Allelic Variants

There are no related allelic variants
Related diseases of KIF 2ITZA_IRE (PDB code: 2ITZ, chain A)
Number of involved diseases in the family 99
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,
INSRR
171Link
n/aEpstein-Barr virus infectionFGR, JAK3, MAP3K7, SYK10Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, MET, SRC285Link
NeuroblastomaALK, NTRK1, NTRK2, NTRK310Link
n/aMeaslesFYN, JAK2, JAK3, MAP3K79Link
LeukemiaABL1, ABL2, JAK222Link
MelanomaEGFR, FGFR1, MET171Link
n/aTuberculosisJAK2, SRC, SYK132Link
Gastric cancerEGFR, FGFR2, MET166Link
Lung cancerALK, EGFR, PTK2169Link
n/aViral myocarditisABL1, ABL2, FYN22Link
n/aPathogenic Escherichia coli infectionABL1, FYN22Link
Colon cancerAURKA, SRC138Link
SCIDJAK3, LCK23Link
Pfeiffer syndromeFGFR1, FGFR229Link
n/aHerpes simplex infectionJAK2, MAP3K73Link
n/aCervical cancerEGFR, FGFR3166Link
n/aShigellosisABL1, SRC133Link
Jackson-Weiss syndromeFGFR1, FGFR229Link
n/aLeishmaniasisJAK2, MAP3K73Link
n/aToxoplasmosisJAK2, MAP3K73Link
n/aImmunodeficienciesJAK3, LCK23Link
n/aThyroid cancerNTRK1, RET10Link
n/aBladder cancerEGFR, FGFR3166Link
LADD syndromeFGFR2, FGFR34Link
n/aChoriocarcinomaCSF1R, EGFR174Link
Crouzon syndromeFGFR2, FGFR34Link
n/aMedullary thyroid carcinomaNTRK1, RET10Link
Apert syndromeFGFR24Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR24Link
Osteoglophonic dysplasiaFGFR129Link
TrigonocephalyFGFR129Link
CraniosynostosisFGFR24Link
Bent bone dysplasia syndromeFGFR24Link
Beare-Stevenson cutis gyrata syndromeFGFR24Link
Kallmann syndromeFGFR129Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR24Link
n/aSaethre-Chotzen syndromeFGFR24Link
Hypogonadotropic hypogonadismFGFR129Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK7Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R13Link
AgammaglobulinemiaBTK7Link
n/aPituitary DwarfismBTK7Link
n/aMaturity onset diabetes of the youngBLK11Link
n/aAgammaglobulinemiasBTK7Link
n/aSpondylometaepiphyseal dysplasiaDDR24Link
n/aOral cancerEGFR166Link
n/aType I diabetes mellitusERBB35Link
n/aLethal congenital contractural syndromeERBB35Link
Adenocarcinoma of lungEGFR166Link
n/aHepatitis CEGFR166Link
n/aEsophageal cancerEGFR166Link
n/aGliomaEGFR166Link
n/aLaryngeal cancerEGFR166Link
n/aAchondroplasiaFGFR33Link
ScaphocephalyFGFR24Link
n/aAlcoholismNTRK22Link
n/aObesityNTRK22Link
n/aAmoebiasisPTK22Link
n/aInsensitivity to painNTRK12Link
Hepatocellular carcinomaMET8Link
Renal cell carcinomaMET8Link
n/aCholangiocarcinomaMET8Link
n/aMalariaMET8Link
n/aAutism suseptibilityMET8Link
n/aRenal agenesis and Renal adysplasiaRET9Link
Hirschsprung diseaseRET9Link
n/aTransient erythroblastopenia of childhoodTEC4Link
Venous malformationsTEK11Link
n/aRheumatoid arthritisTEK11Link
n/aPopliteal pterygium syndromeRIPK41Link
Renal agenesisRET9Link
n/aCongenital central hypoventilation syndromeRET9Link
Central hypoventilation syndromeRET9Link
Multiple endocrine neoplasiaRET9Link
PheochromocytomaRET9Link
ThrombocythemiaJAK21Link
n/aMyeloproliferative disorderJAK21Link
n/aMuenke syndromeFGFR33Link
n/aNevusFGFR33Link
n/aSpermatocytic seminomaFGFR33Link
n/aHypochondroplasiaFGFR33Link
Colorectal cancerFGFR33Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR24Link
n/aMultiple myelomaFGFR33Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR33Link
n/aCATSHL syndromeFGFR33Link
n/aThanatophoric dysplasiaFGFR33Link
n/aCancer progression/metastasisFGFR41Link
Polycythemia veraJAK21Link
n/aInfluenza AJAK21Link
n/aBudd-Chiari syndromeJAK21Link
MyelofibrosisJAK21Link
Lymphoproliferative syndromeITK3Link
Hyperinsulinemic hypoglycemiaINSR3Link
n/aPrion diseasesFYN8Link
n/aLeprechaunismINSR3Link
Rabson-Mendenhall syndromeINSR3Link
Diabetes mellitusINSR3Link