KIDFamMap

Allelic Variants
There are no related allelic variants

Related diseases of KIF 3LCTA_ADP (PDB code: 3LCT, chain A)
Number of involved diseases in the family	64
Number of ALK related diseases	2

All kinase in this family ALK

Allelic Variants	Disease Description	Involved kinases (This family)	Inhibitor of Involved Kinases	Search Disease
	Melanoma	EGFR, FGFR1, IGF1R, MET	3	Link
	Prostate cancer	EGFR, FGFR1, FGFR2, IGF1R	4	Link
	Gastric cancer	EGFR, FGFR2, MET	4	Link
n/a	Epithelial cell signaling in Helicobacter pylori infection	EGFR, MET, SRC	5	Link
	Lung cancer	ALK, EGFR, PTK2	3	Link
	Pfeiffer syndrome	FGFR1, FGFR2	3	Link
n/a	Shigellosis	ABL1, SRC	6	Link
	Colon cancer	AURKA, SRC	6	Link
	Jackson-Weiss syndrome	FGFR1, FGFR2	3	Link
	Hypogonadotropic hypogonadism	FGFR1	1	Link
	Osteoglophonic dysplasia	FGFR1	1	Link
	Cataract	EPHA2	1	Link
	Kallmann syndrome	FGFR1	1	Link
	Trigonocephaly	FGFR1	1	Link
	Bent bone dysplasia syndrome	FGFR2	2	Link
	Beare-Stevenson cutis gyrata syndrome	FGFR2	2	Link
	Apert syndrome	FGFR2	2	Link
n/a	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis	FGFR2	2	Link
n/a	Hepatitis C	EGFR	1	Link
	Adenocarcinoma of lung	EGFR	1	Link
n/a	Oral cancer	EGFR	1	Link
	Neuroblastoma	ALK	1	Link
n/a	Viral myocarditis	ABL1	2	Link
n/a	Pathogenic Escherichia coli infection	ABL1	2	Link
n/a	Esophageal cancer	EGFR	1	Link
n/a	Bladder cancer	EGFR	1	Link
	Leukemia	ABL1	2	Link
n/a	Laryngeal cancer	EGFR	1	Link
n/a	Glioma	EGFR	1	Link
n/a	Choriocarcinoma	EGFR	1	Link
n/a	Cervical cancer	EGFR	1	Link
	Craniofacial-skeletal-dermatologic dysplasia	FGFR2	2	Link
	Craniosynostosis	FGFR2	2	Link
	Hirschsprung disease	RET	2	Link
n/a	Congenital central hypoventilation syndrome	RET	2	Link
n/a	Renal agenesis and Renal adysplasia	RET	2	Link
n/a	Thyroid cancer	RET	2	Link
	Hepatocellular carcinoma	MET	1	Link
n/a	Amoebiasis	PTK2	2	Link
	Central hypoventilation syndrome	RET	2	Link
n/a	Medullary thyroid carcinoma	RET	2	Link
n/a	Immunodeficiencies	ZAP70	1	Link
	Selective T-cell defect	ZAP70	1	Link
n/a	Tuberculosis	SRC	4	Link
	Renal agenesis	RET	2	Link
	Multiple endocrine neoplasia	RET	2	Link
	Pheochromocytoma	RET	2	Link
n/a	Autism suseptibility	MET	1	Link
n/a	Malaria	MET	1	Link
n/a	Scaphocephaly and Axenfeld-Rieger anomaly	FGFR2	2	Link
n/a	Malignant pleural mesothelioma	IGF1R	2	Link
	Scaphocephaly	FGFR2	2	Link
n/a	Saethre-Chotzen syndrome	FGFR2	2	Link
	Crouzon syndrome	FGFR2	2	Link
	LADD syndrome	FGFR2	2	Link
n/a	Synovial sarcoma	IGF1R	2	Link
	Insulin-like growth factor I	IGF1R	2	Link
	Renal cell carcinoma	MET	1	Link
n/a	Cholangiocarcinoma	MET	1	Link
	Retinitis pigmentosa	MERTK	2	Link
	Hyperinsulinemic hypoglycemia	INSR	3	Link
n/a	Leprechaunism	INSR	3	Link
	Rabson-Mendenhall syndrome	INSR	3	Link
	Diabetes mellitus	INSR	3	Link

BioXGEM.

KIDFamMap

Allelic Variants