Genes | GeDiPNet - Gene Disease Pathway & Associations

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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

7001 to 7010 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
7001	8270	LAGE3	L antigen family member 3	CVG5, DXS9879E, DXS9951E, ESO3, GAMOS2, ITBA2, Pcc1	Galloway-mowat syndrome
7002	3903	LAIR1	Leukocyte associated immunoglobulin like receptor 1	CD305, LAIR-1	Iga nephropathy
7003	3904	LAIR2	Leukocyte associated immunoglobulin like receptor 2	CD306	Colorectal cancer
7004	3906	LALBA	Lactalbumin alpha	HAMLET, LYZG	Psychiatric disorders
7005	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
7006	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)
7007	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
7008	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
7009	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)
7010	3912	LAMB1	Laminin subunit beta 1	CLM, LIS5	Autism, Central nervous system cancer, Ulcerative colitis, Lissencephaly, Cobblestone lissencephaly, Coloboma, Congenital ocular coloboma, Corneal disease, Corneal dystrophy, Eating disorder, Endometriosis, Eye disease, Fuchs endothelial dystrophy, Glioblastoma, Glioma View all (5 more)

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