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

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YIR033W MGA2 / SGDID:S000001472
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
YIR033W MGA2 SGDID:S000001472
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 95.80 4.70E-05 6.60E-09 67.90 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
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 95.60 8.00E-05 1.20E-08 64.20 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
ACAP2 CENTB2 KIAA0041
Arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2 (Centaurin-beta-2) (Cnt-b2)
Homo sapiens
Tethered Spinal Cord Syndrome
6if3_a Q15057 ENSG00000114331 ACAP2 96.00 3.10E-05 4.20E-09 66.30 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
Nfkbib Ikbb
NF-kappa-B inhibitor beta (NF-kappa-BIB) (I-kappa-B-beta) (IkB-B) (IkB-beta) (IkappaBbeta)
Mus musculus
1k3z_d Q60778 96.70 2.40E-06 3.50E-10 74.40 0 0 1 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
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 96.20 1.60E-05 2.40E-09 71.10 0 0 1 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
Plxna4 Kiaa1550
Plexin-A4
Mus musculus
5l5k_a Q80UG2 95.80 6.20E-05 7.10E-09 87.40 0 0 1 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
EF_0377
EF_0377
Enterococcus faecalis
3hra_a Q838Q8 95.60 8.40E-05 1.30E-08 59.90 0 0 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
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 96.10 2.20E-05 3.30E-09 66.30 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
PPP1R13L IASPP NKIP1 PPP1R13BL RAI
RelA-associated inhibitor (Inhibitor of ASPP protein) (Protein iASPP) (NFkB-interacting protein 1) (PPP1R13B-like protein)
Homo sapiens
Basal Cell Carcinoma,Dilated Cardiomyopathy,Noonan Syndrome With Multiple Lentigines
2vge_a Q8WUF5 ENSG00000104881 PPP1R13L 95.50 0.00011 1.50E-08 63.60 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
ASB11
Ankyrin repeat and SOCS box protein 11 (ASB-11)
Homo sapiens
Lacrimal Duct Obstruction
4uuc_a Q8WXH4 ENSG00000165192 ASB11 95.70 6.40E-05 9.80E-09 61.90 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
ILK ILK1 ILK2
Integrin-linked protein kinase (EC 2.7.11.1) (59 kDa serine/threonine-protein kinase) (Beta-integrin-linked kinase) (ILK-1) (ILK-2) (p59ILK)
2.7.11.1 Homo sapiens
Polycystic Kidney Disease,Thyroid Gland Anaplastic Carcinoma,Hypertrophic Cardiomyopathy,Dilated Cardiomyopathy,Hypermobile Ehlers-Danlos Syndrome,Focal Segmental Glomerulosclerosis,Brain Cancer,Ovarian Cancer,Colorectal Cancer,Prostate Cancer,Hyperphosphatemia,Exudative Vitreoretinopathy,Renal Fibrosis,Lung Cancer,Pancreatic Cancer
4hi8_a Q13418 ENSG00000166333 ILK 95.50 0.0001 1.50E-08 59.10 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
TV1425 TVG1472127
Putative ankyrin repeat protein TV1425
Thermoplasma volcanium
2rfm_b Q978J0 96.00 2.70E-05 4.00E-09 64.20 0 0 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
Exoc2 Sec5 Sec5l1
Exocyst complex component 2 (Exocyst complex component Sec5)
Mus musculus
1hk6_a Q9D4H1 96.50 6.30E-06 7.80E-10 66.50 0 0 1 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
TNKS2 PARP5B TANK2 TNKL
Poly [ADP-ribose] polymerase tankyrase-2 (EC 2.4.2.30) (ADP-ribosyltransferase diphtheria toxin-like 6) (ARTD6) (Poly [ADP-ribose] polymerase 5B) (Protein poly-ADP-ribosyltransferase tankyrase-2) (EC 2.4.2.-) (TNKS-2) (TRF1-interacting ankyrin-related ADP-ribose polymerase 2) (Tankyrase II) (Tankyrase-2) (TANK2) (Tankyrase-like protein) (Tankyrase-related protein)
2.4.2.30 Homo sapiens
Familial Isolated Hypoparathyroidism,Arthrogryposis, Renal Dysfunction, And Cholestasis 2,Cherubism,Arthrogryposis, Renal Dysfunction, And Cholestasis 1
4z68_a Q9H2K2 ENSG00000107854 TNKS2 96.10 2.40E-05 3.50E-09 62.00 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
EBF3 COE3
Transcription factor COE3 (Early B-cell factor 3) (EBF-3) (Olf-1/EBF-like 2) (O/E-2) (OE-2)
Homo sapiens
Renal Tubular Dysgenesis,Moebius Syndrome,Cohen Syndrome,Constipation,Neurogenic Bladder,Anus Benign Neoplasm,Urinary Tract Infection,Hereditary Melanoma,Hypotonia, Ataxia, And Delayed Development Syndrome,Griscelli Syndrome, Type 3,Familial Vesicoureteral Reflux,Renal Dysplasia,Isolated Pierre Robin Sequence,Hypotonia,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Urinary Tract Infections, Recurrent,Acid-Labile Subunit Deficiency,Urofacial Syndrome 1,Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant,Renal Hypodysplasia/Aplasia 1,Vesicoureteral Reflux 1,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Ataxia And Polyneuropathy, Adult-Onset,Pierre Robin Syndrome
3muj_b Q9H4W6 ENSG00000108001 EBF3 99.20 1.80E-15 2.00E-19 138.30 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
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
6by9_a Q9H9B1 ENSG00000181090 EHMT1 95.70 6.20E-05 8.90E-09 68.30 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
ANKRA2 ANKRA
Ankyrin repeat family A protein 2 (RFXANK-like protein 2)
Homo sapiens
Donnai-Barrow Syndrome,Three M Syndrome 1,Branchiooculofacial Syndrome
3so8_a Q9H9E1 ENSG00000164331 ANKRA2 96.50 6.80E-06 1.00E-09 66.40 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
AKR2A AFT AKR2 At4g35450 F15J1.20
Ankyrin repeat domain-containing protein 2A (AtAKR2)
Arabidopsis thaliana
4tum_c Q9SAR5 95.50 9.40E-05 1.50E-08 55.20 0 0 0 0 0 0 1 0
YIR033W MGA2 SGDID:S000001472
CAMTA1 KIAA0833 MSTP023
Calmodulin-binding transcription activator 1
Homo sapiens
Cerebellar Ataxia, Nonprogressive, With Mental Retardation,Vascular Cancer,Malignant Hemangioma,Malignant Epithelioid Hemangioendothelioma,Dystonia 11, Myoclonic,Telangiectatic Osteogenic Sarcoma,Conventional Angiosarcoma,Proliferative Fasciitis,Histiocytoid Hemangioma,Neuroblastoma,Epithelioid Hemangioendothelioma,Hemangioendothelioma,Mediastinal Mesenchymal Tumor,Hepatocellular Carcinoma,Oligodendroglioma,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Brain Malformations With Or Without Urinary Tract Defects,Angiosarcoma,Chromosome 1p36 Deletion Syndrome
2cxk_a Q9Y6Y1 ENSG00000171735 CAMTA1 96.30 1.40E-05 1.70E-09 63.20 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
CDKN2C CDKN6
Cyclin-dependent kinase 4 inhibitor C (Cyclin-dependent kinase 6 inhibitor) (p18-INK4c) (p18-INK6)
Homo sapiens
Plasma Cell Neoplasm,Retinal Cancer,Parathyroid Adenoma,Leukemia, Acute Lymphoblastic,Ovarian Cancer,Breast Cancer,Multiple Endocrine Neoplasia,Oligodendroglioma,Pheochromocytoma,Retinoblastoma,Chromophobe Adenoma,Multiple Endocrine Neoplasia, Type Iv,Lymphoma, Non-Hodgkin, Familial,Multiple Endocrine Neoplasia, Type I,Meningioma, Familial,Lymphoma,Myeloma, Multiple,Medulloblastoma,Melanoma, Cutaneous Malignant 1,Lung Cancer
1ihb_b P42773 95.80 4.50E-05 6.90E-09 59.50 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
ABAYE2397
ABAYE2397
Acinetobacter baumannii
5d66_a B0VB33 96.50 6.20E-06 9.30E-10 67.70 0 0 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
Lebu_0176
Lebu_0176
Leptotrichia buccalis
3t8k_a C7NDE2 95.70 7.10E-05 1.00E-08 61.40 0 0 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
Kank1
Kank1
Mus musculus
5yay_a E9Q238 95.50 0.0001 1.50E-08 65.10 0 0 1 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
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 95.80 4.30E-05 6.50E-09 60.70 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
Exoc2 Sec5 Sec5l1
Exocyst complex component 2 (Exocyst complex component Sec5) (rSec5)
Rattus norvegicus
1uad_d O54921 96.50 7.80E-06 9.40E-10 67.10 0 0 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
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 96.10 2.20E-05 3.20E-09 65.90 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
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
5gp7_a O95271 ENSG00000173273 TNKS 95.90 4.40E-05 6.30E-09 62.30 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
MET
Hepatocyte growth factor receptor (HGF receptor) (EC 2.7.10.1) (HGF/SF receptor) (Proto-oncogene c-Met) (Scatter factor receptor) (SF receptor) (Tyrosine-protein kinase Met)
2.7.10.1 Homo sapiens
Pancreatic Adenocarcinoma,Mesothelioma, Malignant,Skin Melanoma,Familial Renal Papillary Carcinoma,Spinal Chordoma,Follicular Adenoma,Thyroid Gland Cancer,Peritoneal Mesothelioma,Lung Cancer Susceptibility 3,Occipital Lobe Neoplasm,Mucositis,Acral Lentiginous Melanoma,Chondrosarcoma,Chordoma,Chronic Erosive Gastritis,Melanoma,Gastroesophageal Adenocarcinoma,Thyroid Gland Anaplastic Carcinoma,Dedifferentiated Liposarcoma,Myxofibrosarcoma,Tongue Carcinoma,Hereditary Renal Cell Carcinoma,Clear Cell Renal Cell Carcinoma,Hepatoblastoma,Bile Duct Cancer,Tall Cell Variant Papillary Carcinoma,Doxorubicin Induced Cardiomyopathy,Differentiated Thyroid Carcinoma,Malignant Pleural Mesothelioma,Refractive Error,Ependymoblastoma,Neuroblastoma,Inherited Cancer-Predisposing Syndrome,Arthrogryposis, Distal, Type 1a,Glioma,Kidney Cancer,Lung Disease,Ovarian Clear Cell Adenocarcinoma,Hypopharynx Cancer,Ovarian Cancer,Adenocarcinoma,Breast Ductal Carcinoma,Breast Carcinoma In Situ,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,High Grade Glioma,Colorectal Cancer,Papillary Carcinoma,Hepatocellular Carcinoma,Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb,Malignant Peripheral Nerve Sheath Tumor,Rhabdomyosarcoma,Biliary Tract Cancer,Gastric Cancer,Prostate Cancer,Papillary Thyroid Microcarcinoma,Cholangiocarcinoma,Microvascular Complications Of Diabetes 1,Lung Benign Neoplasm,Large Cell Medulloblastoma,Thyroid Gland Follicular Carcinoma,Autism 9,Renal Cell Carcinoma, Papillary, 1,Sarcoma, Synovial,Familial Mediterranean Fever, Autosomal Dominant,Barrett Esophagus,Distal Arthrogryposis,Alveolar Soft Part Sarcoma,Tumor Predisposition Syndrome,Vitreoretinopathy, Neovascular Inflammatory,Von Hippel-Lindau Syndrome,Salivary Gland Carcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Renal Cell Carcinoma, Nonpapillary,Autism Spectrum Disorder,Osteofibrous Dysplasia,Deafness, Autosomal Recessive 97,Inguinal Hernia,Medulloblastoma,Autism,Melanoma, Uveal,Pediatric Hepatocellular Carcinoma,Lung Cancer,Helicobacter Pylori Infection,Pancreatic Cancer
5lsp_a P08581 ENSG00000105976 MET 95.60 0.00011 1.30E-08 69.60 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
spa
Immunoglobulin G-binding protein A (IgG-binding protein A) (Staphylococcal protein A) (SpA)
Staphylococcus aureus
5cbn_a P38507 96.30 1.20E-05 1.60E-09 67.90 0 0 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
CDKN2D
Cyclin-dependent kinase 4 inhibitor D (p19-INK4d)
Homo sapiens
Non-Invasive Bladder Urothelial Carcinoma,T-Cell Lymphoblastic Leukemia/Lymphoma,Retinal Cancer,Parathyroid Adenoma,Adult Central Nervous System Primitive Neuroectodermal Neoplasm,Melanoma, Cutaneous Malignant 1
1bd8_a P55273 96.80 1.70E-06 2.00E-10 76.50 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
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 95.60 7.00E-05 1.10E-08 61.50 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
NAS6 YGR232W G8564
Probable 26S proteasome regulatory subunit p28 (Proteasome non-ATPase subunit 6)
Saccharomyces cerevisiae
2dzn_e P50086 95.90 3.50E-05 5.40E-09 63.30 0 0 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
MTPN
Myotrophin (Protein V-1)
Homo sapiens
Dilated Cardiomyopathy,Muscle Hypertrophy
3aaa_c P58546 ENSG00000105887 MTPN 95.60 7.70E-05 1.20E-08 54.50 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
Mtpn Gcdp
Myotrophin (Granule cell differentiation protein) (Protein V-1)
Mus musculus
2kxp_c P62774 95.60 6.90E-05 1.10E-08 53.90 0 0 1 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
Plxna1 Kiaa4053
Plexin-A1 (Plex 1) (Plexin-1)
Mus musculus
5l56_a P70206 96.00 3.80E-05 4.50E-09 88.90 0 0 1 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
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
4rly_a Q01484 ENSG00000145362 ANK2 96.00 2.50E-05 3.80E-09 68.90 1 1 0 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
Notch1 Motch
Neurogenic locus notch homolog protein 1 (Notch 1) (Motch A) (mT14) (p300) [Cleaved into: Notch 1 extracellular truncation (NEXT); Notch 1 intracellular domain (NICD)]
Mus musculus
1ymp_a Q01705 95.90 3.40E-05 5.20E-09 58.60 0 0 1 0 0 0 0 0
YIR033W MGA2 SGDID:S000001472
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 96.30 1.10E-05 1.70E-09 68.90 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab