KIDFamMap

Allelic Variants
There are no related allelic variants

Related diseases of KIF 3G0EA_B49 (PDB code: 3G0E, chain A)
Number of involved diseases in the family	78
Number of DDR1 related diseases	0

All kinase in this family DDR1

Allelic Variants	Disease Description	Involved kinases (This family)	Inhibitor of Involved Kinases	Search Disease
	Leukemia	ABL1, ABL2, JAK2, KIT, PDGFRB	31	Link
	Prostate cancer	FGFR1, FGFR2, PDGFRA, PDGFRB	31	Link
	Melanoma	FGFR1, PDGFRA, PDGFRB	31	Link
n/a	Epstein-Barr virus infection	FGR, LYN, RIPK1	8	Link
n/a	Viral myocarditis	ABL1, ABL2, FYN	8	Link
	Gastrointestinal stromal tumor	KIT, PDGFRA	19	Link
	Pfeiffer syndrome	FGFR1, FGFR2	17	Link
	Hemangioma	FLT4, KDR	32	Link
n/a	Myeloproliferative disorder	JAK2, PDGFRB	29	Link
	LADD syndrome	FGFR2, FGFR3	7	Link
	Crouzon syndrome	FGFR2, FGFR3	7	Link
n/a	Tuberculosis	JAK2, SRC	12	Link
n/a	Measles	FYN, JAK2	7	Link
n/a	Rheumatoid arthritis	FLT1, TEK	6	Link
	Jackson-Weiss syndrome	FGFR1, FGFR2	17	Link
n/a	Glioma	PDGFRA, PDGFRB	28	Link
n/a	Shigellosis	ABL1, SRC	11	Link
	Neuroblastoma	NTRK2, NTRK3	8	Link
n/a	Pathogenic Escherichia coli infection	ABL1, FYN	8	Link
n/a	Epithelial cell signaling in Helicobacter pylori infection	LYN, SRC	11	Link
n/a	Scaphocephaly and Axenfeld-Rieger anomaly	FGFR2	6	Link
n/a	Multiple myeloma	FGFR3	7	Link
	Colorectal cancer	FGFR3	7	Link
n/a	Bladder cancer	FGFR3	7	Link
n/a	FGFR3-related short limb skeletal dysplasias	FGFR3	7	Link
	Scaphocephaly	FGFR2	6	Link
n/a	CATSHL syndrome	FGFR3	7	Link
n/a	Achondroplasia	FGFR3	7	Link
n/a	Cervical cancer	FGFR3	7	Link
	Bent bone dysplasia syndrome	FGFR2	6	Link
n/a	Saethre-Chotzen syndrome	FGFR2	6	Link
	Trigonocephaly	FGFR1	16	Link
	Osteoglophonic dysplasia	FGFR1	16	Link
	Hypogonadotropic hypogonadism	FGFR1	16	Link
n/a	Choriocarcinoma	CSF1R	10	Link
n/a	Leukoencephalopathy, diffuse hereditary, with spheroids	CSF1R	10	Link
	Kallmann syndrome	FGFR1	16	Link
	Gastric cancer	FGFR2	6	Link
	Craniofacial-skeletal-dermatologic dysplasia	FGFR2	6	Link
	Craniosynostosis	FGFR2	6	Link
n/a	Hypochondroplasia	FGFR3	7	Link
	Beare-Stevenson cutis gyrata syndrome	FGFR2	6	Link
n/a	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis	FGFR2	6	Link
	Apert syndrome	FGFR2	6	Link
n/a	Cancer progression/metastasis	FGFR4	2	Link
n/a	Muenke syndrome	FGFR3	7	Link
	Mastocytosis with associated hematologic disorder	KIT	19	Link
n/a	Immunodeficiencies	LCK	8	Link
	Mast cell leukemia	KIT	19	Link
n/a	Germ cell tumors	KIT	19	Link
	Thrombocythemia	JAK2	6	Link
	Piebaldism	KIT	19	Link
	SCID	LCK	8	Link
n/a	Congenital myasthenic syndrome	MUSK	4	Link
	Colon cancer	SRC	10	Link
	Venous malformations	TEK	1	Link
n/a	Hepatitis C	RIPK1	5	Link
n/a	Hypereosinophilic syndrome	PDGFRA	7	Link
n/a	Myasthenic syndrome	MUSK	4	Link
n/a	Alcoholism	NTRK2	8	Link
n/a	Obesity	NTRK2	8	Link
	Myelofibrosis	JAK2	6	Link
n/a	Budd-Chiari syndrome	JAK2	6	Link
n/a	Lymphedema	FLT4	7	Link
n/a	Prion diseases	FYN	5	Link
n/a	Lymphedemas	FLT4	7	Link
n/a	Thanatophoric dysplasia	FGFR3	7	Link
n/a	Nevus	FGFR3	7	Link
n/a	Spermatocytic seminoma	FGFR3	7	Link
n/a	Leprechaunism	INSR	6	Link
	Rabson-Mendenhall syndrome	INSR	6	Link
n/a	Influenza A	JAK2	6	Link
n/a	Herpes simplex infection	JAK2	6	Link
n/a	Toxoplasmosis	JAK2	6	Link
n/a	Leishmaniasis	JAK2	6	Link
	Diabetes mellitus	INSR	6	Link
	Hyperinsulinemic hypoglycemia	INSR	6	Link
	Polycythemia vera	JAK2	6	Link

BioXGEM.

KIDFamMap

Allelic Variants