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

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YER075C PTP3 / SGDID:S000000877
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
YER075C PTP3 SGDID:S000000877
PTPN9
Tyrosine-protein phosphatase non-receptor type 9 (EC 3.1.3.48) (Protein-tyrosine phosphatase MEG2) (PTPase MEG2)
3.1.3.48 Homo sapiens
Breast Cancer
4ge6_a P43378 ENSG00000169410 PTPN9 100.00 2.00E-37 1.90E-41 334.70 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPN22 PTPN8
Tyrosine-protein phosphatase non-receptor type 22 (EC 3.1.3.48) (Hematopoietic cell protein-tyrosine phosphatase 70Z-PEP) (Lymphoid phosphatase) (LyP) (PEST-domain phosphatase) (PEP)
3.1.3.48 Homo sapiens
Psoriasis,Lymphopenia,Myopathy,Palindromic Rheumatism,Achalasia,Diabetes Mellitus,Multifocal Motor Neuropathy,Chronic Mucocutaneous Candidiasis,Autoimmune Polyendocrine Syndrome, Type Ii,Thyroiditis,Type 1 Diabetes Mellitus 12,Latent Autoimmune Diabetes In Adults,Primary Biliary Cholangitis,Pediatric Systemic Lupus Erythematosus,Vogt-Koyanagi-Harada Disease,Graves' Disease,Alopecia Areata,Granulomatosis With Polyangiitis,Autoimmune Disease,Behcet Syndrome,Arthritis,Central Nervous System Vasculitis,Type 1 Diabetes Mellitus,Aplastic Anemia,Scleritis,Adrenal Cortical Hypofunction,Crohn'S Disease,Lupus Erythematosus,Anca-Associated Vasculitis,Pernicious Anemia,Oligoarticular Juvenile Idiopathic Arthritis,Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis,Brucellosis,Bone Inflammation Disease,Turner Syndrome,Thrombocytopenia,Rheumatoid Arthritis,Type 1 Diabetes Mellitus 2,Multiple Sclerosis,Adrenal Cortex Disease,Type 1 Diabetes Mellitus 18,Hypoadrenocorticism, Familial,Immunodeficiency 31c,Inflammatory Bowel Disease,Temporal Arteritis,Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1,Hashimoto Thyroiditis,Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6,Autoimmune Disease Of Endocrine System,Autoimmune Disease Of Musculoskeletal System,Autoimmune Disease Of Skin And Connective Tissue,Psoriatic Arthritis,Systemic Lupus Erythematosus,Penicillin Allergy,Type 1 Diabetes Mellitus 3,Type 1 Diabetes Mellitus 5,Celiac Disease 1,Type 1 Diabetes Mellitus 8
2p6x_a Q9Y2R2 ENSG00000134242 PTPN22 100.00 6.20E-36 5.90E-40 322.60 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPRQ
Phosphatidylinositol phosphatase PTPRQ (EC 3.1.3.-) (Receptor-type tyrosine-protein phosphatase Q) (PTP-RQ) (R-PTP-Q) (EC 3.1.3.48)
3.1.3.48 Homo sapiens
Usher Syndrome, Type Id,Malignant Inflammatory Fibrous Histiocytoma,Retinitis Pigmentosa,Deafness, Autosomal Recessive 39,Deafness, Autosomal Recessive 12,Mesangial Proliferative Glomerulonephritis,Usher Syndrome Type 2,Deafness, Autosomal Dominant 50,Sensorineural Hearing Loss,Usher Syndrome, Type I,Deafness, Autosomal Recessive 84a,Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna,Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb,Deafness, Autosomal Dominant 73,Branchiootic Syndrome 1,Deafness, Autosomal Recessive 23,Deafness, Autosomal Recessive 42,Deafness, Autosomal Recessive 16,Deafness, Autosomal Recessive 66,Normal Pressure Hydrocephalus,Deafness, Autosomal Dominant 1, With Or Without Thrombocytopenia,Deafness, Autosomal Recessive 61,Usher Syndrome,Autosomal Dominant Nonsyndromic Deafness,Deafness, Autosomal Dominant 22,Vertical Talus, Congenital,Deafness, Autosomal Recessive 22,Deafness, Autosomal Recessive,Deafness, Autosomal Recessive 37,Dyschromatosis Universalis Hereditaria,Paine Syndrome
4ikc_a Q9UMZ3 100.00 5.50E-36 5.30E-40 316.30 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPN18 BDP1
Tyrosine-protein phosphatase non-receptor type 18 (EC 3.1.3.48) (Brain-derived phosphatase)
3.1.3.48 Homo sapiens
2oc3_a Q99952 ENSG00000072135 PTPN18 100.00 2.00E-37 1.90E-41 333.20 0 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
Protein-tyrosine-phosphatase (EC 3.1.3.48)
Protein-tyrosine-phosphatase (EC 3.1.3.48)
3.1.3.48 Rattus norvegicus
3i36_a Q62884 100.00 1.90E-37 1.80E-41 339.70 0 0 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
Tc00.1047053510187.234
Tc00.1047053510187.234
Trypanosoma cruzi
4az1_a Q4E4C8 99.90 1.30E-32 1.20E-36 294.80 0 0 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
Tb10.70.0070
Tb10.70.0070
3.1.3.48 Trypanosoma brucei
3m4u_a Q38AT7 99.90 5.50E-32 5.30E-36 290.00 0 0 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPRN ICA3 ICA512
Receptor-type tyrosine-protein phosphatase-like N (R-PTP-N) (Islet cell antigen 512) (ICA 512) (Islet cell autoantigen 3) (PTP IA-2) [Cleaved into: ICA512-N-terminal fragment (ICA512-NTF); ICA512-transmembrane fragment (ICA512-TMF); ICA512-cleaved cytosolic fragment (ICA512-CCF)]
Homo sapiens
Anal Spasm,Cervix Uteri Carcinoma In Situ,Uterus Carcinoma In Situ,Gestational Diabetes,Diabetes Mellitus,Lymphocele,Cervical Large Cell Neuroendocrine Carcinoma,Type 1 Diabetes Mellitus 13,Isthmus Cancer,Cervical Incompetence,Type 1 Diabetes Mellitus 12,Cervix Disease,Hemometra,Pancreatic Colloid Cystadenoma,Parametritis,Autoimmune Disease,Microinvasive Cervical Squamous Cell Carcinoma,Benign Struma Ovarii,Type 1 Diabetes Mellitus,Brachydactyly, Type C,Cervix Carcinoma,Adrenal Cortical Hypofunction,Wissler-Fanconi Syndrome,Fallopian Tube Endometrioid Adenocarcinoma,Pernicious Anemia,Neuronal Ceroid Lipofuscinosis,Type 1 Diabetes Mellitus 2,Type 2 Diabetes Mellitus,Vaginal Discharge,Insulinoma,Pancreatic Cystadenoma,Gastrointestinal System Benign Neoplasm,Bleeding Disorder, Platelet-Type, 17,Maturity-Onset Diabetes Of The Young,Diabetes Mellitus, Ketosis-Prone,Autoimmune Disease Of Endocrine System,Type 1 Diabetes Mellitus 7,Celiac Disease 1
2i1y_b Q16849 ENSG00000054356 PTPRN 100.00 1.20E-37 1.10E-41 334.60 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPRO GLEPP1 PTPU2
Receptor-type tyrosine-protein phosphatase O (R-PTP-O) (EC 3.1.3.48) (Glomerular epithelial protein 1) (Protein tyrosine phosphatase U2) (PTP-U2) (PTPase U2)
3.1.3.48 Homo sapiens
Nephrotic Syndrome,Galloway-Mowat Syndrome,Genetic Steroid-Resistant Nephrotic Syndrome,Familial Nephrotic Syndrome,Focal Segmental Glomerulosclerosis,Crescentic Glomerulonephritis,Alport Syndrome,Focal Segmental Glomerulosclerosis 1,Nephrotic Syndrome, Type 6,Wilms Tumor 1
2gjt_a Q16827 ENSG00000151490 PTPRO 99.90 9.80E-34 9.40E-38 301.80 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPN14 PEZ PTPD2
Tyrosine-protein phosphatase non-receptor type 14 (EC 3.1.3.48) (Protein-tyrosine phosphatase pez)
3.1.3.48 Homo sapiens
Metatypical Basal Cell Carcinoma,Choanal Atresia And Lymphedema,Wilson-Turner X-Linked Mental Retardation Syndrome
2bzl_a Q15678 ENSG00000152104 PTPN14 100.00 2.80E-37 2.60E-41 336.30 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPRR ECPTP PTPRQ
Receptor-type tyrosine-protein phosphatase R (R-PTP-R) (EC 3.1.3.48) (Ch-1PTPase) (NC-PTPCOM1) (Protein-tyrosine phosphatase PCPTP1)
3.1.3.48 Homo sapiens
Usher Syndrome, Type Id,Myopia,Refractive Error,Usher Syndrome Type 2,Deafness, Autosomal Recessive 84a,Deafness, Autosomal Dominant 1, With Or Without Thrombocytopenia,Usher Syndrome,Autosomal Dominant Nonsyndromic Deafness,Dyschromatosis Universalis Hereditaria
2a8b_a Q15256 ENSG00000153233 PTPRR 99.90 1.00E-33 9.90E-38 300.20 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPRJ DEP1
Receptor-type tyrosine-protein phosphatase eta (Protein-tyrosine phosphatase eta) (R-PTP-eta) (EC 3.1.3.48) (Density-enhanced phosphatase 1) (DEP-1) (HPTP eta) (Protein-tyrosine phosphatase receptor type J) (R-PTP-J) (CD antigen CD148)
3.1.3.48 Homo sapiens
Interstitial Keratitis,Angiocentric Glioma,Pendred Syndrome,Griscelli Syndrome, Type 3,Colorectal Cancer,Methotrexate-Associated Lymphoproliferation,Thrombocytopenia,Lynch Syndrome,Cd45 Deficiency,Cogan Syndrome,Griscelli Syndrome,Niemann-Pick Disease, Type C1
2nz6_a Q12913 ENSG00000149177 PTPRJ 100.00 3.60E-38 3.40E-42 341.70 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPN11 PTP2C SHPTP2
Tyrosine-protein phosphatase non-receptor type 11 (EC 3.1.3.48) (Protein-tyrosine phosphatase 1D) (PTP-1D) (Protein-tyrosine phosphatase 2C) (PTP-2C) (SH-PTP2) (SHP-2) (Shp2) (SH-PTP3)
3.1.3.48 Homo sapiens
Tricuspid Valve Insufficiency,Metachondromatosis,Heart Septal Defect,Heart Disease,Learning Disability,Endometrial Cancer,Pfeiffer Syndrome,Childhood Acute Lymphocytic Leukemia,Lung Cancer Susceptibility 3,Chronic Myelomonocytic Leukemia,Pulmonary Valve Stenosis,Atrial Heart Septal Defect,Leukemia, Chronic Myeloid,Plasma Cell Neoplasm,Juvenile Xanthogranuloma,Neurofibromatosis-Noonan Syndrome,B-Lymphoblastic Leukemia/Lymphoma,Hypertrophic Cardiomyopathy,Rasopathy,Noonan Syndrome-Like Disorder With Loose Anagen Hair,Keratosis Pilaris Atrophicans Faciei,Specific Learning Disability,Costello Syndrome,Hemorrhagic Disease,Essential Thrombocythemia,Myeloproliferative Neoplasm,Neutropenia,Pulmonary Interstitial Glycogenosis,Neurofibromatosis, Type I,Aggressive Systemic Mastocytosis,Villonodular Synovitis,Leukemia,Neuroblastoma,Pilocytic Astrocytoma,Gliofibroma,Cryptorchidism, Unilateral Or Bilateral,Skin Granular Cell Tumor,Childhood Leukemia,Pseudo-Turner Syndrome,Inherited Cancer-Predisposing Syndrome,Testicular Spermatocytic Seminoma,Leukemia, Acute Myeloid,Noonan Syndrome 1,Bone Marrow Cancer,Myelodysplastic/Myeloproliferative Neoplasm,Hematologic Cancer,Leukemia, Acute Lymphoblastic,Noonan Syndrome And Noonan-Related Syndrome,Autoimmune Disease,Dilated Cardiomyopathy,Sensorineural Hearing Loss,Pigmented Villonodular Synovitis,Brain Cancer,Acute Megakaryoblastic Leukemia In Down Syndrome,Enchondromatosis, Multiple, Ollier Type,Noonan Syndrome-Like Disorder With Loose Anagen Hair 2,Myeloid Leukemia,Neurofibromatosis,Breast Cancer,Protein-Losing Enteropathy,Patent Foramen Ovale,Mature Cataract,Colorectal Cancer,Cystic Lymphangioma,Pulmonary Valve Disease,Hepatocellular Carcinoma,Pectus Excavatum,Cardiofaciocutaneous Syndrome 1,Microcephaly,Embryonal Rhabdomyosarcoma,Rhabdomyosarcoma,Noonan Syndrome With Multiple Lentigines,Noonan Syndrome-Like Disorder With Or Without Juvenile Myelomonocytic Leukemia,Cherubism,Noonan Syndrome 3,Gastric Cancer,Cone-Rod Dystrophy 2,Systemic Mastocytosis,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Thrombocytopenia,Gastric Adenocarcinoma,Lung Squamous Cell Carcinoma,Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy,Arrhythmogenic Right Ventricular Cardiomyopathy,Legius Syndrome,Hypertelorism, Microtia, Facial Clefting Syndrome,Odontochondrodysplasia,Leopard Syndrome 2,Severe Congenital Neutropenia,Tetralogy Of Fallot,Myelodysplastic Syndrome,Tumor Predisposition Syndrome,Down Syndrome,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Meningioma, Familial,Autism Spectrum Disorder,Lymphoma,Patent Ductus Arteriosus 1,Lymphoproliferative Syndrome, X-Linked, 1,Body Dysmorphic Disorder,Scoliosis,Lentigines,Noonan Syndrome-Like Disorder With Loose Anagen Hair 1,Ptosis,Leopard Syndrome 1,Leukemia, Chronic Lymphocytic,Juvenile Myelomonocytic Leukemia,Atrial Septal Defect 2,Myeloma, Multiple,Lymphoproliferative Syndrome,Neuroblastoma 1,Lung Cancer,Helicobacter Pylori Infection,Polycythemia Vera
3b7o_a Q06124 ENSG00000179295 PTPN11 100.00 1.80E-37 1.70E-41 335.40 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPN12
Tyrosine-protein phosphatase non-receptor type 12 (EC 3.1.3.48) (PTP-PEST) (Protein-tyrosine phosphatase G1) (PTPG1)
3.1.3.48 Homo sapiens
Leiomyomatosis,Charcot-Marie-Tooth Disease,Colorectal Cancer,Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, And Acne,Lynch Syndrome,Myopathy, Centronuclear, 2
5hde_a Q05209 ENSG00000127947 PTPN12 100.00 6.20E-38 5.90E-42 338.10 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
sptP STM2878
Secreted effector protein SptP [Includes: GTPase-activating protein (GAP); Tyrosine-protein phosphatase (EC 3.1.3.48)]
3.1.3.48 Salmonella typhimurium
1g4u_s P74873 100.00 3.60E-35 3.30E-39 327.90 0 0 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPN5
Tyrosine-protein phosphatase non-receptor type 5 (EC 3.1.3.48) (Neural-specific protein-tyrosine phosphatase) (Striatum-enriched protein-tyrosine phosphatase) (STEP)
3.1.3.48 Homo sapiens
Kagami-Ogata Syndrome,Viral Gastritis,Phencyclidine Abuse,Disease Of Mental Health,Fragile X Syndrome
2bv5_a P54829 ENSG00000110786 PTPN5 99.90 1.40E-33 1.30E-37 298.70 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPRT KIAA0283
Receptor-type tyrosine-protein phosphatase T (R-PTP-T) (EC 3.1.3.48) (Receptor-type tyrosine-protein phosphatase rho) (RPTP-rho)
3.1.3.48 Homo sapiens
Colorectal Cancer,Schizophrenia,Autism Spectrum Disorder,Autism
2ooq_a O14522 ENSG00000196090 PTPRT 100.00 1.10E-35 1.00E-39 314.40 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
Ptp10D CG1817
Tyrosine-protein phosphatase 10D (EC 3.1.3.48) (Receptor-linked protein-tyrosine phosphatase 10D) (DPTP10D)
3.1.3.48 Drosophila melanogaster
3s3e_a P35992 100.00 1.80E-36 1.70E-40 326.60 0 0 0 0 1 0 0 0
YER075C PTP3 SGDID:S000000877
PTPN7
Tyrosine-protein phosphatase non-receptor type 7 (EC 3.1.3.48) (Hematopoietic protein-tyrosine phosphatase) (HEPTP) (Protein-tyrosine phosphatase LC-PTP)
3.1.3.48 Homo sapiens
Rasopathy
1zc0_a P35236 ENSG00000143851 PTPN7 100.00 1.50E-36 1.40E-40 329.40 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPN6 HCP PTP1C
Tyrosine-protein phosphatase non-receptor type 6 (EC 3.1.3.48) (Hematopoietic cell protein-tyrosine phosphatase) (Protein-tyrosine phosphatase 1C) (PTP-1C) (Protein-tyrosine phosphatase SHP-1) (SH-PTP1)
3.1.3.48 Homo sapiens
Neutrophilic Dermatosis, Acute Febrile,Leishmaniasis,Myeloproliferative Neoplasm,Leukemia, Acute Lymphoblastic,Polycythemia,Subcorneal Pustular Dermatosis,Breast Adenocarcinoma,Severe Congenital Neutropenia,Acute Promyelocytic Leukemia,Cd45 Deficiency,Polycythemia Vera
2b3o_a P29350 ENSG00000111679 PTPN6 99.90 7.10E-34 7.00E-38 325.70 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPN4
Tyrosine-protein phosphatase non-receptor type 4 (EC 3.1.3.48) (Protein-tyrosine phosphatase MEG1) (MEG) (PTPase-MEG1)
3.1.3.48 Homo sapiens
Rabies,Disease Of Mental Health
2i75_a P29074 ENSG00000088179 PTPN4 100.00 1.10E-37 1.10E-41 339.30 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPN3 PTPH1
Tyrosine-protein phosphatase non-receptor type 3 (EC 3.1.3.48) (Protein-tyrosine phosphatase H1) (PTP-H1)
3.1.3.48 Homo sapiens
Type 1 Diabetes Mellitus,Autoimmune Lymphoproliferative Syndrome,Breast Cancer,Non-Functioning Pituitary Adenoma,Hyperinsulinemic Hypoglycemia, Familial, 5,Cholangiocarcinoma,Fragile X Syndrome,Scott Syndrome
4ri5_a P26045 ENSG00000070159 PTPN3 100.00 2.10E-38 2.00E-42 343.10 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPRZ1 HTPZP2 PTPRZ PTPRZ2 PTPZ
Receptor-type tyrosine-protein phosphatase zeta (R-PTP-zeta) (EC 3.1.3.48) (Protein-tyrosine phosphatase receptor type Z polypeptide 1) (Protein-tyrosine phosphatase receptor type Z polypeptide 2) (R-PTP-zeta-2)
3.1.3.48 Homo sapiens
Oligodendroglioma,Hyperkalemic Periodic Paralysis,Generalized Epilepsy With Febrile Seizures Plus, Type 1,Generalized Epilepsy With Febrile Seizures Plus
5awx_a P23471 ENSG00000106278 PTPRZ1 100.00 3.80E-36 3.70E-40 320.60 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPRG PTPG
Receptor-type tyrosine-protein phosphatase gamma (Protein-tyrosine phosphatase gamma) (R-PTP-gamma) (EC 3.1.3.48)
3.1.3.48 Homo sapiens
Infantile Myofibromatosis,Fuchs' Endothelial Dystrophy,Lung Cancer Susceptibility 3,Corneal Dystrophy,Schizoaffective Disorder,Breast Cancer,Breast Disease,Lynch Syndrome,Renal Cell Carcinoma, Nonpapillary
2h4v_b P23470 ENSG00000144724 PTPRG 100.00 3.90E-38 3.70E-42 342.00 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPRE
Receptor-type tyrosine-protein phosphatase epsilon (Protein-tyrosine phosphatase epsilon) (R-PTP-epsilon) (EC 3.1.3.48)
3.1.3.48 Homo sapiens
6d3f_a P23469 ENSG00000132334 PTPRE 99.90 6.80E-34 6.60E-38 300.20 0 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPRB PTPB
Receptor-type tyrosine-protein phosphatase beta (Protein-tyrosine phosphatase beta) (R-PTP-beta) (EC 3.1.3.48) (Vascular endothelial protein tyrosine phosphatase) (VE-PTP)
3.1.3.48 Homo sapiens
Vascular Cancer,Skin Angiosarcoma,Ovarian Angiosarcoma,Glial Tumor,Hyperkalemic Periodic Paralysis,Generalized Epilepsy With Febrile Seizures Plus, Type 1,Angiosarcoma,Generalized Epilepsy With Febrile Seizures Plus
2hc1_a P23467 ENSG00000127329 PTPRB 100.00 4.00E-35 4.00E-39 310.20 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
Ptpra Lrp Ptpa
Receptor-type tyrosine-protein phosphatase alpha (Protein-tyrosine phosphatase alpha) (R-PTP-alpha) (EC 3.1.3.48) (LCA-related phosphatase) (PTPTY-28)
3.1.3.48 Mus musculus
1p15_b P18052 99.90 1.30E-33 1.30E-37 292.10 0 0 1 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPN1 PTP1B
Tyrosine-protein phosphatase non-receptor type 1 (EC 3.1.3.48) (Protein-tyrosine phosphatase 1B) (PTP-1B)
3.1.3.48 Homo sapiens
Primary Mediastinal B-Cell Lymphoma,Diabetes Mellitus,Rasopathy,Myeloproliferative Neoplasm,Leptin Deficiency Or Dysfunction,Ovarian Cancer,Bubonic Plague,Lipid Metabolism Disorder,Noonan Syndrome With Multiple Lentigines,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Hypertension, Essential
2cm2_a P18031 ENSG00000196396 PTPN1 100.00 1.20E-35 1.10E-39 320.00 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
yopH yop51
Tyrosine-protein phosphatase YopH (EC 3.1.3.48) (Virulence protein)
3.1.3.48 Yersinia enterocolitica
1yts_a P15273 99.90 1.00E-31 9.60E-36 284.10 0 0 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPRF LAR
Receptor-type tyrosine-protein phosphatase F (EC 3.1.3.48) (Leukocyte common antigen related) (LAR)
3.1.3.48 Homo sapiens
Isolated Congenital Breast Hypoplasia/Aplasia,Van Maldergem Syndrome 1,Pheochromocytoma,Breasts And/Or Nipples, Aplasia Or Hypoplasia Of, 2,Ureterocele
1lar_a P10586 ENSG00000142949 PTPRF 99.90 7.10E-34 6.90E-38 329.70 1 1 0 0 0 0 0 0
YER075C PTP3 SGDID:S000000877
PTPRC CD45
Receptor-type tyrosine-protein phosphatase C (EC 3.1.3.48) (Leukocyte common antigen) (L-CA) (T200) (CD antigen CD45)
3.1.3.48 Homo sapiens
X-Linked Recessive Disease,Reticulum Cell Sarcoma,Severe Combined Immunodeficiency,Childhood Acute Lymphocytic Leukemia,Lymphosarcoma,Lymphoblastic Lymphoma,Listeriosis,Retinitis Pigmentosa,Hair Disease,Pancreas Lymphoma,Kagami-Ogata Syndrome,Neuroendocrine Carcinoma,Vulvar Apocrine Adenocarcinoma,Signet Ring Basal Cell Carcinoma,Malignant Fibrous Histiocytoma,Leukemia, Chronic Myeloid,Heart Lymphoma,Diabetes Mellitus,Autoimmune Disease Of The Nervous System,Barre-Lieou Syndrome,B-Lymphoblastic Leukemia/Lymphoma,Benign Giant Cell Tumor,Bone Lymphoma,Desmoplastic Small Round Cell Tumor,Autoimmune Hepatitis,Leukocyte Disease,Glomangiomatosis,Dendritic Cell Tumor,Encephalitis,T-Cell Non-Hodgkin Lymphoma,Mature B-Cell Neoplasm,B-Cell Lymphoma,Cobblestone Retinal Degeneration,Epiglottis Neoplasm,Endometrial Small Cell Carcinoma,Plasmablastic Lymphoma,T-Cell Lymphoblastic Leukemia/Lymphoma,Primitive Neuroectodermal Tumor Of The Cervix Uteri,Blood Platelet Disease,Benign Mastocytoma,Diamond-Blackfan Anemia 1,Bladder Small Cell Carcinoma,Monoclonal Gammopathy Of Uncertain Significance,Lymphatic System Disease,Retroperitoneum Carcinoma,Cerebellopontine Angle Primitive Neuroectodermal Tumor,Villonodular Synovitis,Lymph Node Disease,Blood Coagulation Disease,Glomeruloid Hemangioma,Tibial Nerve Palsy,Leukemia, Acute Myeloid,Bone Marrow Cancer,Gallbladder Lymphoma,Extraosseous Ewings Sarcoma-Primitive Neuroepithelial Tumor,Leber Plus Disease,Retroperitoneal Fibrosis,Leukemia, Acute Lymphoblastic,Combined Immunodeficiency,Microinvasive Cervical Squamous Cell Carcinoma,Dilated Cardiomyopathy,Myoepithelioma,Nodular Tenosynovitis,Pigmented Villonodular Synovitis,Actinomycosis,Human Immunodeficiency Virus Infectious Disease,Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Positive,Epithelioid Leiomyosarcoma,Small Intestinal Sarcoma,Thymus Gland Disease,Idiopathic Interstitial Pneumonia,Type 1 Diabetes Mellitus,Breast Lipoma,Cranial Nerve Malignant Neoplasm,Reticulosarcoma,Autoimmune Lymphoproliferative Syndrome,Hodgkin'S Lymphoma, Lymphocytic-Histiocytic Predominance,Brachydactyly, Type C,Immune System Disease,Epididymis Cancer,Epididymis Adenocarcinoma,Mediastinal Cancer,Myeloid Sarcoma,Prostate Neuroendocrine Neoplasm,T-Cell Acute Lymphoblastic Leukemia,Histiocytic And Dendritic Cell Cancer,Malignant Giant Cell Tumor Of Soft Parts,Breast Cancer,Peripheral Nervous System Disease,Cystadenocarcinoma,Cerebral Lipidosis,Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive,Primary Cutaneous Anaplastic Large Cell Lymphoma,Demyelinating Disease,Bicipital Tenosynovitis,Cataract 4, Multiple Types,Rhabdomyosarcoma,Hepatitis C Virus,Thymoma,Thymus Cancer,Multifocal Osteogenic Sarcoma,T Cell Deficiency,Cranial Nerve Neoplasm,Histiocytosis,Skin Carcinoma,Omenn Syndrome,Cone-Rod Dystrophy 2,Disease Of Mental Health,Retinitis Pigmentosa 24,Brittle Bone Disorder,Conventional Fibrosarcoma,Mucinous Cystadenocarcinoma,Pulmonary Fibrosis, Idiopathic,Macular Degeneration, Age-Related, 8,Olfactory Nerve Neoplasm,Rhabdoid Cancer,Olfactory Neuroblastoma,Integumentary System Disease,Retinitis Pigmentosa 23,Retinitis Pigmentosa 10,Plasmacytoma,Multiple Sclerosis,Diclofenac Allergy,Sarcoidosis 1,Drug-Induced Lupus Erythematosus,Disease By Infectious Agent,Langerhans Cell Histiocytosis,Merkel Cell Carcinoma,Lymphoma, Non-Hodgkin, Familial,Lymphoma, Hodgkin, Classic,Primary Bacterial Infectious Disease,Small Cell Cancer Of The Lung,Spastic Paraplegia 3, Autosomal Dominant,Hypotrichosis 1,Parkinson Disease 4, Autosomal Dominant,Hereditary Lymphedema,Inflammatory Bowel Disease,Immune Deficiency Disease,Lymphoma, Mucosa-Associated Lymphoid Type,Small Cell Carcinoma,X-Linked Monogenic Disease,Anaplastic Large Cell Lymphoma,Diffuse Large B-Cell Lymphoma,Ewing Sarcoma,Mantle Cell Lymphoma,Peripheral T-Cell Lymphoma,Mental Retardation, Autosomal Dominant 36,Acute Promyelocytic Leukemia,Gastrointestinal Carcinoma,Duodenum Adenoma,Wilms Tumor 1,Autoimmune Disease Of Central Nervous System,Cd45 Deficiency,Ectodermal Dysplasia 1, Hypohidrotic, X-Linked,Hypertension, Essential,Autoimmune Disease Of Musculoskeletal System,Lymphoma,Metachromatic Leukodystrophy,Leukemia, Chronic Lymphocytic,Autosomal Dominant Non-Syndromic Intellectual Disability,Systemic Lupus Erythematosus,Mycobacterium Tuberculosis 1,Pelizaeus-Merzbacher Disease,Myeloma, Multiple,Lymphoproliferative Syndrome,Waldenstroem'S Macroglobulinemia,Hereditary Lymphedema I,Lung Cancer,Celiac Disease 1,Budd-Chiari Syndrome
1ygr_a P08575 ENSG00000081237 PTPRC 100.00 1.90E-35 1.80E-39 347.30 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab