Allelic Variants

There are no related allelic variants
Related diseases of KIF 2VTTA_LZD (PDB code: 2VTT, chain A)
Number of involved diseases in the family 111
Number of GRK7 related diseases 0
All kinase in this family  GRK7
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
n/aEpstein-Barr virus infectionAKT2, CDC2, CDK2, CHUK,
CSNK2A1, CSNK2A2, EIF2AK2,
FGR, GSK3B, JAK1, JAK3, LYN,
MAP2K3, MAP2K6, MAP3K7,
MAPK10, MAPK14, MAPK9
23Link
n/aMeaslesAKT2, CDK2, CDK4, CDK6,
CHUK, CSNK2A1, CSNK2A2,
EIF2AK2, FYN, GSK3B, IRAK4,
JAK1, JAK2, JAK3, MAP3K7,
PRKCQ
25Link
n/aInfluenza AAKT2, EIF2AK2, GSK3B, IRAK4,
JAK1, JAK2, MAP2K1, MAP2K3,
MAP2K6, MAPK10, MAPK14,
MAPK9, PRKCA
10Link
n/aTuberculosisAKT2, CAMK2A, CAMK2B,
CAMK2D, IRAK4, JAK1, JAK2,
MAPK10, MAPK14, MAPK9, SRC
6Link
n/aToxoplasmosisAKT2, CHUK, IRAK4, JAK1,
JAK2, MAP2K3, MAP2K6,
MAP3K7, MAPK10, MAPK14,
MAPK9
6Link
n/aHerpes simplex infectionCDC2, CDK2, CHUK, CSNK2A1,
CSNK2A2, EIF2AK2, JAK1,
JAK2, MAP3K7, MAPK10, MAPK9
22Link
LeukemiaABL1, ABL2, AKT2, CDK4,
CDK6, CHUK, JAK2, MAP2K1,
PIM2, RPS6KB1
8Link
Prostate cancerAKT2, CDK2, CHEK2, CHUK,
FGFR1, FGFR2, GSK3B, MAP2K1,
PDPK1
28Link
n/aShigellosisABL1, CHUK, MAPK10, MAPK14,
MAPK9, ROCK1, ROCK2, SRC
5Link
n/aHepatitis CAKT2, CHUK, EIF2AK2, GSK3B,
JAK1, MAPK10, MAPK14, MAPK9
5Link
n/aSalmonella infectionMAPK10, MAPK14, MAPK9, PKN1,
PKN2, ROCK1, ROCK2
4Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCHUK, LYN, MAPK10, MAPK14,
MAPK9, MET, SRC
5Link
MelanomaAKT2, CDK4, CDK6, FGFR1,
MAP2K1, MET
10Link
n/aChagas diseaseAKT2, CHUK, IRAK4, MAPK10,
MAPK14, MAPK9
5Link
n/aLeishmaniasisIRAK4, JAK1, JAK2, MAP3K7,
MAPK14
6Link
Lung cancerAKT2, CDK2, CDK4, CDK6, CHUK20Link
n/aPathogenic Escherichia coli infectionABL1, FYN, PRKCA, ROCK1,
ROCK2
4Link
n/aAlcoholismCAMKK1, CAMKK2, MAP2K1,
NTRK2
7Link
Mental retardationCASK, DYRK1A, PAK3, RPS6KA35Link
n/aPertussisIRAK4, MAPK10, MAPK14, MAPK94Link
n/aImmunodeficienciesJAK3, LCK, ZAP705Link
n/aViral myocarditisABL1, ABL2, FYN4Link
n/aAmyotrophic lateral sclerosisMAP2K3, MAP2K6, MAPK142Link
Diabetes mellitusAKT2, MAPK10, MAPK92Link
n/aPrion diseasesFYN, MAP2K15Link
n/aEpileptic encephalopathyCDKL5, MAPK102Link
Gastric cancerFGFR2, MET3Link
Jackson-Weiss syndromeFGFR1, FGFR27Link
n/aEarly infantile epileptic encephalopathyCDKL5, MAPK102Link
Pfeiffer syndromeFGFR1, FGFR27Link
LADD syndromeFGFR2, FGFR34Link
Crouzon syndromeFGFR2, FGFR34Link
NeuroblastomaNTRK2, NTRK34Link
n/aCervical cancerCDK4, FGFR35Link
n/aNon-syndromic X-linked mental retardationPAK3, RPS6KA34Link
Colon cancerAURKA, SRC5Link
SCIDJAK3, LCK4Link
n/aBladder cancerDAPK1, FGFR34Link
Apert syndromeFGFR23Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR23Link
n/aSpondylometaepiphyseal dysplasiaDDR21Link
Hypogonadotropic hypogonadismFGFR17Link
Osteoglophonic dysplasiaFGFR17Link
Kallmann syndromeFGFR17Link
TrigonocephalyFGFR17Link
n/aMalignant melanomaCDK42Link
n/aLegionellosisCLK15Link
n/aFG syndromeCASK1Link
Beare-Stevenson cutis gyrata syndromeFGFR23Link
n/aMaturity onset diabetes of the youngBLK4Link
Hypoinsulinemic hypoglycemiaAKT22Link
Ovarian cancerAKT22Link
n/aFamilial partial lipodystrophyAKT22Link
n/aGliomaCDK42Link
n/aCocaine addictionCDK53Link
OsteosarcomaCHEK24Link
n/aCocoon syndromeCHUK2Link
Breast cancerCHEK24Link
Li-Fraumeni syndromeCHEK24Link
n/aPrader-Willi and Angelman syndromesCDKL51Link
n/aAngelman syndrome-likeCDKL51Link
n/aSaethre-Chotzen syndromeFGFR23Link
Bent bone dysplasia syndromeFGFR23Link
n/aCholangiocarcinomaMET1Link
n/aMalariaMET1Link
n/aAutism suseptibilityMET1Link
Hepatocellular carcinomaMET1Link
Renal cell carcinomaMET1Link
Cardiofaciocutaneous syndromeMAP2K15Link
n/aMyeloproliferative disorderJAK23Link
ThrombocythemiaJAK23Link
REtinitis pigmentosaMAK1Link
n/aNoonan syndrome and related disordersMAP2K15Link
n/aCongenital myasthenic syndromeMUSK2Link
n/aMyasthenic syndromeMUSK2Link
n/aPituitary tumorPRKCA1Link
n/aType I diabetes mellitusPRKCQ4Link
n/aCoffin-Lowry syndromeRPS6KA34Link
Selective T-cell defectZAP701Link
n/aAmoebiasisPRKCA1Link
n/aAfrican trypanosomiasisPRKCA1Link
n/aObesityNTRK24Link
n/aGlycogen storage diseasesPHKG25Link
n/aCirrhosis due to liver phosphorylase kinase deficiencyPHKG25Link
n/aVibrio cholerae infectionPRKCA1Link
Glycogen storage diseasePHKG25Link
MyelofibrosisJAK23Link
n/aBudd-Chiari syndromeJAK23Link
n/aCATSHL syndromeFGFR34Link
n/aAchondroplasiaFGFR34Link
Colorectal cancerFGFR34Link
n/aHypochondroplasiaFGFR34Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR34Link
n/aMultiple myelomaFGFR34Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR23Link
CraniosynostosisFGFR23Link
ScaphocephalyFGFR23Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR23Link
n/aMuenke syndromeFGFR34Link
n/aNevusFGFR34Link
n/aInvasive pneumococcal diseaseIRAK43Link
IRAK4 deficiencyIRAK43Link
Lymphoproliferative syndromeITK4Link
Polycythemia veraJAK23Link
n/aEndocrine-cerebroosteodysplasiaICK3Link
n/aBasal cell carcinomaGSK3B2Link
n/aSpermatocytic seminomaFGFR34Link
n/aThanatophoric dysplasiaFGFR34Link
n/aCancer progression/metastasisFGFR41Link
n/aOguchi diseaseGRK12Link
n/aCongenital stationary night blindnessGRK12Link