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 462 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

51
Linker for activation of T cells family member 2
HSPC046, LAB, NTAL, WBSCR15, WBSCR5, WSCR5
Promyelocytic leukemia, Moyamoya disease, Systemic lupus erythematosus, Williams syndrome

52
Large tumor suppressor kinase 1
WARTS, wts
Astrocytoma, Basal cell carcinoma, Testicular carcinoma, Testicular germ cell tumor

53
Large tumor suppressor kinase 2
KPM
Astrocytoma, Scoliosis

54
Lymphocyte transmembrane adaptor 1
LAX
Breast cancer, Obstructive sleep apnea syndrome

55
Layilin
-
Asthma, Eczema, Bipolar disorder, Coronary artery disease, Obesity

56
LBH regulator of Wnt signaling pathway
-
Asthma, Celiac disease, Immune system disease, Multiple sclerosis, Polycystic ovary syndrome, Rheumatoid arthritis, Systemic lupus erythematosus

57
LBH domain containing 1
C11orf48
Mitochondrial complex deficiency

58
Lipopolysaccharide binding protein
BPIFD2
Exanthema, Metabolic syndrome, Obesity, Periodontitis, Sepsis, Stevens-johnson syndrome, Diabetes mellitus type 2

59
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

60
Ladybird homeobox 1
CCHS3, HPX-6, HPX6, LBX1H, homeobox
Bipolar disorder, Breast neoplasms, Haddad syndrome, Central hypoventilation syndrome, Congenital central hypoventilation syndrome, Desbuquois syndrome