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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YLL001W | DNM1 | SGDID:S000003924 | DNM1 DNM |
Dynamin-1 (EC 3.6.5.5) |
3.6.5.5 | Homo sapiens | Zellweger Syndrome,Seizure Disorder,Optic Nerve Disease,Cohen Syndrome,Myopathy, Centronuclear, 1,Undetermined Early-Onset Epileptic Encephalopathy,Peroxisome Biogenesis Disorder 1b,Optic Atrophy 1,Charcot-Marie-Tooth Disease,Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 2,Neuronal Intranuclear Inclusion Disease,Centronuclear Myopathy,Disease Of Mental Health,Neuropathy, Hereditary Sensory, Type Id,Aceruloplasminemia,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Lennox-Gastaut Syndrome,Early Infantile Epileptic Encephalopathy,Charcot-Marie-Tooth Disease, Dominant Intermediate B,Developmental And Epileptic Encephalopathy 31,Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive,Rett Syndrome |
6dlu_p | Q05193 | ENSG00000106976 | DNM1 | 100.00 | 1.00E-50 | 1.20E-54 | 433.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLL001W | DNM1 | SGDID:S000003924 | DNM1L DLP1 DRP1 |
Dynamin-1-like protein (EC 3.6.5.5) (Dnm1p/Vps1p-like protein) (DVLP) (Dynamin family member proline-rich carboxyl-terminal domain less) (Dymple) (Dynamin-like protein) (Dynamin-like protein 4) (Dynamin-like protein IV) (HdynIV) (Dynamin-related protein 1) |
3.6.5.5 | Homo sapiens | Myopathy, Lactic Acidosis, And Sideroblastic Anemia,Zellweger Syndrome,Myopathy,Optic Nerve Disease,Scotoma,Cockayne Syndrome A,Alzheimer Disease,Mitochondrial Myopathy,Paroxysmal Dystonia,Hereditary Spastic Paraplegia,Skin Amelanotic Melanoma,Autosomal Recessive Spastic Ataxia,Optic Atrophy 1,Brain Cancer,Obesity Due To Melanocortin 4 Receptor Deficiency,Spastic Paraplegia 8,Charcot-Marie-Tooth Disease,Cranial Nerve Disease,Parkinson Disease, Late-Onset,Peripheral Nervous System Disease,Microcephaly,Encephalopathy,Tooth Disease,Myopathy, Lactic Acidosis, And Sideroblastic Anemia 2,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Lactic Acidosis,Optic Atrophy With Or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, And Neuropathy,Spinocerebellar Ataxia 12,Optic Atrophy 5,Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 1,Spastic Ataxia,Leigh Syndrome,3-Methylglutaconic Aciduria, Type Iii |
4bej_b | O00429 | ENSG00000087470 | DNM1L | 100.00 | 1.40E-40 | 1.80E-44 | 339.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLL001W | DNM1 | SGDID:S000003924 | Dynamin_M |
Dynamin central region |
pfam Family | PF01031 | 99.90 | 5.50E-30 | 7.10E-34 | 236.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
YLL001W | DNM1 | SGDID:S000003924 | Dnm1 |
Dnm1 |
Cyanidioschyzon merolae | 6fgz_a | Q84Y91 | 100.00 | 1.90E-47 | 2.30E-51 | 409.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YLL001W | DNM1 | SGDID:S000003924 | MX2 |
Interferon-induced GTP-binding protein Mx2 (Interferon-regulated resistance GTP-binding protein MxB) (Myxovirus resistance protein 2) (p78-related protein) |
Homo sapiens | Influenza,Pediculus Humanus Corporis Infestation,Hantavirus Hemorrhagic Fever With Renal Syndrome,Danubian Endemic Familial Nephropathy,Aicardi-Goutieres Syndrome,Microphthalmia With Limb Anomalies |
4whj_a | P20592 | ENSG00000183486 | MX2 | 100.00 | 8.40E-38 | 1.00E-41 | 325.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLL001W | DNM1 | SGDID:S000003924 | CTHT_0065850 |
CTHT_0065850 |
Chaetomium thermophilum | 6ql4_a | G0SGC7 | 99.90 | 7.60E-31 | 7.20E-35 | 297.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YLL001W | DNM1 | SGDID:S000003924 | DNM3 KIAA0820 |
Dynamin-3 (EC 3.6.5.5) (Dynamin, testicular) (T-dynamin) |
3.6.5.5 | Homo sapiens | Myopathy, Centronuclear, 1,Sezary'S Disease,Centronuclear Myopathy,Neuropathy, Hereditary Sensory, Type Id |
5a3f_d | Q9UQ16 | ENSG00000197959 | DNM3 | 100.00 | 2.80E-51 | 3.40E-55 | 439.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |