KIDFamMap

Allelic Variants
There are no related allelic variants

Related diseases of KIF 3L8XA_N4D (PDB code: 3L8X, chain A)
Number of involved diseases in the family	65
Number of GRK7 related diseases	0

All kinase in this family GRK7

Allelic Variants	Disease Description	Involved kinases (This family)	Inhibitor of Involved Kinases	Search Disease
n/a	Epstein-Barr virus infection	CDC2, CDK2, CHUK, CSNK2A1, CSNK2A2, FGR, GSK3B, LYN, MAPK10, MAPK11, MAPK14, MAPK8, MAPK9, PRKX	74	Link
	Prostate cancer	CDK2, CHEK2, CHUK, EPHB2, FGFR1, FGFR2, GSK3B, MAPK1, PDPK1	17	Link
n/a	Shigellosis	ABL1, CHUK, MAPK1, MAPK10, MAPK11, MAPK14, MAPK8, MAPK9, SRC	67	Link
n/a	Epithelial cell signaling in Helicobacter pylori infection	CHUK, LYN, MAPK10, MAPK11, MAPK14, MAPK8, MAPK9, SRC	65	Link
n/a	Herpes simplex infection	CDC2, CDK2, CHUK, CSNK2A1, CSNK2A2, MAPK10, MAPK8, MAPK9	18	Link
n/a	Hepatitis C	CHUK, GSK3B, MAPK1, MAPK10, MAPK11, MAPK14, MAPK8, MAPK9	58	Link
n/a	Toxoplasmosis	CHUK, MAPK1, MAPK10, MAPK11, MAPK14, MAPK8, MAPK9	52	Link
n/a	Influenza A	GSK3B, MAPK1, MAPK10, MAPK11, MAPK14, MAPK8, MAPK9	58	Link
n/a	Tuberculosis	MAPK1, MAPK10, MAPK11, MAPK14, MAPK8, MAPK9, SRC	66	Link
n/a	Chagas disease	CHUK, MAPK1, MAPK10, MAPK11, MAPK14, MAPK8, MAPK9	52	Link
n/a	Measles	CDK2, CHUK, CSNK2A1, CSNK2A2, FYN, GSK3B	19	Link
n/a	Pertussis	MAPK1, MAPK10, MAPK11, MAPK14, MAPK8, MAPK9	52	Link
n/a	Salmonella infection	MAPK1, MAPK10, MAPK11, MAPK14, MAPK8, MAPK9	52	Link
	Leukemia	ABL1, ABL2, CHUK, MAPK1, RPS6KB1	5	Link
	Diabetes mellitus	MAPK1, MAPK10, MAPK8, MAPK9	7	Link
n/a	Prion diseases	FYN, MAPK1, PRKX	4	Link
n/a	Viral myocarditis	ABL1, ABL2, FYN	6	Link
n/a	Leishmaniasis	MAPK1, MAPK11, MAPK14	48	Link
	Lung cancer	CDK2, CHUK	10	Link
n/a	Pathogenic Escherichia coli infection	ABL1, FYN	6	Link
	Mental retardation	DYRK1A, RPS6KA3	1	Link
	Melanoma	FGFR1, MAPK1	2	Link
	Jackson-Weiss syndrome	FGFR1, FGFR2	1	Link
n/a	Amyotrophic lateral sclerosis	MAPK11, MAPK14	47	Link
	Pfeiffer syndrome	FGFR1, FGFR2	1	Link
	Osteoglophonic dysplasia	FGFR1	1	Link
	Kallmann syndrome	FGFR1	1	Link
	Trigonocephaly	FGFR1	1	Link
n/a	Bladder cancer	DAPK1	1	Link
	Hypogonadotropic hypogonadism	FGFR1	1	Link
	Osteosarcoma	CHEK2	1	Link
	Breast cancer	CHEK2	1	Link
	Gastric cancer	FGFR2	1	Link
n/a	Maturity onset diabetes of the young	BLK	2	Link
	Li-Fraumeni syndrome	CHEK2	1	Link
n/a	Cocoon syndrome	CHUK	1	Link
	Craniofacial-skeletal-dermatologic dysplasia	FGFR2	1	Link
n/a	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis	FGFR2	1	Link
	Glycogen storage disease	PHKG2	1	Link
n/a	Cirrhosis due to liver phosphorylase kinase deficiency	PHKG2	1	Link
n/a	Glycogen storage diseases	PHKG2	1	Link
n/a	Epileptic encephalopathy	MAPK10	2	Link
n/a	Short rib-polydactyly syndorme	NEK1	1	Link
n/a	Cocaine addiction	PRKX	1	Link
n/a	Vibrio cholerae infection	PRKX	1	Link
	Colon cancer	SRC	15	Link
n/a	Coffin-Lowry syndrome	RPS6KA3	1	Link
n/a	Non-syndromic X-linked mental retardation	RPS6KA3	1	Link
n/a	Amoebiasis	PRKX	1	Link
n/a	Cardiomyopathy	PRKX	1	Link
n/a	Early infantile epileptic encephalopathy	MAPK10	2	Link
n/a	Alcoholism	MAPK1	1	Link
	Crouzon syndrome	FGFR2	1	Link
	Craniosynostosis	FGFR2	1	Link
	Bent bone dysplasia syndrome	FGFR2	1	Link
	Apert syndrome	FGFR2	1	Link
	Beare-Stevenson cutis gyrata syndrome	FGFR2	1	Link
	LADD syndrome	FGFR2	1	Link
n/a	Saethre-Chotzen syndrome	FGFR2	1	Link
n/a	Immunodeficiencies	LCK	16	Link
	SCID	LCK	16	Link
n/a	Endocrine-cerebroosteodysplasia	ICK	1	Link
n/a	Basal cell carcinoma	GSK3B	6	Link
	Scaphocephaly	FGFR2	1	Link
n/a	Scaphocephaly and Axenfeld-Rieger anomaly	FGFR2	1	Link

BioXGEM.

KIDFamMap

Allelic Variants