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 CDKL1 related diseases 0
All kinase in this family  CDKL1
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