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Metazoan complexes |
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Details of MAPK10 gene in Homo sapiens
IDs | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Link outs | Gene Name | Alias | Uniprot ID | SwissProt ID | NCBI gene ID | ENSEMBL ID | Description | Source | |
|
| MAPK10 | JNK3,JNK3A,PRKM10,SAPK1B | P53779 | MK10_HUMAN | 5602 | ENSG00000109339 | Mitogen-activated protein kinase 10 | SPROT | |
Disease | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Disease | OMIM id | ||||||||
| Epileptic encephalopathy, Lennox-Gastaut type (EELG) [MIM:606369]: A childhood disorder characterized by a combination of seizures, usually including atypical absence seizures, tonic seizures, atonic or astatic seizures, and mental retardation. Note=The disease is caused by mutations affecting the gene represented in this entry. A chromosomal aberration involving MAPK10 has been found in a single patient. Translocation t(Y4)(q11.2q21) which causes MAPK10 truncation. | 606369 | ||||||||
Orthologs in other species | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| M. musculus | D. melonogaster | C. elegans | S. purpuratus | ||||||
| ENSMUSG00000046709 | bsk | jnk-1 | Sp-Jnk | ||||||
| Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
Complex ID | Corum | BioGrid | IRefWeb | Novelty |
|---|---|---|---|---|---|---|---|---|---|
| Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
|---|---|---|---|---|