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

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YML002W YML002W / SGDID:S000004461
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
YML002W YML002W SGDID:S000004461
ASB9
Ankyrin repeat and SOCS box protein 9 (ASB-9)
Homo sapiens
Uterine Corpus Endometrial Carcinoma
3d9h_a Q96DX5 ENSG00000102048 ASB9 99.30 1.50E-16 1.60E-20 155.70 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
legA12 lpg0483
legA12 lpg0483
Legionella pneumophila
5vrq_a Q5ZY89 98.60 1.30E-11 1.30E-15 129.00 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
Nfkbib Ikbb
NF-kappa-B inhibitor beta (NF-kappa-BIB) (I-kappa-B-beta) (IkB-B) (IkB-beta) (IkappaBbeta)
Mus musculus
1k3z_d Q60778 99.60 1.80E-19 2.00E-23 172.20 0 0 1 0 0 0 0 0
YML002W YML002W SGDID:S000004461
KANK2 ANKRD25 KIAA1518 MXRA3 SIP
KN motif and ankyrin repeat domain-containing protein 2 (Ankyrin repeat domain-containing protein 25) (Matrix-remodeling-associated protein 3) (SRC-1-interacting protein) (SIP) (SRC-interacting protein) (SRC1-interacting protein)
Homo sapiens
Nephrotic Syndrome,Pseudoainhum,Familial Woolly Hair Syndrome,Succinic Semialdehyde Dehydrogenase Deficiency,Focal Segmental Glomerulosclerosis,Ectodermal Dysplasia 4, Hair/Nail Type,Striate Palmoplantar Keratoderma,Nephrotic Syndrome, Type 16,Palmoplantar Keratoderma And Woolly Hair,Woolly Hair, Autosomal Dominant,Gamma-Amino Butyric Acid Metabolism Disorder,Multiple Pterygium Syndrome, Escobar Variant
4hbd_a Q63ZY3 ENSG00000197256 KANK2 98.90 2.20E-13 2.30E-17 131.30 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
KLLA0_C04147g
KLLA0_C04147g
Kluyveromyces lactis
5h2a_a Q6CUK7 99.20 1.80E-15 2.00E-19 145.90 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
K1L
K1L
Vaccinia virus
3kea_b Q6IV60 98.90 1.10E-13 1.30E-17 132.20 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
Bd3460
Bd3460
Bdellovibrio bacteriovorus
5cec_b Q6MHS9 99.10 1.70E-14 1.90E-18 134.00 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
Tnks Tnks1
Poly [ADP-ribose] polymerase tankyrase-1 (EC 2.4.2.30) (ADP-ribosyltransferase diphtheria toxin-like 5) (ARTD5) (Protein poly-ADP-ribosyltransferase tankyrase-1) (EC 2.4.2.-) (TRF1-interacting ankyrin-related ADP-ribose polymerase 1) (Tankyrase I) (Tankyrase-1) (TANK1)
2.4.2.30 Mus musculus
6cf6_a Q6PFX9 99.50 3.40E-18 3.70E-22 168.20 0 0 1 0 0 0 0 0
YML002W YML002W SGDID:S000004461
EF_0377
EF_0377
Enterococcus faecalis
3hra_a Q838Q8 99.20 2.90E-15 3.30E-19 133.60 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
ZDHHC17 HIP14 HIP3 HYPH KIAA0946 HSPC294
Palmitoyltransferase ZDHHC17 (EC 2.3.1.225) (Acyltransferase ZDHHC17) (EC 2.3.1.-) (DHHC domain-containing cysteine-rich protein 17) (DHHC17) (Huntingtin yeast partner H) (Huntingtin-interacting protein 14) (HIP-14) (Huntingtin-interacting protein 3) (HIP-3) (Huntingtin-interacting protein H) (Putative MAPK-activating protein PM11) (Putative NF-kappa-B-activating protein 205) (Zinc finger DHHC domain-containing protein 17)
2.3.1.225 Homo sapiens
Huntington Disease,Hypoparathyroidism, X-Linked
3eu9_a Q8IUH5 ENSG00000186908 ZDHHC17 99.50 9.70E-19 1.10E-22 162.80 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
ASB11
Ankyrin repeat and SOCS box protein 11 (ASB-11)
Homo sapiens
Lacrimal Duct Obstruction
4uuc_a Q8WXH4 ENSG00000165192 ASB11 99.40 1.30E-17 1.40E-21 152.20 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
Trpv6
Transient receptor potential cation channel subfamily V member 6 (TrpV6) (Calcium transport protein 1) (CaT1) (Epithelial calcium channel 2) (ECaC2)
Mus musculus
2rfa_a Q91WD2 99.10 5.10E-15 5.70E-19 136.20 0 0 1 0 0 0 0 0
YML002W YML002W SGDID:S000004461
legA1 lpg2416
legA1 lpg2416
Legionella pneumophila
2aja_b Q5ZSV0 98.70 1.60E-12 1.70E-16 132.20 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
ANKRD27 PP12899
Ankyrin repeat domain-containing protein 27 (VPS9 domain-containing protein)
Homo sapiens
Parastremmatic Dwarfism,Hermansky-Pudlak Syndrome,Pontiac Fever
4b93_b Q96NW4 ENSG00000105186 ANKRD27 99.20 1.30E-15 1.40E-19 147.50 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
TV1425 TVG1472127
Putative ankyrin repeat protein TV1425
Thermoplasma volcanium
2rfm_b Q978J0 98.90 9.00E-14 9.90E-18 124.90 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
Espn
Espin (Ectoplasmic specialization protein)
Mus musculus
5et1_b Q9ET47 99.30 3.30E-16 3.70E-20 155.20 0 0 1 0 0 0 0 0
YML002W YML002W SGDID:S000004461
TRPV6 ECAC2
Transient receptor potential cation channel subfamily V member 6 (TrpV6) (CaT-like) (CaT-L) (Calcium transport protein 1) (CaT1) (Epithelial calcium channel 2) (ECaC2)
Homo sapiens
Metatropic Dysplasia,Pseudohypoaldosteronism,Hypervitaminosis D,Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques,Pendred Syndrome,Hyperparathyroidism,Bone Mineral Density Quantitative Trait Locus 15,Aromatase Deficiency,Prostate Cancer,Hyperparathyroidism, Transient Neonatal,Scapuloperoneal Spinal Muscular Atrophy,Hyperparathyroidism, Neonatal Severe,Spondyloepiphyseal Dysplasia, Maroteaux Type,Spondylometaphyseal Dysplasia, Kozlowski Type,Brachyolmia,Autosomal Recessive Disease,Estrogen-Receptor Negative Breast Cancer,Mucolipidosis Iv
6e2f_c Q9H1D0 ENSG00000165125 TRPV6 98.90 1.50E-13 1.40E-17 157.90 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
EHMT1 EUHMTASE1 GLP KIAA1876 KMT1D
Histone-lysine N-methyltransferase EHMT1 (EC 2.1.1.-) (Euchromatic histone-lysine N-methyltransferase 1) (Eu-HMTase1) (G9a-like protein 1) (GLP) (GLP1) (Histone H3-K9 methyltransferase 5) (H3-K9-HMTase 5) (Lysine N-methyltransferase 1D)
2.1.1.- Homo sapiens
Kleefstra Syndrome,Deafness, Autosomal Dominant 47,Hypoplastic Left Heart Syndrome,Polymicrogyria,Kleefstra Syndrome Due To A Point Mutation,Pontocerebellar Hypoplasia, Type 2a,Weaver Syndrome,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Kleefstra Syndrome 1,Chromosome 16p13.3 Deletion Syndrome, Proximal,Pitt-Hopkins Syndrome,Schizophrenia,Ogden Syndrome,Autism Spectrum Disorder,Kabuki Syndrome 1,Autosomal Dominant Non-Syndromic Intellectual Disability,Chromosomal Deletion Syndrome,Autism,Christianson Syndrome
3b7b_a Q9H9B1 ENSG00000181090 EHMT1 99.40 1.10E-17 1.30E-21 154.60 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
ANKRA2 ANKRA
Ankyrin repeat family A protein 2 (RFXANK-like protein 2)
Homo sapiens
Donnai-Barrow Syndrome,Three M Syndrome 1,Branchiooculofacial Syndrome
3v31_a Q9H9E1 ENSG00000164331 ANKRA2 98.70 1.40E-12 1.60E-16 114.10 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
Shank3 Prosap2
SH3 and multiple ankyrin repeat domains protein 3 (Shank3) (Proline-rich synapse-associated protein 2) (ProSAP2) (SPANK-2)
Rattus norvegicus
5g4x_a Q9JLU4 99.30 1.30E-16 1.40E-20 159.60 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
RABGEF1 RABEX5
Rab5 GDP/GTP exchange factor (RAP1) (Rabaptin-5-associated exchange factor for Rab5) (Rabex-5)
Homo sapiens
Dyggve-Melchior-Clausen Disease,Smith-Mccort Dysplasia 1
4q9u_a Q9UJ41 ENSG00000154710 RABGEF1 98.60 7.90E-12 7.00E-16 130.70 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
Trpv5 Ecac1
Transient receptor potential cation channel subfamily V member 5 (TrpV5) (Epithelial calcium channel 1) (ECaC1) (Osm-9-like TRP channel 3) (OTRPC3)
Oryctolagus cuniculus
6o1u_d Q9XSM3 98.70 2.80E-12 2.70E-16 146.30 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
TRPC6 TRP6
Short transient receptor potential channel 6 (TrpC6) (Transient receptor protein 6) (TRP-6)
Homo sapiens
Nephrotic Syndrome,T Cell And Nk Cell Immunodeficiency,Progressive Familial Heart Block,End Stage Renal Disease,Hypertrophic Pyloric Stenosis,Pyloric Stenosis,Genetic Steroid-Resistant Nephrotic Syndrome,Glutamate-Cysteine Ligase Deficiency,Familial Episodic Pain Syndrome,Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques,Familial Nephrotic Syndrome,Focal Segmental Glomerulosclerosis,Kidney Disease,Malignant Hypertension,Lipoid Nephrosis,Alport Syndrome,Focal Segmental Glomerulosclerosis 1,Pulmonary Hypertension,Focal Segmental Glomerulosclerosis 2,Hypothalamic Neoplasm,Diencephalic Neoplasm,Frasier Syndrome,Denys-Drash Syndrome,Hypertension, Essential,Membranous Nephropathy,Mucolipidosis Iv
5yx9_b Q9Y210 ENSG00000137672 TRPC6 98.90 3.30E-13 3.20E-17 158.60 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
TRPV2 VRL
Transient receptor potential cation channel subfamily V member 2 (TrpV2) (Osm-9-like TRP channel 2) (OTRPC2) (Vanilloid receptor-like protein 1) (VRL-1)
Homo sapiens
Dentin Sensitivity,Inflammatory Bowel Disease 28,Familial Episodic Pain Syndrome,Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques,Dilated Cardiomyopathy,Facial Dermatosis,Scapuloperoneal Spinal Muscular Atrophy,Brachyolmia
2f37_b Q9Y5S1 ENSG00000187688 TRPV2 98.90 1.80E-13 2.00E-17 125.60 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
lin-12 R107.8
Protein lin-12 (Abnormal cell lineage protein 12) (Notch-like protein lin-12)
Caenorhabditis elegans
2fo1_e P14585 99.20 6.20E-16 6.80E-20 154.40 0 0 0 0 0 1 0 0
YML002W YML002W SGDID:S000004461
85/88 kDa calcium-independent phospholipase A2 (CaI-PLA2) (EC 3.1.1.4) (2-lysophosphatidylcholine acylhydrolase) (EC 3.1.1.5) (Group VI phospholipase A2) (GVI PLA2) (Intracellular membrane-associated calcium-independent phospholipase A2 beta) (iPLA2-beta) (PLA2G6) (Palmitoyl-CoA hydrolase) (EC 3.1.2.2) (Patatin-like phospholipase domain-containing protein 9) (PNPLA9)
Cricetulus griseus
6aun_a A0A384E119 99.10 3.90E-15 4.00E-19 168.60 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
ABAYE2397
ABAYE2397
Acinetobacter baumannii
5d66_a B0VB33 99.30 8.50E-17 9.50E-21 144.80 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
nompC CG17468 CT30855 Dmel\CG11020 DmNompC jf24 l(2)25Dc l(2)jf24 nomp NOMPC NompC ORE-13 TRPN TRPN1 CG11020 Dmel_CG11020
nompC CG17468 CT30855 Dmel\CG11020 DmNompC jf24 l(2)25Dc l(2)jf24 nomp NOMPC NompC ORE-13 TRPN TRPN1 CG11020 Dmel_CG11020
Drosophila melanogaster
5vkq_d E0A9E1 99.00 2.90E-14 3.00E-18 176.30 0 0 0 0 1 0 0 0
YML002W YML002W SGDID:S000004461
LMJF_29_1100
LMJF_29_1100
Leishmania major
3ljn_a E9ADW8 99.30 3.70E-16 4.10E-20 155.10 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
Kank1
Kank1
Mus musculus
5yay_a E9Q238 98.80 3.80E-13 4.00E-17 128.80 0 0 1 0 0 0 0 0
YML002W YML002W SGDID:S000004461
ASPG
ASPG
3.5.1.1 Cavia porcellus
5dnc_b H0W0T5 98.60 1.10E-11 1.00E-15 139.50 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
RFXANK ANKRA1 RFXB
DNA-binding protein RFXANK (Ankyrin repeat family A protein 1) (Regulatory factor X subunit B) (RFX-B) (Regulatory factor X-associated ankyrin-containing protein)
Homo sapiens
Severe Combined Immunodeficiency,Tibial Neuropathy,Tarsal Tunnel Syndrome,Combined Immunodeficiency,Discharging Ear,Purine Nucleoside Phosphorylase Deficiency,Alcoholic Gastritis,Acquired Thrombocytopenia,Omenn Syndrome,Retinitis Pigmentosa 48,Bare Lymphocyte Syndrome, Type I,Immune Deficiency Disease,Bare Lymphocyte Syndrome, Type Ii,Tumoral Calcinosis, Hyperphosphatemic, Familial, 1,Bjornstad Syndrome
3uxg_a O14593 ENSG00000064490 RFXANK 98.60 8.20E-12 9.20E-16 108.30 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
PSMD10
26S proteasome non-ATPase regulatory subunit 10 (26S proteasome regulatory subunit p28) (Gankyrin) (p28(GANK))
Homo sapiens
Dedifferentiated Liposarcoma,Hepatocellular Carcinoma,Retinoblastoma
5vhi_g O75832 ENSG00000101843 PSMD10 99.30 5.90E-17 6.60E-21 149.40 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
TNKS PARP5A PARPL TIN1 TINF1 TNKS1
Poly [ADP-ribose] polymerase tankyrase-1 (EC 2.4.2.30) (ADP-ribosyltransferase diphtheria toxin-like 5) (ARTD5) (Poly [ADP-ribose] polymerase 5A) (Protein poly-ADP-ribosyltransferase tankyrase-1) (EC 2.4.2.-) (TNKS-1) (TRF1-interacting ankyrin-related ADP-ribose polymerase) (Tankyrase I) (Tankyrase-1) (TANK1)
2.4.2.30 Homo sapiens
Cornelia De Lange Syndrome,Lung Acinar Adenocarcinoma,Amyotrophic Lateral Sclerosis 1,Arthrogryposis, Renal Dysfunction, And Cholestasis 2,Cherubism,Meningioma, Familial,Arthrogryposis, Renal Dysfunction, And Cholestasis 1
5jhq_d O95271 ENSG00000173273 TNKS 99.10 9.60E-15 1.10E-18 150.10 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
ALDOA
Fructose-bisphosphate aldolase A (EC 4.1.2.13) (Muscle-type aldolase)
4.1.2.13 Oryctolagus cuniculus
6mwq_d P00883 99.00 4.20E-14 3.80E-18 156.30 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
SWI6 YLR182W L9470.8
Regulatory protein SWI6 (Cell-cycle box factor subunit SWI6) (MBF subunit P90) (Trans-acting activator of HO endonuclease gene)
Saccharomyces cerevisiae
1sw6_b P09959 98.90 1.90E-13 2.00E-17 136.30 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
Ankyrin-1
Homo sapiens
Migraine With Or Without Aura 1,Hereditary Elliptocytosis,Glutamate-Cysteine Ligase Deficiency,Familial Episodic Pain Syndrome,8p11.2 Deletion Syndrome,Hereditary Spherocytosis,Ehrlichiosis,Facial Dermatosis,Hemolytic Anemia,Congenital Hemolytic Anemia,Developmental And Epileptic Encephalopathy 5,Myopathy, Distal, 3,Disease Of Mental Health,Kallmann Syndrome,Malaria,Spherocytosis, Type 1,Brugada Syndrome,Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema,Spinocerebellar Ataxia 5
1n11_a P16157 99.60 4.60E-20 4.80E-24 193.60 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
NFKBIA IKBA MAD3 NFKBI
NF-kappa-B inhibitor alpha (I-kappa-B-alpha) (IkB-alpha) (IkappaBalpha) (Major histocompatibility complex enhancer-binding protein MAD3)
Homo sapiens
Vascular Disease,Stomach Carcinoma In Situ,Bone Cancer,Leukemia, Chronic Myeloid,Diabetes Mellitus,Hepatitis B,Mycobacterium Malmoense,Ectodermal Dysplasia,B-Cell Lymphoma,Osteomyelitis, Sterile Multifocal, With Periostitis And Pustulosis,T-Cell Lymphoblastic Leukemia/Lymphoma,Carbuncle,Shigellosis,Periostitis,Hypohidrotic Ectodermal Dysplasia With Immunodeficiency,Newcastle Disease,Legionellosis,Ovarian Cancer,Burkitt Lymphoma,T-Cell Acute Lymphoblastic Leukemia,Crohn'S Disease,Squamous Cell Carcinoma, Head And Neck,Malignant Astrocytoma,Gliosarcoma,Giant Cell Glioblastoma,Parkinson Disease, Late-Onset,Colorectal Cancer,Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive,Hepatocellular Carcinoma,Human Immunodeficiency Virus Type 1,Tropical Spastic Paraparesis,Chromosome 14q11-Q22 Deletion Syndrome,Cardiomyopathy, Dilated, 1gg,Breast Adenocarcinoma,Cone-Rod Dystrophy 2,Prostate Cancer,Disease Of Mental Health,Rheumatoid Arthritis,Adult T-Cell Leukemia,Inflammatory Bowel Disease,Immune Deficiency Disease,Myelodysplastic Syndrome,Intellectual Developmental Disorder, X-Linked 108,Ectodermal Dysplasia And Immunodeficiency 2,Mantle Cell Lymphoma,Nasopharyngeal Carcinoma,Psoriatic Arthritis,Leukemia, Chronic Lymphocytic,Systemic Lupus Erythematosus,Myeloma, Multiple,Lung Cancer,Helicobacter Pylori Infection,Asthma,Pancreatic Cancer
1nfi_e P25963 ENSG00000100906 NFKBIA 99.10 8.40E-15 9.50E-19 131.70 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
SWH1 OSH1 YAR042W YAR044W
Oxysterol-binding protein homolog 1
Saccharomyces cerevisiae
5h28_a P35845 99.00 6.50E-14 7.10E-18 132.00 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
NOTCH1 TAN1
Neurogenic locus notch homolog protein 1 (Notch 1) (hN1) (Translocation-associated notch protein TAN-1) [Cleaved into: Notch 1 extracellular truncation (NEXT); Notch 1 intracellular domain (NICD)]
Homo sapiens
Ventricular Septal Defect,Heart Septal Defect,Heart Disease,Richter'S Syndrome,Squamous Cell Carcinoma,Severe Combined Immunodeficiency,Lymphoblastic Lymphoma,Retinitis Pigmentosa,Myeloid And Lymphoid Neoplasms Associated With Fgfr1 Abnormalities,Ossifying Fibroma,Adenoid Cystic Carcinoma,Double Outlet Right Ventricle,Hajdu-Cheney Syndrome,Bone Cancer,Atrial Heart Septal Defect,Invasive Bladder Transitional Cell Carcinoma,Prion Disease,Connective Tissue Disease,Uterine Adnexa Cancer,Kleefstra Syndrome,Tongue Carcinoma,Orofacial Cleft 4,Clear Cell Renal Cell Carcinoma,Aortic Dissection,Alzheimer Disease,Rasopathy,Nodular Regenerative Hyperplasia,Mucoepidermoid Carcinoma,T-Cell Non-Hodgkin Lymphoma,Holoprosencephaly,Plasmablastic Lymphoma,T-Cell Lymphoblastic Leukemia/Lymphoma,Biliary Tract Disease,Infratentorial Cancer,Familial Thoracic Aortic Aneurysm And Aortic Dissection,Leukemia,Colon Adenocarcinoma,Neuroblastoma,Hypoplastic Left Heart Syndrome,Lacrimal Gland Adenoid Cystic Carcinoma,Shone Complex,Acute Leukemia,Intrahepatic Cholangiocarcinoma,Leukemia, Acute Myeloid,Bone Marrow Cancer,Basal Cell Carcinoma,Hematologic Cancer,Hemangioma,Leukemia, Acute Lymphoblastic,Combined Immunodeficiency,Basal Cell Nevus Syndrome,Aortic Disease,Aortic Valve Disease 1,Focal Segmental Glomerulosclerosis,Brain Cancer,Precursor T-Cell Acute Lymphoblastic Leukemia,Lung Adenoma,Oropharynx Cancer,Aplastic Anemia,Ovarian Cancer,T-Cell Acute Lymphoblastic Leukemia,Breast Cancer,Tonsil Cancer,Exudative Vitreoretinopathy 5,Microphthalmia,Malignant Astrocytoma,Adult Liposarcoma,Breast Liposarcoma,Anaplastic Astrocytoma,Colorectal Cancer,Peripheral Nervous System Disease,Hepatocellular Carcinoma,Splenic Diffuse Red Pulp Small B-Cell Lymphoma,Pheochromocytoma,Aneurysm,Hydrocephalus,Tongue Disease,Cerebral Degeneration,Spondylocostal Dysostosis 3, Autosomal Recessive,Alagille Syndrome 1,Skin Carcinoma,Hemophagocytic Lymphohistiocytosis, Familial, 2,Gastric Cancer,Friedreich Ataxia,Prostate Cancer,Disease Of Mental Health,Cervical Cancer,Aortic Aneurysm,Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, Type 1,Orofacial Cleft 8,Scalp-Ear-Nipple Syndrome,Lung Squamous Cell Carcinoma,Adenoiditis,Merkel Cell Carcinoma,Lymphoma, Non-Hodgkin, Familial,Mouth Disease,Adams-Oliver Syndrome 5,Loeys-Dietz Syndrome,Hypoplastic Left Heart Syndrome 1,Tetralogy Of Fallot,Myelodysplastic Syndrome,Mantle Cell Lymphoma,Peripheral T-Cell Lymphoma,Heart, Malformation Of,Tongue Squamous Cell Carcinoma,Acute Promyelocytic Leukemia,Bone Squamous Cell Carcinoma,Aortic Aneurysm, Familial Thoracic 1,Endosteal Hyperostosis, Autosomal Dominant,Wilms Tumor 1,Mental Retardation, Autosomal Dominant 40,Lipoprotein Quantitative Trait Locus,Cardiovascular Organ Benign Neoplasm,Brain Glioma,Patent Ductus Arteriosus 1,Adams-Oliver Syndrome,Wilson-Turner X-Linked Mental Retardation Syndrome,Dowling-Degos Disease,Leukemia, Chronic Lymphocytic,Marfan Syndrome,Left Ventricular Noncompaction,Myeloma, Multiple,Medulloblastoma,Lung Cancer,Oliver Syndrome,Pancreatic Cancer
2f8y_a P46531 ENSG00000148400 NOTCH1 99.20 1.80E-15 2.10E-19 137.20 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
NAS6 YGR232W G8564
Probable 26S proteasome regulatory subunit p28 (Proteasome non-ATPase subunit 6)
Saccharomyces cerevisiae
1wg0_a P50086 99.50 4.00E-19 4.50E-23 165.80 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
NFKB2 LYT10
Nuclear factor NF-kappa-B p100 subunit (DNA-binding factor KBF2) (H2TF1) (Lymphocyte translocation chromosome 10 protein) (Nuclear factor of kappa light polypeptide gene enhancer in B-cells 2) (Oncogene Lyt-10) (Lyt10) [Cleaved into: Nuclear factor NF-kappa-B p52 subunit]
Homo sapiens
Immunodeficiency 10,B Cell Deficiency,Ectodermal Dysplasia,B-Cell Non-Hodgkin Lymphoma,B-Cell Lymphoma,Common Variable Immunodeficiency,Asbestos-Related Lung Carcinoma,Combined Immunodeficiency,Legionellosis,Osteopetrosis,Neuroaspergillosis,Immunodeficiency, Common Variable, 10,Splenic Marginal Zone Lymphoma,Lymphoma,Acth Deficiency, Isolated,Incontinentia Pigmenti,Immunodeficiency, Common Variable, 1
4ot9_a Q00653 ENSG00000077150 NFKB2 99.20 5.10E-16 5.60E-20 154.20 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
ANK2 ANKB
Ankyrin-2 (ANK-2) (Ankyrin-B) (Brain ankyrin) (Non-erythroid ankyrin)
Homo sapiens
Timothy Syndrome,Heart Disease,Hypertrophic Cardiomyopathy,Familial Long Qt Syndrome,Legionnaire Disease,Long Qt Syndrome 12,Dilated Cardiomyopathy,Jervell And Lange-Nielsen Syndrome 1,Hereditary Spherocytosis,Long Qt Syndrome,Heart Conduction Disease,Progressive Familial Heart Block, Type Ia,Sick Sinus Syndrome,Andersen Cardiodysrhythmic Periodic Paralysis,Cardiac Arrhythmia,Developmental And Epileptic Encephalopathy 5,Long Qt Syndrome 13,Disease Of Mental Health,Long Qt Syndrome 3,Long Qt Syndrome 2,Long Qt Syndrome 6,Long Qt Syndrome 5,Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Long Qt Syndrome 9,Long Qt Syndrome 10,Long Qt Syndrome 11,Coffin-Siris Syndrome 1,Brugada Syndrome 3,Familial Atrial Fibrillation,Sinoatrial Node Disease,Long Qt Syndrome 1,Intrinsic Cardiomyopathy,Autism Spectrum Disorder,Atrial Fibrillation,Cardiac Arrest,Autism,Catecholaminergic Polymorphic Ventricular Tachycardia,Spinocerebellar Ataxia 5,Cardiac Arrhythmia, Ankyrin-B-Related
5y4d_a Q01484 ENSG00000145362 ANK2 99.10 4.00E-15 4.30E-19 163.90 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
AVO2 YMR068W YM9916.07
Target of rapamycin complex 2 subunit AVO2 (TORC2 subunit AVO2) (Adheres voraciously to TOR2 protein 2)
Saccharomyces cerevisiae
6emk_h Q04749 98.60 7.40E-12 6.70E-16 135.50 0 0 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
RNASEL RNS4
2-5A-dependent ribonuclease (2-5A-dependent RNase) (EC 3.1.26.-) (Ribonuclease 4) (Ribonuclease L) (RNase L)
3.1.26.- Homo sapiens
Viral Infectious Disease,Myalgic Encephalomyelitis/Chronic Fatigue Syndrome,Rasopathy,Dengue Disease,Prostate Cancer, Hereditary, 1,West Nile Encephalitis,West Nile Fever,Noonan Syndrome 1,Chronic Fatigue Syndrome,Herpes Simplex,West Nile Virus Infection,Vaccinia,Prostate Cancer,Lynch Syndrome,La Crosse Encephalitis,Noonan Syndrome 2,Paralytic Poliomyelitis,Aicardi-Goutieres Syndrome,Immune Deficiency Disease,Microphthalmia With Limb Anomalies
4oau_c Q05823 ENSG00000135828 RNASEL 98.80 4.70E-13 4.80E-17 149.90 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
KANK1 ANKRD15 KANK KIAA0172
KN motif and ankyrin repeat domain-containing protein 1 (Ankyrin repeat domain-containing protein 15) (Kidney ankyrin repeat-containing protein)
Homo sapiens
Metanephric Adenoma,Chromosome 9p Deletion Syndrome,Nephrotic Syndrome,Cerebral Palsy,Inherited Congenital Spastic Tetraplegia,Cerebral Palsy, Spastic Quadriplegic, 2,Myeloproliferative Neoplasm,Quadriplegia,Renal Adenoma,Tukel Syndrome,Spastic Quadriplegia,Spastic Cerebral Palsy,Brain Glioma,Autosomal Dominant Non-Syndromic Intellectual Disability
5ybu_a Q14678 ENSG00000107104 KANK1 98.90 1.50E-13 1.60E-17 129.40 1 1 0 0 0 0 0 0
YML002W YML002W SGDID:S000004461
AKT1 At2g26650 F18A8.2
Potassium channel AKT1
Arabidopsis thaliana
5aar_a Q38998 98.70 2.00E-12 2.30E-16 112.60 0 0 0 0 0 0 1 0

Weizmann Institute of Science | Maya Schuldiner Lab