Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "L"
191 to 200 of 464 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

191
Lin-54 DREAM MuvB core complex component
CXCDC1, JC8.6, MIP120, TCX1
Atrial fibrillation, Cardiovascular disease

192
Lin-7 cell polarity scaffold A
LIN-7A, LIN7, MALS-1, MALS1, TIP-33, VELI1
Carcinoma, Liver cirrhosis, Diabetes mellitus type 2

193
Lin-7 cell polarity scaffold C
LIN-7-C, LIN-7C, MALS-3, MALS3, VELI3
Metabolic syndrome, Pancreatic cancer, Hypertension, Diabetes mellitus type 2

194
LINC02210-CRHR1 readthrough
CRHR1-IT1-CRHR1, MGC57346-CRHR1
Alzheimer disease, Androgenetic alopecia, Autism, Breast cancer, Cancer, Colorectal cancer, Corticobasal degeneration, Dementia, Estrogen-receptor negative breast cancer, Gastroesophageal reflux disease, Hypertrophic cardiomyopathy, Lung cancer, Major depressive disorder, Migraine, Mood disorder
View all (15 more)

195
Long intergenic non-protein coding RNA 2798
-
Alzheimer disease

196
Leucine rich repeat and Ig domain containing 1
LERN1, LRRN6A, MRT64, UNQ201
Alzheimer disease, Attention deficit hyperactivity disorder, Essential tremor, Glaucoma, Hypertension, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Mood disorder, Neurotic disorder, Post-traumatic stress disorder, Schizophrenia, Substance abuse, Systemic lupus erythematosus, Diabetes mellitus type 2
View all (1 more)

197
Leucine rich repeat and Ig domain containing 2
LERN3, LRRN6C
Alzheimer disease, Amphetamine or sympathomimetic abuse, Astrocytoma, Attention deficit hyperactivity disorder, Bipolar disorder, Brain aneurysm, Breast cancer, Carotid atherosclerosis, Central nervous system cancer, Obstructive pulmonary disease, Color vision deficiency, Diabetes mellitus, Dry eye syndrome, Endometrial cancer, Endometrial neoplasms
View all (16 more)

198
Leucine rich repeat and Ig domain containing 4
DAAT9248, LRRN6D, PRO34002
Coronary artery disease, Intestinal obstruction, Polymicrogyria

199
Lines homolog 1
LINS, MRT27, WINS1
Autism, Nonsyndromic intellectual disability, Neurodevelopmental disorder, Intellectual developmental disorder, Non-specific syndromic intellectual disability

200
Lipase A, lysosomal acid type
CESD, LAL
Cholesterol ester storage disease, Ischemic heart disease, Coronary artery disease, Heart disease, Large artery stroke, Myocardial infarction, Myocardial ischemia, Niemann-pick disease, Wolman disease