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"
51 to 60 of 464 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

51
Linker for activation of T cells
IMD52, LAT1, pp36
Alzheimer disease, Amyotrophic lateral sclerosis, Atrial fibrillation, Diffuse gastric adenocarcinoma, Gastric cancer, Immunodeficiency, Liver disease, Motor neuron disease, Sarcoidosis, Severe combined immunodeficiency

52
Linker for activation of T cells family member 2
HSPC046, LAB, NTAL, WBSCR15, WBSCR5, WSCR5
Promyelocytic leukemia, Moyamoya disease, Systemic lupus erythematosus, Williams syndrome

53
Large tumor suppressor kinase 1
WARTS, wts
Astrocytoma, Basal cell carcinoma, Testicular carcinoma, Testicular germ cell tumor

54
Large tumor suppressor kinase 2
KPM
Astrocytoma, Scoliosis

55
Lymphocyte transmembrane adaptor 1
LAX
Breast cancer, Obstructive sleep apnea syndrome

56
Layilin
-
Asthma, Eczema, Bipolar disorder, Coronary artery disease, Obesity

57
LBH regulator of Wnt signaling pathway
-
Asthma, Celiac disease, Immune system disease, Liver cirrhosis, Multiple sclerosis, Polycystic ovary syndrome, Rheumatoid arthritis, Systemic lupus erythematosus

58
LBH domain containing 1
C11orf48
Mitochondrial complex deficiency

59
Lipopolysaccharide binding protein
BPIFD2
Exanthema, Liver cirrhosis, Metabolic syndrome, Obesity, Periodontitis, Sepsis, Stevens-johnson syndrome, Diabetes mellitus type 2

60
Lamin B receptor
C14SR, DHCR14B, LMN2R, PHA, PHASK, TDRD18
Biliary cirrhosis, Congenital retrognathism, Connective tissue disease, Desbuquois syndrome, Jeune thoracic dystrophy, Parkinson disease, Pelger-huet anomaly, Biliary cholangitis, Reynolds syndrome, Rhizomelic skeletal dysplasia with or without pelger-huet anomaly