Allelic Variants

There are no related allelic variants
Related diseases of KIF 2WKMA_PFY (PDB code: 2WKM, chain A)
Number of involved diseases in the family 98
Number of MET related diseases 8
All kinase in this family  MET
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
n/aMeaslesIRAK1, IRAK4, JAK1, JAK2,
JAK3, MAP3K7
6Link
n/aToxoplasmosisIRAK1, IRAK4, JAK1, JAK2,
MAP3K7
6Link
n/aLeishmaniasisIRAK1, IRAK4, JAK1, JAK2,
MAP3K7
6Link
n/aEpstein-Barr virus infectionIRAK1, JAK1, JAK3, MAP3K76Link
Lung cancerALK, EGFR, PTK2, ROS117Link
n/aTuberculosisIRAK1, IRAK4, JAK1, JAK26Link
Prostate cancerEGFR, FGFR1, FGFR217Link
MelanomaEGFR, FGFR1, MET22Link
n/aInfluenza AIRAK4, JAK1, JAK26Link
Gastric cancerEGFR, FGFR2, MET20Link
n/aHerpes simplex infectionJAK1, JAK2, MAP3K76Link
NeuroblastomaALK, NTRK2, NTRK37Link
n/aHepatitis CEGFR, JAK114Link
n/aChagas diseaseIRAK1, IRAK45Link
LADD syndromeFGFR2, FGFR35Link
HemangiomaFLT4, KDR21Link
Jackson-Weiss syndromeFGFR1, FGFR29Link
n/aPertussisIRAK1, IRAK45Link
Pfeiffer syndromeFGFR1, FGFR29Link
Crouzon syndromeFGFR2, FGFR35Link
n/aChoriocarcinomaCSF1R, EGFR17Link
n/aCervical cancerEGFR, FGFR316Link
n/aBladder cancerEGFR, FGFR316Link
LeukemiaABL1, JAK27Link
n/aEpithelial cell signaling in Helicobacter pylori infectionEGFR, MET19Link
Beare-Stevenson cutis gyrata syndromeFGFR24Link
Apert syndromeFGFR24Link
n/aMultiple myelomaFGFR35Link
n/aPathogenic Escherichia coli infectionABL16Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR35Link
Bent bone dysplasia syndromeFGFR24Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR24Link
ScaphocephalyFGFR24Link
n/aSaethre-Chotzen syndromeFGFR24Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR24Link
CraniosynostosisFGFR24Link
n/aAgammaglobulinemiasBTK1Link
n/aShigellosisABL16Link
AgammaglobulinemiaBTK1Link
Adenocarcinoma of lungEGFR13Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK1Link
n/aLaryngeal cancerEGFR13Link
n/aOral cancerEGFR13Link
n/aEsophageal cancerEGFR13Link
n/aGliomaEGFR13Link
Hypogonadotropic hypogonadismFGFR18Link
Osteoglophonic dysplasiaFGFR18Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R6Link
n/aViral myocarditisABL16Link
n/aPituitary DwarfismBTK1Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR24Link
TrigonocephalyFGFR18Link
n/aCATSHL syndromeFGFR35Link
Kallmann syndromeFGFR18Link
n/aNevusFGFR35Link
n/aAchondroplasiaFGFR35Link
n/aMyasthenic syndromeMUSK2Link
n/aAlcoholismNTRK26Link
n/aObesityNTRK26Link
n/aCongenital myasthenic syndromeMUSK2Link
Hepatocellular carcinomaMET8Link
Renal cell carcinomaMET8Link
n/aCholangiocarcinomaMET8Link
n/aMalariaMET8Link
n/aAutism suseptibilityMET8Link
n/aAmoebiasisPTK25Link
n/aThyroid cancerRET7Link
PheochromocytomaRET7Link
Renal agenesisRET7Link
n/aPopliteal pterygium syndromeRIPK42Link
Multiple endocrine neoplasiaRET7Link
n/aMedullary thyroid carcinomaRET7Link
n/aRenal agenesis and Renal adysplasiaRET7Link
Hirschsprung diseaseRET7Link
n/aCongenital central hypoventilation syndromeRET7Link
Central hypoventilation syndromeRET7Link
SCIDJAK35Link
n/aImmunodeficienciesJAK35Link
n/aLymphedemasFLT45Link
n/aLymphedemaFLT45Link
n/aLeprechaunismINSR4Link
n/aCancer progression/metastasisFGFR41Link
n/aThanatophoric dysplasiaFGFR35Link
Colorectal cancerFGFR35Link
n/aHypochondroplasiaFGFR35Link
n/aMuenke syndromeFGFR35Link
n/aSpermatocytic seminomaFGFR35Link
Rabson-Mendenhall syndromeINSR4Link
Diabetes mellitusINSR4Link
MyelofibrosisJAK24Link
n/aMyeloproliferative disorderJAK24Link
ThrombocythemiaJAK24Link
n/aBudd-Chiari syndromeJAK24Link
Polycythemia veraJAK24Link
Hyperinsulinemic hypoglycemiaINSR4Link
n/aInvasive pneumococcal diseaseIRAK44Link
IRAK4 deficiencyIRAK44Link
Lymphoproliferative syndromeITK4Link