Allelic Variants

There are no related allelic variants
Related diseases of KIF 2GQGA_1N1 (PDB code: 2GQG, chain A)
Number of involved diseases in the family 117
Number of MAP4K3 related diseases 0
All kinase in this family  MAP4K3
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Prostate cancerBRAF, EGFR, EPHB2, ERBB2,
FGFR1, FGFR2, MAP2K1,
PDGFRA, PDGFRB
5Link
LeukemiaABL1, ABL2, BRAF, JAK2, KIT,
MAP2K1, PDGFRB, TGFBR1
7Link
n/aEpstein-Barr virus infectionFGR, JAK3, LYN, MAP3K7,
MAPK14, SYK, TYK2
7Link
MelanomaBRAF, EGFR, FGFR1, MAP2K1,
PDGFRA, PDGFRB
4Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, LYN, MAPK14, SRC10Link
n/aMeaslesFYN, JAK2, JAK3, MAP3K7,
TYK2
5Link
n/aTuberculosisJAK2, MAPK14, RIPK2, SRC,
SYK
10Link
n/aShigellosisABL1, MAPK14, RIPK2, SRC10Link
n/aToxoplasmosisJAK2, MAP3K7, MAPK14, TYK24Link
n/aInfluenza AJAK2, MAP2K1, MAPK14, TYK24Link
n/aHepatitis CBRAF, EGFR, MAPK14, TYK24Link
Adenocarcinoma of lungBRAF, EGFR, ERBB24Link
n/aHerpes simplex infectionJAK2, MAP3K7, TYK22Link
Gastric cancerEGFR, ERBB2, FGFR24Link
n/aGliomaEGFR, PDGFRA, PDGFRB4Link
n/aLeishmaniasisJAK2, MAP3K7, MAPK144Link
n/aBladder cancerEGFR, ERBB2, FGFR34Link
n/aCervical cancerEGFR, ERBB2, FGFR34Link
n/aViral myocarditisABL1, ABL2, FYN9Link
n/aChoriocarcinomaCSF1R, EGFR, ERBB25Link
Crouzon syndromeFGFR2, FGFR32Link
n/aPathogenic Escherichia coli infectionABL1, FYN9Link
Jackson-Weiss syndromeFGFR1, FGFR22Link
n/aImmunodeficienciesJAK3, LCK29Link
n/aPrion diseasesFYN, MAP2K15Link
LADD syndromeFGFR2, FGFR32Link
n/aMyeloproliferative disorderJAK2, PDGFRB4Link
Colon cancerAURKA, SRC9Link
n/aChagas diseaseMAPK14, TGFBR14Link
n/aAlcoholismBRAF, MAP2K12Link
SCIDJAK3, LCK29Link
Pfeiffer syndromeFGFR1, FGFR22Link
n/aThyroid cancerBRAF, RET3Link
n/aNoonan syndrome and related disordersBRAF, MAP2K12Link
Gastrointestinal stromal tumorKIT, PDGFRA4Link
n/aPancreatic cancerACVR1B, ERBB23Link
Lung cancerBRAF, EGFR3Link
Colorectal cancerBRAF, FGFR32Link
Cardiofaciocutaneous syndromeBRAF, MAP2K12Link
Endometrial CancerERBB23Link
n/aLaryngeal cancerEGFR3Link
Osteoglophonic dysplasiaFGFR12Link
TrigonocephalyFGFR12Link
GlioblastomaERBB23Link
Hypogonadotropic hypogonadismFGFR12Link
n/aLethal congenital contractural syndromeERBB31Link
n/aCholangiocarcinomaERBB23Link
n/aType I diabetes mellitusERBB31Link
Breast cancerERBB23Link
Ovarian cancerERBB23Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK5Link
n/aEsophageal cancerEGFR3Link
n/aMalignant melanomaBRAF2Link
LEOPARD syndromeBRAF2Link
n/aChrondrodysplasiaBMPR1B1Link
BrachydactylyBMPR1B1Link
n/aJuvenile polyposis syndromeBMPR1A1Link
n/aPolyposisBMPR1A1Link
Noonan syndromeBRAF2Link
n/aAgammaglobulinemiasBTK5Link
n/aSpondylometaepiphyseal dysplasiaDDR24Link
n/aOral cancerEGFR3Link
Fibrodysplasia ossificans progressivaACVR12Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R4Link
n/aPituitary DwarfismBTK5Link
AgammaglobulinemiaBTK5Link
n/aMaturity onset diabetes of the youngBLK5Link
CraniosynostosisFGFR22Link
Kallmann syndromeFGFR12Link
n/aSalmonella infectionMAPK144Link
n/aPertussisMAPK144Link
n/aHypereosinophilic syndromePDGFRA4Link
n/aRenal agenesis and Renal adysplasiaRET3Link
n/aAmyotrophic lateral sclerosisMAPK144Link
Mastocytosis with associated hematologic disorderKIT4Link
HemangiomaKDR2Link
PiebaldismKIT4Link
n/aGerm cell tumorsKIT4Link
Mast cell leukemiaKIT4Link
Hirschsprung diseaseRET3Link
n/aCongenital central hypoventilation syndromeRET3Link
Loeys-Dietz syndromeTGFBR12Link
n/aFamilial thoracic aortic aneurysm and dissectionTGFBR12Link
Multiple self-healing squamous epitheliomaTGFBR12Link
n/aTyrosine kinase 2 deficiencyTYK21Link
n/aTransient erythroblastopenia of childhoodTEC3Link
n/aBasal cell carcinomaSTK362Link
Central hypoventilation syndromeRET3Link
n/aMedullary thyroid carcinomaRET3Link
Multiple endocrine neoplasiaRET3Link
Renal agenesisRET3Link
PheochromocytomaRET3Link
ThrombocythemiaJAK22Link
MyelofibrosisJAK22Link
ScaphocephalyFGFR22Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
n/aMultiple myelomaFGFR31Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR31Link
n/aSaethre-Chotzen syndromeFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
Apert syndromeFGFR22Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
n/aCATSHL syndromeFGFR31Link
n/aAchondroplasiaFGFR31Link
Diabetes mellitusINSR1Link
Hyperinsulinemic hypoglycemiaINSR1Link
Polycythemia veraJAK22Link
n/aBudd-Chiari syndromeJAK22Link
Rabson-Mendenhall syndromeINSR1Link
n/aLeprechaunismINSR1Link
n/aHypochondroplasiaFGFR31Link
n/aMuenke syndromeFGFR31Link
n/aNevusFGFR31Link
n/aThanatophoric dysplasiaFGFR31Link
n/aSpermatocytic seminomaFGFR31Link