Allelic Variants

There are no related allelic variants
Related diseases of KIF 2XB7A_GUI (PDB code: 2XB7, chain A)
Number of involved diseases in the family 107
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
n/aMeaslesFYN, JAK1, JAK2, JAK3,
MAP3K7, TYK2
2Link
Prostate cancerEGFR, EPHB2, FGFR1, FGFR2,
IGF1R, INSRR
38Link
n/aEpstein-Barr virus infectionFGR, JAK1, JAK3, MAP3K7,
SYK, TYK2
2Link
n/aTuberculosisJAK1, JAK2, SRC, SYK2Link
MelanomaEGFR, FGFR1, IGF1R, MET39Link
n/aHerpes simplex infectionJAK1, JAK2, MAP3K7, TYK22Link
n/aToxoplasmosisJAK1, JAK2, MAP3K7, TYK22Link
Lung cancerALK, EGFR, PTK2, ROS110Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, MET, SRC3Link
n/aHepatitis CEGFR, JAK1, TYK22Link
LeukemiaABL1, ABL2, JAK22Link
n/aViral myocarditisABL1, ABL2, FYN2Link
Gastric cancerEGFR, FGFR2, MET3Link
n/aLeishmaniasisJAK1, JAK2, MAP3K72Link
NeuroblastomaALK, NTRK1, NTRK210Link
n/aInfluenza AJAK1, JAK2, TYK22Link
n/aCervical cancerEGFR, FGFR31Link
Jackson-Weiss syndromeFGFR1, FGFR22Link
HemangiomaFLT4, KDR2Link
n/aImmunodeficienciesJAK3, ZAP7020Link
n/aBladder cancerEGFR, FGFR31Link
n/aPathogenic Escherichia coli infectionABL1, FYN2Link
n/aShigellosisABL1, SRC2Link
Colon cancerAURKA, SRC2Link
Pfeiffer syndromeFGFR1, FGFR22Link
n/aChoriocarcinomaCSF1R, EGFR1Link
n/aMedullary thyroid carcinomaNTRK1, RET2Link
LADD syndromeFGFR2, FGFR31Link
Crouzon syndromeFGFR2, FGFR31Link
n/aThyroid cancerNTRK1, RET2Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
Apert syndromeFGFR21Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR31Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
n/aMultiple myelomaFGFR31Link
n/aSaethre-Chotzen syndromeFGFR21Link
CraniosynostosisFGFR21Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
ScaphocephalyFGFR21Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
Bent bone dysplasia syndromeFGFR21Link
CataractEPHA21Link
Kallmann syndromeFGFR12Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R1Link
n/aSpondylometaepiphyseal dysplasiaDDR21Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK1Link
AgammaglobulinemiaBTK1Link
n/aMaturity onset diabetes of the youngBLK1Link
n/aAgammaglobulinemiasBTK1Link
n/aPituitary DwarfismBTK1Link
n/aOral cancerEGFR1Link
n/aEsophageal cancerEGFR1Link
Osteoglophonic dysplasiaFGFR12Link
TrigonocephalyFGFR12Link
Hypogonadotropic hypogonadismFGFR12Link
n/aCATSHL syndromeFGFR31Link
n/aGliomaEGFR1Link
n/aLaryngeal cancerEGFR1Link
Adenocarcinoma of lungEGFR1Link
n/aSpermatocytic seminomaFGFR31Link
n/aAchondroplasiaFGFR31Link
n/aCongenital myasthenic syndromeMUSK1Link
n/aMyasthenic syndromeMUSK1Link
n/aInsensitivity to painNTRK11Link
n/aAlcoholismNTRK22Link
Hepatocellular carcinomaMET3Link
n/aAutism suseptibilityMET3Link
Retinitis pigmentosaMERTK1Link
Renal cell carcinomaMET3Link
n/aCholangiocarcinomaMET3Link
n/aMalariaMET3Link
n/aObesityNTRK22Link
n/aAmoebiasisPTK21Link
Renal agenesisRET2Link
n/aTransient erythroblastopenia of childhoodTEC1Link
n/aTyrosine kinase 2 deficiencyTYK22Link
Selective T-cell defectZAP7020Link
PheochromocytomaRET2Link
Multiple endocrine neoplasiaRET2Link
n/aRenal agenesis and Renal adysplasiaRET2Link
Hirschsprung diseaseRET2Link
n/aCongenital central hypoventilation syndromeRET2Link
Central hypoventilation syndromeRET2Link
n/a46XY sex reversal 6MAP3K11Link
SCIDJAK31Link
n/aLymphedemasFLT41Link
n/aLymphedemaFLT41Link
n/aPrion diseasesFYN1Link
n/aMalignant pleural mesotheliomaIGF1R37Link
n/aCancer progression/metastasisFGFR41Link
n/aThanatophoric dysplasiaFGFR31Link
Colorectal cancerFGFR31Link
n/aHypochondroplasiaFGFR31Link
n/aMuenke syndromeFGFR31Link
n/aNevusFGFR31Link
n/aSynovial sarcomaIGF1R37Link
Insulin-like growth factor IIGF1R37Link
n/aBudd-Chiari syndromeJAK22Link
MyelofibrosisJAK22Link
n/aMyeloproliferative disorderJAK22Link
ThrombocythemiaJAK22Link
Polycythemia veraJAK22Link
Lymphoproliferative syndromeITK1Link
n/aLeprechaunismINSR11Link
Rabson-Mendenhall syndromeINSR11Link
Diabetes mellitusINSR11Link
Hyperinsulinemic hypoglycemiaINSR11Link