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KIDFamMap: Kinase-inhibitor-disease family map
Statistics
6 kinase conformation types
and 1208 kinase-inhibitor families
962 kinase-inhibitor-disease relationships
399 human protein kinases
35,788 kinase inhibitors
186,985 kinase-inhibitor assays
55,603 kinase-inhibitor interactions (<=10uM)
339 diseases
638 disease allelic variants
updated at August 23, 2012
Search by disease
Disease
Compound
Kinase
Input a disease name (Ex:
Leukemia
)
Browse by Alphabet:
Alphabet
A (20)
B (8)
C (34)
D (8)
E (7)
F (5)
G (6)
H (15)
I (6)
J (2)
K (1)
L (17)
M (23)
N (8)
O (6)
P (26)
R (7)
S (15)
T (17)
V (3)
W (1)
Other (1)
All diseases
Achondroplasia
Acromesomelic dysplasia
Acute lymphoblastic leukemia
Acute myeloid leukemia
Adenocarcinoma of lung
African trypanosomiasis
Agammaglobulinemia
Alcoholism
Alveolar rhabdomyosarcoma
Amoebiasis
Amyotrophic lateral sclerosis
Angelman syndrome-like
Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
Aortic aneurysm
Apert syndrome
Asthma susceptibility
Ataxia telangiectasia
Ataxia with ocular apraxia
Ataxia-telangiectasia
Autism suseptibility
Basal cell carcinoma
Beare-Stevenson cutis gyrata syndrome
Bent bone dysplasia syndrome
Bladder cancer
Brachydactyly
Breast and colorectal cancer
Breast cancer
Budd-Chiari syndrome
Cancer progression/metastasis
Cardiofaciocutaneous syndrome
Cardiomyopathy
Cataract
CATSHL syndrome
Central hypoventilation syndrome
Cerebral infarction
Cervical cancer
Chagas disease
Charcot-Marie-Tooth disease
Cholangiocarcinoma
Choriocarcinoma
Chrondrodysplasia
Chronic lymphocytic leukemia
Chronic myeloid leukemia
Cirrhosis due to liver phosphorylase kinase deficiency
Cocaine addiction
Cocoon syndrome
Coenzyme Q10 deficiency
Coffin-Lowry syndrome
Colon cancer
Colorectal cancer
Combined immunodeficiencies
Cone-rod dystrophy
Cone-rod dystrophy and cone dystrophy
Congenital central hypoventilation syndrome
Congenital myasthenic syndrome
Congenital stationary night blindness
Coronary heart disease
Craniofacial-skeletal-dermatologic dysplasia
Craniosynostosis
Crouzon syndrome
Crouzon syndrome with acanthosis nigricans
Cutaneous telangiectasia and cancer syndrome
Deafness
Diabetes mellitus
Diarrhea
Dilated cardiomyopathy
Distal hereditary motor neuropathies
Distal muscular dystrophies
Dopamine receptor D2
Dystonia-Parkinsonism
Early infantile epileptic encephalopathy
Endocrine-cerebroosteodysplasia
Endometrial Cancer
Epileptic encephalopathy
Epithelial cell signaling in Helicobacter pylori infection
Epstein-Barr virus infection
Esophageal cancer
Familial partial lipodystrophy
Familial thoracic aortic aneurysm and dissection
FG syndrome
FGFR3-related short limb skeletal dysplasias
Fibrodysplasia ossificans progressiva
Gastric cancer
Gastrointestinal stromal tumor
Germ cell tumors
Glioblastoma
Glioma
Glycogen storage diseases
Hemangioma
Hepatitis C
Hepatocellular carcinoma
Hereditary hemorrhagic telangiectasia
Herpes simplex infection
Heterotaxy
Hirschsprung disease
Hypereosinophilic syndrome
Hyperinsulinemic hypoglycemia
Hyperkalemic distal renal tubular acidosis
Hypertrophic cardiomyopathy
Hypochondroplasia
Hypogonadotropic hypogonadism
Hypoinsulinemic hypoglycemia with hemihypertrophy
Hypomagnesemia
Influenza A
Insensitivity to pain
Insulin-like growth factor I
Insulin-resistant diabetes mellitus with acanthosis nigricans
Invasive pneumococcal disease
IRAK4 deficiency
Jackson-Weiss syndrome
Juvenile polyposis syndrome
Kallmann syndrome
LADD syndrome
Laryngeal cancer
Leber congenital amaurosis
Legionellosis
Leishmaniasis
LEOPARD syndrome
Leprechaunism
Lethal congenital contractural syndrome
Leukemia
Leukoencephalopathy
Lewy body dementia
Li-Fraumeni syndrome
Loeys-Dietz syndrome
Lung cancer
Lymphedema
Lymphoma
Lymphoproliferative syndrome
Malaria
Malignant melanoma
Malignant pleural mesothelioma
Mast cell leukemia
Mastocytosis with associated hematologic disorder
Maturity onset diabetes of the young
Measles
Meconium ileus
Medullary thyroid carcinoma
Melanoma
Mental retardation
Mental retardation and microcephaly with pontine and cerebellar hypoplasia
Mosaic variegated aneuploidy syndrome
Muenke syndrome
Multiple endocrine neoplasia
Multiple myeloma
Muscular dystrophy
Myasthenic syndrome
Myelofibrosis
Myelomonocytic leukemia
Myeloproliferative disorder
Myopathy
Myotonic dystrophy
Nephronophthisis medullary cystic kidney disease
Neuroblastoma
Neuropathy
Nevus
Non-small cell lung cancer
Non-syndromic X-linked mental retardation
Noonan syndrome
Noonan syndrome and related disorders
Obesity
Oguchi disease
Oral cancer
Osteoglophonic dysplasia
Osteosarcoma
Ovarian cancer
Pancreatic cancer
Parkinson disease
Pathogenic Escherichia coli infection
Permanent neonatal diabetes mellitus
Persistent Mullerian duct syndrom
Pertussis
Peutz-Jeghers syndrome
Pfeiffer syndrome
Pheochromocytoma
Piebaldism
Pituitary Dwarfism
Pituitary tumor
Polycythemia vera
Polyhydramnios
Polyposis
Pontocerebellar hypoplasia
Popliteal pterygium syndrome
Prader-Willi and Angelman syndromes
Premature chromatid separation trait
Prion diseases
Prostate cancer
Proteus syndrome
Pseudohypoaldosteronism
PTEN hamartoma tumor syndrome
Pulmonary hypertension
Pulmonary venoocclusive disease
Rabson-Mendenhall syndrome
Renal agenesis
Renal agenesis and Renal adysplasia
Renal cell carcinoma
Retinitis pigmentosa
Rheumatoid arthritis
Robinow syndrome
Saethre-Chotzen syndrome
Salmonella infection
Scaphocephaly
Scaphocephaly and Axenfeld-Rieger anomaly
Schizophrenia
SCID
Seckel syndrome
Selective T-cell defect
Shigellosis
Short rib-polydactyly syndorme
Small cell lung cancer
Spermatocytic seminoma
Spinocerebellar ataxia
Spondylometaepiphyseal dysplasia
Synovial sarcoma
T-B+Severe combined immunodeficiencies
T-cell prolymphocytic leukemia
Telangiectasia
Testicular tumor
Thanatophoric dysplasia
Thrombocythemia
Thrombocytopenia
Thyroid cancer
Thyroid carcinoma
Tibial muscular dystrophy
Toxoplasmosis
Transient erythroblastopenia of childhood
Trigonocephaly
Tuberculosis
Type I diabetes mellitus
Type II diabetes mellitus
Tyrosine kinase 2 deficiency
Venous malformations
Vibrio cholerae infection
Viral myocarditis
Wolcott-Rallison syndrome