Allelic Variants

There are no related allelic variants
Related diseases of KIF 2JEDA_LG8 (PDB code: 2JED, chain A)
Number of involved diseases in the family 87
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, CSNK2A2, FGR,
GSK3B, JAK3, MAPK10, MAPK8
12Link
n/aMeaslesCDK2, CSNK2A2, FYN, GSK3B,
JAK2, JAK3, PRKCQ
6Link
n/aHerpes simplex infectionCDC2, CDK2, CSNK2A2, JAK2,
MAPK10, MAPK8
10Link
n/aTuberculosisCAMK2A, JAK2, MAPK10, MAPK8,
SRC
3Link
n/aInfluenza AGSK3B, JAK2, MAPK10, MAPK8,
PRKCB
4Link
Prostate cancerCDK2, FGFR2, GSK3B, PDPK14Link
n/aSalmonella infectionMAPK10, MAPK8, PKN1, PKN21Link
Diabetes mellitusMAPK10, MAPK8, PRKCD, PRKCE2Link
n/aShigellosisABL1, MAPK10, MAPK8, SRC3Link
NeuroblastomaNTRK1, NTRK2, NTRK32Link
n/aHepatitis CGSK3B, MAPK10, MAPK83Link
LeukemiaABL1, ABL2, JAK21Link
n/aToxoplasmosisJAK2, MAPK10, MAPK81Link
n/aEpithelial cell signaling in Helicobacter pylori infectionMAPK10, MAPK8, SRC3Link
n/aViral myocarditisABL1, ABL2, FYN1Link
n/aAlcoholismCAMKK1, CAMKK2, NTRK21Link
n/aLeishmaniasisJAK2, PRKCB2Link
n/aThyroid cancerNTRK1, RET3Link
n/aPertussisMAPK10, MAPK81Link
LADD syndromeFGFR2, FGFR31Link
n/aImmunodeficienciesJAK3, ZAP701Link
Crouzon syndromeFGFR2, FGFR31Link
n/aChagas diseaseMAPK10, MAPK81Link
n/aPathogenic Escherichia coli infectionABL1, FYN1Link
n/aMedullary thyroid carcinomaNTRK1, RET3Link
n/aAchondroplasiaFGFR31Link
ScaphocephalyFGFR21Link
n/aCervical cancerFGFR31Link
Colorectal cancerFGFR31Link
n/aHypochondroplasiaFGFR31Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
n/aMultiple myelomaFGFR31Link
n/aBladder cancerFGFR31Link
n/aMaturity onset diabetes of the youngBLK1Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR31Link
n/aCATSHL syndromeFGFR31Link
Jackson-Weiss syndromeFGFR21Link
n/aSaethre-Chotzen syndromeFGFR21Link
Apert syndromeFGFR21Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
Gastric cancerFGFR21Link
Venous malformationsTEK1Link
Lung cancerCDK22Link
Bent bone dysplasia syndromeFGFR21Link
n/aRheumatoid arthritisTEK1Link
Colon cancerSRC3Link
Pfeiffer syndromeFGFR21Link
CraniosynostosisFGFR21Link
Selective T-cell defectZAP701Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
n/aMuenke syndromeFGFR31Link
n/aCongenital stationary night blindnessGRK11Link
n/aNevusFGFR31Link
n/aVibrio cholerae infectionPRKCB1Link
n/aAfrican trypanosomiasisPRKCB1Link
Glycogen storage diseasePHKG21Link
n/aCirrhosis due to liver phosphorylase kinase deficiencyPHKG21Link
n/aObesityNTRK21Link
n/aGlycogen storage diseasesPHKG21Link
n/aAmoebiasisPRKCB1Link
n/aCerebral infarctionPRKCH1Link
Multiple endocrine neoplasiaRET3Link
PheochromocytomaRET3Link
Central hypoventilation syndromeRET3Link
n/aCongenital central hypoventilation syndromeRET3Link
n/aType I diabetes mellitusPRKCQ3Link
n/aRenal agenesis and Renal adysplasiaRET3Link
Hirschsprung diseaseRET3Link
n/aInsensitivity to painNTRK11Link
n/aEpileptic encephalopathyMAPK101Link
n/aOguchi diseaseGRK11Link
n/aBasal cell carcinomaGSK3B3Link
Renal agenesisRET3Link
n/aPrion diseasesFYN1Link
n/aSpermatocytic seminomaFGFR31Link
n/aThanatophoric dysplasiaFGFR31Link
n/aCancer progression/metastasisFGFR41Link
n/aEndocrine-cerebroosteodysplasiaICK1Link
Lymphoproliferative syndromeITK1Link
SCIDJAK31Link
n/aEarly infantile epileptic encephalopathyMAPK101Link
ThrombocythemiaJAK21Link
n/aMyeloproliferative disorderJAK21Link
Polycythemia veraJAK21Link
n/aBudd-Chiari syndromeJAK21Link
MyelofibrosisJAK21Link