KIDFamMap

Allelic Variants
There are no related allelic variants

Related diseases of KIF 3OCTA_1N1 (PDB code: 3OCT, chain A)
Number of involved diseases in the family	103
Number of TEC related diseases	1

All kinase in this family TEC

Allelic Variants	Disease Description	Involved kinases (This family)	Inhibitor of Involved Kinases	Search Disease
	Prostate cancer	BRAF, EGFR, EPHB2, ERBB2, FGFR2, PDGFRA, PDGFRB	5	Link
	Leukemia	ABL1, ABL2, BRAF, JAK2, KIT, PDGFRB	7	Link
n/a	Epstein-Barr virus infection	FGR, JAK3, LYN, SYK, TYK2	6	Link
n/a	Measles	FYN, JAK2, JAK3, TYK2	5	Link
n/a	Epithelial cell signaling in Helicobacter pylori infection	CSK, EGFR, LYN, SRC	9	Link
	Melanoma	BRAF, EGFR, PDGFRA, PDGFRB	4	Link
	Gastric cancer	EGFR, ERBB2, FGFR2	4	Link
n/a	Hepatitis C	BRAF, EGFR, TYK2	3	Link
	Adenocarcinoma of lung	BRAF, EGFR, ERBB2	4	Link
n/a	Tuberculosis	JAK2, SRC, SYK	9	Link
n/a	Cervical cancer	EGFR, ERBB2, FGFR3	4	Link
n/a	Bladder cancer	EGFR, ERBB2, FGFR3	4	Link
n/a	Viral myocarditis	ABL1, ABL2, FYN	9	Link
n/a	Glioma	EGFR, PDGFRA, PDGFRB	4	Link
n/a	Choriocarcinoma	CSF1R, EGFR, ERBB2	5	Link
n/a	Myeloproliferative disorder	JAK2, PDGFRB	4	Link
	Lung cancer	BRAF, EGFR	3	Link
n/a	Influenza A	JAK2, TYK2	2	Link
n/a	Herpes simplex infection	JAK2, TYK2	2	Link
n/a	Toxoplasmosis	JAK2, TYK2	2	Link
n/a	Immunodeficiencies	JAK3, LCK	29	Link
	Gastrointestinal stromal tumor	KIT, PDGFRA	4	Link
n/a	Thyroid cancer	BRAF, RET	3	Link
	Crouzon syndrome	FGFR2, FGFR3	2	Link
	Colon cancer	AURKA, SRC	9	Link
	LADD syndrome	FGFR2, FGFR3	2	Link
n/a	Shigellosis	ABL1, SRC	10	Link
	SCID	JAK3, LCK	29	Link
	Colorectal cancer	BRAF, FGFR3	2	Link
n/a	Pathogenic Escherichia coli infection	ABL1, FYN	9	Link
n/a	Lethal congenital contractural syndrome	ERBB3	1	Link
n/a	Type I diabetes mellitus	ERBB3	1	Link
n/a	Laryngeal cancer	EGFR	3	Link
	Glioblastoma	ERBB2	3	Link
	Ovarian cancer	ERBB2	3	Link
n/a	Cholangiocarcinoma	ERBB2	3	Link
	Endometrial Cancer	ERBB2	3	Link
	Breast cancer	ERBB2	3	Link
n/a	Pancreatic cancer	ERBB2	3	Link
n/a	Agammaglobulinemias	BTK	5	Link
n/a	Esophageal cancer	EGFR	3	Link
n/a	Alcoholism	BRAF	2	Link
	Cardiofaciocutaneous syndrome	BRAF	2	Link
n/a	Noonan syndrome and related disorders	BRAF	2	Link
n/a	Malignant melanoma	BRAF	2	Link
n/a	Maturity onset diabetes of the young	BLK	5	Link
	Brachydactyly	BMPR1B	1	Link
n/a	Chrondrodysplasia	BMPR1B	1	Link
	LEOPARD syndrome	BRAF	2	Link
	Noonan syndrome	BRAF	2	Link
n/a	Spondylometaepiphyseal dysplasia	DDR2	4	Link
n/a	Oral cancer	EGFR	3	Link
n/a	Leukoencephalopathy, diffuse hereditary, with spheroids	CSF1R	4	Link
n/a	Agammaglobulinemia and isolated hormone deficiency	BTK	5	Link
n/a	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis	FGFR2	2	Link
n/a	Pituitary Dwarfism	BTK	5	Link
	Agammaglobulinemia	BTK	5	Link
	Jackson-Weiss syndrome	FGFR2	2	Link
	Apert syndrome	FGFR2	2	Link
n/a	Germ cell tumors	KIT	4	Link
	Mast cell leukemia	KIT	4	Link
	Mastocytosis with associated hematologic disorder	KIT	4	Link
	Piebaldism	KIT	4	Link
	Hemangioma	KDR	2	Link
n/a	Leishmaniasis	JAK2	2	Link
n/a	Budd-Chiari syndrome	JAK2	2	Link
	Myelofibrosis	JAK2	2	Link
	Thrombocythemia	JAK2	2	Link
n/a	Hypereosinophilic syndrome	PDGFRA	4	Link
n/a	Renal agenesis and Renal adysplasia	RET	3	Link
	Renal agenesis	RET	3	Link
n/a	Basal cell carcinoma	STK36	2	Link
n/a	Transient erythroblastopenia of childhood	TEC	3	Link
n/a	Tyrosine kinase 2 deficiency	TYK2	1	Link
	Pheochromocytoma	RET	3	Link
	Multiple endocrine neoplasia	RET	3	Link
	Hirschsprung disease	RET	3	Link
n/a	Congenital central hypoventilation syndrome	RET	3	Link
	Central hypoventilation syndrome	RET	3	Link
n/a	Medullary thyroid carcinoma	RET	3	Link
	Polycythemia vera	JAK2	2	Link
	Hyperinsulinemic hypoglycemia	INSR	1	Link
	Scaphocephaly	FGFR2	2	Link
n/a	Scaphocephaly and Axenfeld-Rieger anomaly	FGFR2	2	Link
n/a	Multiple myeloma	FGFR3	1	Link
n/a	Saethre-Chotzen syndrome	FGFR2	2	Link
	Pfeiffer syndrome	FGFR2	2	Link
	Beare-Stevenson cutis gyrata syndrome	FGFR2	2	Link
	Bent bone dysplasia syndrome	FGFR2	2	Link
	Craniofacial-skeletal-dermatologic dysplasia	FGFR2	2	Link
	Craniosynostosis	FGFR2	2	Link
n/a	FGFR3-related short limb skeletal dysplasias	FGFR3	1	Link
n/a	CATSHL syndrome	FGFR3	1	Link
n/a	Prion diseases	FYN	5	Link
n/a	Leprechaunism	INSR	1	Link
	Rabson-Mendenhall syndrome	INSR	1	Link
	Diabetes mellitus	INSR	1	Link
n/a	Thanatophoric dysplasia	FGFR3	1	Link
n/a	Spermatocytic seminoma	FGFR3	1	Link
n/a	Achondroplasia	FGFR3	1	Link
n/a	Hypochondroplasia	FGFR3	1	Link
n/a	Muenke syndrome	FGFR3	1	Link
n/a	Nevus	FGFR3	1	Link

BioXGEM.

KIDFamMap

Allelic Variants