Allelic Variants
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There are no related allelic variants
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Number of involved diseases in the family |
58 |
Number of BLK related diseases |
1 |
All kinase in this family
BLK
Allelic Variants |
Disease Description |
Involved kinases (This family) |
Inhibitor of Involved Kinases |
Search Disease |
| Leukemia | ABL1, ABL2, BRAF, KIT, PDGFRB, RAF1 | 5 | Link | | Prostate cancer | BRAF, FGFR1, FGFR2, PDGFRB, RAF1 | 5 | Link | | Melanoma | BRAF, FGFR1, PDGFRB, RAF1 | 5 | Link | n/a | Hepatitis C | BRAF, RAF1, RIPK1 | 5 | Link | n/a | Epithelial cell signaling in Helicobacter pylori infection | CSK, LYN, SRC | 2 | Link | n/a | Epstein-Barr virus infection | FGR, LYN, RIPK1 | 1 | Link | n/a | Viral myocarditis | ABL1, ABL2, FYN | 1 | Link | | Noonan syndrome | BRAF, RAF1 | 5 | Link | n/a | Pathogenic Escherichia coli infection | ABL1, FYN | 1 | Link | | Jackson-Weiss syndrome | FGFR1, FGFR2 | 2 | Link | n/a | Shigellosis | ABL1, SRC | 2 | Link | | LEOPARD syndrome | BRAF, RAF1 | 5 | Link | n/a | Tuberculosis | RAF1, SRC | 2 | Link | | Colon cancer | AURKA, SRC | 2 | Link | | Pfeiffer syndrome | FGFR1, FGFR2 | 2 | Link | n/a | Alcoholism | BRAF, RAF1 | 5 | Link | n/a | Choriocarcinoma | CSF1R | 2 | Link | n/a | Leukoencephalopathy, diffuse hereditary, with spheroids | CSF1R | 2 | Link | | Trigonocephaly | FGFR1 | 2 | Link | | Hypogonadotropic hypogonadism | FGFR1 | 2 | Link | | Osteoglophonic dysplasia | FGFR1 | 2 | Link | | Colorectal cancer | BRAF | 5 | Link | | Lung cancer | BRAF | 5 | Link | n/a | Thyroid cancer | BRAF | 5 | Link | n/a | Chrondrodysplasia | BMPR1B | 1 | Link | | Brachydactyly | BMPR1B | 1 | Link | n/a | Malignant melanoma | BRAF | 5 | Link | n/a | Noonan syndrome and related disorders | BRAF | 5 | Link | n/a | Maturity onset diabetes of the young | BLK | 1 | Link | | Cardiofaciocutaneous syndrome | BRAF | 5 | Link | | Adenocarcinoma of lung | BRAF | 5 | Link | | Kallmann syndrome | FGFR1 | 2 | Link | | Gastric cancer | FGFR2 | 1 | Link | | Mast cell leukemia | KIT | 1 | Link | n/a | Germ cell tumors | KIT | 1 | Link | | Gastrointestinal stromal tumor | KIT | 1 | Link | | Piebaldism | KIT | 1 | Link | | Mastocytosis with associated hematologic disorder | KIT | 1 | Link | n/a | Immunodeficiencies | LCK | 1 | Link | n/a | Basal cell carcinoma | STK36 | 1 | Link | n/a | Influenza A | RAF1 | 1 | Link | n/a | Myeloproliferative disorder | PDGFRB | 1 | Link | | SCID | LCK | 1 | Link | n/a | Glioma | PDGFRB | 1 | Link | | Hemangioma | KDR | 2 | Link | n/a | Measles | FYN | 1 | Link | | Craniofacial-skeletal-dermatologic dysplasia | FGFR2 | 1 | Link | | Bent bone dysplasia syndrome | FGFR2 | 1 | Link | | Beare-Stevenson cutis gyrata syndrome | FGFR2 | 1 | Link | n/a | Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | FGFR2 | 1 | Link | | Apert syndrome | FGFR2 | 1 | Link | | Craniosynostosis | FGFR2 | 1 | Link | | Crouzon syndrome | FGFR2 | 1 | Link | n/a | Prion diseases | FYN | 1 | Link | n/a | Scaphocephaly and Axenfeld-Rieger anomaly | FGFR2 | 1 | Link | | Scaphocephaly | FGFR2 | 1 | Link | | LADD syndrome | FGFR2 | 1 | Link | n/a | Saethre-Chotzen syndrome | FGFR2 | 1 | Link |
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