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AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

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YIL001W YIL001W / SGDID:S000001263
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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

Weizmann Institute of Science | Maya Schuldiner Lab