Allelic Variants

There are no related allelic variants
Related diseases of KIF 2IW6A_QQ2 (PDB code: 2IW6, chain A)
Number of involved diseases in the family 86
Number of FRK related diseases 0
All kinase in this family  FRK
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
n/aMeaslesCDK2, CDK4, FYN, GSK3B,
IRAK4, JAK2, JAK3, MAP3K7,
PRKCQ
62Link
n/aEpstein-Barr virus infectionCDK2, FGR, GSK3B, JAK3, LYN,
MAP2K3, MAP2K6, MAP3K7
38Link
n/aInfluenza AGSK3B, IRAK4, JAK2, MAP2K1,
MAP2K3, MAP2K6, PRKCA
7Link
Prostate cancerCDK2, CHEK2, FGFR1, FGFR2,
GSK3B, MAP2K1
43Link
LeukemiaABL1, ABL2, CDK4, JAK2,
MAP2K1, RPS6KB1
56Link
n/aPathogenic Escherichia coli infectionABL1, FYN, PRKCA, ROCK1,
ROCK2
15Link
n/aToxoplasmosisIRAK4, JAK2, MAP2K3, MAP2K6,
MAP3K7
3Link
MelanomaCDK4, FGFR1, MAP2K1, MET53Link
n/aSalmonella infectionPKN1, PKN2, ROCK1, ROCK21Link
n/aEpithelial cell signaling in Helicobacter pylori infectionLYN, MET, PAK1, SRC131Link
n/aShigellosisABL1, ROCK1, ROCK2, SRC129Link
n/aTuberculosisCAMK2A, IRAK4, JAK2, SRC129Link
n/aHerpes simplex infectionCDK2, JAK2, MAP3K732Link
n/aLeishmaniasisIRAK4, JAK2, MAP3K73Link
Mental retardationCASK, PAK3, RPS6KA32Link
n/aImmunodeficienciesJAK3, LCK, ZAP7020Link
n/aAlcoholismCAMKK2, MAP2K1, NTRK24Link
n/aViral myocarditisABL1, ABL2, FYN14Link
SCIDJAK3, LCK19Link
n/aBasal cell carcinomaGSK3B, STK362Link
n/aAmyotrophic lateral sclerosisMAP2K3, MAP2K61Link
n/aNon-syndromic X-linked mental retardationPAK3, RPS6KA32Link
n/aPrion diseasesFYN, MAP2K16Link
Diabetes mellitusPRKCD, PRKCE11Link
Pfeiffer syndromeFGFR1, FGFR29Link
Gastric cancerFGFR2, MET4Link
Lung cancerCDK2, CDK448Link
Jackson-Weiss syndromeFGFR1, FGFR29Link
NeuroblastomaNTRK2, NTRK33Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
Bent bone dysplasia syndromeFGFR21Link
Apert syndromeFGFR21Link
OsteosarcomaCHEK22Link
Kallmann syndromeFGFR18Link
n/aGliomaCDK440Link
n/aMalignant melanomaCDK440Link
n/aCervical cancerCDK440Link
n/aMaturity onset diabetes of the youngBLK3Link
n/aFG syndromeCASK1Link
Li-Fraumeni syndromeCHEK22Link
Breast cancerCHEK22Link
Osteoglophonic dysplasiaFGFR18Link
TrigonocephalyFGFR18Link
Hypogonadotropic hypogonadismFGFR18Link
n/aSpondylometaepiphyseal dysplasiaDDR21Link
CraniosynostosisFGFR21Link
n/aLegionellosisCLK11Link
n/aHepatitis CGSK3B1Link
Crouzon syndromeFGFR21Link
n/aCirrhosis due to liver phosphorylase kinase deficiencyPHKG21Link
Glycogen storage diseasePHKG21Link
n/aGlycogen storage diseasesPHKG21Link
n/aObesityNTRK22Link
n/aAutism suseptibilityMET3Link
Hepatocellular carcinomaMET3Link
n/aShort rib-polydactyly syndormeNEK11Link
n/aVibrio cholerae infectionPRKCA2Link
n/aAfrican trypanosomiasisPRKCA2Link
Colon cancerSRC129Link
Selective T-cell defectZAP703Link
n/aCoffin-Lowry syndromeRPS6KA31Link
n/aType I diabetes mellitusPRKCQ10Link
n/aAmoebiasisPRKCA2Link
n/aPituitary tumorPRKCA2Link
n/aCerebral infarctionPRKCH1Link
n/aMalariaMET3Link
n/aCholangiocarcinomaMET3Link
n/aChagas diseaseIRAK42Link
n/aInvasive pneumococcal diseaseIRAK42Link
n/aPertussisIRAK42Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
LADD syndromeFGFR21Link
n/aSaethre-Chotzen syndromeFGFR21Link
ScaphocephalyFGFR21Link
IRAK4 deficiencyIRAK42Link
Lymphoproliferative syndromeITK1Link
n/aNoonan syndrome and related disordersMAP2K13Link
Cardiofaciocutaneous syndromeMAP2K13Link
Renal cell carcinomaMET3Link
ThrombocythemiaJAK21Link
n/aMyeloproliferative disorderJAK21Link
Polycythemia veraJAK21Link
n/aBudd-Chiari syndromeJAK21Link
MyelofibrosisJAK21Link