Allelic Variants

There are no related allelic variants
Related diseases of KIF 2XYNA_VX6 (PDB code: 2XYN, chain A)
Number of involved diseases in the family 105
Number of PKN1 related diseases 1
All kinase in this family  PKN1
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
n/aEpstein-Barr virus infectionCDC2, CDK2, FGR, JAK3, LYN,
MAPK14, RIPK1, SYK
19Link
LeukemiaABL1, ABL2, JAK2, KIT,
PDGFRB, TGFBR1
17Link
n/aMeaslesCDK2, FYN, IRAK4, JAK2,
JAK3, PRKCQ
34Link
Prostate cancerCDK2, EPHB2, FGFR1, FGFR2,
PDGFRA, PDGFRB
13Link
n/aTuberculosisIRAK4, JAK2, MAPK14, SRC,
SYK
27Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, LYN, MAPK14, SRC15Link
n/aLeishmaniasisIRAK4, JAK2, MAPK1416Link
n/aToxoplasmosisIRAK4, JAK2, MAPK1416Link
n/aInfluenza AIRAK4, JAK2, MAPK1416Link
n/aChagas diseaseIRAK4, MAPK14, TGFBR13Link
MelanomaFGFR1, PDGFRA, PDGFRB2Link
n/aHerpes simplex infectionCDC2, CDK2, JAK225Link
n/aSalmonella infectionMAPK14, PKN1, PKN24Link
Lung cancerALK, CDK2, ROS114Link
n/aViral myocarditisABL1, ABL2, FYN5Link
n/aShigellosisABL1, MAPK14, SRC17Link
n/aMyeloproliferative disorderJAK2, PDGFRB14Link
LADD syndromeFGFR2, FGFR32Link
n/aImmunodeficienciesJAK3, LCK9Link
n/aType I diabetes mellitusERBB3, PRKCQ10Link
Gastrointestinal stromal tumorKIT, PDGFRA3Link
n/aPathogenic Escherichia coli infectionABL1, FYN5Link
Crouzon syndromeFGFR2, FGFR32Link
n/aPertussisIRAK4, MAPK143Link
SCIDJAK3, LCK9Link
Colon cancerAURKA, SRC71Link
Jackson-Weiss syndromeFGFR1, FGFR22Link
n/aGliomaPDGFRA, PDGFRB2Link
n/aCardiomyopathyPRKAA1, PRKAA22Link
n/aHepatitis CMAPK14, RIPK14Link
Pfeiffer syndromeFGFR1, FGFR22Link
Kallmann syndromeFGFR12Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
Apert syndromeFGFR22Link
Gastric cancerFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
CraniosynostosisFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
TrigonocephalyFGFR12Link
Osteoglophonic dysplasiaFGFR12Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
n/aEpileptic encephalopathyCDKL51Link
Hypogonadotropic hypogonadismFGFR12Link
n/aAgammaglobulinemiasBTK2Link
n/aPituitary DwarfismBTK2Link
n/aChrondrodysplasiaBMPR1B1Link
BrachydactylyBMPR1B1Link
Fibrodysplasia ossificans progressivaACVR12Link
NeuroblastomaALK2Link
n/aMaturity onset diabetes of the youngBLK2Link
AgammaglobulinemiaBTK2Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK2Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R2Link
n/aLethal congenital contractural syndromeERBB31Link
n/aChoriocarcinomaCSF1R2Link
n/aAngelman syndrome-likeCDKL51Link
n/aCocaine addictionCDK51Link
n/aPrader-Willi and Angelman syndromesCDKL51Link
n/aEarly infantile epileptic encephalopathyCDKL51Link
n/aAchondroplasiaFGFR32Link
n/aSaethre-Chotzen syndromeFGFR22Link
n/aThyroid cancerRET3Link
n/aRenal agenesis and Renal adysplasiaRET3Link
Hirschsprung diseaseRET3Link
Diabetes mellitusPRKCD9Link
n/aHypereosinophilic syndromePDGFRA2Link
n/aGerm cell tumorsKIT3Link
Mast cell leukemiaKIT3Link
Mastocytosis with associated hematologic disorderKIT3Link
n/aAmyotrophic lateral sclerosisMAPK142Link
n/aCongenital central hypoventilation syndromeRET3Link
Central hypoventilation syndromeRET3Link
n/aRheumatoid arthritisTEK3Link
Loeys-Dietz syndromeTGFBR11Link
n/aFamilial thoracic aortic aneurysm and dissectionTGFBR11Link
Multiple self-healing squamous epitheliomaTGFBR11Link
Venous malformationsTEK3Link
n/aTransient erythroblastopenia of childhoodTEC1Link
n/aMedullary thyroid carcinomaRET3Link
Multiple endocrine neoplasiaRET3Link
PheochromocytomaRET3Link
Renal agenesisRET3Link
PiebaldismKIT3Link
ThrombocythemiaJAK214Link
n/aCervical cancerFGFR32Link
Colorectal cancerFGFR32Link
n/aHypochondroplasiaFGFR32Link
n/aCATSHL syndromeFGFR32Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR32Link
ScaphocephalyFGFR22Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
n/aMultiple myelomaFGFR32Link
n/aBladder cancerFGFR32Link
n/aMuenke syndromeFGFR32Link
n/aNevusFGFR32Link
Lymphoproliferative syndromeITK2Link
Polycythemia veraJAK214Link
n/aBudd-Chiari syndromeJAK214Link
MyelofibrosisJAK214Link
IRAK4 deficiencyIRAK41Link
n/aInvasive pneumococcal diseaseIRAK41Link
n/aSpermatocytic seminomaFGFR32Link
n/aThanatophoric dysplasiaFGFR32Link
n/aCancer progression/metastasisFGFR42Link
n/aPrion diseasesFYN2Link