| 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 |