Allelic Variants

There are no related allelic variants
Related diseases of KIF 3LW0A_CCX (PDB code: 3LW0, chain A)
Number of involved diseases in the family 101
Number of TEC related diseases 1
All kinase in this family  TEC
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Prostate cancerEGFR, EPHB2, FGFR1, FGFR2,
IGF1R, INSRR
5Link
Lung cancerALK, EGFR, PTK2, ROS13Link
NeuroblastomaALK, NTRK1, NTRK2, NTRK32Link
MelanomaEGFR, FGFR1, IGF1R5Link
n/aHepatitis CEGFR, RIPK1, TYK23Link
n/aBladder cancerEGFR, FGFR33Link
Gastric cancerEGFR, FGFR23Link
n/aCervical cancerEGFR, FGFR33Link
n/aMedullary thyroid carcinomaNTRK1, RET2Link
n/aToxoplasmosisJAK2, TYK22Link
n/aEpithelial cell signaling in Helicobacter pylori infectionEGFR, SRC4Link
n/aThyroid cancerNTRK1, RET2Link
Crouzon syndromeFGFR2, FGFR31Link
LADD syndromeFGFR2, FGFR31Link
n/aInfluenza AJAK2, TYK22Link
n/aMeaslesJAK2, TYK22Link
n/aShigellosisABL1, SRC8Link
n/aTuberculosisJAK2, SRC2Link
LeukemiaABL1, JAK27Link
n/aHerpes simplex infectionJAK2, TYK22Link
HemangiomaFLT4, KDR3Link
Pfeiffer syndromeFGFR1, FGFR22Link
Jackson-Weiss syndromeFGFR1, FGFR22Link
n/aEpstein-Barr virus infectionRIPK1, TYK22Link
Apert syndromeFGFR21Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
n/aMultiple myelomaFGFR31Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR31Link
n/aCATSHL syndromeFGFR31Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
ScaphocephalyFGFR21Link
Bent bone dysplasia syndromeFGFR21Link
CraniosynostosisFGFR21Link
n/aSaethre-Chotzen syndromeFGFR21Link
Hypogonadotropic hypogonadismFGFR12Link
Kallmann syndromeFGFR12Link
AgammaglobulinemiaBTK1Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK1Link
n/aPituitary DwarfismBTK1Link
n/aAgammaglobulinemiasBTK1Link
n/aPathogenic Escherichia coli infectionABL17Link
n/aViral myocarditisABL17Link
n/aMaturity onset diabetes of the youngBLK3Link
n/aSpondylometaepiphyseal dysplasiaDDR24Link
n/aOral cancerEGFR3Link
n/aAchondroplasiaFGFR31Link
Osteoglophonic dysplasiaFGFR12Link
TrigonocephalyFGFR12Link
Adenocarcinoma of lungEGFR3Link
n/aLaryngeal cancerEGFR3Link
n/aEsophageal cancerEGFR3Link
n/aChoriocarcinomaEGFR3Link
n/aGliomaEGFR3Link
n/aSpermatocytic seminomaFGFR31Link
Colorectal cancerFGFR31Link
n/aRenal agenesis and Renal adysplasiaRET1Link
Hirschsprung diseaseRET1Link
n/aCongenital central hypoventilation syndromeRET1Link
n/aAmoebiasisPTK21Link
n/aObesityNTRK21Link
n/aCongenital myasthenic syndromeMUSK1Link
n/aMyasthenic syndromeMUSK1Link
n/aInsensitivity to painNTRK12Link
n/aAlcoholismNTRK21Link
Central hypoventilation syndromeRET1Link
Multiple endocrine neoplasiaRET1Link
n/aTransient erythroblastopenia of childhoodTEC1Link
Venous malformationsTEK1Link
n/aRheumatoid arthritisTEK1Link
n/aTyrosine kinase 2 deficiencyTYK22Link
Colon cancerSRC2Link
Mental retardationRPS6KA32Link
PheochromocytomaRET1Link
Renal agenesisRET1Link
n/aNon-syndromic X-linked mental retardationRPS6KA32Link
n/aCoffin-Lowry syndromeRPS6KA32Link
Retinitis pigmentosaMERTK1Link
SCIDLCK6Link
n/aMalignant pleural mesotheliomaIGF1R2Link
n/aSynovial sarcomaIGF1R2Link
Insulin-like growth factor IIGF1R2Link
n/aLymphedemaFLT42Link
n/aLymphedemasFLT42Link
n/aHypochondroplasiaFGFR31Link
n/aMuenke syndromeFGFR31Link
n/aNevusFGFR31Link
n/aThanatophoric dysplasiaFGFR31Link
n/aLeprechaunismINSR1Link
Rabson-Mendenhall syndromeINSR1Link
MyelofibrosisJAK21Link
n/aMyeloproliferative disorderJAK21Link
ThrombocythemiaJAK21Link
n/aImmunodeficienciesLCK6Link
n/aBudd-Chiari syndromeJAK21Link
n/aLeishmaniasisJAK21Link
Diabetes mellitusINSR1Link
Hyperinsulinemic hypoglycemiaINSR1Link
Lymphoproliferative syndromeITK18Link
Polycythemia veraJAK21Link