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

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YPR065W ROX1 / SGDID:S000006269
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
YPR065W ROX1 SGDID:S000006269
KMT2C HALR KIAA1506 MLL3
Histone-lysine N-methyltransferase 2C (Lysine N-methyltransferase 2C) (EC 2.1.1.354) (Homologous to ALR protein) (Myeloid/lymphoid or mixed-lineage leukemia protein 3)
2.1.1.354 Homo sapiens
Plasma Cell Neoplasm,Kleefstra Syndrome,Leukemia,Leukemia, Acute Myeloid,Kleefstra Syndrome Due To A Point Mutation,Cystic Kidney Disease,Colorectal Cancer,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Kleefstra Syndrome 2,Disease Of Mental Health,Kleefstra Syndrome 1,Autism Spectrum Disorder,Kabuki Syndrome 1,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Nut Midline Carcinoma,Myeloma, Multiple,Cardiomyopathy, Infantile Histiocytoid
2yuk_a Q8NEZ4 ENSG00000055609 KMT2C 98.20 3.10E-10 2.90E-14 88.50 1 1 0 0 0 0 0 0
YPR065W ROX1 SGDID:S000006269
Sox18 Sox-18
Transcription factor SOX-18
Mus musculus
4y60_c P43680 98.20 2.80E-10 3.50E-14 78.30 0 0 1 0 0 0 0 0
YPR065W ROX1 SGDID:S000006269
SOX17
Transcription factor SOX-17
Homo sapiens
Cakut,Speech Disorder,Seminoma,Arteriovenous Malformations Of The Brain,Adenocarcinoma In Situ,Heritable Pulmonary Arterial Hypertension,Brachydactyly, Type E1,Germ Cell Cancer,Familial Vesicoureteral Reflux,Germ Cell And Embryonal Cancer,Intracranial Aneurysm,Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 4,Vesicoureteral Reflux 3,Cerebral Arterial Disease,Hypotrichosis-Lymphedema-Telangiectasia-Renal Defect Syndrome,Hypotrichosis-Lymphedema-Telangiectasia Syndrome
2yul_a Q9H6I2 ENSG00000164736 SOX17 98.20 2.30E-10 2.80E-14 79.60 1 1 0 0 0 0 0 0
YPR065W ROX1 SGDID:S000006269
PMS1 PMSL1
PMS1 protein homolog 1 (DNA mismatch repair protein PMS1)
Homo sapiens
Cowden Syndrome,Muir-Torre Syndrome,Urachus Cancer,Hereditary Nonpolyposis Colon Cancer,Sebaceous Adenocarcinoma,Rectum Signet Ring Adenocarcinoma,Ovarian Cancer,Hereditary Breast Ovarian Cancer Syndrome,Colorectal Cancer,Sebaceous Gland Neoplasm,Lynch Syndrome I,Meier-Gorlin Syndrome 2,Lynch Syndrome,Familial Adenomatous Polyposis,Colorectal Cancer, Hereditary Nonpolyposis, Type 6,Colorectal Cancer, Hereditary Nonpolyposis, Type 4,Miller-Dieker Lissencephaly Syndrome,Epilepsy, Idiopathic Generalized 9
2cs1_a P54277 ENSG00000064933 PMS1 98.20 2.20E-10 2.70E-14 82.10 1 1 0 0 0 0 0 0
YPR065W ROX1 SGDID:S000006269
Hmgb1 Hmg-1 Hmg1
High mobility group protein B1 (Amphoterin) (Heparin-binding protein p30) (High mobility group protein 1) (HMG-1)
Rattus norvegicus
1ckt_a P63159 98.90 1.60E-13 1.60E-17 101.60 0 0 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab