Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "L"

31 to 40 of 462 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
31	24141	LAMP5	Lysosomal associated membrane protein family member 5	BAD-LAMP, BADLAMP, C20orf103, LAMP-5, UNC-46	Erectile dysfunction, Major depressive disorder
32	28956	LAMTOR2	Late endosomal/lysosomal adaptor, MAPK and MTOR activator 2	ENDAP, HSPC003, MAPBPIP, MAPKSP1AP, ROBLD3, Ragulator2, p14	Parkinson disease
33	8649	LAMTOR3	Late endosomal/lysosomal adaptor, MAPK and MTOR activator 3	MAP2K1IP1, MAPBP, MAPKSP1, MP1, PRO0633, Ragulator3	Peripheral arterial disease
34	389541	LAMTOR4	Late endosomal/lysosomal adaptor, MAPK and MTOR activator 4	C7orf59	Alzheimer disease, Venous thromboembolism
35	10542	LAMTOR5	Late endosomal/lysosomal adaptor, MAPK and MTOR activator 5	HBXIP, XIP	Breast neoplasms
36	10314	LANCL1	LanC like glutathione S-transferase 1	GPR69A, p40	Contracture
37	55915	LANCL2	LanC like glutathione S-transferase 2	GPR69B, TASP	Color vision deficiency
38	51056	LAP3	Leucine aminopeptidase 3	HEL-S-106, LAP, LAPEP, PEPS	Alzheimer disease
39	7805	LAPTM5	Lysosomal protein transmembrane 5	CLAST6	Iga nephropathy, Hypertension
40	9215	LARGE1	LARGE xylosyl- and glucuronyltransferase 1	LARGE, MDC1D, MDDGA6, MDDGB6	Amphetamine or sympathomimetic abuse, Congenital muscular dystrophy due to dystroglycanopathy, Congenital muscular dystrophy, Congenital myopathy, Liver neoplasms, Major depressive disorder, Metabolic syndrome, Muscle eye brain disease, Muscular dystrophy, Neurotic disorder, Oligodendroglioma, Retinitis pigmentosa, Schizophrenia, Scoliosis, Diabetes mellitus type 2, Walker-warburg syndrome View all (1 more)

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