Allelic Variants

There are no related allelic variants
Related diseases of KIF 3FQSA_585 (PDB code: 3FQS, chain A)
Number of involved diseases in the family 102
Number of FRK related diseases 0
All kinase in this family  FRK
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Prostate cancerBRAF, EGFR, EPHB2, FGFR1,
FGFR2, PDGFRA, PDGFRB
2Link
n/aEpstein-Barr virus infectionFGR, JAK1, JAK3, LYN, SYK,
TYK2
3Link
LeukemiaABL1, ABL2, BRAF, JAK2, KIT,
PDGFRB
1Link
Lung cancerALK, BRAF, EGFR, PTK2, ROS120Link
MelanomaBRAF, EGFR, FGFR1, PDGFRA,
PDGFRB
2Link
n/aMeaslesFYN, JAK1, JAK2, JAK3, TYK21Link
n/aTuberculosisJAK1, JAK2, SRC, SYK3Link
n/aHepatitis CBRAF, EGFR, JAK1, TYK22Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, LYN, SRC2Link
n/aGliomaEGFR, PDGFRA, PDGFRB2Link
n/aViral myocarditisABL1, ABL2, FYN1Link
n/aToxoplasmosisJAK1, JAK2, TYK21Link
NeuroblastomaALK, NTRK2, NTRK33Link
n/aInfluenza AJAK1, JAK2, TYK21Link
n/aImmunodeficienciesJAK3, LCK, ZAP701Link
n/aHerpes simplex infectionJAK1, JAK2, TYK21Link
Crouzon syndromeFGFR2, FGFR31Link
Gastric cancerEGFR, FGFR22Link
n/aBladder cancerEGFR, FGFR32Link
n/aChoriocarcinomaCSF1R, EGFR2Link
n/aPathogenic Escherichia coli infectionABL1, FYN1Link
LADD syndromeFGFR2, FGFR31Link
Pfeiffer syndromeFGFR1, FGFR21Link
Jackson-Weiss syndromeFGFR1, FGFR21Link
n/aCervical cancerEGFR, FGFR32Link
n/aShigellosisABL1, SRC1Link
n/aLeishmaniasisJAK1, JAK21Link
Adenocarcinoma of lungBRAF, EGFR2Link
n/aThyroid cancerBRAF, RET1Link
Colorectal cancerBRAF, FGFR31Link
Gastrointestinal stromal tumorKIT, PDGFRA1Link
SCIDJAK3, LCK1Link
n/aAlcoholismBRAF, NTRK21Link
n/aMyeloproliferative disorderJAK2, PDGFRB1Link
Kallmann syndromeFGFR11Link
TrigonocephalyFGFR11Link
n/aMaturity onset diabetes of the youngBLK1Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
Osteoglophonic dysplasiaFGFR11Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
Bent bone dysplasia syndromeFGFR21Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
Apert syndromeFGFR21Link
n/aMalignant melanomaBRAF1Link
n/aLaryngeal cancerEGFR2Link
Hypogonadotropic hypogonadismFGFR11Link
n/aPituitary DwarfismBTK2Link
AgammaglobulinemiaBTK2Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK2Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R1Link
n/aNoonan syndrome and related disordersBRAF1Link
n/aOral cancerEGFR2Link
Cardiofaciocutaneous syndromeBRAF1Link
LEOPARD syndromeBRAF1Link
Noonan syndromeBRAF1Link
n/aEsophageal cancerEGFR2Link
n/aAgammaglobulinemiasBTK2Link
n/aMultiple myelomaFGFR31Link
CraniosynostosisFGFR21Link
n/aHypereosinophilic syndromePDGFRA1Link
n/aAmoebiasisPTK217Link
n/aRenal agenesis and Renal adysplasiaRET1Link
n/aObesityNTRK21Link
n/aMyasthenic syndromeMUSK1Link
n/aGerm cell tumorsKIT1Link
Mast cell leukemiaKIT1Link
Mastocytosis with associated hematologic disorderKIT1Link
n/aCongenital myasthenic syndromeMUSK1Link
Hirschsprung diseaseRET1Link
n/aCongenital central hypoventilation syndromeRET1Link
n/aTransient erythroblastopenia of childhoodTEC1Link
n/aTyrosine kinase 2 deficiencyTYK21Link
Selective T-cell defectZAP701Link
Colon cancerSRC1Link
Renal agenesisRET1Link
Central hypoventilation syndromeRET1Link
n/aMedullary thyroid carcinomaRET1Link
Multiple endocrine neoplasiaRET1Link
PheochromocytomaRET1Link
PiebaldismKIT1Link
ThrombocythemiaJAK21Link
n/aHypochondroplasiaFGFR31Link
n/aMuenke syndromeFGFR31Link
n/aNevusFGFR31Link
n/aAchondroplasiaFGFR31Link
n/aCATSHL syndromeFGFR31Link
n/aSaethre-Chotzen syndromeFGFR21Link
ScaphocephalyFGFR21Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR31Link
n/aSpermatocytic seminomaFGFR31Link
n/aThanatophoric dysplasiaFGFR31Link
Lymphoproliferative syndromeITK1Link
Polycythemia veraJAK21Link
n/aBudd-Chiari syndromeJAK21Link
MyelofibrosisJAK21Link
Hyperinsulinemic hypoglycemiaINSR8Link
Diabetes mellitusINSR8Link
n/aCancer progression/metastasisFGFR41Link
n/aPrion diseasesFYN1Link
n/aLeprechaunismINSR8Link
Rabson-Mendenhall syndromeINSR8Link