Allelic Variants
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There are no related allelic variants
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| Number of involved diseases in the family |
44 |
| Number of MAPK14 related diseases |
12 |
All kinase in this family
MAPK14
Allelic
Variants |
Disease Description |
Involved kinases
(This family) |
Inhibitor of
Involved Kinases |
Search
Disease |
| n/a | Tuberculosis | MAPK10, MAPK14, MAPK9, PLK3 | 80 | Link | | Prostate cancer | CDK2, CHEK2, FGFR2, PDPK1 | 4 | Link | | n/a | Epstein-Barr virus infection | CDK2, MAPK10, MAPK14, MAPK9 | 83 | Link | | n/a | Chagas disease | MAPK10, MAPK14, MAPK9 | 80 | Link | | n/a | Toxoplasmosis | MAPK10, MAPK14, MAPK9 | 80 | Link | | n/a | Pertussis | MAPK10, MAPK14, MAPK9 | 80 | Link | | n/a | Shigellosis | MAPK10, MAPK14, MAPK9 | 80 | Link | | n/a | Epithelial cell signaling in Helicobacter pylori infection | MAPK10, MAPK14, MAPK9 | 80 | Link | | n/a | Salmonella infection | MAPK10, MAPK14, MAPK9 | 80 | Link | | n/a | Hepatitis C | MAPK10, MAPK14, MAPK9 | 80 | Link | | n/a | Herpes simplex infection | CDK2, MAPK10, MAPK9 | 6 | Link | | n/a | Influenza A | MAPK10, MAPK14, MAPK9 | 80 | Link | | n/a | Measles | CDK2, FYN | 3 | Link | | Diabetes mellitus | MAPK10, MAPK9 | 3 | Link | | Apert syndrome | FGFR2 | 1 | Link | | Beare-Stevenson cutis gyrata syndrome | FGFR2 | 1 | Link | | Bent bone dysplasia syndrome | FGFR2 | 1 | Link | | Craniosynostosis | FGFR2 | 1 | Link | | Craniofacial-skeletal-dermatologic dysplasia | FGFR2 | 1 | Link | | Gastric cancer | FGFR2 | 1 | Link | | n/a | Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | FGFR2 | 1 | Link | | Breast cancer | CHEK2 | 1 | Link | | Osteosarcoma | CHEK2 | 1 | Link | | Li-Fraumeni syndrome | CHEK2 | 1 | Link | | Crouzon syndrome | FGFR2 | 1 | Link | | n/a | Bladder cancer | DAPK1 | 1 | Link | | Lung cancer | CDK2 | 3 | Link | | Scaphocephaly | FGFR2 | 1 | Link | | Jackson-Weiss syndrome | FGFR2 | 1 | Link | | n/a | Leishmaniasis | MAPK14 | 78 | Link | | n/a | Amyotrophic lateral sclerosis | MAPK14 | 78 | Link | | n/a | Short rib-polydactyly syndorme | NEK1 | 1 | Link | | n/a | Non-syndromic X-linked mental retardation | RPS6KA3 | 1 | Link | | Mental retardation | RPS6KA3 | 1 | Link | | n/a | Coffin-Lowry syndrome | RPS6KA3 | 1 | Link | | n/a | Epileptic encephalopathy | MAPK10 | 1 | Link | | n/a | Early infantile epileptic encephalopathy | MAPK10 | 1 | Link | | Pfeiffer syndrome | FGFR2 | 1 | Link | | LADD syndrome | FGFR2 | 1 | Link | | n/a | Saethre-Chotzen syndrome | FGFR2 | 1 | Link | | n/a | Scaphocephaly and Axenfeld-Rieger anomaly | FGFR2 | 1 | Link | | n/a | Viral myocarditis | FYN | 1 | Link | | n/a | Pathogenic Escherichia coli infection | FYN | 1 | Link | | n/a | Prion diseases | FYN | 1 | Link |
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