| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YPR093C | ASR1 | SGDID:S000006297 | BAZ1B WBSC10 WBSCR10 WBSCR9 WSTF |
Tyrosine-protein kinase BAZ1B (EC 2.7.10.2) (Bromodomain adjacent to zinc finger domain protein 1B) (Williams syndrome transcription factor) (Williams-Beuren syndrome chromosomal region 10 protein) (Williams-Beuren syndrome chromosomal region 9 protein) (hWALp2) |
2.7.10.2 | Homo sapiens | Myopathy, Centronuclear, 1,Klippel-Feil Syndrome,Helsmoortel-Van Der Aa Syndrome,Supravalvular Aortic Stenosis,Williams-Beuren Syndrome,Autosomal Dominant Non-Syndromic Intellectual Disability,Chromosomal Deletion Syndrome |
1f62_a | Q9UIG0 | 97.80 | 1.20E-08 | 9.20E-13 | 65.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YPR093C | ASR1 | SGDID:S000006297 | 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 |
2ysm_a | Q8NEZ4 | ENSG00000055609 | KMT2C | 97.30 | 2.80E-07 | 2.30E-11 | 67.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YPR093C | ASR1 | SGDID:S000006297 | KAT6B KIAA0383 MORF MOZ2 MYST4 |
Histone acetyltransferase KAT6B (EC 2.3.1.48) (Histone acetyltransferase MOZ2) (MOZ, YBF2/SAS3, SAS2 and TIP60 protein 4) (MYST-4) (Monocytic leukemia zinc finger protein-related factor) |
2.3.1.48 | Homo sapiens | Renal Hypoplasia,Clubfoot,Rasopathy,Pylorospasm,Familial Clubfoot With Or Without Associated Lower Limb Anomalies,Kat6b-Related Multiple Congenital Anomalies Syndrome,Craniosynostosis,Cryptorchidism, Unilateral Or Bilateral,Nephronophthisis,Kat6b Disorders,Eyelid Disease,Monocytic Leukemia,Blepharophimosis,Lin-Gettig Syndrome,Familial Vesicoureteral Reflux,Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant,Cardiofaciocutaneous Syndrome 1,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Clubfoot, Congenital, With Or Without Deficiency Of Long Bones And/Or Mirror-Image Polydactyly,Disease Of Mental Health,Ohdo Syndrome, Sbbys Variant,Craniosynostosis 1,Chromosome 16p13.3 Deletion Syndrome, Proximal,Epicanthus,46,Xx Sex Reversal 3,Cornelia De Lange Syndrome 5,Telecanthus,Genitopatellar Syndrome,Vesicoureteral Reflux 1,Hypertelorism,Ohdo Syndrome,Kbg Syndrome,Methylmalonic Acidemia And Homocysteinemia, Cblx Type,Ptosis |
5u2j_a | Q8WYB5 | ENSG00000156650 | KAT6B | 96.80 | 2.70E-06 | 2.20E-10 | 61.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YPR093C | ASR1 | SGDID:S000006297 | DPF3 BAF45C CERD4 |
Zinc finger protein DPF3 (BRG1-associated factor 45C) (BAF45C) (Zinc finger protein cer-d4) |
Homo sapiens | Neurilemmomatosis,Tetralogy Of Fallot,Atrial Septal Defect 9,Autosomal Dominant Non-Syndromic Intellectual Disability |
2kwk_a | Q92784 | ENSG00000205683 | DPF3 | 97.40 | 1.20E-07 | 9.40E-12 | 69.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YPR093C | ASR1 | SGDID:S000006297 | KAT6A MOZ MYST3 RUNXBP2 ZNF220 |
Histone acetyltransferase KAT6A (EC 2.3.1.48) (MOZ, YBF2/SAS3, SAS2 and TIP60 protein 3) (MYST-3) (Monocytic leukemia zinc finger protein) (Runt-related transcription factor-binding protein 2) (Zinc finger protein 220) |
2.3.1.48 | Homo sapiens | Chronic Myelomonocytic Leukemia,Leukemia,Neonatal Leukemia,Leukemia, Acute Myeloid,Acute Myeloid Leukemia With T(8;16)(P11;P13) Translocation,Monocytic Leukemia,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Ohdo Syndrome, Sbbys Variant,Chromosome 16p13.3 Deletion Syndrome, Proximal,Myelodysplastic Syndrome,Arboleda-Tham Syndrome,Acute Promyelocytic Leukemia,Syndromic Intellectual Disability,Autism Spectrum Disorder,Ohdo Syndrome,Leukemia, Acute Monocytic,Autosomal Dominant Non-Syndromic Intellectual Disability,Autism |
5b78_a | Q92794 | ENSG00000083168 | KAT6A | 97.20 | 3.90E-07 | 3.10E-11 | 68.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YPR093C | ASR1 | SGDID:S000006297 | MTF2 PCL2 |
Metal-response element-binding transcription factor 2 (Metal regulatory transcription factor 2) (Metal-response element DNA-binding protein M96) (Polycomb-like protein 2) (hPCl2) |
Homo sapiens | Weaver Syndrome,Retinitis Pigmentosa 48,Hereditary Lymphedema,Hereditary Lymphedema I |
5xfr_a | Q9Y483 | ENSG00000143033 | MTF2 | 97.60 | 3.90E-08 | 3.10E-12 | 85.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |