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

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YGR233C PHO81 / SGDID:S000003465
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
YGR233C PHO81 SGDID:S000003465
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
1wdy_a Q05823 ENSG00000135828 RNASEL 99.40 6.80E-18 9.00E-22 161.20 1 1 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
LMJF_29_1100
LMJF_29_1100
Leishmania major
3ljn_a E9ADW8 99.30 7.30E-17 9.30E-21 162.70 0 0 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
ASB11
Ankyrin repeat and SOCS box protein 11 (ASB-11)
Homo sapiens
Lacrimal Duct Obstruction
4uuc_a Q8WXH4 ENSG00000165192 ASB11 99.10 6.00E-15 7.90E-19 135.80 1 1 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
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 99.00 2.60E-14 3.30E-18 143.70 1 1 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
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 99.00 2.90E-14 3.40E-18 164.90 0 0 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
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 99.20 4.80E-16 6.20E-20 154.60 0 0 1 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
lin-12 R107.8
Protein lin-12 (Abnormal cell lineage protein 12) (Notch-like protein lin-12)
Caenorhabditis elegans
2fo1_e P14585 99.20 2.70E-15 3.40E-19 152.00 0 0 0 0 0 1 0 0
YGR233C PHO81 SGDID:S000003465
Nfkbib Ikbb
NF-kappa-B inhibitor beta (NF-kappa-BIB) (I-kappa-B-beta) (IkB-B) (IkB-beta) (IkappaBbeta)
Mus musculus
1k3z_d Q60778 99.00 2.30E-14 3.00E-18 137.80 0 0 1 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
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 98.90 1.30E-13 1.70E-17 128.40 1 1 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
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 99.10 1.40E-14 1.70E-18 146.90 0 0 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
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 1.30E-13 1.60E-17 132.00 1 1 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
CTHT_0005190
CTHT_0005190
Chaetomium thermophilum
5ijj_b G0RY29 98.80 5.80E-13 5.80E-17 133.30 0 0 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
Espn
Espin (Ectoplasmic specialization protein)
Mus musculus
5et1_b Q9ET47 99.30 2.10E-16 2.70E-20 159.10 0 0 1 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
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 3.90E-15 4.80E-19 166.70 1 1 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
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 99.20 3.10E-15 3.50E-19 189.40 0 0 0 0 1 0 0 0
YGR233C PHO81 SGDID:S000003465
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 99.20 9.00E-16 1.20E-19 144.30 1 1 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
NAS6 YGR232W G8564
Probable 26S proteasome regulatory subunit p28 (Proteasome non-ATPase subunit 6)
Saccharomyces cerevisiae
1wg0_a P50086 99.00 6.60E-14 8.40E-18 131.50 0 0 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
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
1ikn_d P25963 99.10 5.60E-15 6.20E-19 147.70 1 1 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
K1L
K1L
Vaccinia virus
3kea_b Q6IV60 98.90 2.00E-13 2.50E-17 132.60 0 0 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
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 99.20 5.70E-16 7.20E-20 161.70 1 1 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
XPR1 SYG1 XR
Xenotropic and polytropic retrovirus receptor 1 (Protein SYG1 homolog) (Xenotropic and polytropic murine leukemia virus receptor X3) (X-receptor)
Homo sapiens
Basal Ganglia Disease,Leukemia,Dystonia,Fanconi Syndrome,Basal Ganglia Calcification, Idiopathic, 6,Basal Ganglia Calcification,Basal Ganglia Calcification, Idiopathic, 1
5ijh_b Q9UBH6 ENSG00000143324 XPR1 99.20 1.50E-15 1.60E-19 153.00 1 1 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
legA1 lpg2416
legA1 lpg2416
Legionella pneumophila
2aja_b Q5ZSV0 99.00 6.80E-14 8.20E-18 145.30 0 0 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
MACROH2A1 H2AFY
Core histone macro-H2A.1 (Histone macroH2A1) (mH2A1) (Histone H2A.y) (H2A/y) (Medulloblastoma antigen MU-MB-50.205)
Homo sapiens
Breast Cancer,Fanconi Anemia, Complementation Group A,Liebenberg Syndrome,Medulloblastoma
5iit_a O75367 ENSG00000113648 MACROH2A1 98.80 3.70E-13 4.00E-17 145.10 1 1 0 0 0 0 0 0
YGR233C PHO81 SGDID:S000003465
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 99.00 3.60E-14 4.70E-18 132.40 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab