Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7181 to 7190 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7181
Lin-7 cell polarity scaffold C
LIN-7-C, LIN-7C, MALS-3, MALS3, VELI3
Metabolic syndrome, Pancreatic cancer, Hypertension, Diabetes mellitus type 2

7182
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)

7183
Long intergenic non-protein coding RNA 2798
-
Alzheimer disease

7184
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)

7185
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)

7186
Leucine rich repeat and Ig domain containing 4
DAAT9248, LRRN6D, PRO34002
Coronary artery disease, Intestinal obstruction, Polymicrogyria

7187
Lines homolog 1
LINS, MRT27, WINS1
Autism, Nonsyndromic intellectual disability, Neurodevelopmental disorder, Intellectual developmental disorder, Non-specific syndromic intellectual disability

7188
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

7189
Lipase C, hepatic type
HDLCQ12, HL, HTGL, LIPH
Alzheimer disease, Amyotrophic lateral sclerosis, Arterial occlusive disease, Atrial fibrillation, Atrophic macular degeneration, Cancer, Ischemic heart disease, Coronary artery disease, Diabetes mellitus, Diabetes mellitus type 1, Diabetes mellitus type 2, Hyperlipidemia, Heart failure, Hepatic lipase deficiency, Hypercholesterolemia
View all (13 more)

7190
Lipase E, hormone sensitive type
AOMS4, FPLD6, HSL, LHS, REH
Partial lipodystrophy, Hypertension, Lipodystrophy