Allelic Variants

There are no related allelic variants
Related diseases of KIF 2X2MA_X2M (PDB code: 2X2M, chain A)
Number of involved diseases in the family 59
Number of RET related diseases 9
All kinase in this family  RET
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
n/aTuberculosisIRAK4, JAK2, RAF1, SRC12Link
n/aMeaslesIRAK4, JAK2, JAK3, TYK212Link
LeukemiaJAK2, KIT, PDGFRB, RAF121Link
n/aInfluenza AIRAK4, JAK2, RAF1, TYK24Link
Prostate cancerFGFR1, PDGFRB, PDPK1, RAF146Link
NeuroblastomaALK, NTRK1, NTRK2, NTRK314Link
MelanomaFGFR1, PDGFRB, RAF119Link
n/aToxoplasmosisIRAK4, JAK2, TYK23Link
Lung cancerALK, PTK211Link
n/aThyroid cancerNTRK1, RET21Link
n/aMedullary thyroid carcinomaNTRK1, RET21Link
n/aMyeloproliferative disorderJAK2, PDGFRB18Link
n/aLeishmaniasisIRAK4, JAK22Link
n/aAlcoholismNTRK2, RAF14Link
n/aHerpes simplex infectionJAK2, TYK22Link
n/aEpstein-Barr virus infectionJAK3, TYK211Link
n/aHepatitis CRAF1, TYK22Link
n/aPertussisIRAK41Link
n/aChagas diseaseIRAK41Link
Pfeiffer syndromeFGFR114Link
n/aEpithelial cell signaling in Helicobacter pylori infectionSRC9Link
Renal agenesisRET19Link
PheochromocytomaRET19Link
n/aInvasive pneumococcal diseaseIRAK41Link
Central hypoventilation syndromeRET19Link
Multiple endocrine neoplasiaRET19Link
Kallmann syndromeFGFR114Link
IRAK4 deficiencyIRAK41Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R4Link
n/aChoriocarcinomaCSF1R4Link
n/aTyrosine kinase 2 deficiencyTYK21Link
Hypogonadotropic hypogonadismFGFR114Link
Osteoglophonic dysplasiaFGFR114Link
Jackson-Weiss syndromeFGFR114Link
n/aShigellosisSRC9Link
Colon cancerSRC9Link
TrigonocephalyFGFR114Link
Polycythemia veraJAK21Link
n/aGliomaPDGFRB17Link
Mastocytosis with associated hematologic disorderKIT3Link
Mast cell leukemiaKIT3Link
n/aGerm cell tumorsKIT3Link
n/aLewy body dementiaLRRK23Link
n/aParkinson diseaseLRRK23Link
n/aObesityNTRK23Link
n/aAmoebiasisPTK21Link
n/aInsensitivity to painNTRK13Link
LEOPARD syndromeRAF11Link
Gastrointestinal stromal tumorKIT3Link
PiebaldismKIT3Link
Hirschsprung diseaseRET19Link
n/aBudd-Chiari syndromeJAK21Link
n/aCongenital central hypoventilation syndromeRET19Link
MyelofibrosisJAK21Link
n/aRenal agenesis and Renal adysplasiaRET19Link
SCIDJAK311Link
Noonan syndromeRAF11Link
n/aImmunodeficienciesJAK311Link
ThrombocythemiaJAK21Link