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 "C"
151 to 160 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

151
Chromosome 8 open reading frame 34
VEST-1, VEST1
Colorectal cancer, Coronary artery disease, Dupuytren contracture, Moyamoya disease, Nonalcoholic fatty liver disease, Obesity, Osteoarthritis, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm

152
C8orf44-SGK3 readthrough
-
Alzheimer disease, Colorectal cancer, Major depressive disorder

153
Chromosome 8 open reading frame 89
-
Scoliosis

154
Chromosome 8 open reading frame 90
-
Alzheimer disease, Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Major depressive disorder, Metabolic syndrome, Obesity, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome, Diabetes mellitus type 2

155
Complement C9
ARMD15, C9D
Atrophic macular degeneration, C1 esterase inhibitor deficiency, C9 deficiency, Hepatocellular carcinoma, Cardiac embolism, Cardioembolic stroke, Central nervous system cancer, Complement component deficiency, Macular and posterior pole degeneration, Dermatomyositis, Glioblastoma, Glioma, Macular degeneration, Age-related macular degeneration, Mesothelioma
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156
Chromosome 9 open reading frame 152
bA470J20.2
Alzheimer disease, Prostate cancer

157
Chromosome 9 open reading frame 40
-
Gout

158
Chromosome 9 open reading frame 57
-
Metabolic syndrome, Schizophrenia, Scoliosis, Diabetes mellitus type 2

159
C9orf72-SMCR8 complex subunit
ALSFTD, DENND9, DENNL72, FTDALS, FTDALS1
Amyotrophic lateral sclerosis, Juvenile arthritis, Autism, Disorder of eye, Eye disease, Frontotemporal dementia, Frontotemporal dementia with or without amyotrophic lateral sclerosis, Frontotemporal dementia with motor neuron disease, Huntington disease, Juvenile idiopathic arthritis, Non-organic psychosis, Oligoarticular juvenile idiopathic arthritis, Progressive myoclonic epilepsy, Psychotic disorders, Schizoaffective disorder
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160
Carbonic anhydrase 1
CA-I, CAB, Car1, HEL-S-11
Biliary cirrhosis, Congestive ophthalmopathy, Esophageal squamous cell carcinoma, Graves ophthalmopathy, Systemic lupus erythematosus, Myopathic ophthalmopathy, Biliary cholangitis, Rheumatoid arthritis, Rickets, Sjogren syndrome, Stomach neoplasms