Allelic Variants

There are no related allelic variants
Related diseases of KIF 3PJ1A_LHL (PDB code: 3PJ1, chain A)
Number of involved diseases in the family 96
Number of BTK related diseases 4
All kinase in this family  BTK
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Prostate cancerEGFR, FGFR2, IGF1R, PDGFRA,
PDGFRB
44Link
MelanomaEGFR, IGF1R, MET, PDGFRA,
PDGFRB
50Link
LeukemiaABL1, JAK2, KIT, PDGFRB40Link
n/aEpithelial cell signaling in Helicobacter pylori infectionEGFR, LYN, MET, SRC51Link
Gastric cancerEGFR, FGFR2, MET13Link
n/aEpstein-Barr virus infectionLYN, SYK, TYK22Link
n/aMeaslesFYN, JAK2, TYK21Link
n/aGliomaEGFR, PDGFRA, PDGFRB32Link
n/aTuberculosisJAK2, SRC, SYK45Link
Lung cancerALK, EGFR, ROS16Link
Crouzon syndromeFGFR2, FGFR36Link
Gastrointestinal stromal tumorKIT, PDGFRA7Link
n/aMyeloproliferative disorderJAK2, PDGFRB32Link
n/aToxoplasmosisJAK2, TYK21Link
n/aInfluenza AJAK2, TYK21Link
n/aHerpes simplex infectionJAK2, TYK21Link
LADD syndromeFGFR2, FGFR36Link
n/aHepatitis CEGFR, TYK26Link
n/aShigellosisABL1, SRC46Link
n/aViral myocarditisABL1, FYN6Link
HemangiomaFLT4, KDR9Link
NeuroblastomaALK, NTRK21Link
n/aPathogenic Escherichia coli infectionABL1, FYN6Link
n/aCervical cancerEGFR, FGFR39Link
n/aBladder cancerEGFR, FGFR39Link
Colorectal cancerFGFR35Link
n/aHypochondroplasiaFGFR35Link
Jackson-Weiss syndromeFGFR22Link
Pfeiffer syndromeFGFR22Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR35Link
n/aAchondroplasiaFGFR35Link
n/aCATSHL syndromeFGFR35Link
n/aMultiple myelomaFGFR35Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
n/aSaethre-Chotzen syndromeFGFR22Link
ScaphocephalyFGFR22Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
CraniosynostosisFGFR22Link
n/aOral cancerEGFR5Link
n/aEsophageal cancerEGFR5Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK2Link
AgammaglobulinemiaBTK2Link
n/aAgammaglobulinemiasBTK2Link
n/aPituitary DwarfismBTK2Link
n/aChoriocarcinomaEGFR5Link
n/aLaryngeal cancerEGFR5Link
Bent bone dysplasia syndromeFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
n/aMuenke syndromeFGFR35Link
Apert syndromeFGFR22Link
Adenocarcinoma of lungEGFR5Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
n/aLymphedemasFLT41Link
n/aNevusFGFR35Link
n/aAlcoholismNTRK21Link
n/aObesityNTRK21Link
n/aHypereosinophilic syndromePDGFRA1Link
Hepatocellular carcinomaMET7Link
n/aAutism suseptibilityMET7Link
SCIDLCK36Link
Renal cell carcinomaMET7Link
n/aCholangiocarcinomaMET7Link
n/aMalariaMET7Link
n/aThyroid cancerRET2Link
n/aRenal agenesis and Renal adysplasiaRET2Link
Renal agenesisRET2Link
Colon cancerSRC45Link
n/aTyrosine kinase 2 deficiencyTYK21Link
PheochromocytomaRET2Link
Multiple endocrine neoplasiaRET2Link
Hirschsprung diseaseRET2Link
n/aCongenital central hypoventilation syndromeRET2Link
Central hypoventilation syndromeRET2Link
n/aMedullary thyroid carcinomaRET2Link
n/aImmunodeficienciesLCK36Link
Mastocytosis with associated hematologic disorderKIT7Link
n/aSynovial sarcomaIGF1R12Link
Insulin-like growth factor IIGF1R12Link
n/aLeprechaunismINSR5Link
n/aMalignant pleural mesotheliomaIGF1R12Link
n/aPrion diseasesFYN1Link
n/aSpermatocytic seminomaFGFR35Link
n/aThanatophoric dysplasiaFGFR35Link
n/aCancer progression/metastasisFGFR41Link
n/aLymphedemaFLT41Link
Rabson-Mendenhall syndromeINSR5Link
Diabetes mellitusINSR5Link
PiebaldismKIT7Link
n/aGerm cell tumorsKIT7Link
Mast cell leukemiaKIT7Link
ThrombocythemiaJAK21Link
MyelofibrosisJAK21Link
Hyperinsulinemic hypoglycemiaINSR5Link
Polycythemia veraJAK21Link
n/aLeishmaniasisJAK21Link
n/aBudd-Chiari syndromeJAK21Link