Allelic Variants

There are no related allelic variants
Related diseases of KIF 3OG7A_032 (PDB code: 3OG7, chain A)
Number of involved diseases in the family 58
Number of DDR1 related diseases 0
All kinase in this family  DDR1
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
LeukemiaABL1, ABL2, BRAF, KIT,
PDGFRB, RAF1
5Link
Prostate cancerBRAF, FGFR1, FGFR2, PDGFRB,
RAF1
5Link
MelanomaBRAF, FGFR1, PDGFRB, RAF15Link
n/aHepatitis CBRAF, RAF1, RIPK15Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, LYN, SRC2Link
n/aEpstein-Barr virus infectionFGR, LYN, RIPK11Link
n/aViral myocarditisABL1, ABL2, FYN1Link
Noonan syndromeBRAF, RAF15Link
n/aPathogenic Escherichia coli infectionABL1, FYN1Link
Jackson-Weiss syndromeFGFR1, FGFR22Link
n/aShigellosisABL1, SRC2Link
LEOPARD syndromeBRAF, RAF15Link
n/aTuberculosisRAF1, SRC2Link
Colon cancerAURKA, SRC2Link
Pfeiffer syndromeFGFR1, FGFR22Link
n/aAlcoholismBRAF, RAF15Link
n/aChoriocarcinomaCSF1R2Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R2Link
TrigonocephalyFGFR12Link
Hypogonadotropic hypogonadismFGFR12Link
Osteoglophonic dysplasiaFGFR12Link
Colorectal cancerBRAF5Link
Lung cancerBRAF5Link
n/aThyroid cancerBRAF5Link
n/aChrondrodysplasiaBMPR1B1Link
BrachydactylyBMPR1B1Link
n/aMalignant melanomaBRAF5Link
n/aNoonan syndrome and related disordersBRAF5Link
n/aMaturity onset diabetes of the youngBLK1Link
Cardiofaciocutaneous syndromeBRAF5Link
Adenocarcinoma of lungBRAF5Link
Kallmann syndromeFGFR12Link
Gastric cancerFGFR21Link
Mast cell leukemiaKIT1Link
n/aGerm cell tumorsKIT1Link
Gastrointestinal stromal tumorKIT1Link
PiebaldismKIT1Link
Mastocytosis with associated hematologic disorderKIT1Link
n/aImmunodeficienciesLCK1Link
n/aBasal cell carcinomaSTK361Link
n/aInfluenza ARAF11Link
n/aMyeloproliferative disorderPDGFRB1Link
SCIDLCK1Link
n/aGliomaPDGFRB1Link
HemangiomaKDR2Link
n/aMeaslesFYN1Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
Bent bone dysplasia syndromeFGFR21Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
Apert syndromeFGFR21Link
CraniosynostosisFGFR21Link
Crouzon syndromeFGFR21Link
n/aPrion diseasesFYN1Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
ScaphocephalyFGFR21Link
LADD syndromeFGFR21Link
n/aSaethre-Chotzen syndromeFGFR21Link