Allelic Variants

There are no related allelic variants
Related diseases of KIF 3A7JA_ADP (PDB code: 3A7J, chain A)
Number of involved diseases in the family 87
Number of STK24 related diseases 0
All kinase in this family  STK24
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Prostate cancerCDK2, CHEK2, EGFR, FGFR1,
FGFR2, IGF1R, MAP2K1, PDPK1
7Link
MelanomaEGFR, FGFR1, IGF1R, MAP2K1,
MET
5Link
n/aInfluenza AEIF2AK2, IRAK4, MAP2K1,
MAPK12
4Link
n/aEpithelial cell signaling in Helicobacter pylori infectionEGFR, MAPK12, MET, SRC5Link
Lung cancerALK, CDK2, EGFR, PTK23Link
LeukemiaABL1, MAP2K1, PIM16Link
Gastric cancerEGFR, FGFR2, MET4Link
n/aEpstein-Barr virus infectionCDK2, EIF2AK2, MAPK122Link
n/aShigellosisABL1, MAPK12, SRC6Link
n/aTuberculosisIRAK4, MAPK12, SRC4Link
n/aHepatitis CEGFR, EIF2AK2, MAPK121Link
n/aMeaslesCDK2, EIF2AK2, IRAK42Link
n/aImmunodeficienciesLCK, ZAP701Link
n/aHerpes simplex infectionCDK2, EIF2AK22Link
Colon cancerAURKA, SRC6Link
n/aChagas diseaseIRAK4, MAPK121Link
n/aLeishmaniasisIRAK4, MAPK121Link
Pfeiffer syndromeFGFR1, FGFR23Link
Jackson-Weiss syndromeFGFR1, FGFR23Link
n/aPertussisIRAK4, MAPK121Link
n/aToxoplasmosisIRAK4, MAPK121Link
n/aBladder cancerDAPK1, EGFR2Link
n/aLethal congenital contractural syndromeERBB31Link
Osteoglophonic dysplasiaFGFR11Link
n/aType I diabetes mellitusERBB31Link
Hypogonadotropic hypogonadismFGFR11Link
TrigonocephalyFGFR11Link
Li-Fraumeni syndromeCHEK21Link
Apert syndromeFGFR22Link
NeuroblastomaALK1Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
Kallmann syndromeFGFR11Link
n/aViral myocarditisABL12Link
n/aPathogenic Escherichia coli infectionABL12Link
n/aCervical cancerEGFR1Link
n/aChoriocarcinomaEGFR1Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
n/aLaryngeal cancerEGFR1Link
n/aGliomaEGFR1Link
Mental retardationCASK2Link
n/aFG syndromeCASK2Link
Adenocarcinoma of lungEGFR1Link
Breast cancerCHEK21Link
OsteosarcomaCHEK21Link
n/aEsophageal cancerEGFR1Link
n/aOral cancerEGFR1Link
Crouzon syndromeFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
Hepatocellular carcinomaMET1Link
n/aAmoebiasisPTK22Link
n/aThyroid cancerRET2Link
n/aAutism suseptibilityMET1Link
n/aMalariaMET1Link
n/aSalmonella infectionMAPK121Link
Renal cell carcinomaMET1Link
n/aCholangiocarcinomaMET1Link
n/aRenal agenesis and Renal adysplasiaRET2Link
Hirschsprung diseaseRET2Link
Renal agenesisRET2Link
n/aPolyhydramniosSTRADA2Link
Selective T-cell defectZAP701Link
PheochromocytomaRET2Link
Multiple endocrine neoplasiaRET2Link
n/aCongenital central hypoventilation syndromeRET2Link
Central hypoventilation syndromeRET2Link
n/aMedullary thyroid carcinomaRET2Link
n/aAmyotrophic lateral sclerosisMAPK121Link
Cardiofaciocutaneous syndromeMAP2K14Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
n/aMalignant pleural mesotheliomaIGF1R2Link
n/aSynovial sarcomaIGF1R2Link
ScaphocephalyFGFR22Link
n/aSaethre-Chotzen syndromeFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
CraniosynostosisFGFR22Link
LADD syndromeFGFR22Link
Insulin-like growth factor IIGF1R2Link
n/aLeprechaunismINSR3Link
n/aNoonan syndrome and related disordersMAP2K14Link
n/aPrion diseasesMAP2K14Link
n/aAlcoholismMAP2K14Link
SCIDLCK1Link
IRAK4 deficiencyIRAK41Link
Rabson-Mendenhall syndromeINSR3Link
Diabetes mellitusINSR3Link
Hyperinsulinemic hypoglycemiaINSR3Link
n/aInvasive pneumococcal diseaseIRAK41Link