Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Showing genes starting with "L"

11 to 20 of 462 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
11	646262	LACTBL1	Lactamase beta like 1	-	Metabolic syndrome, Diabetes mellitus type 2
12	8270	LAGE3	L antigen family member 3	CVG5, DXS9879E, DXS9951E, ESO3, GAMOS2, ITBA2, Pcc1	Galloway-mowat syndrome
13	3903	LAIR1	Leukocyte associated immunoglobulin like receptor 1	CD305, LAIR-1	Iga nephropathy
14	3904	LAIR2	Leukocyte associated immunoglobulin like receptor 2	CD306	Colorectal cancer
15	3906	LALBA	Lactalbumin alpha	HAMLET, LYZG	Psychiatric disorders
16	284217	LAMA1	Laminin subunit alpha 1	LAMA, PTBHS, S-LAM-alpha	Alzheimer disease, Ataxia with oculomotor apraxia, Brain injuries, Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts, Colorectal neoplasms, Intellectual developmental disorder, Lung cancer, Nonalcoholic fatty liver disease, Non-small cell lung carcinoma, Optic atrophy, Retinitis pigmentosa, Schizophrenia, Squamous cell carcinoma, Diabetes mellitus type 2
17	3908	LAMA2	Laminin subunit alpha 2	LAMM, MDC1A	Asthma, Attention deficit hyperactivity disorder, Dilated cardiomyopathy, Charcot-marie-tooth disease, Color vision deficiency, Congenital merosin-deficient muscular dystrophy, Congenital muscular dystrophy, Eye disease, Hyperopia, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Juvenile idiopathic arthritis, Limb-girdle muscular dystrophy, Muscular dystrophy, Myopathy View all (11 more)
18	3909	LAMA3	Laminin subunit alpha 3	BM600, E170, JEB2A, JEB2B, JEB2C, LAMNA, LOCS	Amyotrophic lateral sclerosis, Skin ulcer, Junctional epidermolysis bullosa, Interstitial lung disease, Laryngo-onycho-cutaneous syndrome, Ovarian epithelial cancer, Ovarian cancer, Ovarian serous carcinoma, Seasonal allergic rhinitis
19	3910	LAMA4	Laminin subunit alpha 4	CMD1JJ, LAMA3, LAMA4*-1	Arrhythmogenic right ventricular cardiomyopathy, Brugada syndrome, Cardiomyopathy, Dilated cardiomyopathy, Left ventricular noncompaction cardiomyopathy, Pelvic organ prolapse, Spinocerebellar ataxia, Catecholaminergic polymorphic ventricular tachycardia, Wolff-parkinson-white syndrome
20	3911	LAMA5	Laminin subunit alpha 5	BBDS2, NPHS26	Bent bone dysplasia, Colorectal adenoma, Colorectal cancer, Presynaptic congenital myasthenic syndromes, Congenital omphalocele, Desbuquois syndrome, Developmental disability, Focal glomerulosclerosis, Fuchs endothelial dystrophy, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Holoprosencephaly, Insomnia, Multiple sclerosis, Nephrotic syndrome View all (5 more)

«««123 4 5...»»»