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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YMR044W | IOC4 | SGDID:S000004647 | DNMT3B |
DNA (cytosine-5)-methyltransferase 3B (Dnmt3b) (EC 2.1.1.37) (DNA methyltransferase HsaIIIB) (DNA MTase HsaIIIB) (M.HsaIIIB) |
2.1.1.37 | Homo sapiens | Endometrial Cancer,Adult Syndrome,Facioscapulohumeral Muscular Dystrophy 1,Facioscapulohumeral Muscular Dystrophy 2,Early-Onset Schizophrenia,Mucoepidermoid Carcinoma,Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome,Muscular Dystrophy,Testicular Spermatocytic Seminoma,Leukemia, Acute Myeloid,Primary Hyperoxaluria,Ovarian Cancer,Burkitt Lymphoma,Breast Cancer,Squamous Cell Carcinoma, Head And Neck,Colorectal Cancer,Hepatocellular Carcinoma,Sotos Syndrome 1,Mood Disorder,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Cerebellar Ataxia, Deafness, And Narcolepsy, Autosomal Dominant,Mutagen Sensitivity,Beckwith-Wiedemann Syndrome,Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2,Immune Deficiency Disease,Tetralogy Of Fallot,Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1,Myelodysplastic Syndrome,Thrombocytopenic Purpura, Autoimmune,Nasopharyngeal Carcinoma,Cartilage-Hair Hypoplasia,Kabuki Syndrome 1,Lung Cancer,Hyperoxaluria, Primary, Type I |
5nrr_b | Q9UBC3 | ENSG00000088305 | DNMT3B | 99.10 | 3.50E-15 | 3.70E-19 | 126.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YMR044W | IOC4 | SGDID:S000004647 | 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 |
2gfu_a | P52701 | ENSG00000116062 | MSH6 | 99.20 | 9.40E-16 | 1.10E-19 | 125.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YMR044W | IOC4 | SGDID:S000004647 | NSD3 WHSC1L1 DC28 |
Histone-lysine N-methyltransferase NSD3 (EC 2.1.1.370) (EC 2.1.1.371) (Nuclear SET domain-containing protein 3) (Protein whistle) (WHSC1-like 1 isoform 9 with methyltransferase activity to lysine) (Wolf-Hirschhorn syndrome candidate 1-like protein 1) (WHSC1-like protein 1) |
2.1.1.370,2.1.1.371, | Homo sapiens | Weaver Syndrome,Sotos Syndrome 1,Kleefstra Syndrome 1,Wolf-Hirschhorn Syndrome,Nut Midline Carcinoma,Childhood Acute Myeloid Leukemia |
2daq_a | Q9BZ95 | ENSG00000147548 | NSD3 | 99.40 | 1.30E-17 | 1.60E-21 | 129.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YMR044W | IOC4 | SGDID:S000004647 | NSD2 KIAA1090 MMSET TRX5 WHSC1 |
Histone-lysine N-methyltransferase NSD2 (EC 2.1.1.357) (Multiple myeloma SET domain-containing protein) (MMSET) (Nuclear SET domain-containing protein 2) (Protein trithorax-5) (Wolf-Hirschhorn syndrome candidate 1 protein) |
2.1.1.356 | Homo sapiens | Chromosomal Disease,Blood Protein Disease,Chromosome 4p Deletion,Leukocyte Disease,Smoldering Myeloma,Monoclonal Gammopathy Of Uncertain Significance,Bone Marrow Cancer,Skin Squamous Cell Carcinoma,Microcephaly,Weaver Syndrome,Sotos Syndrome 1,Sweeney-Cox Syndrome,Wolf-Hirschhorn Syndrome,Kabuki Syndrome 1,Chromosomal Deletion Syndrome,Myeloma, Multiple |
5vc8_b | O96028 | ENSG00000109685 | NSD2 | 99.10 | 3.60E-15 | 4.00E-19 | 123.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YMR044W | IOC4 | SGDID:S000004647 | PWWP2B PWWP2 |
PWWP domain-containing protein 2B |
Homo sapiens | Weaver Syndrome,Sotos Syndrome 1,Kleefstra Syndrome 1,Mental Retardation, X-Linked, Syndromic, Claes-Jensen Type,Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 |
4ld6_a | Q6NUJ5 | ENSG00000171813 | PWWP2B | 99.30 | 1.40E-16 | 1.60E-20 | 126.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YMR044W | IOC4 | SGDID:S000004647 | HDGFL3 HDGF2 HDGFRP3 CGI-142 |
Hepatoma-derived growth factor-related protein 3 (HRP-3) (Hepatoma-derived growth factor 2) (HDGF-2) |
Homo sapiens | Spinal Muscular Atrophy, Type I |
6iip_a | Q9Y3E1 | ENSG00000166503 | HDGFL3 | 99.30 | 1.40E-16 | 1.60E-20 | 120.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YMR044W | IOC4 | SGDID:S000004647 | Tb927.2.3580 |
Tb927.2.3580 |
Trypanosoma brucei | 2m1h_a | Q586X9 | 99.20 | 2.00E-15 | 2.20E-19 | 122.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YMR044W | IOC4 | SGDID:S000004647 | BRPF3 KIAA1286 |
Bromodomain and PHD finger-containing protein 3 |
Homo sapiens | Lethal Congenital Contracture Syndrome 2 |
3pfs_a | Q9ULD4 | ENSG00000096070 | BRPF3 | 99.30 | 4.70E-16 | 4.90E-20 | 134.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YMR044W | IOC4 | SGDID:S000004647 | BRPF1 BR140 |
Peregrin (Bromodomain and PHD finger-containing protein 1) (Protein Br140) |
Homo sapiens | Intellectual Developmental Disorder With Dysmorphic Facies And Ptosis,Eyelid Disease,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Ohdo Syndrome, Sbbys Variant,Adult Medulloblastoma,Syndromic Intellectual Disability,Ohdo Syndrome,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Ptosis |
3l42_a | P55201 | ENSG00000156983 | BRPF1 | 99.30 | 4.20E-16 | 4.80E-20 | 126.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YMR044W | IOC4 | SGDID:S000004647 | Hdgfl3 Hdgfrp3 |
Hepatoma-derived growth factor-related protein 3 (HRP-3) |
Mus musculus | 1n27_a | Q9JMG7 | 99.30 | 8.40E-17 | 9.70E-21 | 124.10 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YMR044W | IOC4 | SGDID:S000004647 | HDGF HMG1L2 |
Hepatoma-derived growth factor (HDGF) (High mobility group protein 1-like 2) (HMG-1L2) |
Homo sapiens | Childhood Malignant Schwannoma,Hepatocellular Carcinoma,Lung Cancer |
1ri0_a | P51858 | ENSG00000143321 | HDGF | 99.20 | 1.90E-15 | 2.00E-19 | 122.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YMR044W | IOC4 | SGDID:S000004647 | Hdgf |
Hepatoma-derived growth factor (HDGF) |
Rattus norvegicus | 5xsk_a | Q8VHK7 | 99.20 | 3.30E-15 | 3.40E-19 | 123.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YMR044W | IOC4 | SGDID:S000004647 | DNMT3A |
DNA (cytosine-5)-methyltransferase 3A (Dnmt3a) (EC 2.1.1.37) (DNA methyltransferase HsaIIIA) (DNA MTase HsaIIIA) (M.HsaIIIA) |
2.1.1.37 | Homo sapiens | Breast Implant-Associated Anaplastic Large Cell Lymphoma,Lymphosarcoma,Retinitis Pigmentosa,Lung Cancer Susceptibility 3,Chronic Myelomonocytic Leukemia,Plasma Cell Neoplasm,Adult Syndrome,Sporadic Pheochromocytoma/Secreting Paraganglioma,Rare Genetic Intellectual Disability,Myeloproliferative Neoplasm,Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome,Alpha Thalassemia-X-Linked Intellectual Disability Syndrome,Leukemia,Mixed Phenotype Acute Leukemia,Acute Leukemia,Testicular Spermatocytic Seminoma,Leukemia, Acute Myeloid,Mixed Phenotype Acute Leukemia With T,Bone Marrow Cancer,Myelodysplastic/Myeloproliferative Neoplasm,Cebpa-Associated Familial Acute Myeloid Leukemia,Etv6 Thrombocytopenia And Predisposition To Leukemia,Chronic Leukemia,Primary Hyperoxaluria,Ovarian Cancer,Myeloid Leukemia,Testicular Cancer,T-Cell Acute Lymphoblastic Leukemia,Rahman Syndrome,Glioblastoma,Gliosarcoma,Giant Cell Glioblastoma,Colorectal Cancer,Hepatocellular Carcinoma,Microcephaly,Weaver Syndrome,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Retinitis Pigmentosa 58,West Syndrome,Systemic Mastocytosis,Disease Of Mental Health,Thrombocytopenia,Tatton-Brown-Rahman Syndrome,Beckwith-Wiedemann Syndrome,Neuropathy, Hereditary Sensory, Type Ie,Myelodysplastic Syndrome,Mature T-Cell And Nk-Cell Lymphoma,Peripheral T-Cell Lymphoma,Heyn-Sproul-Jackson Syndrome,Cartilage-Hair Hypoplasia,Juvenile Myelomonocytic Leukemia,Umbilical Hernia,Myelofibrosis,Myeloma, Multiple,Medulloblastoma,Childhood Acute Myeloid Leukemia,Lung Cancer,Hyperoxaluria, Primary, Type I,Polycythemia Vera |
3llr_b | Q9Y6K1 | ENSG00000119772 | DNMT3A | 99.20 | 5.50E-16 | 5.90E-20 | 132.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YMR044W | IOC4 | SGDID:S000004647 | Tb927.2.3480 |
Tb927.2.3480 |
Trypanosoma brucei | 2nas_a | Q586Y0 | 99.30 | 4.60E-16 | 5.20E-20 | 122.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YMR044W | IOC4 | SGDID:S000004647 | ZMYND8 KIAA1125 PRKCBP1 RACK7 |
Protein kinase C-binding protein 1 (Cutaneous T-cell lymphoma-associated antigen se14-3) (CTCL-associated antigen se14-3) (Rack7) (Zinc finger MYND domain-containing protein 8) |
Homo sapiens | Breast Cancer,Lymphoma,Cutaneous T Cell Lymphoma |
4cos_a | Q9ULU4 | ENSG00000101040 | ZMYND8 | 99.00 | 3.50E-14 | 4.10E-18 | 129.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YMR044W | IOC4 | SGDID:S000004647 | ZMYND11 BRAM1 BS69 |
Zinc finger MYND domain-containing protein 11 (Adenovirus 5 E1A-binding protein) (Bone morphogenetic protein receptor-associated molecule 1) (Protein BS69) |
Homo sapiens | Intellectual Disability-Expressive Aphasia-Facial Dysmorphism Syndrome,Short-Rib Thoracic Dysplasia 2 With Or Without Polydactyly,Mental Retardation, Autosomal Dominant 30,Paragangliomas 5,Fibrodysplasia Ossificans Progressiva,Autism Spectrum Disorder,Ptosis,Autosomal Dominant Non-Syndromic Intellectual Disability |
4ns5_a | Q15326 | ENSG00000015171 | ZMYND11 | 98.90 | 1.50E-13 | 1.70E-17 | 120.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |