Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2341 to 2350 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2341
Cerebral endothelial cell adhesion molecule
CEECAM1, GLT25D3
Systemic lupus erythematosus

2342
Ceramide kinase
LK4, dA59H18.2, dA59H18.3, hCERK
Liver cirrhosis

2343
CERK like autophagy regulator
RP26
Retinitis pigmentosa, Cone dystrophy, Cone-rod dystrophy, Macular dystrophy, Peptic ulcer disease, Stargardt disease

2344
Ceramide synthase 1
EPM8, GDF-1, GDF1, LAG1, LASS1, UOG1
Congenital heart defects, Congenital heart disease, Double outlet right ventricle, Progressive myoclonic epilepsy, Heterotaxy syndrome, Right atrial isomerism, Situs ambiguus, Tetralogy of fallot, Transposition of the great arteries

2345
Ceramide synthase 2
L3, LASS2, SP260, TMSG1
Basal cell carcinoma, Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Kidney disease, Colorectal cancer, Melanoma, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Gout, Hepatocellular carcinoma, Lung cancer
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2346
Ceramide synthase 3
ARCI9, LASS3
Congenital ichthyosis, Behcet disease, Congenital ichthyosiform erythroderma, Congenital nonbullous ichthyosiform erythroderma, Ichthyosis, Lamellar ichthyosis

2347
Ceramide synthase 4
LASS4, Trh1
Alzheimer disease, Central nervous system cancer, Glioma, Gout, Macular telangiectasia

2348
Ceramide synthase 5
LASS5, Trh4
Hypertension, Schizophrenia

2349
Ceramide synthase 6
CERS5, LASS6
Bipolar disorder, Central nervous system cancer, Obstructive pulmonary disease, Glioblastoma, Glioma, Hyperthyroidism, Schizophrenia, Scoliosis, Diabetes mellitus type 2

2350
Ceramide transporter 1
CERT, CERTL, COL4A3BP, GPBP, MRD34, NEDHSF, STARD11
Atrial fibrillation, Cancer, Non-small-cell lung carcinoma, Cardiovascular disease, Coronary artery disease, Diabetes mellitus, Epilepsy, Hyperlipidemia, Gallstones, Heart failure, Intellectual developmental disorder, Metabolic syndrome, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Stroke
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