Allelic Variants

There are no related allelic variants
Related diseases of KIF 3CKXA_STU (PDB code: 3CKX, chain A)
Number of involved diseases in the family 141
Number of FGFR3 related diseases 14
All kinase in this family  FGFR3
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
n/aEpstein-Barr virus infectionCDC2, CDK2, EIF2AK2,
EIF2AK4, FGR, JAK1, JAK3,
MAP2K3, MAP2K6, MAP3K14,
MAPK12, MAPK13, MAPK14, SYK,
TBK1
20Link
n/aInfluenza AEIF2AK2, EIF2AK4, IRAK4,
JAK1, JAK2, MAP2K1, MAP2K3,
MAP2K6, MAPK1, MAPK12,
MAPK13, MAPK14, PRKCA, RAF1,
TBK1
61Link
n/aTuberculosisCAMK2A, CAMK2B, IRAK4, JAK1,
JAK2, MAPK1, MAPK12, MAPK13,
MAPK14, PLK3, RAF1, SRC, SYK
21Link
Prostate cancerCDK2, CHEK2, EGFR, EPHB2,
FGFR1, FGFR2, IGF1R, INSRR,
MAP2K1, MAPK1, PDPK1, RAF1
46Link
n/aMeaslesCDK2, CDK4, CDK6, EIF2AK2,
EIF2AK4, FYN, IRAK4, JAK1,
JAK2, JAK3, PRKCQ, TBK1
19Link
LeukemiaABL1, ABL2, CDK4, CDK6,
JAK2, MAP2K1, MAPK1, PIM1,
RAF1, RPS6KB1, RPS6KB2
15Link
n/aHepatitis CEGFR, EIF2AK2, EIF2AK4,
JAK1, MAPK1, MAPK12, MAPK13,
MAPK14, RAF1, TBK1
42Link
n/aToxoplasmosisIRAK4, JAK1, JAK2, MAP2K3,
MAP2K6, MAPK1, MAPK12,
MAPK13, MAPK14
13Link
MelanomaCDK4, CDK6, EGFR, FGFR1,
IGF1R, MAP2K1, MAPK1, MET,
RAF1
43Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, MAP3K14, MAPK12,
MAPK13, MAPK14, MET, PAK1,
SRC
42Link
Lung cancerALK, CDK2, CDK4, CDK6, EGFR,
MAP3K8, PTK2, ROS1
43Link
n/aHerpes simplex infectionCDC2, CDK2, EIF2AK2,
EIF2AK4, JAK1, JAK2, TBK1
15Link
n/aAlcoholismCAMK4, CAMKK1, CAMKK2,
MAP2K1, MAPK1, NTRK2, RAF1
12Link
n/aLeishmaniasisIRAK4, JAK1, JAK2, MAPK1,
MAPK12, MAPK13, MAPK14
12Link
n/aShigellosisABL1, MAPK1, MAPK12, MAPK13,
MAPK14, SRC
20Link
n/aSalmonella infectionMAPK1, MAPK12, MAPK13,
MAPK14, PKN1, PKN2
13Link
n/aChagas diseaseIRAK4, MAPK1, MAPK12,
MAPK13, MAPK14
6Link
Diabetes mellitusINSR, MAPK1, PRKCD, PRKCE,
PRKCZ
15Link
n/aPertussisIRAK4, MAPK1, MAPK12,
MAPK13, MAPK14
6Link
n/aAmyotrophic lateral sclerosisMAP2K3, MAP2K6, MAPK12,
MAPK13, MAPK14
11Link
NeuroblastomaALK, NTRK1, NTRK2, NTRK316Link
n/aPathogenic Escherichia coli infectionABL1, FYN, PRKCA61Link
n/aCervical cancerCDK4, EGFR, FGFR340Link
n/aViral myocarditisABL1, ABL2, FYN13Link
n/aImmunodeficienciesJAK3, LCK, ZAP7016Link
Gastric cancerEGFR, FGFR2, MET39Link
n/aPrion diseasesFYN, MAP2K1, MAPK111Link
n/aBladder cancerDAPK1, EGFR, FGFR339Link
Jackson-Weiss syndromeFGFR1, FGFR29Link
SCIDJAK3, LCK16Link
Pfeiffer syndromeFGFR1, FGFR29Link
n/aThyroid cancerNTRK1, RET18Link
n/aMedullary thyroid carcinomaNTRK1, RET18Link
Mental retardationCASK, PAK38Link
Crouzon syndromeFGFR2, FGFR38Link
LADD syndromeFGFR2, FGFR38Link
Colon cancerAURKA, SRC19Link
n/aAmoebiasisPRKCA, PTK257Link
n/aGliomaCDK4, EGFR40Link
n/aSaethre-Chotzen syndromeFGFR28Link
ScaphocephalyFGFR28Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR28Link
Osteoglophonic dysplasiaFGFR19Link
n/aMultiple myelomaFGFR37Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR28Link
Beare-Stevenson cutis gyrata syndromeFGFR28Link
Kallmann syndromeFGFR19Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR28Link
Bent bone dysplasia syndromeFGFR28Link
TrigonocephalyFGFR19Link
CraniosynostosisFGFR28Link
Apert syndromeFGFR28Link
OsteosarcomaCHEK25Link
Hypogonadotropic hypogonadismFGFR19Link
AgammaglobulinemiaBTK5Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK5Link
n/aFG syndromeCASK1Link
n/aMalignant melanomaCDK46Link
n/aPituitary DwarfismBTK5Link
n/aAgammaglobulinemiasBTK5Link
Fibrodysplasia ossificans progressivaACVR13Link
n/aMaturity onset diabetes of the youngBLK8Link
n/aJuvenile polyposis syndromeBMPR1A2Link
n/aPolyposisBMPR1A2Link
n/aCocaine addictionCDK55Link
n/aPrader-Willi and Angelman syndromesCDKL51Link
n/aEsophageal cancerEGFR38Link
n/aChoriocarcinomaEGFR38Link
n/aLaryngeal cancerEGFR38Link
Adenocarcinoma of lungEGFR38Link
n/aOral cancerEGFR38Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR37Link
n/aEarly infantile epileptic encephalopathyCDKL51Link
n/aAngelman syndrome-likeCDKL51Link
n/aEpileptic encephalopathyCDKL51Link
Breast cancerCHEK25Link
Li-Fraumeni syndromeCHEK25Link
n/aSpermatocytic seminomaFGFR37Link
n/aCATSHL syndromeFGFR37Link
n/aGlycogen storage diseasesPHKG29Link
n/aNon-syndromic X-linked mental retardationPAK38Link
n/aCirrhosis due to liver phosphorylase kinase deficiencyPHKG29Link
Glycogen storage diseasePHKG29Link
n/aAfrican trypanosomiasisPRKCA55Link
n/aVibrio cholerae infectionPRKCA55Link
n/aObesityNTRK29Link
n/aInsensitivity to painNTRK115Link
Hepatocellular carcinomaMET8Link
n/aAutism suseptibilityMET8Link
n/aCongenital myasthenic syndromeMUSK5Link
n/aMyasthenic syndromeMUSK5Link
DeafnessMYO3A2Link
n/aDeafness, autosomal recessiveMYO3A2Link
n/aPituitary tumorPRKCA55Link
n/aType I diabetes mellitusPRKCQ8Link
n/aBasal cell carcinomaSTK363Link
Renal agenesisRET11Link
n/aTransient erythroblastopenia of childhoodTEC2Link
Venous malformationsTEK32Link
Selective T-cell defectZAP7010Link
n/aRheumatoid arthritisTEK32Link
PheochromocytomaRET11Link
Multiple endocrine neoplasiaRET11Link
Noonan syndromeRAF12Link
LEOPARD syndromeRAF12Link
n/aRenal agenesis and Renal adysplasiaRET11Link
Hirschsprung diseaseRET11Link
Central hypoventilation syndromeRET11Link
n/aCongenital central hypoventilation syndromeRET11Link
n/aMalariaMET8Link
n/aCholangiocarcinomaMET8Link
n/aEndocrine-cerebroosteodysplasiaICK2Link
n/aOguchi diseaseGRK14Link
n/aMalignant pleural mesotheliomaIGF1R5Link
n/aSynovial sarcomaIGF1R5Link
n/aLeprechaunismINSR5Link
Insulin-like growth factor IIGF1R5Link
n/aCongenital stationary night blindnessGRK14Link
n/aCancer progression/metastasisFGFR43Link
Colorectal cancerFGFR37Link
n/aAchondroplasiaFGFR37Link
n/aHypochondroplasiaFGFR37Link
n/aMuenke syndromeFGFR37Link
n/aThanatophoric dysplasiaFGFR37Link
n/aNevusFGFR37Link
Rabson-Mendenhall syndromeINSR5Link
Hyperinsulinemic hypoglycemiaINSR5Link
n/aParkinson diseaseLRRK25Link
n/aLewy body dementiaLRRK25Link
REtinitis pigmentosaMAK1Link
n/aNoonan syndrome and related disordersMAP2K14Link
Renal cell carcinomaMET8Link
Cardiofaciocutaneous syndromeMAP2K14Link
ThrombocythemiaJAK210Link
n/aMyeloproliferative disorderJAK210Link
IRAK4 deficiencyIRAK44Link
n/aInvasive pneumococcal diseaseIRAK44Link
Lymphoproliferative syndromeITK6Link
Polycythemia veraJAK210Link
MyelofibrosisJAK210Link
n/aBudd-Chiari syndromeJAK210Link