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 CDK2 related diseases 5
All kinase in this family  CDK2
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