Allelic Variants

There are no related allelic variants
Related diseases of KIF 1MP8A_ADP (PDB code: 1MP8, chain A)
Number of involved diseases in the family 50
Number of PTK2 related diseases 2
All kinase in this family  PTK2
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Lung cancerALK, CDK2, EGFR, PTK23Link
Prostate cancerCDK2, EGFR, FGFR1, FGFR25Link
MelanomaEGFR, FGFR1, MET3Link
n/aEpithelial cell signaling in Helicobacter pylori infectionEGFR, MET, SRC5Link
Gastric cancerEGFR, FGFR2, MET4Link
Jackson-Weiss syndromeFGFR1, FGFR23Link
Colon cancerAURKA, SRC6Link
Pfeiffer syndromeFGFR1, FGFR23Link
n/aMalariaMET1Link
n/aLaryngeal cancerEGFR1Link
n/aGliomaEGFR1Link
n/aCervical cancerEGFR1Link
n/aShigellosisSRC4Link
n/aHepatitis CEGFR1Link
Hypogonadotropic hypogonadismFGFR11Link
Adenocarcinoma of lungEGFR1Link
n/aAmoebiasisPTK22Link
n/aChoriocarcinomaEGFR1Link
n/aBladder cancerEGFR1Link
n/aMeaslesCDK21Link
Selective T-cell defectZAP701Link
NeuroblastomaALK1Link
n/aHerpes simplex infectionCDK21Link
n/aEpstein-Barr virus infectionCDK21Link
n/aTuberculosisSRC4Link
n/aEsophageal cancerEGFR1Link
n/aOral cancerEGFR1Link
n/aImmunodeficienciesZAP701Link
Osteoglophonic dysplasiaFGFR11Link
TrigonocephalyFGFR11Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
ScaphocephalyFGFR22Link
n/aSaethre-Chotzen syndromeFGFR22Link
n/aLeprechaunismINSR3Link
Rabson-Mendenhall syndromeINSR3Link
n/aCholangiocarcinomaMET1Link
Renal cell carcinomaMET1Link
Hyperinsulinemic hypoglycemiaINSR3Link
Diabetes mellitusINSR3Link
LADD syndromeFGFR22Link
Crouzon syndromeFGFR22Link
n/aAutism suseptibilityMET1Link
Kallmann syndromeFGFR11Link
Hepatocellular carcinomaMET1Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
Apert syndromeFGFR22Link
CraniosynostosisFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link