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 NEK1 related diseases 1
All kinase in this family  NEK1
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