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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YMR075W | RCO1 | SGDID:S000004680 | NSD3 WHSC1L1 DC28 |
Histone-lysine N-methyltransferase NSD3 (EC 2.1.1.370) (EC 2.1.1.371) (Nuclear SET domain-containing protein 3) (Protein whistle) (WHSC1-like 1 isoform 9 with methyltransferase activity to lysine) (Wolf-Hirschhorn syndrome candidate 1-like protein 1) (WHSC1-like protein 1) |
2.1.1.370,2.1.1.371, | Homo sapiens | Weaver Syndrome,Sotos Syndrome 1,Kleefstra Syndrome 1,Wolf-Hirschhorn Syndrome,Nut Midline Carcinoma,Childhood Acute Myeloid Leukemia |
4gnd_c | Q9BZ95 | ENSG00000147548 | NSD3 | 97.50 | 4.90E-08 | 6.40E-12 | 73.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YMR075W | RCO1 | SGDID:S000004680 | zf-PHD-like |
PHD/FYVE-zinc-finger like domain |
pfam Domain | PF15446 | 97.20 | 3.30E-07 | 3.90E-11 | 76.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
YMR075W | RCO1 | SGDID:S000004680 | 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 | 2.10E-07 | 2.90E-11 | 71.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |