Allelic Variants

There are no related allelic variants
Related diseases of KIF 1AQ1A_STU (PDB code: 1AQ1, chain A)
Number of involved diseases in the family 118
Number of GSK3A related diseases 0
All kinase in this family  GSK3A
Allelic
Variants		 Disease Description Involved kinases
(This family)		 Inhibitor of
Involved Kinases		 Search
Disease
n/aEpstein-Barr virus infectionAKT1, AKT2, AKT3, CDC2,
CDK2, CHUK, CSNK2A1,
CSNK2A2, EIF2AK2, FGR,
GSK3B, JAK1, JAK3, LYN,
MAP2K3, MAP2K6, MAP3K7,
MAPK10, MAPK12, MAPK13,
MAPK14, MAPK8, MAPK9		21Link
n/aInfluenza AAKT1, AKT2, AKT3, EIF2AK2,
GSK3B, IRAK4, JAK1, JAK2,
MAP2K1, MAP2K3, MAP2K6,
MAPK1, MAPK10, MAPK12,
MAPK13, MAPK14, MAPK8,
MAPK9, PRKCA, PRKCB		62Link
n/aMeaslesAKT1, AKT2, AKT3, CDK2,
CDK4, CDK6, CHUK, CSNK2A1,
CSNK2A2, EIF2AK2, FYN,
GSK3B, IRAK4, JAK1, JAK2,
JAK3, MAP3K7, PRKCQ		19Link
n/aTuberculosisAKT1, AKT2, AKT3, CAMK2A,
CAMK2B, CAMK2D, IRAK4, JAK1,
JAK2, MAPK1, MAPK10, MAPK12,
MAPK13, MAPK14, MAPK8,
MAPK9, PLK3, SRC		22Link
n/aToxoplasmosisAKT1, AKT2, AKT3, CHUK,
IRAK4, JAK1, JAK2, MAP2K3,
MAP2K6, MAP3K7, MAPK1,
MAPK10, MAPK12, MAPK13,
MAPK14, MAPK8, MAPK9		14Link
LeukemiaABL1, ABL2, AKT1, AKT2,
AKT3, CDK4, CDK6, CHUK,
JAK2, MAP2K1, MAPK1, PIM1,
PIM2, RPS6KB1, RPS6KB2		15Link
n/aHepatitis CAKT1, AKT2, AKT3, CHUK,
EIF2AK2, GSK3B, JAK1, MAPK1,
MAPK10, MAPK12, MAPK13,
MAPK14, MAPK8, MAPK9		14Link
n/aHerpes simplex infectionCDC2, CDK2, CHUK, CSNK2A1,
CSNK2A2, EIF2AK2, JAK1,
JAK2, MAP3K7, MAPK10, MAPK8,
MAPK9		16Link
Prostate cancerAKT1, AKT2, AKT3, CDK2,
CHEK2, CHUK, FGFR1, FGFR2,
GSK3B, MAP2K1, MAPK1, PDPK1		17Link
n/aShigellosisABL1, CHUK, MAPK1, MAPK10,
MAPK12, MAPK13, MAPK14,
MAPK8, MAPK9, ROCK1, ROCK2,
SRC		22Link
n/aChagas diseaseAKT1, AKT2, AKT3, CHUK,
IRAK4, MAPK1, MAPK10,
MAPK12, MAPK13, MAPK14,
MAPK8, MAPK9		10Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCHUK, LYN, MAPK10, MAPK12,
MAPK13, MAPK14, MAPK8,
MAPK9, MET, PAK1, SRC		22Link
n/aSalmonella infectionMAPK1, MAPK10, MAPK12,
MAPK13, MAPK14, MAPK8,
MAPK9, PKN1, PKN2, ROCK1,
ROCK2		14Link
n/aLeishmaniasisIRAK4, JAK1, JAK2, MAP3K7,
MAPK1, MAPK12, MAPK13,
MAPK14, PRKCB		16Link
MelanomaAKT1, AKT2, AKT3, CDK4,
CDK6, FGFR1, MAP2K1, MAPK1,
MET		13Link
n/aPertussisIRAK4, MAPK1, MAPK10,
MAPK12, MAPK13, MAPK14,
MAPK8, MAPK9		10Link
Diabetes mellitusAKT2, MAPK1, MAPK10, MAPK8,
MAPK9, PRKCD, PRKCE		16Link
Lung cancerAKT1, AKT2, AKT3, CDK2,
CDK4, CDK6, CHUK		12Link
n/aAmyotrophic lateral sclerosisMAP2K3, MAP2K6, MAPK12,
MAPK13, MAPK14		11Link
n/aAlcoholismCAMKK1, CAMKK2, MAP2K1,
MAPK1, NTRK2		12Link
n/aPathogenic Escherichia coli infectionABL1, FYN, PRKCA, ROCK1,
ROCK2		61Link
Mental retardationCASK, DYRK1A, PAK3, RPS6KA311Link
n/aPrion diseasesFYN, MAP2K1, MAPK111Link
n/aViral myocarditisABL1, ABL2, FYN13Link
n/aImmunodeficienciesJAK3, LCK, ZAP7016Link
Colon cancerAURKA, SRC19Link
Crouzon syndromeFGFR2, FGFR38Link
Breast cancerAKT1, CHEK28Link
n/aEpileptic encephalopathyCDKL5, MAPK106Link
n/aEarly infantile epileptic encephalopathyCDKL5, MAPK106Link
n/aBasal cell carcinomaGSK3B, STK3610Link
Gastric cancerFGFR2, MET9Link
n/aCervical cancerCDK4, FGFR39Link
Ovarian cancerAKT1, AKT27Link
Colorectal cancerAKT1, FGFR37Link
n/aBladder cancerDAPK1, FGFR39Link
Pfeiffer syndromeFGFR1, FGFR29Link
Jackson-Weiss syndromeFGFR1, FGFR29Link
LADD syndromeFGFR2, FGFR38Link
NeuroblastomaNTRK2, NTRK39Link
SCIDJAK3, LCK16Link
n/aAfrican trypanosomiasisPRKCA, PRKCB55Link
n/aVibrio cholerae infectionPRKCA, PRKCB55Link
n/aNon-syndromic X-linked mental retardationPAK3, RPS6KA310Link
n/aAmoebiasisPRKCA, PRKCB55Link
n/aAutism suseptibilityMET8Link
n/aMaturity onset diabetes of the youngBLK8Link
n/aMalariaMET8Link
n/aCongenital myasthenic syndromeMUSK5Link
Hepatocellular carcinomaMET8Link
n/aFG syndromeCASK1Link
n/aMalignant melanomaCDK46Link
n/aMyasthenic syndromeMUSK5Link
Renal cell carcinomaMET8Link
Li-Fraumeni syndromeCHEK25Link
n/aAngelman syndrome-likeCDKL51Link
n/aCholangiocarcinomaMET8Link
n/aGliomaCDK46Link
n/aCocaine addictionCDK55Link
n/aPrader-Willi and Angelman syndromesCDKL51Link
n/aFamilial partial lipodystrophyAKT27Link
Hypoinsulinemic hypoglycemiaAKT27Link
n/aPituitary tumorPRKCA55Link
Glycogen storage diseasePHKG29Link
n/aCerebral infarctionPRKCH12Link
n/aPTEN hamartoma tumor syndromeAKT17Link
Selective T-cell defectZAP7010Link
n/aCoffin-Lowry syndromeRPS6KA38Link
n/aType I diabetes mellitusPRKCQ8Link
n/aCirrhosis due to liver phosphorylase kinase deficiencyPHKG29Link
n/aGlycogen storage diseasesPHKG29Link
OsteosarcomaCHEK25Link
n/aShort rib-polydactyly syndormeNEK13Link
n/aSchizophreniaAKT17Link
n/aProteus syndromeAKT17Link
n/aObesityNTRK29Link
n/aNephronophthisisNEK81Link
n/aNephronophthisis-medullary cystic kidney diseaseNEK81Link
Cardiofaciocutaneous syndromeMAP2K14Link
n/aInvasive pneumococcal diseaseIRAK44Link
n/aHypochondroplasiaFGFR37Link
n/aMuenke syndromeFGFR37Link
n/aNevusFGFR37Link
n/aAchondroplasiaFGFR37Link
n/aCATSHL syndromeFGFR37Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR28Link
n/aMultiple myelomaFGFR37Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR37Link
n/aSpermatocytic seminomaFGFR37Link
n/aThanatophoric dysplasiaFGFR37Link
n/aEndocrine-cerebroosteodysplasiaICK2Link
Lymphoproliferative syndromeITK6Link
IRAK4 deficiencyIRAK44Link
Polycythemia veraJAK210Link
n/aOguchi diseaseGRK14Link
n/aCancer progression/metastasisFGFR43Link
n/aBudd-Chiari syndromeJAK210Link
n/aCongenital stationary night blindnessGRK14Link
ScaphocephalyFGFR28Link
n/aSaethre-Chotzen syndromeFGFR28Link
Osteoglophonic dysplasiaFGFR19Link
TrigonocephalyFGFR19Link
REtinitis pigmentosaMAK1Link
Hypogonadotropic hypogonadismFGFR19Link
n/aSpondylometaepiphyseal dysplasiaDDR23Link
n/aCocoon syndromeCHUK6Link
n/aLegionellosisCLK18Link
n/aNoonan syndrome and related disordersMAP2K14Link
Kallmann syndromeFGFR19Link
ThrombocythemiaJAK210Link
CraniosynostosisFGFR28Link
n/aMyeloproliferative disorderJAK210Link
MyelofibrosisJAK210Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR28Link
Bent bone dysplasia syndromeFGFR28Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR28Link
Apert syndromeFGFR28Link
Beare-Stevenson cutis gyrata syndromeFGFR28Link