| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YBR103W | SIF2 | SGDID:S000000307 | TLE1 |
Transducin-like enhancer protein 1 (E(Sp1) homolog) (Enhancer of split groucho-like protein 1) (ESG1) |
Homo sapiens | Tibial Adamantinoma,Spindle Cell Sarcoma,Kidney Sarcoma,Adamantinoma Of Long Bones,Myxofibrosarcoma,Malignant Triton Tumor,Atypical Teratoid Rhabdoid Tumor,Core Binding Factor Acute Myeloid Leukemia,Kidney Clear Cell Sarcoma,Glomus Tumor,Cellular Congenital Mesoblastic Nephroma,Epithelioid Malignant Peripheral Nerve Sheath Tumor,Malignant Glandular Tumor Of Peripheral Nerve Sheath,Cellular Neurofibroma,Synovium Cancer,Subungual Glomus Tumor,Spindle Cell Synovial Sarcoma,Biphasic Synovial Sarcoma,Monophasic Synovial Sarcoma,Mediastinal Mesenchymal Tumor,Spindle Cell Liposarcoma,Synovium Neoplasm,Malignant Peripheral Nerve Sheath Tumor,West Syndrome,Hemangiopericytoma, Malignant,Rapp-Hodgkin Syndrome,Septooptic Dysplasia,Sarcoma, Synovial,Ewing Sarcoma,Chondrosarcoma, Extraskeletal Myxoid,Dermatofibrosarcoma Protuberans |
1gxr_a | Q04724 | 98.10 | 1.50E-09 | 1.10E-13 | 105.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YBR103W | SIF2 | SGDID:S000000307 | PLRG1 |
Pleiotropic regulator 1 |
Homo sapiens | Poikiloderma With Neutropenia,Cardiac Valvular Dysplasia, X-Linked |
4yvd_a | O43660 | ENSG00000171566 | PLRG1 | 98.00 | 2.50E-09 | 2.00E-13 | 103.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YBR103W | SIF2 | SGDID:S000000307 | RRP9 RNU3IP2 U355K |
U3 small nucleolar RNA-interacting protein 2 (RRP9 homolog) (U3 small nucleolar ribonucleoprotein-associated 55 kDa protein) (U3 snoRNP-associated 55 kDa protein) (U3-55K) |
Homo sapiens | 4j0w_a | O43818 | ENSG00000114767 | RRP9 | 98.00 | 2.40E-09 | 1.90E-13 | 101.30 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YBR103W | SIF2 | SGDID:S000000307 | TBL1X TBL1 |
F-box-like/WD repeat-containing protein TBL1X (SMAP55) (Transducin beta-like protein 1X) (Transducin-beta-like protein 1, X-linked) |
Homo sapiens | Parasitic Ectoparasitic Infectious Disease,Ovarian Endometrial Cancer,Microcephaly And Chorioretinopathy 1,Retinitis Pigmentosa,Speech Disorder,Multisystem Inflammatory Syndrome In Children,Amyotrophic Lateral Sclerosis 1,Ectodermal Dysplasia 5, Hair/Nail Type,Ectodermal Dysplasia 6, Hair/Nail Type,Ectodermal Dysplasia 7, Hair/Nail Type,Ectodermal Dysplasia 9, Hair/Nail Type,Malt Worker'S Lung,Epilepsy, Idiopathic Generalized 3,Ventriculomegaly With Cystic Kidney Disease,Sensorineural Hearing Loss,Fundus Dystrophy,Pituitary Adenoma 5, Multiple Types,Paramyotonia Congenita Of Von Eulenburg,Acute Gonococcal Prostatitis,Hypothyroidism,Cone-Rod Dystrophy 2,Disease Of Mental Health,Spermatogenic Failure 24,Jackson-Weiss Syndrome,Congenital Myasthenic Syndrome,Tinea Barbae,Hypotrichosis 1,Ocular Albinism,Hypothyroidism, Congenital, Nongoitrous, 8,Epilepsy, Idiopathic Generalized 2,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,Short-Rib Thoracic Dysplasia 14 With Polydactyly,Methylmalonic Aciduria, Cbla Type,Pelizaeus-Merzbacher Disease,Rett Syndrome,Syndromic X-Linked Intellectual Disability Snyder Type |
2xtc_b | O60907 | ENSG00000101849 | TBL1X | 99.30 | 5.30E-16 | 3.70E-20 | 119.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YBR103W | SIF2 | SGDID:S000000307 | RSA4 YCR072C YCR72C |
Ribosome assembly protein 4 (Notchless protein homolog 1) (Ribosome biogenesis factor RSA4) |
Saccharomyces cerevisiae | 4wjv_d | P25382 | 98.00 | 2.50E-09 | 2.00E-13 | 102.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YBR103W | SIF2 | SGDID:S000000307 | SIF2 EMB1 YBR103W YBR0832 |
SIR4-interacting protein SIF2 |
Saccharomyces cerevisiae | 1r5m_a | P38262 | 99.50 | 5.80E-19 | 4.50E-23 | 176.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YBR103W | SIF2 | SGDID:S000000307 | SMX2 SNP2 YFL017W-A YFL017Bw |
Small nuclear ribonucleoprotein G (snRNP-G) (Sm protein G) (Sm-G) (SmG) |
Saccharomyces cerevisiae | 6bk8_d | P40204 | 97.90 | 5.60E-09 | 4.40E-13 | 103.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YBR103W | SIF2 | SGDID:S000000307 | COP1 At2g32950 T21L14.11 |
E3 ubiquitin-protein ligase COP1 (EC 2.3.2.27) (Constitutive photomorphogenesis protein 1) (RING-type E3 ubiquitin transferase COP1) |
2.3.2.27 | Arabidopsis thaliana | 5igo_c | P43254 | 97.90 | 5.70E-09 | 4.50E-13 | 98.60 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
| YBR103W | SIF2 | SGDID:S000000307 | pkwA pkw1 |
Probable serine/threonine-protein kinase PkwA (EC 2.7.11.1) |
2.7.11.1 | Thermomonospora curvata | 5yzv_b | P49695 | 98.10 | 1.30E-09 | 1.10E-13 | 100.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YBR103W | SIF2 | SGDID:S000000307 | GNB1 |
Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 (Transducin beta chain 1) |
Bos taurus | 1tbg_c | P62871 | 98.10 | 1.00E-09 | 7.90E-14 | 103.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YBR103W | SIF2 | SGDID:S000000307 | SPBPJ4664.04 |
Putative coatomer subunit alpha (Alpha-coat protein) (Alpha-COP) |
Schizosaccharomyces pombe | 4j87_a | Q96WV5 | 98.10 | 1.20E-09 | 9.80E-14 | 101.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YBR103W | SIF2 | SGDID:S000000307 | TBL1XR1 IRA1 TBLR1 |
F-box-like/WD repeat-containing protein TBL1XR1 (Nuclear receptor corepressor/HDAC3 complex subunit TBLR1) (TBL1-related protein 1) (Transducin beta-like 1X-related protein 1) |
Homo sapiens | Learning Disability,Fitzsimmons Syndrome,Noonan Syndrome 1,Pierpont Syndrome,Central Nervous System Hematologic Cancer,Lipomatosis,West Syndrome,Disease Of Mental Health,Acute Promyelocytic Leukemia,Mental Retardation, Autosomal Dominant 41,Rett Syndrome,Autism |
4lg9_a | Q9BZK7 | ENSG00000177565 | TBL1XR1 | 98.10 | 1.40E-09 | 1.10E-13 | 105.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |