| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YBR089C-A | NHP6B | SGDID:S000002157 | 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 | 99.60 | 2.60E-20 | 1.80E-24 | 96.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YBR089C-A | NHP6B | SGDID:S000002157 | 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 | 99.10 | 5.80E-15 | 4.00E-19 | 76.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YBR089C-A | NHP6B | SGDID:S000002157 | 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 | 99.20 | 2.90E-15 | 2.00E-19 | 78.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YBR089C-A | NHP6B | SGDID:S000002157 | NHP6A NHPA YPR052C YP9499.09C |
Non-histone chromosomal protein 6A |
Saccharomyces cerevisiae | 1j5n_a | P11632 | 99.30 | 3.70E-16 | 2.60E-20 | 82.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YBR089C-A | NHP6B | SGDID:S000002157 | NHP1 |
High mobility group protein homolog NHP1 |
Babesia bovis | 2lhj_a | P40632 | 99.30 | 6.40E-16 | 4.40E-20 | 82.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YBR089C-A | NHP6B | SGDID:S000002157 | 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 | 99.50 | 4.70E-18 | 3.10E-22 | 91.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YBR089C-A | NHP6B | SGDID:S000002157 | 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 | 99.10 | 5.80E-15 | 4.00E-19 | 76.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |