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 |
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YIL001W | YIL001W | SGDID:S000001263 | SPOP |
Speckle-type POZ protein (HIB homolog 1) (Roadkill homolog 1) |
Homo sapiens | Suppression Of Tumorigenicity 12,Microcephaly,Prostate Cancer,Nabais Sa-De Vries Syndrome, Type 1,Nabais Sa-De Vries Syndrome, Type 2 |
4j8z_a | O43791 | ENSG00000121067 | SPOP | 98.60 | 9.80E-12 | 8.40E-16 | 112.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL001W | YIL001W | SGDID:S000001263 | Cp190 E(mod)4-1 CG6384 |
Centrosome-associated zinc finger protein CP190 (Protein enhancer of mod(mdg4)4-1) (dMAP190) |
Drosophila melanogaster | 6er1_a | Q24478 | 97.80 | 1.10E-08 | 9.80E-13 | 84.30 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YIL001W | YIL001W | SGDID:S000001263 | KLHL3 KIAA1129 |
Kelch-like protein 3 |
Homo sapiens | Retinitis Pigmentosa,Bartter Disease,Renal Tubular Transport Disease,Pseudohypoaldosteronism,Familial Hypertension,Arthrogryposis, Distal, Type 3,Liddle Syndrome 1,Distal Arthrogryposis,Metabolic Acidosis,Pseudohypoaldosteronism, Type Iid,Pseudohypoaldosteronism, Type Iie,Pseudohypoaldosteronism, Type Iia,Hypertension, Essential,Cold-Induced Sweating Syndrome,Gitelman Syndrome |
4hxi_a | Q9UH77 | ENSG00000146021 | KLHL3 | 98.50 | 4.30E-11 | 3.60E-15 | 114.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL001W | YIL001W | SGDID:S000001263 | KEAP1 INRF2 KIAA0132 KLHL19 |
Kelch-like ECH-associated protein 1 (Cytosolic inhibitor of Nrf2) (INrf2) (Kelch-like protein 19) |
Homo sapiens | Retinitis Pigmentosa,Haemophilus Meningitis,Primary Biliary Cholangitis,Cataract,Paget'S Disease Of Bone,Breast Cancer,Colorectal Cancer,Papillary Adenocarcinoma,Hepatocellular Carcinoma,Gastric Cancer,Disease Of Mental Health,Lung Squamous Cell Carcinoma,Renal Cell Carcinoma, Papillary, 1,Parkinson Disease 17,Goiter, Multinodular 1, With Or Without Sertoli-Leydig Cell Tumors,Fumarase Deficiency,Lung Cancer |
5nlb_a | Q14145 | ENSG00000079999 | KEAP1 | 98.00 | 2.30E-09 | 2.00E-13 | 90.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL001W | YIL001W | SGDID:S000001263 | MYNN OSZF ZBTB31 SBBIZ1 |
Myoneurin (Zinc finger and BTB domain-containing protein 31) |
Homo sapiens | Cogan-Reese Syndrome |
2vpk_a | Q9NPC7 | ENSG00000085274 | MYNN | 97.80 | 1.20E-08 | 1.00E-12 | 81.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL001W | YIL001W | SGDID:S000001263 | KBTB1 VACWR180 A55R |
Kelch repeat and BTB domain-containing protein A55 |
Vaccinia virus | 6i2m_a | P24768 | 98.50 | 3.40E-11 | 2.80E-15 | 113.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YIL001W | YIL001W | SGDID:S000001263 | BTBD6 BDPL |
BTB/POZ domain-containing protein 6 (Lens BTB domain protein) |
Homo sapiens | Cerebellofaciodental Syndrome |
2vkp_b | Q96KE9 | ENSG00000184887 | BTBD6 | 97.80 | 9.80E-09 | 8.50E-13 | 80.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL001W | YIL001W | SGDID:S000001263 | ZBTB7A FBI1 LRF ZBTB7 ZNF857A |
Zinc finger and BTB domain-containing protein 7A (Factor binding IST protein 1) (FBI-1) (Factor that binds to inducer of short transcripts protein 1) (HIV-1 1st-binding protein 1) (Leukemia/lymphoma-related factor) (POZ and Krueppel erythroid myeloid ontogenic factor) (POK erythroid myeloid ontogenic factor) (Pokemon) (Pokemon 1) (TTF-I-interacting peptide 21) (TIP21) (Zinc finger protein 857A) |
Homo sapiens | Hemoglobinopathy |
2if5_a | O95365 | ENSG00000178951 | ZBTB7A | 98.00 | 2.70E-09 | 2.30E-13 | 86.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL001W | YIL001W | SGDID:S000001263 | SLX4 BTBD12 KIAA1784 KIAA1987 |
Structure-specific endonuclease subunit SLX4 (BTB/POZ domain-containing protein 12) |
Homo sapiens | Interstitial Nephritis, Karyomegalic,Maternal Uniparental Disomy,Maternal Uniparental Disomy Of Chromosome 16,Fanconi Anemia, Complementation Group V,Fanconi Anemia, Complementation Group R,Fanconi Anemia, Complementation Group U,Dyskeratosis Congenita,Fanconi Anemia, Complementation Group J,Fanconi Anemia, Complementation Group Q,Aplastic Anemia,Breast Cancer,Glioblastoma,Fanconi Anemia, Complementation Group O,Microcephaly,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Xeroderma Pigmentosum, Complementation Group F,Xeroderma Pigmentosum, Complementation Group G,Fanconi Anemia, Complementation Group N,Fanconi Anemia, Complementation Group P,Xfe Progeroid Syndrome,Fanconi Anemia, Complementation Group D1,Fanconi Anemia, Complementation Group T |
4uyi_a | Q8IY92 | ENSG00000188827 | SLX4 | 97.80 | 1.20E-08 | 9.80E-13 | 87.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL001W | YIL001W | SGDID:S000001263 | ZBTB16 PLZF ZNF145 |
Zinc finger and BTB domain-containing protein 16 (Promyelocytic leukemia zinc finger protein) (Zinc finger protein 145) (Zinc finger protein PLZF) |
Homo sapiens | Leukemia,Cryptorchidism, Unilateral Or Bilateral,Leukemia, Acute Myeloid,Precursor T-Cell Acute Lymphoblastic Leukemia,Microcephaly,Fanconi Anemia, Complementation Group A,Lymphoma, Non-Hodgkin, Familial,Acute Promyelocytic Leukemia,Skeletal Defects, Genital Hypoplasia, And Mental Retardation |
1buo_a | Q05516 | 98.90 | 1.30E-13 | 1.00E-17 | 116.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YIL001W | YIL001W | SGDID:S000001263 | IVNS1ABP ARA3 FLARA3 KIAA0850 KLHL39 NS1 NS1BP HSPC068 |
Influenza virus NS1A-binding protein (NS1-BP) (NS1-binding protein) (Aryl hydrocarbon receptor-associated protein 3) (Kelch-like protein 39) |
Homo sapiens | Viral Infectious Disease,Avian Influenza,Pseudobulbar Palsy,Influenza,Newcastle Disease,Japanese Encephalitis,Tick-Borne Encephalitis,Dengue Virus,Leber Hereditary Optic Neuropathy, Modifier Of,Immunodeficiency 70,Crustacean Allergy |
6n34_a | Q9Y6Y0 | ENSG00000116679 | IVNS1ABP | 97.80 | 9.80E-09 | 8.30E-13 | 86.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL001W | YIL001W | SGDID:S000001263 | Zbtb48 Hkr3 Tzap |
Telomere zinc finger-associated protein (TZAP) (Krueppel-related zinc finger protein 3 homolog) (Zinc finger and BTB domain-containing protein 48) |
Mus musculus | 2yy9_a | Q1H9T6 | 97.80 | 1.30E-08 | 1.10E-12 | 84.80 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YIL001W | YIL001W | SGDID:S000001263 | KLHL11 |
Kelch-like protein 11 |
Homo sapiens | Polyradiculopathy |
3i3n_a | Q9NVR0 | ENSG00000178502 | KLHL11 | 98.30 | 1.60E-10 | 1.40E-14 | 109.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL001W | YIL001W | SGDID:S000001263 | BCL6 BCL5 LAZ3 ZBTB27 ZNF51 |
B-cell lymphoma 6 protein (BCL-6) (B-cell lymphoma 5 protein) (BCL-5) (Protein LAZ-3) (Zinc finger and BTB domain-containing protein 27) (Zinc finger protein 51) |
Homo sapiens | Gastrointestinal Lymphoma,Lymphoblastic Lymphoma,Hypertrichosis,Acquired Immunodeficiency Syndrome,Cll/Sll,Human Herpesvirus 8,Primary Mediastinal B-Cell Lymphoma,Nodal Marginal Zone Lymphoma,Heart Lymphoma,Bladder Lymphoma,Spleen Cancer,Chest Wall Lymphoma,Bone Lymphoma,Lung Lymphoma,Tracheal Lymphoma,Primary Cutaneous B-Cell Lymphoma,Eye Lymphoma,Primary Cutaneous Cd4+ Small/Medium-Sized Pleomorphic T-Cell Lymphoma,Osteonecrosis Of The Jaw,B-Cell Non-Hodgkin Lymphoma,Mature B-Cell Neoplasm,B-Cell Lymphoma,Epiglottis Neoplasm,Ovarian Lymphoma,Plasmablastic Lymphoma,Testicular Lymphoma,Lymphatic System Disease,Primary Central Nervous System Lymphoma,Intraocular Lymphoma,Breast Osteosarcoma,Angioimmunoblastic T-Cell Lymphoma,Leukemia, Acute Myeloid,Primary Mediastinal Large B-Cell Lymphoma,Intravascular Large B-Cell Lymphoma,Follicular Lymphoma 1,Gallbladder Lymphoma,High Grade B-Cell Lymphoma With Myc And/ Or Bcl2 And/Or Bcl6 Rearrangement,Splenic Disease,Leber Plus Disease,Leukemia, Acute Lymphoblastic,Intestinal Disease,Reticulosarcoma,Sezary'S Disease,Hodgkin'S Lymphoma, Lymphocytic-Histiocytic Predominance,Prostate Lymphoma,Soft Palate Cancer,T-Cell/Histiocyte Rich Large B Cell Lymphoma,Burkitt Lymphoma,Gastric Lymphoma,Paranasal Sinus Lymphoma,Hodgkin'S Lymphoma, Nodular Sclerosis,Microphthalmia,Idiopathic Cd4-Positive T-Lymphocytopenia,Central Nervous System Hematologic Cancer,Composite Lymphoma,Gray Zone Lymphoma,Pediatric Lymphoma,Adult Lymphoma,Breast Lymphoma,Nasal Cavity Lymphoma,Spinal Cord Lymphoma,Central Nervous System Lymphoma,Nodal Marginal Zone B-Cell Lymphoma,Nodular Lymphocyte Predominant Hodgkin Lymphoma,Fanconi Anemia, Complementation Group A,Ureteral Lymphoma,Appendix Lymphoma,Microphthalmia, Syndromic 2,Colon Lymphoma,Orofaciodigital Syndrome Viii,Pleural Empyema,Lymphoma, Non-Hodgkin, Familial,Lymphoma, Hodgkin, Classic,Immunodeficiency With Hyper-Igm, Type 2,Immune Deficiency Disease,Lymphoma, Mucosa-Associated Lymphoid Type,Mature T-Cell And Nk-Cell Lymphoma,Diffuse Large B-Cell Lymphoma,Mantle Cell Lymphoma,Lymphoplasmacytic Lymphoma,Marginal Zone B-Cell Lymphoma,Peripheral T-Cell Lymphoma,Splenic Marginal Zone Lymphoma,Acute Promyelocytic Leukemia,Follicular Lymphoma,Wilms Tumor 1,Lymphoma,Lymphatic System Cancer,Alpha Chain Disease,Leukemia, Chronic Lymphocytic,Autosomal Dominant Non-Syndromic Intellectual Disability,Systemic Lupus Erythematosus,Myeloma, Multiple,Lymphoproliferative Syndrome,Lung Cancer,Progesterone Resistance |
5n1x_b | P41182 | ENSG00000113916 | BCL6 | 98.00 | 3.00E-09 | 2.50E-13 | 86.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL001W | YIL001W | SGDID:S000001263 | GAN GAN1 KLHL16 |
Gigaxonin (Kelch-like protein 16) |
Homo sapiens | Retinitis Pigmentosa,Neuromuscular Disease,Cohen Syndrome,Axonal Neuropathy,Giant Axonal Neuropathy 2,Hereditary Spastic Paraplegia,Inflammatory And Toxic Neuropathy,Giant Axonal Neuropathy,Ataxia-Oculomotor Apraxia 3,Neuropathy,Charcot-Marie-Tooth Disease,Peripheral Nervous System Disease,Tooth Disease,Alcoholic Neuropathy,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Charcot-Marie-Tooth Disease, Type 4b2,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Spinal Muscular Atrophy, X-Linked 2,Charcot-Marie-Tooth Disease, Axonal, Type 2p,Alexander Disease,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Cold-Induced Sweating Syndrome,Charcot-Marie-Tooth Disease, Axonal, Type 2cc,Charcot-Marie-Tooth Disease, Axonal, Type 2t,Giant Axonal Neuropathy 1, Autosomal Recessive |
2ppi_a | Q9H2C0 | ENSG00000261609 | GAN | 97.80 | 1.50E-08 | 1.20E-12 | 85.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL001W | YIL001W | SGDID:S000001263 | ZBTB48 HKR3 TZAP ZNF855 |
Telomere zinc finger-associated protein (TZAP) (Krueppel-related zinc finger protein 3) (hKR3) (Zinc finger and BTB domain-containing protein 48) (Zinc finger protein 855) |
Homo sapiens | Neuroblastoma |
3b84_a | P10074 | ENSG00000204859 | ZBTB48 | 97.80 | 1.00E-08 | 8.90E-13 | 82.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL001W | YIL001W | SGDID:S000001263 | KCTD17 |
BTB/POZ domain-containing protein KCTD17 |
Homo sapiens | Dystonia 11, Myoclonic,Dystonia,Vertebral Artery Occlusion,Dystonia 26, Myoclonic |
5a6r_a | Q8N5Z5 | ENSG00000100379 | KCTD17 | 98.80 | 8.90E-13 | 7.10E-17 | 113.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |