Allelic Variants

There are no related allelic variants
Related diseases of KIF 3PLSA_ANP (PDB code: 3PLS, chain A)
Number of involved diseases in the family 40
Number of MST1R related diseases 0
All kinase in this family  MST1R
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Prostate cancerCDK2, FGFR2, IGF1R5Link
Lung cancerALK, CDK22Link
Crouzon syndromeFGFR22Link
CraniosynostosisFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
Jackson-Weiss syndromeFGFR22Link
LADD syndromeFGFR22Link
ScaphocephalyFGFR22Link
n/aSaethre-Chotzen syndromeFGFR22Link
Pfeiffer syndromeFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
n/aMeaslesCDK21Link
NeuroblastomaALK1Link
n/aHerpes simplex infectionCDK21Link
n/aEpstein-Barr virus infectionCDK21Link
Apert syndromeFGFR22Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
Gastric cancerFGFR22Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
n/aMalignant pleural mesotheliomaIGF1R2Link
n/aMedullary thyroid carcinomaRET1Link
Central hypoventilation syndromeRET1Link
n/aCongenital central hypoventilation syndromeRET1Link
Multiple endocrine neoplasiaRET1Link
PheochromocytomaRET1Link
Selective T-cell defectZAP701Link
n/aImmunodeficienciesZAP701Link
Renal agenesisRET1Link
Hirschsprung diseaseRET1Link
n/aRenal agenesis and Renal adysplasiaRET1Link
Insulin-like growth factor IIGF1R2Link
MelanomaIGF1R2Link
n/aSynovial sarcomaIGF1R2Link
n/aLeprechaunismINSR3Link
Rabson-Mendenhall syndromeINSR3Link
n/aThyroid cancerRET1Link
Retinitis pigmentosaMERTK2Link
Hyperinsulinemic hypoglycemiaINSR3Link
Diabetes mellitusINSR3Link