| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YNL023C | FAP1 | SGDID:S000004968 | Probable RNA-binding protein |
Probable RNA-binding protein |
Clostridium symbiosum | 3gku_a | D0VX24 | 97.10 | 6.70E-07 | 7.30E-11 | 83.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YNL023C | FAP1 | SGDID:S000004968 | SPAG7 |
Sperm-associated antigen 7 |
Homo sapiens | Aphthous Stomatitis,Cervical Adenitis,Pharyngitis |
2cpm_a | O75391 | ENSG00000091640 | SPAG7 | 98.40 | 9.80E-11 | 1.10E-14 | 96.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YNL023C | FAP1 | SGDID:S000004968 | IGHMBP2 SMBP2 SMUBP2 |
DNA-binding protein SMUBP-2 (EC 3.6.4.12) (EC 3.6.4.13) (ATP-dependent helicase IGHMBP2) (Glial factor 1) (GF-1) (Immunoglobulin mu-binding protein 2) |
3.6.4.13 | Homo sapiens | Spinal Muscular Atrophy With Lower Extremity Predominance,Adult Respiratory Distress Syndrome,Myopathy,Progressive Multifocal Leukoencephalopathy,Neuromuscular Disease,Amyotrophic Lateral Sclerosis 1,Neuronopathy, Distal Hereditary Motor, Type Iib,Spinal Muscular Atrophy,Charcot-Marie-Tooth Disease Type 2a2a,Muscular Atrophy,Anterior Horn Cell Disease,Autosomal Recessive Distal Hereditary Motor Neuronopathy,Autosomal Dominant Distal Hereditary Motor Neuronopathy,Distal Hereditary Motor Neuronopathy Type 2,Motor Peripheral Neuropathy,Charcot-Marie-Tooth Hereditary Neuropathy,Diaphragmatic Eventration,Neuropathy,Charcot-Marie-Tooth Disease,Amyotrophic Lateral Sclerosis 4, Juvenile,Polyneuropathy,Neonatal Myasthenia Gravis,Autosomal Dominant Intermediate Charcot-Marie-Tooth,Tooth Disease,Respiratory Failure,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1,Scapuloperoneal Spinal Muscular Atrophy,Brown-Vialetto-Van Laere Syndrome,Spinal Muscular Atrophy, X-Linked 2,Neuropathy, Hereditary Sensory And Autonomic, Type Iia,Childhood Spinal Muscular Atrophy,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Ptosis,Spinal Muscular Atrophy, Type I,Spinal Muscular Atrophy, Type Iii,Spinal Muscular Atrophy, Type Ii,Charcot-Marie-Tooth Disease, Axonal, Type 2t,Neuronopathy, Distal Hereditary Motor, Type Va |
2lrr_a | P38935 | ENSG00000132740 | IGHMBP2 | 98.20 | 2.80E-10 | 2.90E-14 | 93.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YNL023C | FAP1 | SGDID:S000004968 | R3HDM2 KIAA1002 |
R3H domain-containing protein 2 |
Homo sapiens | 1whr_a | Q9Y2K5 | ENSG00000179912 | R3HDM2 | 99.00 | 6.70E-14 | 7.60E-18 | 119.90 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |