Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2921 to 2930 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2921
Copine 4
COPN4, CPN4
Alzheimer disease, Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Brain aneurysm, Color vision deficiency, Coronary aneurysm, Dementia, Dental caries, Eosinophilia, Lung cancer, Metabolic syndrome, Oligodendroglioma, Prostate cancer, Substance abuse, Diabetes mellitus type 2

2922
Copine 5
COPN5, CPN5
Biliary tract cancer, Breast cancer, Bullous pemphigoid, Systemic lupus erythematosus

2923
Copine 6
copine-6
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

2924
Copine 7
-
Basal cell carcinoma, Schizophrenia

2925
Copine 8
-
Atypical femoral fracture, Bipolar disorder

2926
Carboxypeptidase O
-
Gestational diabetes, Insomnia, Venous thromboembolism

2927
Coproporphyrinogen oxidase
COX, CPO, CPX, HARPO, HCP
Coproporphyria, Hereditary coproporphyria, Liver disease, Porphyria cutanea tarda

2928
Calcineurin like phosphoesterase domain containing 1
CSTP1
Cerebral amyloid angiopathy, Melanoma, Dementia, Diabetic ketoacidosis, Neuroblastoma, Obesity, Oligodendroglioma, Diabetes mellitus type 2

2929
Carboxypeptidase Q
LDP, PGCP
Attention deficit hyperactivity disorder, Renal cell carcinoma, Migraine, Diabetes mellitus type 2

2930
Carbamoyl-phosphate synthase 1
CPSASE1, GATD6, PHN
Alzheimer disease, Carbamoyl phosphate synthetase deficiency, Cholecystolithiasis, Kidney disease, Color vision deficiency, Colorectal cancer, Congenital hyperammonemia, Coronary artery disease, Urea cycle disorder, Gallstones, Gout, Hyperammonemia, Intellectual developmental disorder, Kidney failure, Macular telangiectasia
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