| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YKR054C | DYN1 | SGDID:S000001762 | DHC_N2 |
Dynein heavy chain, N-terminal region 2 |
pfam Family | PF08393 | 99.90 | 4.80E-30 | 6.00E-34 | 296.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
| YKR054C | DYN1 | SGDID:S000001762 | dhcA DDB_G0276355 |
Dynein heavy chain, cytoplasmic (Dynein heavy chain, cytosolic) (DYHC) |
Dictyostelium discoideum | 3vkg_a | P34036 | 100.00 | 3.00E-177 | 3.00E-181 | 1829.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YKR054C | DYN1 | SGDID:S000001762 | DYN1 DHC1 YKR054C |
Dynein heavy chain, cytoplasmic (Dynein heavy chain, cytosolic) (DYHC) |
Saccharomyces cerevisiae | 4akg_a | P36022 | 100.00 | 1.00E-231 | 1.00E-235 | 2346.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YKR054C | DYN1 | SGDID:S000001762 | DYNC1H1 DHC1 DNCH1 DNCL DNECL DYHC KIAA0325 |
Cytoplasmic dynein 1 heavy chain 1 (Cytoplasmic dynein heavy chain 1) (Dynein heavy chain, cytosolic) |
Homo sapiens | Spinal Muscular Atrophy With Lower Extremity Predominance,Charcot-Marie-Tooth Disease Type 5,Myopathy,Neuronal Migration Disorders,Seizure Disorder,Neuromuscular Disease,Cohen Syndrome,Spinal Muscular Atrophy, Lower Extremity-Predominant, 1, Autosomal Dominant,Amyotrophic Lateral Sclerosis 1,Spinal Muscular Atrophy,Motor Neuron Disease,Muscular Atrophy,Distal Hereditary Motor Neuronopathy Type 7,Motor Peripheral Neuropathy,Polymicrogyria,Autosomal Dominant Childhood-Onset Proximal Spinal Muscular Atrophy,Neuropathy,Charcot-Marie-Tooth Disease,Parkinson Disease, Late-Onset,Microcephaly,Tooth Disease,Myiasis,Alacrima, Achalasia, And Mental Retardation Syndrome,Autosomal Dominant Cerebellar Ataxia,Disease Of Mental Health,Ophthalmomyiasis,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Lissencephaly,Periventricular Nodular Heterotopia,Charcot-Marie-Tooth Disease, Axonal, Type 2o,Charcot-Marie-Tooth Disease, Dominant Intermediate E,Charcot-Marie-Tooth Disease, X-Linked Recessive, 2,Mental Retardation, Autosomal Dominant 13,Autism Spectrum Disorder,Neuronopathy, Distal Hereditary Motor, Type Viib,Charcot-Marie-Tooth Disease, Demyelinating, Type 1f,Autosomal Dominant Non-Syndromic Intellectual Disability,Charcot-Marie-Tooth Disease, Axonal, Type 2k,Chromosome 15q24 Deletion Syndrome,Autism,Band Heterotopia |
6f1t_f | Q14204 | ENSG00000197102 | DYNC1H1 | 100.00 | 1.50E-48 | 1.90E-52 | 493.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |