Allelic Variants

There are no related allelic variants
Related diseases of KIF 3CJGA_KIM (PDB code: 3CJG, chain A)
Number of involved diseases in the family 49
Number of KDR related diseases 1
All kinase in this family  KDR
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
MelanomaBRAF, FGFR1, IGF1R, MET28Link
Prostate cancerBRAF, FGFR1, FGFR2, IGF1R29Link
Lung cancerALK, BRAF9Link
Jackson-Weiss syndromeFGFR1, FGFR22Link
Pfeiffer syndromeFGFR1, FGFR22Link
Gastric cancerFGFR2, MET2Link
Osteoglophonic dysplasiaFGFR11Link
Hypogonadotropic hypogonadismFGFR11Link
Noonan syndromeBRAF8Link
Apert syndromeFGFR21Link
TrigonocephalyFGFR11Link
Kallmann syndromeFGFR11Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
LEOPARD syndromeBRAF8Link
Colorectal cancerBRAF8Link
n/aMalignant melanomaBRAF8Link
n/aThyroid cancerBRAF8Link
NeuroblastomaALK1Link
n/aNoonan syndrome and related disordersBRAF8Link
n/aAlcoholismBRAF8Link
Cardiofaciocutaneous syndromeBRAF8Link
Adenocarcinoma of lungBRAF8Link
LeukemiaBRAF8Link
n/aHepatitis CBRAF8Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
Bent bone dysplasia syndromeFGFR21Link
n/aCholangiocarcinomaMET1Link
Renal cell carcinomaMET1Link
HemangiomaKDR13Link
Hyperinsulinemic hypoglycemiaINSR2Link
n/aEpithelial cell signaling in Helicobacter pylori infectionMET1Link
n/aMalariaMET1Link
n/aRheumatoid arthritisTEK1Link
Venous malformationsTEK1Link
Hepatocellular carcinomaMET1Link
n/aAutism suseptibilityMET1Link
Diabetes mellitusINSR2Link
Rabson-Mendenhall syndromeINSR2Link
LADD syndromeFGFR21Link
Crouzon syndromeFGFR21Link
CraniosynostosisFGFR21Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
n/aSaethre-Chotzen syndromeFGFR21Link
ScaphocephalyFGFR21Link
n/aLeprechaunismINSR2Link
Insulin-like growth factor IIGF1R19Link
n/aSynovial sarcomaIGF1R19Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
n/aMalignant pleural mesotheliomaIGF1R19Link