| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YOR064C | YNG1 | SGDID:S000005590 | 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 | 96.20 | 2.40E-05 | 2.20E-09 | 50.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YOR064C | YNG1 | SGDID:S000005590 | SET3 YKR029C |
SET domain-containing protein 3 |
Saccharomyces cerevisiae | 5tdr_a | P36124 | 96.60 | 4.40E-06 | 5.10E-10 | 51.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YOR064C | YNG1 | SGDID:S000005590 | YNG1 YOR064C YOR29-15 |
Protein YNG1 (ING1 homolog 1) |
Saccharomyces cerevisiae | 2jmj_a | Q08465 | 97.30 | 1.90E-07 | 1.90E-11 | 65.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YOR064C | YNG1 | SGDID:S000005590 | SHPRH KIAA2023 |
E3 ubiquitin-protein ligase SHPRH (EC 2.3.2.27) (EC 3.6.4.-) (RING-type E3 ubiquitin transferase SHPRH) (SNF2, histone-linker, PHD and RING finger domain-containing helicase) |
2.3.2.27 | Homo sapiens | Xeroderma Pigmentosum, Variant Type |
2m85_a | Q149N8 | ENSG00000146414 | SHPRH | 95.80 | 7.00E-05 | 8.00E-09 | 46.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YOR064C | YNG1 | SGDID:S000005590 | SIZ1 Os05g0125000 LOC_Os05g03430 OSJNBb0079L11.3 |
E3 SUMO-protein ligase SIZ1 (EC 2.3.2.-) (E3 SUMO-protein transferase SIZ1) |
2.3.2.- | Oryza sativa | 2rsd_a | Q6L4L4 | 95.50 | 0.00013 | 1.50E-08 | 45.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YOR064C | YNG1 | SGDID:S000005590 | KMT2E MLL5 |
Inactive histone-lysine N-methyltransferase 2E (Inactive lysine N-methyltransferase 2E) (Myeloid/lymphoid or mixed-lineage leukemia protein 5) |
Homo sapiens | Epilepsy,Non-Specific Syndromic Intellectual Disability,Kleefstra Syndrome 2,Disease Of Mental Health,O'Donnell-Luria-Rodan Syndrome,Cerebroretinal Microangiopathy With Calcifications And Cysts 1,Kabuki Syndrome 1,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Autism |
2lv9_a | Q8IZD2 | ENSG00000005483 | KMT2E | 96.60 | 5.70E-06 | 5.80E-10 | 57.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YOR064C | YNG1 | SGDID:S000005590 | PHF20 C20orf104 GLEA2 HCA58 NZF TZP |
PHD finger protein 20 (Glioma-expressed antigen 2) (Hepatocellular carcinoma-associated antigen 58) (Novel zinc finger protein) (Transcription factor TZP) |
Homo sapiens | Hepatocellular Carcinoma,Glycogen Storage Disease Iv |
5tbn_a | Q9BVI0 | ENSG00000025293 | PHF20 | 95.40 | 0.00015 | 1.70E-08 | 42.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YOR064C | YNG1 | SGDID:S000005590 | ING4 My036 |
Inhibitor of growth protein 4 (p29ING4) |
Homo sapiens | 2vnf_a | Q9UNL4 | ENSG00000111653 | ING4 | 95.10 | 0.00031 | 3.40E-08 | 42.30 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YOR064C | YNG1 | SGDID:S000005590 | PHF8 KIAA1111 ZNF422 |
Histone lysine demethylase PHF8 (EC 1.14.11.27) (EC 1.14.11.65) (PHD finger protein 8) ([histone H3]-dimethyl-L-lysine(36) demethylase PHF8) ([histone H3]-dimethyl-L-lysine(9) demethylase PHF8) |
1.14.11.27,1.14.11.65, | Homo sapiens | Cleft Lip,Cleft Lip/Palate,X-Linked Intellectual Disability, Siderius Type,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Van Der Woude Syndrome 1,Disease Of Mental Health,Orofacial Cleft,Non-Syndromic X-Linked Intellectual Disability,Borjeson-Forssman-Lehmann Syndrome,Acute Promyelocytic Leukemia,Kabuki Syndrome 1,Syndromic X-Linked Intellectual Disability,Autism,Syndromic X-Linked Intellectual Disability Siderius Type |
3kv4_a | Q9UPP1 | ENSG00000172943 | PHF8 | 95.70 | 9.20E-05 | 9.60E-09 | 63.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YOR064C | YNG1 | SGDID:S000005590 | lid CG9088 |
Lysine-specific demethylase lid (EC 1.14.11.67) (Histone demethylase lid) (Jumonji/ARID domain-containing protein lid) (Protein little imaginal disks) (Retinoblastoma-binding protein 2 homolog) ([histone H3]-trimethyl-L-lysine(4) demethylase lid) |
1.14.11.67 | Drosophila melanogaster | 2miq_a | Q9VMJ7 | 95.20 | 0.00026 | 2.90E-08 | 47.00 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 |