Allelic Variants

There are no related allelic variants
Related diseases of KIF 3EFWA_AK8 (PDB code: 3EFW, chain A)
Number of involved diseases in the family 105
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 infectionCDK2, EIF2AK2, JAK1, JAK3,
MAP2K4, MAPK10, MAPK12,
MAPK13, MAPK8, MAPK9,
PRKACA, PRKACB, PRKX, RIPK1,
SYK
5Link
n/aHepatitis CBRAF, EGFR, EIF2AK2, JAK1,
MAPK10, MAPK12, MAPK13,
MAPK8, MAPK9, RAF1, RIPK1
14Link
n/aInfluenza AEIF2AK2, JAK1, JAK2, MAP2K4,
MAPK10, MAPK12, MAPK13,
MAPK8, MAPK9, RAF1
3Link
n/aTuberculosisJAK1, JAK2, MAPK10, MAPK12,
MAPK13, MAPK8, MAPK9, PLK3,
RAF1, SYK
3Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, MAP2K4, MAPK10,
MAPK12, MAPK13, MAPK8, MAPK9
3Link
Prostate cancerBRAF, CDK2, CHEK2, EGFR,
FGFR1, FGFR2, RAF1
13Link
n/aHerpes simplex infectionCDK2, EIF2AK2, JAK1, JAK2,
MAPK10, MAPK8, MAPK9
3Link
n/aToxoplasmosisJAK1, JAK2, MAPK10, MAPK12,
MAPK13, MAPK8, MAPK9
3Link
LeukemiaABL1, ABL2, BRAF, CDK4,
JAK2, RAF1, RPS6KB1
15Link
n/aMeaslesCDK2, CDK4, EIF2AK2, JAK1,
JAK2, JAK3, PRKCQ
4Link
n/aChagas diseaseMAP2K4, MAPK10, MAPK12,
MAPK13, MAPK8, MAPK9
3Link
n/aShigellosisABL1, MAPK10, MAPK12,
MAPK13, MAPK8, MAPK9
5Link
Lung cancerALK, BRAF, CDK2, CDK4, EGFR,
PTK2
13Link
n/aAlcoholismBRAF, CAMKK1, CAMKK2, NTRK2,
PRKACA, RAF1
13Link
MelanomaBRAF, CDK4, EGFR, FGFR1,
RAF1
13Link
n/aPertussisMAPK10, MAPK12, MAPK13,
MAPK8, MAPK9
3Link
n/aSalmonella infectionMAPK10, MAPK12, MAPK13,
MAPK8, MAPK9
3Link
n/aCardiomyopathyMYLK2, PRKAA1, PRKACA,
PRKACB, PRKX
2Link
n/aCocaine addictionCDK5, PRKACA, PRKACB, PRKX2Link
NeuroblastomaALK, NTRK1, NTRK2, NTRK32Link
n/aLeishmaniasisJAK1, JAK2, MAPK12, MAPK132Link
n/aAmoebiasisPRKACA, PRKACB, PRKX, PTK23Link
n/aVibrio cholerae infectionPRKACA, PRKACB, PRKX2Link
n/aCervical cancerCDK4, EGFR, FGFR32Link
n/aPrion diseasesPRKACA, PRKACB, PRKX2Link
Diabetes mellitusMAPK10, MAPK8, MAPK93Link
n/aThyroid cancerBRAF, NTRK1, RET13Link
n/aEarly infantile epileptic encephalopathyCDKL5, MAPK103Link
n/aMalignant melanomaBRAF, CDK413Link
n/aViral myocarditisABL1, ABL24Link
LADD syndromeFGFR2, FGFR32Link
n/aGliomaCDK4, EGFR2Link
Jackson-Weiss syndromeFGFR1, FGFR22Link
Pfeiffer syndromeFGFR1, FGFR22Link
n/aBladder cancerEGFR, FGFR32Link
Crouzon syndromeFGFR2, FGFR32Link
Gastric cancerEGFR, FGFR22Link
n/aEpileptic encephalopathyCDKL5, MAPK103Link
n/aMedullary thyroid carcinomaNTRK1, RET2Link
LEOPARD syndromeBRAF, RAF113Link
Colorectal cancerBRAF, FGFR313Link
n/aImmunodeficienciesJAK3, LCK13Link
Adenocarcinoma of lungBRAF, EGFR13Link
SCIDJAK3, LCK13Link
Noonan syndromeBRAF, RAF113Link
n/aAmyotrophic lateral sclerosisMAPK12, MAPK132Link
n/aPrader-Willi and Angelman syndromesCDKL51Link
Li-Fraumeni syndromeCHEK21Link
n/aChoriocarcinomaEGFR2Link
n/aLaryngeal cancerEGFR2Link
n/aPathogenic Escherichia coli infectionABL14Link
n/aNoonan syndrome and related disordersBRAF13Link
Hypogonadotropic hypogonadismFGFR12Link
Cardiofaciocutaneous syndromeBRAF13Link
Colon cancerAURKA8Link
OsteosarcomaCHEK21Link
Breast cancerCHEK21Link
Osteoglophonic dysplasiaFGFR12Link
n/aOral cancerEGFR2Link
n/aAngelman syndrome-likeCDKL51Link
n/aMaturity onset diabetes of the youngBLK2Link
n/aEsophageal cancerEGFR2Link
CraniosynostosisFGFR22Link
TrigonocephalyFGFR12Link
n/aShort rib-polydactyly syndormeNEK11Link
n/aInsensitivity to painNTRK12Link
n/aObesityNTRK22Link
REtinitis pigmentosaMAK1Link
ThrombocythemiaJAK22Link
n/aBudd-Chiari syndromeJAK22Link
MyelofibrosisJAK22Link
n/aMyeloproliferative disorderJAK22Link
n/aType I diabetes mellitusPRKCQ2Link
n/aRenal agenesis and Renal adysplasiaRET2Link
n/aBasal cell carcinomaSTK362Link
Venous malformationsTEK35Link
n/aRheumatoid arthritisTEK35Link
Renal agenesisRET2Link
PheochromocytomaRET2Link
Hirschsprung diseaseRET2Link
n/aCongenital central hypoventilation syndromeRET2Link
Central hypoventilation syndromeRET2Link
Multiple endocrine neoplasiaRET2Link
Polycythemia veraJAK22Link
Lymphoproliferative syndromeITK2Link
n/aSaethre-Chotzen syndromeFGFR22Link
ScaphocephalyFGFR22Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
Kallmann syndromeFGFR12Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
Apert syndromeFGFR22Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
n/aMultiple myelomaFGFR31Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR31Link
n/aThanatophoric dysplasiaFGFR31Link
n/aCancer progression/metastasisFGFR42Link
n/aEndocrine-cerebroosteodysplasiaICK1Link
n/aSpermatocytic seminomaFGFR31Link
n/aNevusFGFR31Link
n/aCATSHL syndromeFGFR31Link
n/aAchondroplasiaFGFR31Link
n/aHypochondroplasiaFGFR31Link
n/aMuenke syndromeFGFR31Link