Allelic Variants

There are no related allelic variants
Related diseases of KIF 2HY81_1ST (PDB code: 2HY8, chain 1)
Number of involved diseases in the family 75
Number of FGFR3 related diseases 14
All kinase in this family  FGFR3
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Prostate cancerCDK2, CHEK2, EGFR, FGFR1,
GSK3B, MAPK1, PDPK1
14Link
n/aInfluenza AGSK3B, IRAK4, JAK2, MAPK1,
MAPK8, PRKCB
9Link
n/aMeaslesCDK2, CDK6, GSK3B, IRAK4,
JAK2
9Link
n/aTuberculosisIRAK4, JAK2, MAPK1, MAPK86Link
n/aHepatitis CEGFR, GSK3B, MAPK1, MAPK810Link
n/aHerpes simplex infectionCDC2, CDK2, JAK2, MAPK89Link
n/aToxoplasmosisIRAK4, JAK2, MAPK1, MAPK86Link
MelanomaCDK6, EGFR, FGFR1, MAPK19Link
n/aLeishmaniasisIRAK4, JAK2, MAPK1, PRKCB9Link
LeukemiaCDK6, JAK2, MAPK1, PIM17Link
n/aEpstein-Barr virus infectionCDC2, CDK2, GSK3B, MAPK89Link
n/aEpithelial cell signaling in Helicobacter pylori infectionEGFR, MAPK8, PAK110Link
Lung cancerCDK2, CDK6, EGFR12Link
n/aPertussisIRAK4, MAPK1, MAPK86Link
n/aChagas diseaseIRAK4, MAPK1, MAPK86Link
n/aBladder cancerEGFR, FGFR38Link
n/aSalmonella infectionMAPK1, MAPK84Link
n/aShigellosisMAPK1, MAPK84Link
Diabetes mellitusMAPK1, MAPK84Link
n/aCervical cancerEGFR, FGFR38Link
n/aLaryngeal cancerEGFR8Link
Osteoglophonic dysplasiaFGFR14Link
Adenocarcinoma of lungEGFR8Link
Pfeiffer syndromeFGFR14Link
Kallmann syndromeFGFR14Link
Jackson-Weiss syndromeFGFR14Link
Hypogonadotropic hypogonadismFGFR14Link
TrigonocephalyFGFR14Link
n/aChoriocarcinomaEGFR8Link
n/aGliomaEGFR8Link
n/aEpileptic encephalopathyCDKL51Link
n/aAngelman syndrome-likeCDKL51Link
n/aEarly infantile epileptic encephalopathyCDKL51Link
n/aCocaine addictionCDK54Link
n/aPrader-Willi and Angelman syndromesCDKL51Link
Li-Fraumeni syndromeCHEK25Link
Breast cancerCHEK25Link
n/aMultiple myelomaFGFR34Link
Gastric cancerEGFR8Link
n/aEsophageal cancerEGFR8Link
OsteosarcomaCHEK25Link
n/aOral cancerEGFR8Link
Crouzon syndromeFGFR34Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR34Link
n/aAmyotrophic lateral sclerosisMAP3K55Link
n/aPrion diseasesMAPK14Link
n/a46XY sex reversal 6MAP3K11Link
REtinitis pigmentosaMAK1Link
n/aMyeloproliferative disorderJAK24Link
ThrombocythemiaJAK24Link
n/aAlcoholismMAPK14Link
n/aNon-syndromic X-linked mental retardationPAK35Link
n/aCerebral infarctionPRKCH6Link
n/aTransient erythroblastopenia of childhoodTEC2Link
n/aAmoebiasisPRKCB6Link
n/aAfrican trypanosomiasisPRKCB6Link
Mental retardationPAK35Link
n/aVibrio cholerae infectionPRKCB6Link
MyelofibrosisJAK24Link
n/aBudd-Chiari syndromeJAK24Link
LADD syndromeFGFR34Link
n/aMuenke syndromeFGFR34Link
n/aHypochondroplasiaFGFR34Link
Colorectal cancerFGFR34Link
n/aCATSHL syndromeFGFR34Link
n/aAchondroplasiaFGFR34Link
n/aNevusFGFR34Link
n/aSpermatocytic seminomaFGFR34Link
Lymphoproliferative syndromeITK5Link
Polycythemia veraJAK24Link
IRAK4 deficiencyIRAK44Link
n/aInvasive pneumococcal diseaseIRAK44Link
n/aThanatophoric dysplasiaFGFR34Link
n/aBasal cell carcinomaGSK3B6Link
n/aEndocrine-cerebroosteodysplasiaICK1Link