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

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YDR174W HMO1 / SGDID:S000002581
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
YDR174W HMO1 SGDID:S000002581
HMGB3 HMG2A HMG4
High mobility group protein B3 (High mobility group protein 2a) (HMG-2a) (High mobility group protein 4) (HMG-4)
Homo sapiens
Colobomatous Microphthalmia,Microphthalmia,Terminal Osseous Dysplasia,Microphthalmia, Syndromic 13,Linear Skin Defects With Multiple Congenital Anomalies 1
2eqz_a O15347 ENSG00000029993 HMGB3 98.40 4.10E-11 4.60E-15 81.60 1 1 0 0 0 0 0 0
YDR174W HMO1 SGDID:S000002581
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 98.40 7.20E-11 7.90E-15 79.90 1 1 0 0 0 0 0 0
YDR174W HMO1 SGDID:S000002581
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 98.70 3.10E-12 2.70E-16 95.70 1 1 0 0 0 0 0 0
YDR174W HMO1 SGDID:S000002581
Tox
Thymocyte selection-associated high mobility group box protein TOX (Thymus high mobility group box protein TOX)
Mus musculus
2co9_a Q66JW3 98.40 6.40E-11 6.90E-15 84.20 0 0 1 0 0 0 0 0
YDR174W HMO1 SGDID:S000002581
HBP1
HMG box-containing protein 1 (HMG box transcription factor 1) (High mobility group box transcription factor 1)
Homo sapiens
46,Xx Sex Reversal 3,Developmental And Epileptic Encephalopathy 1
2e6o_a O60381 ENSG00000105856 HBP1 98.50 3.50E-11 3.80E-15 83.50 1 1 0 0 0 0 0 0
YDR174W HMO1 SGDID:S000002581
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 99.00 4.10E-14 3.80E-18 100.50 0 0 0 0 0 0 0 0
YDR174W HMO1 SGDID:S000002581
MAEL
Protein maelstrom homolog
Homo sapiens
Retinitis Pigmentosa 49,Brooke-Spiegler Syndrome
2cto_a Q96JY0 ENSG00000143194 MAEL 98.50 2.50E-11 2.60E-15 86.60 1 1 0 0 0 0 0 0
YDR174W HMO1 SGDID:S000002581
PF3D7_0817900
PF3D7_0817900
Plasmodium falciparum
2mrc_a Q8IB14 98.40 7.90E-11 8.30E-15 83.10 0 0 0 0 0 0 0 0
YDR174W HMO1 SGDID:S000002581
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 98.40 6.70E-11 7.30E-15 82.40 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab