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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YOL090W | MSH2 | SGDID:S000005450 | MSH3 DUC1 DUG |
DNA mismatch repair protein Msh3 (hMSH3) (Divergent upstream protein) (DUP) (Mismatch repair protein 1) (MRP1) |
Homo sapiens | Endometrial Cancer,Cowden Syndrome,Familial Adenomatous Polyposis 4,Muir-Torre Syndrome,Cavernous Sinus Meningioma,Myotonic Disease,Myotonic Dystrophy 1,Superficial Urinary Bladder Cancer,Inherited Cancer-Predisposing Syndrome,Small Intestine Cancer,Megaloblastic Anemia,Ovarian Cancer,Breast Cancer,Colorectal Cancer,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Xeroderma Pigmentosum, Complementation Group G,Megaloblastic Anemia Due To Dihydrofolate Reductase Deficiency,Lynch Syndrome,Lipodystrophy, Familial Partial, Type 6,Familial Adenomatous Polyposis,Tumor Predisposition Syndrome,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Autosomal Dominant Non-Syndromic Intellectual Disability 8,Lung Cancer |
3thw_b | P20585 | ENSG00000113318 | MSH3 | 100.00 | 5.90E-84 | 4.10E-88 | 805.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YOL090W | MSH2 | SGDID:S000005450 | mutS NGO1930 |
DNA mismatch repair protein MutS |
Neisseria gonorrhoeae | 5x9w_b | Q5F5J4 | 100.00 | 5.70E-88 | 4.00E-92 | 831.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YOL090W | MSH2 | SGDID:S000005450 | MSH6 GTBP |
DNA mismatch repair protein Msh6 (hMSH6) (G/T mismatch-binding protein) (GTBP) (GTMBP) (MutS protein homolog 6) (MutS-alpha 160 kDa subunit) (p160) |
Homo sapiens | Duodenum Disease,Cervical Adenosarcoma,Uterine Body Mixed Cancer,Endometrial Cancer,Cowden Syndrome,Endometrial Hyperplasia,Gaucher'S Disease,Muir-Torre Syndrome,Adenoma,Cowden Syndrome 1,Rectum Cancer,Rectum Adenocarcinoma,Bilateral Breast Cancer,B-Lymphoblastic Leukemia/Lymphoma,Uterine Corpus Cancer,T-Cell Non-Hodgkin Lymphoma,Intestinal Benign Neoplasm,Ocular Cancer,Mismatch Repair Cancer Syndrome 3,Esophageal Tuberculosis,46,Xy Disorder Of Sexual Development Due To Dihydrotestosterone Backdoor Pathway Biosynthesis Defect,Hereditary Nonpolyposis Colon Cancer,Neurofibromatosis, Type I,Colon Adenocarcinoma,Colonic Benign Neoplasm,Sebaceous Adenocarcinoma,Small Intestine Adenocarcinoma,Pituitary Carcinoma,Renal Pelvis Carcinoma,Inherited Cancer-Predisposing Syndrome,Hereditary Mixed Polyposis Syndrome,B-Lymphoblastic Leukemia/Lymphoma With T,Mismatch Repair Cancer Syndrome,Sebaceous Adenoma,Duodenum Cancer,Dysplastic Nevus Syndrome,Silent Pituitary Adenoma,Rectosigmoid Cancer,Small Intestine Cancer,Brain Cancer,Acidophil Adenoma,Extrahepatic Bile Duct Adenoma,Ulcerative Colitis,Ovarian Cancer,Adenocarcinoma,Neurofibromatosis,Jejunal Cancer,Female Reproductive Endometrioid Cancer,Adenosquamous Colon Carcinoma,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Colorectal Cancer,Mismatch Repair Cancer Syndrome 1,Sebaceous Gland Neoplasm,Pediatric Lymphoma,Endometrioid Ovary Carcinoma,Duodenum Adenocarcinoma,Fallopian Tube Endometrioid Adenocarcinoma,Skin Benign Neoplasm,Oligodendroglioma,Attenuated Familial Adenomatous Polyposis,Renal Pelvis Transitional Cell Carcinoma,Rhabdomyosarcoma,Juvenile Polyposis Syndrome,Xeroderma Pigmentosum, Variant Type,Esophagus Sarcoma,Fanconi Anemia, Complementation Group A,Skin Carcinoma,Gastric Cancer,Lynch Syndrome I,Prostate Cancer,Gaucher Disease, Type I,Cecum Carcinoma,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Breast-Ovarian Cancer, Familial 1,Lynch Syndrome,Familial Adenomatous Polyposis,Gastrointestinal System Benign Neoplasm,Gastric Cancer, Hereditary Diffuse,Tumor Predisposition Syndrome,Colorectal Cancer, Hereditary Nonpolyposis, Type 6,Autosomal Genetic Disease,Colorectal Cancer, Hereditary Nonpolyposis, Type 5,Colorectal Cancer 5,Periampullary Adenoma,Colorectal Adenocarcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Appendix Carcinoid Tumor,Jejunal Adenocarcinoma,Lymphoma,Cerebellar Medulloblastoma,Colitis,Li-Fraumeni Syndrome,Medulloblastoma,Melanoma, Cutaneous Malignant 1,Autosomal Dominant Non-Syndromic Intellectual Disability 8 |
2o8b_b | P52701 | ENSG00000116062 | MSH6 | 100.00 | 7.90E-92 | 5.50E-96 | 880.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YOL090W | MSH2 | SGDID:S000005450 | mutS fdv b2733 JW2703 |
DNA mismatch repair protein MutS |
Escherichia coli | 1ng9_a | P23909 | 100.00 | 4.60E-87 | 3.20E-91 | 823.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | ||||
YOL090W | MSH2 | SGDID:S000005450 | mutS |
DNA mismatch repair protein MutS |
Thermus aquaticus | 1ewq_a | Q56215 | 100.00 | 3.30E-83 | 2.30E-87 | 783.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YOL090W | MSH2 | SGDID:S000005450 | MSH2 |
DNA mismatch repair protein Msh2 (hMSH2) (MutS protein homolog 2) |
Homo sapiens | Duodenum Disease,Cervical Adenosarcoma,Endometrial Cancer,Cheilitis,Sebaceous Gland Disease,Cowden Syndrome,Malignant Fibrous Histiocytoma,Endometrial Hyperplasia,Muir-Torre Syndrome,Adenoma,Cowden Syndrome 1,Cervical Adenoma Malignum,Rectum Cancer,Rectum Adenocarcinoma,Neuroma,Uterine Corpus Cancer,Myh-Associated Polyposis,T-Cell Non-Hodgkin Lymphoma,Intestinal Benign Neoplasm,Ocular Cancer,Ascending Colon Cancer,Intracranial Meningioma,Mismatch Repair Cancer Syndrome 2,Cerebral Primitive Neuroectodermal Tumor,46,Xy Disorder Of Sexual Development Due To Dihydrotestosterone Backdoor Pathway Biosynthesis Defect,Hereditary Nonpolyposis Colon Cancer,Familial Colorectal Cancer,Neurofibromatosis, Type I,Colonic Benign Neoplasm,Sebaceous Adenocarcinoma,Rectum Signet Ring Adenocarcinoma,Small Intestine Adenocarcinoma,Inherited Cancer-Predisposing Syndrome,Acoustic Neuroma,Hereditary Mixed Polyposis Syndrome,Basal Cell Carcinoma,Hematologic Cancer,Leukemia, Acute Lymphoblastic,Colorectal Cancer 1,Mismatch Repair Cancer Syndrome,Sebaceous Adenoma,Transitional Cell Carcinoma,Duodenum Cancer,Dysplastic Nevus Syndrome,Silent Pituitary Adenoma,Ileum Cancer,Small Intestine Cancer,Testicular Germ Cell Tumor,Extrahepatic Bile Duct Adenoma,Lip Cancer,Ulcerative Colitis,Ovarian Cancer,Adenocarcinoma,Neurofibromatosis,Jejunal Cancer,Female Reproductive Endometrioid Cancer,Adenosquamous Colon Carcinoma,Breast Cancer,Glioblastoma,Hereditary Breast Ovarian Cancer Syndrome,Lower Lip Cancer,Actinic Cheilitis,Gliosarcoma,Giant Cell Glioblastoma,Colorectal Cancer,Mismatch Repair Cancer Syndrome 1,Sebaceous Gland Neoplasm,Hepatocellular Carcinoma,Duodenum Adenocarcinoma,Keratoacanthoma,Skin Benign Neoplasm,Oligodendroglioma,Attenuated Familial Adenomatous Polyposis,Renal Pelvis Transitional Cell Carcinoma,Pheochromocytoma,Rhabdomyosarcoma,Juvenile Polyposis Syndrome,Xeroderma Pigmentosum, Variant Type,Esophagus Sarcoma,Sarcoma,Fanconi Anemia, Complementation Group A,Liposarcoma,Skin Carcinoma,Gastric Cancer,Breast Disease,Lynch Syndrome I,Prostate Cancer,Signet Ring Cell Adenocarcinoma,Cecum Carcinoma,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Breast-Ovarian Cancer, Familial 1,Lynch Syndrome,Lymphoma, Non-Hodgkin, Familial,Renal Cell Carcinoma, Papillary, 1,Familial Adenomatous Polyposis,Colorectal Cancer 2,Gastrointestinal System Benign Neoplasm,Gastric Cancer, Hereditary Diffuse,Alveolar Soft Part Sarcoma,Tumor Predisposition Syndrome,Colorectal Cancer, Hereditary Nonpolyposis, Type 6,Autosomal Genetic Disease,Colorectal Cancer, Hereditary Nonpolyposis, Type 5,Ureter, Cancer Of,Colorectal Adenoma,Colorectal Adenocarcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Appendix Carcinoid Tumor,Colitis,Li-Fraumeni Syndrome,Anal Fistula,Melanoma, Cutaneous Malignant 1,Autosomal Dominant Non-Syndromic Intellectual Disability 8,Pancreatic Cancer |
3thw_a | P43246 | ENSG00000095002 | MSH2 | 100.00 | 8.20E-93 | 5.70E-97 | 882.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |