Allelic Variants

There are no related allelic variants
Related diseases of KIF 2B7AA_IZA (PDB code: 2B7A, chain A)
Number of involved diseases in the family 65
Number of JAK2 related diseases 12
All kinase in this family  JAK2
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
n/aMeaslesCDK2, CDK4, FYN, JAK1, JAK2,
JAK3, MAP3K7
11Link
Lung cancerALK, BRAF, CDK2, CDK4, PTK2,
ROS1
7Link
Prostate cancerBRAF, CDK2, FGFR2, PDPK16Link
n/aEpstein-Barr virus infectionCDK2, JAK1, JAK3, MAP3K76Link
n/aHerpes simplex infectionCDK2, JAK1, JAK2, MAP3K710Link
NeuroblastomaALK, NTRK1, NTRK2, NTRK31Link
n/aThyroid cancerBRAF, NTRK1, RET2Link
n/aToxoplasmosisJAK1, JAK2, MAP3K77Link
LeukemiaBRAF, CDK4, JAK29Link
n/aTuberculosisJAK1, JAK2, RIPK27Link
n/aLeishmaniasisJAK1, JAK2, MAP3K77Link
n/aInfluenza AJAK1, JAK27Link
n/aMedullary thyroid carcinomaNTRK1, RET1Link
n/aAlcoholismBRAF, NTRK22Link
n/aHepatitis CBRAF, JAK13Link
n/aMalignant melanomaBRAF, CDK42Link
MelanomaBRAF, CDK42Link
n/aBladder cancerDAPK11Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK1Link
Apert syndromeFGFR21Link
Gastric cancerFGFR21Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
Bent bone dysplasia syndromeFGFR21Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
n/aGliomaCDK41Link
n/aNoonan syndrome and related disordersBRAF1Link
Colorectal cancerBRAF1Link
Cardiofaciocutaneous syndromeBRAF1Link
Adenocarcinoma of lungBRAF1Link
LEOPARD syndromeBRAF1Link
Noonan syndromeBRAF1Link
n/aCervical cancerCDK41Link
Colon cancerAURKA1Link
CraniosynostosisFGFR21Link
LADD syndromeFGFR21Link
Crouzon syndromeFGFR21Link
n/aAmoebiasisPTK21Link
n/aSalmonella infectionPKN11Link
n/aObesityNTRK21Link
n/aShort rib-polydactyly syndormeNEK11Link
n/aInsensitivity to painNTRK11Link
n/aRenal agenesis and Renal adysplasiaRET1Link
Hirschsprung diseaseRET1Link
Renal agenesisRET1Link
n/aShigellosisRIPK21Link
PheochromocytomaRET1Link
Multiple endocrine neoplasiaRET1Link
n/aCongenital central hypoventilation syndromeRET1Link
Central hypoventilation syndromeRET1Link
SCIDJAK33Link
n/aImmunodeficienciesJAK33Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
ScaphocephalyFGFR21Link
n/aSaethre-Chotzen syndromeFGFR21Link
Jackson-Weiss syndromeFGFR21Link
Pfeiffer syndromeFGFR21Link
n/aPrion diseasesFYN1Link
n/aPathogenic Escherichia coli infectionFYN1Link
n/aMyeloproliferative disorderJAK27Link
ThrombocythemiaJAK27Link
MyelofibrosisJAK27Link
n/aBudd-Chiari syndromeJAK27Link
n/aViral myocarditisFYN1Link
Polycythemia veraJAK27Link