| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YER046W | SPO73 | SGDID:S000000848 | MYOF FER1L3 KIAA1207 |
Myoferlin (Fer-1-like protein 3) |
Homo sapiens | Deafness, Autosomal Recessive 9,Myopathy,Autosomal Recessive Limb-Girdle Muscular Dystrophy,Muscular Dystrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b,Dysferlinopathy,Miyoshi Muscular Dystrophy |
2k2o_a | Q9NZM1 | ENSG00000138119 | MYOF | 96.90 | 1.40E-06 | 1.50E-10 | 59.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YER046W | SPO73 | SGDID:S000000848 | Pex24p |
Integral peroxisomal membrane peroxin |
pfam Family | PF06398 | 96.40 | 1.10E-05 | 1.30E-09 | 60.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
| YER046W | SPO73 | SGDID:S000000848 | DYSF FER1L1 |
Dysferlin (Dystrophy-associated fer-1-like protein) (Fer-1-like protein 1) |
Homo sapiens | Muscular Disease,X-Linked Recessive Disease,Deafness, Autosomal Recessive 9,Congenital Fiber-Type Disproportion,Myopathy,Myofibrillar Myopathy,Emery-Dreifuss Muscular Dystrophy,Muscle Tissue Disease,Neuromuscular Disease,Bethlem Myopathy 1,Facioscapulohumeral Muscular Dystrophy 1,Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 2,Qualitative Or Quantitative Defects Of Dysferlin,Polymyositis,Myopathy, Centronuclear, 1,Myositis,Congenital Myopathy, Paradas Type,Autosomal Recessive Limb-Girdle Muscular Dystrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2a,Muscular Dystrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2c,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2d,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2f,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2g,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2h,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2j,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2l,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2x,Tibial Muscular Dystrophy,Limb-Girdle Muscular Dystrophy,Distal Muscular Dystrophy With Anterior Tibial Onset,Isolated Elevated Serum Creatine Phosphokinase Levels,Dysferlinopathy,Muscular Dystrophy, Congenital, Lmna-Related,Diamond-Blackfan Anemia,Localized Lipodystrophy,Myopathy, Myofibrillar, 3,Miyoshi Muscular Dystrophy 3,Foot Drop,Rigid Spine Muscular Dystrophy 1,Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 1,Centronuclear Myopathy,Muscular Dystrophy, Becker Type,Welander Distal Myopathy,Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant,Anterior Compartment Syndrome,Walker-Warburg Syndrome,Muscular Dystrophy-Dystroglycanopathy , Type C, 4,Nonaka Myopathy,Muscular Dystrophy-Dystroglycanopathy,Rippling Muscle Disease 2,Cardiomyopathy, Dilated, 3b,Myopathy, Distal, With Anterior Tibial Onset,Muscular Dystrophy-Dystroglycanopathy , Type C, 5,Muscular Dystrophy, Congenital Merosin-Deficient, 1a,Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2,Ullrich Congenital Muscular Dystrophy 1,Miyoshi Muscular Dystrophy 1,Myopathy, Centronuclear, 2,Batten-Turner Congenital Myopathy,Miyoshi Muscular Dystrophy |
4cah_b | O75923 | ENSG00000135636 | DYSF | 97.00 | 9.70E-07 | 1.10E-10 | 58.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |