Allelic Variants

There are no related allelic variants
Related diseases of KIF 1R78A_FMD (PDB code: 1R78, chain A)
Number of involved diseases in the family 97
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, CHUK, CSNK2A1,
CSNK2A2, EIF2AK2, FGR, JAK1,
JAK3, LYN, MAP2K3, MAP2K6,
MAP3K7, MAPK10, MAPK9
23Link
n/aMeaslesCDK2, CDK4, CHUK, CSNK2A1,
CSNK2A2, EIF2AK2, FYN,
IRAK4, JAK1, JAK2, JAK3,
MAP3K7, PRKCQ
23Link
n/aHerpes simplex infectionCDK2, CHUK, CSNK2A1,
CSNK2A2, EIF2AK2, JAK1,
JAK2, MAP3K7, MAPK10, MAPK9
23Link
n/aInfluenza AEIF2AK2, IRAK4, JAK1, JAK2,
MAP2K1, MAP2K3, MAP2K6,
MAPK10, MAPK9
2Link
n/aToxoplasmosisCHUK, IRAK4, JAK1, JAK2,
MAP2K3, MAP2K6, MAP3K7,
MAPK10, MAPK9
2Link
n/aTuberculosisCAMK2A, CAMK2B, CAMK2D,
IRAK4, JAK1, JAK2, MAPK10,
MAPK9, SRC
2Link
n/aShigellosisABL1, CHUK, MAPK10, MAPK9,
ROCK1, ROCK2, SRC
2Link
Prostate cancerCDK2, CHEK2, CHUK, FGFR1,
FGFR2, MAP2K1, PDPK1
23Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCHUK, LYN, MAPK10, MAPK9,
MET, SRC
2Link
n/aSalmonella infectionMAPK10, MAPK9, PKN1, PKN2,
ROCK1, ROCK2
2Link
LeukemiaABL1, CDK4, CHUK, JAK2,
MAP2K1, RPS6KB1
2Link
n/aHepatitis CCHUK, EIF2AK2, JAK1, MAPK10,
MAPK9
2Link
MelanomaCDK4, FGFR1, MAP2K1, MET2Link
n/aChagas diseaseCHUK, IRAK4, MAPK10, MAPK91Link
n/aLeishmaniasisIRAK4, JAK1, JAK2, MAP3K72Link
n/aPathogenic Escherichia coli infectionABL1, FYN, ROCK1, ROCK22Link
n/aAlcoholismCAMKK1, CAMKK2, MAP2K1,
NTRK2
2Link
Lung cancerCDK2, CDK4, CHUK22Link
n/aPertussisIRAK4, MAPK10, MAPK91Link
Mental retardationDYRK1A, PAK3, RPS6KA32Link
LADD syndromeFGFR2, FGFR32Link
n/aPrion diseasesFYN, MAP2K12Link
Pfeiffer syndromeFGFR1, FGFR22Link
n/aBladder cancerDAPK1, FGFR32Link
Gastric cancerFGFR2, MET2Link
SCIDJAK3, LCK2Link
n/aCervical cancerCDK4, FGFR32Link
NeuroblastomaNTRK2, NTRK32Link
n/aViral myocarditisABL1, FYN2Link
n/aImmunodeficienciesJAK3, LCK2Link
Diabetes mellitusMAPK10, MAPK91Link
Jackson-Weiss syndromeFGFR1, FGFR22Link
Crouzon syndromeFGFR2, FGFR32Link
n/aAmyotrophic lateral sclerosisMAP2K3, MAP2K62Link
n/aNon-syndromic X-linked mental retardationPAK3, RPS6KA32Link
Kallmann syndromeFGFR12Link
CraniosynostosisFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
Apert syndromeFGFR22Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
n/aCocoon syndromeCHUK1Link
TrigonocephalyFGFR12Link
Li-Fraumeni syndromeCHEK21Link
n/aGliomaCDK41Link
n/aMalignant melanomaCDK41Link
n/aMaturity onset diabetes of the youngBLK2Link
Breast cancerCHEK21Link
OsteosarcomaCHEK21Link
Osteoglophonic dysplasiaFGFR12Link
Hypogonadotropic hypogonadismFGFR12Link
n/aSpondylometaepiphyseal dysplasiaDDR21Link
n/aLegionellosisCLK12Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR32Link
n/aSaethre-Chotzen syndromeFGFR22Link
Renal cell carcinomaMET1Link
n/aCholangiocarcinomaMET1Link
n/aMalariaMET1Link
n/aEpileptic encephalopathyMAPK101Link
n/aEarly infantile epileptic encephalopathyMAPK101Link
ThrombocythemiaJAK22Link
n/aNoonan syndrome and related disordersMAP2K12Link
Cardiofaciocutaneous syndromeMAP2K12Link
n/aAutism suseptibilityMET1Link
Hepatocellular carcinomaMET1Link
n/aType I diabetes mellitusPRKCQ2Link
n/aCoffin-Lowry syndromeRPS6KA32Link
Colon cancerSRC2Link
Glycogen storage diseasePHKG22Link
n/aCirrhosis due to liver phosphorylase kinase deficiencyPHKG22Link
n/aCongenital myasthenic syndromeMUSK2Link
n/aMyasthenic syndromeMUSK2Link
n/aObesityNTRK22Link
n/aGlycogen storage diseasesPHKG22Link
n/aMyeloproliferative disorderJAK22Link
MyelofibrosisJAK22Link
n/aHypochondroplasiaFGFR32Link
n/aMuenke syndromeFGFR32Link
n/aNevusFGFR32Link
Colorectal cancerFGFR32Link
n/aAchondroplasiaFGFR32Link
ScaphocephalyFGFR22Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
n/aMultiple myelomaFGFR32Link
n/aCATSHL syndromeFGFR32Link
n/aSpermatocytic seminomaFGFR32Link
n/aThanatophoric dysplasiaFGFR32Link
Lymphoproliferative syndromeITK2Link
Polycythemia veraJAK22Link
n/aBudd-Chiari syndromeJAK22Link
IRAK4 deficiencyIRAK41Link
n/aInvasive pneumococcal diseaseIRAK41Link
n/aCancer progression/metastasisFGFR41Link
n/aCongenital stationary night blindnessGRK11Link
n/aOguchi diseaseGRK11Link
n/aEndocrine-cerebroosteodysplasiaICK1Link