Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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
7011 to 7020 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7011
Laminin subunit beta 2
LAMS, NPHS5, PIERS
Alzheimer disease, Breast cancer, Cognition disorder, Congenital myasthenic syndrome, Coronary artery disease, Delirium, dementia, and cognitive disorders, Diffuse mesangial sclerosis, Focal glomerulosclerosis, Glomerulonephritis, Insomnia, Kidney disease, Myocardial infarction, Nephrotic syndrome, Open angle glaucoma, Prostatic neoplasms

7012
Laminin subunit beta 3
AI1A, BM600-125KDA, JEB1A, JEB1B, LAM5, LAMNB1
Amelogenesis imperfecta, Autism, Dentin dysplasia, Dentinogenesis imperfecta, Epidermolysis bullosa, Junctional epidermolysis bullosa, Neuroblastoma, Other epidermolysis bullosa

7013
Laminin subunit beta 4
-
Juvenile idiopathic arthritis

7014
Laminin subunit gamma 1
LAMB2
Aortic disease, Basal cell carcinoma, Neoplasms, Colorectal adenoma, Colorectal cancer, Diabetic neuropathy, Fuchs endothelial dystrophy, Gout, Hypertriglyceridemia, Marfan syndrome, Prostate cancer, Prostatic neoplasms, Stroke, Systemic lupus erythematosus, Diabetes mellitus type 2
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7015
Laminin subunit gamma 2
B2T, BM600, CSF, EBR2, EBR2A, JEB3A, JEB3B, LAMB2T, LAMNB2
Amelogenesis imperfecta, Atrial fibrillation, Non-small-cell lung carcinoma, Junctional epidermolysis bullosa, Liver cirrhosis, Other epidermolysis bullosa, Systemic lupus erythematosus, Systemic sclerosis

7016
Laminin subunit gamma 3
OCCM
Alzheimer disease, Androgenetic alopecia, Autism, Brain disease, Neurodevelopmental disorder, Conotruncal cardiac defect, Cortical occipital malformations, Endometriosis, Generalized anxiety disorder, Head and neck neoplasm, Intellectual developmental disorder, Mouth neoplasms, Non-specific syndromic intellectual disability, Oral cavity carcinoma, Oropharyngeal cancer
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7017
Lysosomal associated membrane protein 1
CD107a, LAMPA, LGP120
Alzheimer disease

7018
Lysosomal associated membrane protein 2
CD107b, DND, LAMP-2, LAMPB, LGP-96, LGP110
Cardiomyopathy, Dilated cardiomyopathy, Danon disease, Glycogen storage disease, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Status epilepticus

7019
Lysosomal associated membrane protein 3
CD208, DC LAMP, DC-LAMP, DCLAMP, LAMP, LAMP-3, TSC403
Bipolar disorder, Parkinson disease

7020
Lysosomal associated membrane protein family member 5
BAD-LAMP, BADLAMP, C20orf103, LAMP-5, UNC-46
Erectile dysfunction, Major depressive disorder