Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "L"
411 to 420 of 673 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

411
Low density lipoprotein receptor class A domain containing 1
-

412
Long intergenic non-protein coding RNA 1118
-

413
Leucine, glutamate and lysine rich 1
-
Breast cancer, Melanoma, Multiple sclerosis, Psoriasis, Hypertension, Ventricular septal defect

414
Long intergenic non-protein coding RNA 2213
-

415
Lin-28 RNA binding posttranscriptional regulator B
CSDD2
Jeune syndrome, Cholecystolithiasis, Major depressive disorder, Gallstones, Hypogonadism, Insomnia, Neuroblastoma, Neurotic disorder, Schizophrenia

416
Long intergenic non-protein coding RNA 2906
C8orf87

417
L1 cell adhesion molecule
CAML1, CD171, HSAS, HSAS1, HYCX, MASA, MIC5, N-CAM-L1, N-CAML1, NCAM-L1, S10, SPG1
Aphasia, Postictal aphasia, Renal cell carcinoma, Cerebellar ataxia, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Commisural aphasia, Dejerine-lichtheim phenomenon, Dyslexia, Dysphasia, Global developmental delay, Hydrocephalus, Congenital hydrocephalus, Hydrops fetalis, Intellectual developmental disorder, Masa syndrome
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418
Leucine rich repeat containing 10B
-
Coronary artery disease, Hypertension

419
Leukocyte associated immunoglobulin like receptor 1
CD305, LAIR-1
Iga nephropathy

420
Laminin subunit alpha 2
LAMM, MDC1A
Asthma, Attention deficit hyperactivity disorder, Cardiomyopathy, Charcot-marie-tooth disease, Color vision deficiency, Congenital myasthenic syndrome, Eye disease, Hyperopia, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Juvenile idiopathic arthritis, Limb-girdle muscular dystrophy, Muscular dystrophy, Myopathy, Myopia
View all (10 more)