Allelic Variants

There are no related allelic variants
Related diseases of KIF 2WIHA_P48 (PDB code: 2WIH, chain A)
Number of involved diseases in the family 105
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
n/aEpstein-Barr virus infectionAKT1, AKT2, CDC2, CDK2,
CHUK, CSNK2A1, CSNK2A2, FGR,
GSK3B, JAK1, JAK3, LYN,
MAP2K6, MAP3K7, MAPK10,
MAPK14, MAPK8
206Link
n/aMeaslesAKT1, AKT2, CDK2, CDK4,
CHUK, CSNK2A1, CSNK2A2, FYN,
GSK3B, IRAK4, JAK1, JAK2,
JAK3, MAP3K7, PRKCQ
198Link
n/aInfluenza AAKT1, AKT2, GSK3B, IRAK4,
JAK1, JAK2, MAP2K1, MAP2K6,
MAPK10, MAPK14, MAPK8, PRKCA
112Link
n/aToxoplasmosisAKT1, AKT2, CHUK, IRAK4,
JAK1, JAK2, MAP2K6, MAP3K7,
MAPK10, MAPK14, MAPK8
102Link
n/aTuberculosisAKT1, AKT2, IRAK4, JAK1,
JAK2, MAPK10, MAPK14, MAPK8,
PLK3, SRC
151Link
n/aHerpes simplex infectionCDC2, CDK2, CHUK, CSNK2A1,
CSNK2A2, JAK1, JAK2, MAP3K7,
MAPK10, MAPK8
135Link
Prostate cancerAKT1, AKT2, CDK2, CHUK,
FGFR1, FGFR2, GSK3B, MAP2K1,
PDPK1
128Link
LeukemiaABL1, ABL2, AKT1, AKT2,
CDK4, CHUK, JAK2, MAP2K1
114Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCHUK, LYN, MAPK10, MAPK14,
MAPK8, MET, PAK1, SRC
96Link
n/aHepatitis CAKT1, AKT2, CHUK, GSK3B,
JAK1, MAPK10, MAPK14, MAPK8
79Link
n/aChagas diseaseAKT1, AKT2, CHUK, IRAK4,
MAPK10, MAPK14, MAPK8
73Link
n/aShigellosisABL1, CHUK, MAPK10, MAPK14,
MAPK8, ROCK1, SRC
101Link
MelanomaAKT1, AKT2, CDK4, FGFR1,
MAP2K1, MET
80Link
n/aSalmonella infectionMAPK10, MAPK14, MAPK8, PKN1,
PKN2, ROCK1
60Link
n/aLeishmaniasisIRAK4, JAK1, JAK2, MAP3K7,
MAPK14
88Link
Lung cancerAKT1, AKT2, CDK2, CDK4, CHUK146Link
n/aPertussisIRAK4, MAPK10, MAPK14, MAPK859Link
Diabetes mellitusAKT2, MAPK10, MAPK8, PRKCD24Link
n/aPathogenic Escherichia coli infectionABL1, FYN, PRKCA, ROCK121Link
n/aViral myocarditisABL1, ABL2, FYN14Link
n/aAlcoholismCAMKK1, MAP2K1, NTRK23Link
n/aPrion diseasesFYN, MAP2K12Link
Gastric cancerFGFR2, MET7Link
Pfeiffer syndromeFGFR1, FGFR29Link
Crouzon syndromeFGFR2, FGFR32Link
Colon cancerAURKA, SRC108Link
Jackson-Weiss syndromeFGFR1, FGFR29Link
Colorectal cancerAKT1, FGFR313Link
Ovarian cancerAKT1, AKT211Link
n/aCervical cancerCDK4, FGFR359Link
n/aEpileptic encephalopathyCDKL5, MAPK103Link
n/aEarly infantile epileptic encephalopathyCDKL5, MAPK103Link
LADD syndromeFGFR2, FGFR32Link
n/aImmunodeficienciesJAK3, LCK42Link
SCIDJAK3, LCK42Link
Mental retardationPAK3, RPS6KA32Link
NeuroblastomaNTRK2, NTRK33Link
n/aNon-syndromic X-linked mental retardationPAK3, RPS6KA32Link
n/aAmyotrophic lateral sclerosisMAP2K6, MAPK1459Link
n/aMalariaMET7Link
n/aMaturity onset diabetes of the youngBLK2Link
n/aAutism suseptibilityMET7Link
Hepatocellular carcinomaMET7Link
Hypoinsulinemic hypoglycemiaAKT211Link
n/aCholangiocarcinomaMET7Link
n/aFamilial partial lipodystrophyAKT211Link
n/aPrader-Willi and Angelman syndromesCDKL51Link
n/aAngelman syndrome-likeCDKL51Link
n/aCocaine addictionCDK52Link
n/aGliomaCDK457Link
Renal cell carcinomaMET7Link
n/aMalignant melanomaCDK457Link
n/aSchizophreniaAKT111Link
Cardiofaciocutaneous syndromeMAP2K12Link
n/aAmoebiasisPRKCA7Link
n/aAfrican trypanosomiasisPRKCA7Link
n/aPTEN hamartoma tumor syndromeAKT111Link
n/aPituitary tumorPRKCA7Link
n/aCoffin-Lowry syndromeRPS6KA32Link
n/aType I diabetes mellitusPRKCQ11Link
n/aVibrio cholerae infectionPRKCA7Link
Glycogen storage diseasePHKG21Link
n/aCongenital myasthenic syndromeMUSK2Link
n/aProteus syndromeAKT111Link
n/aMyasthenic syndromeMUSK2Link
Breast cancerAKT111Link
n/aCirrhosis due to liver phosphorylase kinase deficiencyPHKG21Link
n/aGlycogen storage diseasesPHKG21Link
n/aObesityNTRK23Link
n/aNoonan syndrome and related disordersMAP2K12Link
IRAK4 deficiencyIRAK41Link
n/aHypochondroplasiaFGFR32Link
n/aMuenke syndromeFGFR32Link
n/aAchondroplasiaFGFR32Link
n/aCATSHL syndromeFGFR32Link
n/aMultiple myelomaFGFR32Link
n/aBladder cancerFGFR32Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR32Link
n/aNevusFGFR32Link
n/aSpermatocytic seminomaFGFR32Link
Lymphoproliferative syndromeITK10Link
n/aInvasive pneumococcal diseaseIRAK41Link
Polycythemia veraJAK231Link
n/aBasal cell carcinomaGSK3B6Link
n/aThanatophoric dysplasiaFGFR32Link
n/aCancer progression/metastasisFGFR42Link
n/aBudd-Chiari syndromeJAK231Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
ScaphocephalyFGFR22Link
Kallmann syndromeFGFR19Link
ThrombocythemiaJAK231Link
TrigonocephalyFGFR19Link
Osteoglophonic dysplasiaFGFR19Link
n/aCocoon syndromeCHUK3Link
n/aSpondylometaepiphyseal dysplasiaDDR22Link
Hypogonadotropic hypogonadismFGFR19Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
Apert syndromeFGFR22Link
MyelofibrosisJAK231Link
n/aSaethre-Chotzen syndromeFGFR22Link
n/aMyeloproliferative disorderJAK231Link
CraniosynostosisFGFR22Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link