| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YGL090W | LIF1 | SGDID:S000003058 | LIF1 YGL090W |
Ligase-interacting factor 1 |
Saccharomyces cerevisiae | 1z56_a | P53150 | 100.00 | 2.10E-50 | 1.90E-54 | 385.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YGL090W | LIF1 | SGDID:S000003058 | XRCC4 |
DNA repair protein XRCC4 (X-ray repair cross-complementing protein 4) |
Homo sapiens | Lymphopenia,Severe Combined Immunodeficiency,Microcephalic Primordial Dwarfism-Insulin Resistance Syndrome,Spinocerebellar Ataxia Type 1 With Axonal Neuropathy,Congenital Nervous System Abnormality,Combined Immunodeficiency,Oculomotor Apraxia,Myoma,Cockayne Syndrome,Dubowitz Syndrome,Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation,Microcephaly,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Omenn Syndrome,Multinodular Goiter,Seckel Syndrome,Lig4 Syndrome,Pigmentary Disorder, Reticulate, With Systemic Manifestations, X-Linked,Short Stature, Microcephaly, And Endocrine Dysfunction,Isolated Growth Hormone Deficiency,Primary Microcephaly,Isolated Growth Hormone Deficiency, Type Ia |
1fu1_b | Q13426 | ENSG00000152422 | XRCC4 | 99.80 | 1.40E-26 | 1.40E-30 | 211.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YGL090W | LIF1 | SGDID:S000003058 | XRCC4 |
DNA double-strand break repair and V(D)J recombination protein XRCC4 |
pfam Family | PF06632 | 99.80 | 9.80E-26 | 8.60E-30 | 222.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |