Allelic Variants

There are no related allelic variants
Related diseases of KIF 1BYGA_STU (PDB code: 1BYG, chain A)
Number of involved diseases in the family 123
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
Prostate cancerAKT2, AKT3, EGFR, EPHB2,
ERBB2, FGFR1, FGFR2, IGF1R,
INSRR, MAPK1, PDGFRA,
PDGFRB, RAF1
42Link
LeukemiaABL1, ABL2, AKT2, AKT3,
JAK2, KIT, MAPK1, PDGFRB,
RAF1, RPS6KB1, RPS6KB2,
TGFBR1
16Link
MelanomaAKT2, AKT3, EGFR, FGFR1,
IGF1R, MAPK1, PDGFRA,
PDGFRB, RAF1
42Link
n/aInfluenza AAKT2, AKT3, IRAK4, JAK2,
MAPK1, PRKCA, PRKCB, RAF1
60Link
n/aTuberculosisAKT2, AKT3, IRAK4, JAK2,
MAPK1, RAF1, SRC, SYK
21Link
n/aMeaslesAKT2, AKT3, FYN, IRAK4,
JAK2, JAK3, PRKCQ
16Link
Lung cancerAKT2, AKT3, ALK, EGFR, PTK2,
ROS1
40Link
n/aHepatitis CAKT2, AKT3, EGFR, MAPK1,
RAF1
39Link
n/aEpstein-Barr virus infectionAKT2, AKT3, FGR, JAK3, SYK16Link
Diabetes mellitusAKT2, MAPK1, PRKCD, PRKCE,
PRKCZ
15Link
n/aToxoplasmosisAKT2, AKT3, IRAK4, JAK2,
MAPK1
12Link
n/aChagas diseaseAKT2, AKT3, IRAK4, MAPK1,
TGFBR1
9Link
n/aLeishmaniasisIRAK4, JAK2, MAPK1, PRKCB16Link
Gastric cancerEGFR, ERBB2, FGFR239Link
n/aGliomaEGFR, PDGFRA, PDGFRB41Link
n/aSalmonella infectionMAPK1, PKN1, PKN213Link
n/aAlcoholismCAMKK2, MAPK1, RAF112Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, SRC41Link
n/aAmoebiasisPRKCA, PRKCB, PTK257Link
n/aViral myocarditisABL1, ABL2, FYN13Link
n/aPathogenic Escherichia coli infectionABL1, FYN, PRKCA61Link
n/aBladder cancerEGFR, ERBB2, FGFR338Link
n/aImmunodeficienciesJAK3, LCK, ZAP7016Link
n/aShigellosisABL1, MAPK1, SRC20Link
n/aCervical cancerEGFR, ERBB2, FGFR338Link
n/aMyeloproliferative disorderJAK2, PDGFRB12Link
Adenocarcinoma of lungEGFR, ERBB238Link
n/aPertussisIRAK4, MAPK16Link
n/aPrion diseasesFYN, MAPK111Link
n/aChoriocarcinomaEGFR, ERBB238Link
SCIDJAK3, LCK16Link
Crouzon syndromeFGFR2, FGFR38Link
n/aThyroid cancerNTRK1, RET18Link
n/aVibrio cholerae infectionPRKCA, PRKCB55Link
NeuroblastomaALK, NTRK116Link
n/aAfrican trypanosomiasisPRKCA, PRKCB55Link
Pfeiffer syndromeFGFR1, FGFR29Link
n/aPancreatic cancerACVR1B, ERBB23Link
Ovarian cancerAKT2, ERBB27Link
n/aMedullary thyroid carcinomaNTRK1, RET18Link
Jackson-Weiss syndromeFGFR1, FGFR29Link
Gastrointestinal stromal tumorKIT, PDGFRA12Link
LADD syndromeFGFR2, FGFR38Link
TrigonocephalyFGFR19Link
Breast cancerERBB22Link
GlioblastomaERBB22Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR28Link
Osteoglophonic dysplasiaFGFR19Link
n/aCholangiocarcinomaERBB22Link
Kallmann syndromeFGFR19Link
Endometrial CancerERBB22Link
Hypogonadotropic hypogonadismFGFR19Link
n/aAgammaglobulinemiasBTK5Link
n/aLaryngeal cancerEGFR38Link
n/aJuvenile polyposis syndromeBMPR1A2Link
n/aPolyposisBMPR1A2Link
n/aMaturity onset diabetes of the youngBLK8Link
Hypoinsulinemic hypoglycemiaAKT27Link
Fibrodysplasia ossificans progressivaACVR13Link
n/aFamilial partial lipodystrophyAKT27Link
BrachydactylyBMPR1B1Link
n/aChrondrodysplasiaBMPR1B1Link
n/aOral cancerEGFR38Link
n/aEsophageal cancerEGFR38Link
n/aSpondylometaepiphyseal dysplasiaDDR23Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK5Link
Apert syndromeFGFR28Link
n/aPituitary DwarfismBTK5Link
AgammaglobulinemiaBTK5Link
ScaphocephalyFGFR28Link
Beare-Stevenson cutis gyrata syndromeFGFR28Link
n/aPituitary tumorPRKCA55Link
n/aCerebral infarctionPRKCH12Link
n/aType I diabetes mellitusPRKCQ8Link
LEOPARD syndromeRAF12Link
n/aHypereosinophilic syndromePDGFRA10Link
n/aInsensitivity to painNTRK115Link
PiebaldismKIT12Link
n/aGerm cell tumorsKIT12Link
Mast cell leukemiaKIT12Link
REtinitis pigmentosaMAK1Link
Mastocytosis with associated hematologic disorderKIT12Link
Noonan syndromeRAF12Link
n/aRenal agenesis and Renal adysplasiaRET11Link
n/aBasal cell carcinomaSTK363Link
Loeys-Dietz syndromeTGFBR12Link
n/aFamilial thoracic aortic aneurysm and dissectionTGFBR12Link
Selective T-cell defectZAP7010Link
Multiple self-healing squamous epitheliomaTGFBR12Link
Colon cancerSRC19Link
Renal agenesisRET11Link
Hirschsprung diseaseRET11Link
n/aCongenital central hypoventilation syndromeRET11Link
Central hypoventilation syndromeRET11Link
PheochromocytomaRET11Link
Multiple endocrine neoplasiaRET11Link
ThrombocythemiaJAK210Link
MyelofibrosisJAK210Link
n/aCATSHL syndromeFGFR37Link
n/aAchondroplasiaFGFR37Link
Colorectal cancerFGFR37Link
n/aHypochondroplasiaFGFR37Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR37Link
n/aMultiple myelomaFGFR37Link
Bent bone dysplasia syndromeFGFR28Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR28Link
CraniosynostosisFGFR28Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR28Link
n/aSaethre-Chotzen syndromeFGFR28Link
n/aMuenke syndromeFGFR37Link
n/aNevusFGFR37Link
n/aInvasive pneumococcal diseaseIRAK44Link
IRAK4 deficiencyIRAK44Link
Polycythemia veraJAK210Link
n/aBudd-Chiari syndromeJAK210Link
n/aHerpes simplex infectionJAK210Link
Insulin-like growth factor IIGF1R5Link
n/aSynovial sarcomaIGF1R5Link
n/aSpermatocytic seminomaFGFR37Link
n/aThanatophoric dysplasiaFGFR37Link
n/aCancer progression/metastasisFGFR43Link
n/aMalignant pleural mesotheliomaIGF1R5Link
n/aEndocrine-cerebroosteodysplasiaICK2Link