Allelic Variants

There are no related allelic variants
Related diseases of KIF 3FZPA_AGS (PDB code: 3FZP, chain A)
Number of involved diseases in the family 51
Number of PTK2B related diseases 0
All kinase in this family  PTK2B
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Prostate cancerEGFR, FGFR2, IGF1R4Link
Lung cancerEGFR, PTK23Link
MelanomaEGFR, IGF1R2Link
n/aHepatitis CEGFR, EIF2AK21Link
n/aEpithelial cell signaling in Helicobacter pylori infectionEGFR, SRC3Link
Gastric cancerEGFR, FGFR23Link
Colon cancerAURKA, SRC5Link
n/aShigellosisABL1, SRC5Link
n/aImmunodeficienciesLCK, ZAP701Link
CataractEPHA21Link
n/aEpstein-Barr virus infectionEIF2AK21Link
Adenocarcinoma of lungEGFR1Link
n/aHerpes simplex infectionEIF2AK21Link
n/aInfluenza AEIF2AK21Link
n/aMeaslesEIF2AK21Link
n/aLaryngeal cancerEGFR1Link
n/aType I diabetes mellitusERBB31Link
n/aOral cancerEGFR1Link
n/aViral myocarditisABL12Link
n/aPathogenic Escherichia coli infectionABL12Link
n/aEsophageal cancerEGFR1Link
n/aBladder cancerEGFR1Link
n/aGliomaEGFR1Link
n/aCervical cancerEGFR1Link
n/aChoriocarcinomaEGFR1Link
n/aLethal congenital contractural syndromeERBB31Link
LeukemiaABL12Link
n/aLeprechaunismINSR3Link
Insulin-like growth factor IIGF1R2Link
n/aSynovial sarcomaIGF1R2Link
n/aMalignant pleural mesotheliomaIGF1R2Link
Rabson-Mendenhall syndromeINSR3Link
Diabetes mellitusINSR3Link
Selective T-cell defectZAP701Link
n/aTuberculosisSRC3Link
n/aAmoebiasisPTK22Link
Hyperinsulinemic hypoglycemiaINSR3Link
SCIDLCK1Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
ScaphocephalyFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
Apert syndromeFGFR22Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
CraniosynostosisFGFR22Link
n/aSaethre-Chotzen syndromeFGFR22Link
Pfeiffer syndromeFGFR22Link
LADD syndromeFGFR22Link
Crouzon syndromeFGFR22Link
Jackson-Weiss syndromeFGFR22Link