Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2281 to 2290 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2281
Cadherin EGF LAG seven-pass G-type receptor 1
ADGRC1, CDHF9, FMI2, HFMI2, LMPHM9, ME2
Alzheimer disease, Bladder exstrophy, Developmental and epileptic encephalopathy, Epilepsy, Gastric cancer, Hydrops fetalis, Lymphatic malformation, Lymphoid leukemia, Neural tube defects, susceptibility to, Situs ambiguus, Walker-warburg syndrome, Yellow nail syndrome

2282
Cadherin EGF LAG seven-pass G-type receptor 2
ADGRC2, CDHF10, EGFL2, Flamingo1, MEGF3
Aneurysm, Aortic aneurysm, Aortic stenosis, Atrial fibrillation, Endometrial hyperplasia, Cancer, Cardiovascular disease, Cerebrovascular disorder, Ischemic heart disease, Congestive heart failure, Coronary artery disease, Diabetes mellitus, Hyperlipidemia, Lipoprotein lipase deficiency, Global developmental delay
View all (16 more)

2283
Cadherin EGF LAG seven-pass G-type receptor 3
ADGRC3, CDHF11, EGFL1, FMI1, HFMI1, MEGF2, RESDA1
Anorexia nervosa, Hepatocellular carcinoma, Neurodevelopmental disorder, Crohn disease, Tourette syndrome, Hypertrophic cardiomyopathy, Inflammatory bowel disease, Major depressive disorder, Non-specific syndromic intellectual disability, Ulcerative colitis

2284
Cell migration inducing hyaluronidase 1
CCSP1, CEMIP1, HYBID, KIAA1199, TMEM2L
Color vision deficiency, Gout, Insomnia, Metabolic syndrome, Periprosthetic osteolysis, Diabetes mellitus type 2

2285
Cell migration inducing hyaluronidase 2
TMEM2
Attention deficit hyperactivity disorder, Color vision deficiency, Liver cirrhosis, Myopia, Substance abuse

2286
Centrosomal AT-AC splicing factor
CCDC84, DLNB14, MVA4
Mosaic variegated aneuploidy

2287
Centromere protein A
CENP-A, CenH3
Ankylosing spondylitis, Hepatocellular carcinoma

2288
Centromere protein B
-
Biliary cirrhosis, Diseases of inner ear, Biliary cholangitis

2289
Centromere protein C
CENP-C, CENPC1, MIF2, hcp-4
Color vision deficiency, Crest syndrome, Crst syndrome, Liver cirrhosis

2290
Centromere protein E
CENP-E, KIF10, MCPH13, PPP1R61
Alzheimer disease, Autism, Primary microcephaly, Hepatocellular carcinoma, Desbuquois syndrome, Gastroesophageal reflux disease, Microcephaly, Seckel syndrome, Testicular carcinoma, Testicular germ cell tumor, Diabetes mellitus type 2