| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YNL024C | YNL024C | SGDID:S000004969 | MJ0882 |
Probable S-adenosylmethionine-dependent methyltransferase MJ0882 (EC 2.1.1.-) |
2.1.1.- | Methanocaldococcus jannaschii | 1dus_a | Q58292 | 98.90 | 4.60E-13 | 2.80E-17 | 93.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YNL024C | YNL024C | SGDID:S000004969 | CMQ451C |
CMQ451C |
Cyanidioschyzon merolae | 3bzb_b | D0VWS8 | 99.40 | 7.30E-17 | 4.50E-21 | 120.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YNL024C | YNL024C | SGDID:S000004969 | METTL21C C13orf39 |
Protein-lysine methyltransferase METTL21C (EC 2.1.1.-) (Methyltransferase-like protein 21C) |
2.1.1.- | Homo sapiens | Atrial Septal Defect 5,Chromosome 4q21 Deletion Syndrome |
4mtl_a | Q5VZV1 | ENSG00000139780 | METTL21C | 98.80 | 2.20E-12 | 1.30E-16 | 93.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YNL024C | YNL024C | SGDID:S000004969 | CAMKMT C2orf34 CLNMT |
Calmodulin-lysine N-methyltransferase (CLNMT) (CaM KMT) (EC 2.1.1.60) |
2.1.1.60 | Homo sapiens | Cystinuria,2p21 Microdeletion Syndrome Without Cystinuria,Meier-Gorlin Syndrome 1,Hypotonia,Myasthenic Syndrome, Congenital, 22,Hypotonia-Cystinuria Syndrome |
4pwy_a | Q7Z624 | ENSG00000143919 | CAMKMT | 98.90 | 6.00E-13 | 3.70E-17 | 97.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YNL024C | YNL024C | SGDID:S000004969 | METTL21A FAM119A HCA557B |
Protein N-lysine methyltransferase METTL21A (EC 2.1.1.-) (HSPA lysine methyltransferase) (HSPA-KMT) (Hepatocellular carcinoma-associated antigen 557b) (Methyltransferase-like protein 21A) |
2.1.1.- | Homo sapiens | Pontocerebellar Hypoplasia, Type 2a,Bardet-Biedl Syndrome 5 |
4lec_a | Q8WXB1 | ENSG00000144401 | METTL21A | 98.70 | 5.60E-12 | 3.40E-16 | 89.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YNL024C | YNL024C | SGDID:S000004969 | EEF1AKMT3 FAM119B HCA557A METTL21B |
EEF1A lysine methyltransferase 3 (EC 2.1.1.-) (Hepatocellular carcinoma-associated antigen 557a) (Methyltransferase-like protein 21B) (Protein-lysine methyltransferase METTL21B) |
2.1.1.- | Homo sapiens | 4qpn_a | Q96AZ1 | ENSG00000123427 | EEF1AKMT3 | 98.70 | 4.40E-12 | 2.70E-16 | 90.90 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YNL024C | YNL024C | SGDID:S000004969 | VCPKMT C14orf138 METTL21D |
Protein-lysine methyltransferase METTL21D (EC 2.1.1.-) (Methyltransferase-like protein 21D) (VCP lysine methyltransferase) (VCP-KMT) (Valosin-containing protein lysine methyltransferase) |
2.1.1.- | Homo sapiens | Pontocerebellar Hypoplasia, Type 2a,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia |
4lg1_c | Q9H867 | ENSG00000100483 | VCPKMT | 99.30 | 3.40E-16 | 2.10E-20 | 112.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |