Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
7041 to 7050 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7041
Large tumor suppressor kinase 1
WARTS, wts
Astrocytoma, Basal cell carcinoma, Testicular carcinoma, Testicular germ cell tumor

7042
Large tumor suppressor kinase 2
KPM
Astrocytoma, Scoliosis

7043
Lymphocyte transmembrane adaptor 1
LAX
Breast cancer, Obstructive sleep apnea syndrome

7044
Layilin
-
Asthma, Eczema, Bipolar disorder, Coronary artery disease, Obesity

7045
LBH regulator of Wnt signaling pathway
-
Asthma, Celiac disease, Immune system disease, Multiple sclerosis, Polycystic ovary syndrome, Rheumatoid arthritis, Systemic lupus erythematosus

7046
LBH domain containing 1
C11orf48
Mitochondrial complex deficiency

7047
Lipopolysaccharide binding protein
BPIFD2
Exanthema, Metabolic syndrome, Obesity, Periodontitis, Sepsis, Stevens-johnson syndrome, Diabetes mellitus type 2

7048
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

7049
Ladybird homeobox 1
CCHS3, HPX-6, HPX6, LBX1H, homeobox
Bipolar disorder, Breast neoplasms, Haddad syndrome, Central hypoventilation syndrome, Congenital central hypoventilation syndrome, Desbuquois syndrome

7050
Lebercilin LCA5
C6orf152
Leber congenital amaurosis, Astrocytoma, Blindness, Central nervous system cancer, Glioblastoma, Glioma, Optic atrophy, Polycystic liver disease, Retinitis pigmentosa, Stargardt disease