Allelic Variants

There are no related allelic variants
Related diseases of KIF 3FSFA_FSS (PDB code: 3FSF, chain A)
Number of involved diseases in the family 40
Number of YES1 related diseases 0
All kinase in this family  YES1
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
n/aShigellosisABL1, MAPK14, SRC34Link
n/aEpithelial cell signaling in Helicobacter pylori infectionLYN, MAPK14, SRC32Link
Pfeiffer syndromeFGFR1, FGFR228Link
Jackson-Weiss syndromeFGFR1, FGFR228Link
Prostate cancerFGFR1, FGFR228Link
n/aEpstein-Barr virus infectionLYN, MAPK147Link
n/aTuberculosisMAPK14, SRC32Link
n/aViral myocarditisABL1, FYN7Link
n/aPathogenic Escherichia coli infectionABL1, FYN7Link
MelanomaFGFR127Link
Apert syndromeFGFR22Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
Gastric cancerFGFR22Link
Hypogonadotropic hypogonadismFGFR127Link
CraniosynostosisFGFR22Link
TrigonocephalyFGFR127Link
Osteoglophonic dysplasiaFGFR127Link
Kallmann syndromeFGFR127Link
Crouzon syndromeFGFR22Link
LeukemiaABL17Link
n/aLeishmaniasisMAPK145Link
n/aPertussisMAPK145Link
n/aChagas diseaseMAPK145Link
n/aToxoplasmosisMAPK145Link
Colon cancerSRC28Link
n/aInfluenza AMAPK145Link
n/aHepatitis CMAPK145Link
n/aSalmonella infectionMAPK145Link
n/aAmyotrophic lateral sclerosisMAPK145Link
ScaphocephalyFGFR22Link
n/aSaethre-Chotzen syndromeFGFR22Link
LADD syndromeFGFR22Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
n/aPrion diseasesFYN1Link
SCIDLCK23Link
n/aImmunodeficienciesLCK23Link
n/aMeaslesFYN1Link