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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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 | 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 | 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 | 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 |
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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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) (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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 |