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

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YMR044W IOC4 / SGDID:S000004647
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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

Weizmann Institute of Science | Maya Schuldiner Lab