (LYR motif-containing protein 3) (NADH-ubiquinone oxidoreductase B22 subunit) |
Homo sapiens | Liver Disease,Mitochondrial Complex I Deficiency, Nuclear Type 24,Epilepsy, Idiopathic Generalized 11,Mitochondrial Complex I Deficiency, Nuclear Type 1,Cardiomyopathy, Infantile Histiocytoid,Leigh Syndrome |
5xtc_p | Q9Y6M9 | ENSG00000147684 | NDUFB9 | 99.20 | 8.00E-16 | 5.50E-20 | 89.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |