Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2271 to 2280 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2271
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

2272
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)

2273
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

2274
Cell migration inducing hyaluronidase 1
CCSP1, CEMIP1, HYBID, KIAA1199, TMEM2L
Color vision deficiency, Gout, Insomnia, Metabolic syndrome, Periprosthetic osteolysis, Diabetes mellitus type 2

2275
Cell migration inducing hyaluronidase 2
TMEM2
Attention deficit hyperactivity disorder, Color vision deficiency, Myopia, Substance abuse

2276
Centrosomal AT-AC splicing factor
CCDC84, DLNB14, MVA4
Mosaic variegated aneuploidy

2277
Centromere protein A
CENP-A, CenH3
Ankylosing spondylitis, Hepatocellular carcinoma

2278
Centromere protein B
-
Biliary cirrhosis, Inner ear disease, Biliary cholangitis

2279
Centromere protein C
CENP-C, CENPC1, MIF2, hcp-4
Color vision deficiency, Crest syndrome, Crst syndrome, Liver cirrhosis

2280
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