Allelic Variants

There are no related allelic variants
Related diseases of KIF 1SM2A_STU (PDB code: 1SM2, chain A)
Number of involved diseases in the family 128
Number of RPS6KA2 related diseases 0
All kinase in this family  RPS6KA2
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Prostate cancerAKT2, AKT3, CDK2, EGFR,
ERBB2, FGFR2, IGF1R, INSRR,
MAP2K1, PDGFRA, PDGFRB
45Link
n/aMeaslesAKT2, AKT3, CDK2, CDK6, FYN,
IRAK4, JAK2, JAK3, PRKCQ,
TYK2
18Link
LeukemiaABL1, ABL2, AKT2, AKT3,
CDK6, JAK2, KIT, MAP2K1,
PDGFRB
15Link
n/aEpstein-Barr virus infectionAKT2, AKT3, CDC2, CDK2, FGR,
JAK3, SYK, TYK2
18Link
MelanomaAKT2, AKT3, CDK6, EGFR,
IGF1R, MAP2K1, PDGFRA,
PDGFRB
43Link
Lung cancerAKT2, AKT3, ALK, CDK2, CDK6,
EGFR, ROS1
43Link
n/aTuberculosisAKT2, AKT3, IRAK4, JAK2,
SRC, SYK
21Link
n/aInfluenza AAKT2, AKT3, IRAK4, JAK2,
MAP2K1, TYK2
12Link
n/aToxoplasmosisAKT2, AKT3, IRAK4, JAK2,
TYK2
11Link
n/aBladder cancerDAPK1, EGFR, ERBB2, FGFR339Link
n/aHerpes simplex infectionCDC2, CDK2, JAK2, TYK214Link
NeuroblastomaALK, NTRK1, NTRK2, NTRK316Link
n/aHepatitis CAKT2, AKT3, EGFR, TYK240Link
n/aEpithelial cell signaling in Helicobacter pylori infectionEGFR, PAK1, SRC42Link
n/aCervical cancerEGFR, ERBB2, FGFR338Link
Gastric cancerEGFR, ERBB2, FGFR239Link
n/aImmunodeficienciesJAK3, LCK, ZAP7016Link
n/aGliomaEGFR, PDGFRA, PDGFRB41Link
Diabetes mellitusAKT2, INSR, PRKCD15Link
n/aViral myocarditisABL1, ABL2, FYN13Link
n/aChagas diseaseAKT2, AKT3, IRAK48Link
HemangiomaFLT4, KDR54Link
Gastrointestinal stromal tumorKIT, PDGFRA12Link
LADD syndromeFGFR2, FGFR38Link
n/aPrion diseasesFYN, MAP2K111Link
Adenocarcinoma of lungEGFR, ERBB238Link
n/aLeishmaniasisIRAK4, JAK211Link
Crouzon syndromeFGFR2, FGFR38Link
n/aMyeloproliferative disorderJAK2, PDGFRB12Link
SCIDJAK3, LCK16Link
n/aChoriocarcinomaEGFR, ERBB238Link
n/aShigellosisABL1, SRC20Link
Ovarian cancerAKT2, ERBB27Link
n/aMedullary thyroid carcinomaNTRK1, RET18Link
n/aPathogenic Escherichia coli infectionABL1, FYN12Link
n/aThyroid cancerNTRK1, RET18Link
n/aAlcoholismMAP2K1, NTRK210Link
Mental retardationPAK3, RPS6KA310Link
n/aNon-syndromic X-linked mental retardationPAK3, RPS6KA310Link
Hypoinsulinemic hypoglycemiaAKT27Link
CraniosynostosisFGFR28Link
Bent bone dysplasia syndromeFGFR28Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR28Link
Jackson-Weiss syndromeFGFR28Link
n/aFamilial partial lipodystrophyAKT27Link
n/aMultiple myelomaFGFR37Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR37Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR28Link
ScaphocephalyFGFR28Link
Beare-Stevenson cutis gyrata syndromeFGFR28Link
Pfeiffer syndromeFGFR28Link
n/aSaethre-Chotzen syndromeFGFR28Link
GlioblastomaERBB22Link
Apert syndromeFGFR28Link
AgammaglobulinemiaBTK5Link
n/aPituitary DwarfismBTK5Link
n/aCATSHL syndromeFGFR37Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK5Link
n/aSpondylometaepiphyseal dysplasiaDDR23Link
n/aOral cancerEGFR38Link
n/aEsophageal cancerEGFR38Link
n/aAgammaglobulinemiasBTK5Link
n/aMaturity onset diabetes of the youngBLK8Link
n/aCholangiocarcinomaERBB22Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR28Link
Breast cancerERBB22Link
Endometrial CancerERBB22Link
n/aLaryngeal cancerEGFR38Link
n/aDopamine receptor D2ANKK12Link
n/aPancreatic cancerERBB22Link
n/aSpermatocytic seminomaFGFR37Link
n/aAchondroplasiaFGFR37Link
n/aNephronophthisisNEK81Link
n/aInsensitivity to painNTRK115Link
n/aObesityNTRK29Link
n/aSalmonella infectionPKN29Link
n/aHypereosinophilic syndromePDGFRA10Link
n/aNephronophthisis-medullary cystic kidney diseaseNEK81Link
n/aShort rib-polydactyly syndormeNEK13Link
REtinitis pigmentosaMAK1Link
n/aNoonan syndrome and related disordersMAP2K14Link
Cardiofaciocutaneous syndromeMAP2K14Link
n/aMyasthenic syndromeMUSK5Link
n/aCongenital myasthenic syndromeMUSK5Link
n/aType I diabetes mellitusPRKCQ8Link
n/aRenal agenesis and Renal adysplasiaRET11Link
n/aTransient erythroblastopenia of childhoodTEC2Link
Venous malformationsTEK32Link
n/aRheumatoid arthritisTEK32Link
Selective T-cell defectZAP7010Link
n/aTyrosine kinase 2 deficiencyTYK28Link
Colon cancerSRC19Link
n/aCoffin-Lowry syndromeRPS6KA38Link
n/aCongenital central hypoventilation syndromeRET11Link
Hirschsprung diseaseRET11Link
Central hypoventilation syndromeRET11Link
Multiple endocrine neoplasiaRET11Link
Renal agenesisRET11Link
PheochromocytomaRET11Link
n/aParkinson diseaseLRRK25Link
n/aLewy body dementiaLRRK25Link
n/aLymphedemaFLT417Link
n/aEndocrine-cerebroosteodysplasiaICK2Link
n/aMalignant pleural mesotheliomaIGF1R5Link
Insulin-like growth factor IIGF1R5Link
n/aSynovial sarcomaIGF1R5Link
n/aLymphedemasFLT417Link
n/aCancer progression/metastasisFGFR43Link
Colorectal cancerFGFR37Link
n/aHypochondroplasiaFGFR37Link
n/aMuenke syndromeFGFR37Link
n/aThanatophoric dysplasiaFGFR37Link
n/aNevusFGFR37Link
n/aLeprechaunismINSR5Link
Rabson-Mendenhall syndromeINSR5Link
ThrombocythemiaJAK210Link
PiebaldismKIT12Link
n/aGerm cell tumorsKIT12Link
Mastocytosis with associated hematologic disorderKIT12Link
Mast cell leukemiaKIT12Link
MyelofibrosisJAK210Link
n/aBudd-Chiari syndromeJAK210Link
n/aPertussisIRAK44Link
Hyperinsulinemic hypoglycemiaINSR5Link
n/aInvasive pneumococcal diseaseIRAK44Link
IRAK4 deficiencyIRAK44Link
Polycythemia veraJAK210Link
Lymphoproliferative syndromeITK6Link