Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
1451 to 1460 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1451
CPQ
Carboxypeptidase Q
LDP, PGCP
Attention deficit hyperactivity disorder, Renal cell carcinoma, Liver cirrhosis, Migraine, Diabetes mellitus, type 2

1452
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, Disorder of the urea cycle metabolism, Gallstones, Gout, Hyperammonemia, Intellectual developmental disorder, Kidney failure, Liver cirrhosis
View all (11 more)

1453
Cleavage and polyadenylation specific factor 1
CPSF160, HSU37012, MYP27, P/cl.18
Myopia, Retinitis pigmentosa, Stomach neoplasms

1454
Cleavage and polyadenylation specific factor 2
CPSF100
B-cell acute lymphoblastic leukemia, Kidney disease, Liver disease, Obesity

1455
Cleavage and polyadenylation specific factor 3
CPSF-73, CPSF73, NEDMHS, NEDMHSN
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

1456
Cleavage and polyadenylation specific factor 6
CFIM, CFIM68, CFIM72, HPBRII-4, HPBRII-7
Attention deficit hyperactivity disorder, Carpal tunnel syndrome, Contracture, Alzheimer disease, Major depressive disorder, Metabolic syndrome, Neurodevelopmental disorder, Osteoarthritis, Psychiatric disorders, Scoliosis, Substance abuse, Diabetes mellitus, type 2

1457
Carnitine palmitoyltransferase 1A
CPT I, CPT1, CPT1-L, CPTI-L, L-CPT1
Breast neoplasm, Carnitine palmitoyltransferase deficiency, Cataract, Diabetes mellitus, Experimental diabetes, Diabetes mellitus type 2, Disorder of fatty acid metabolism, Gout, Kidney failure, Metabolic syndrome, Nonalcoholic fatty liver disease, Obesity, Vitiligo

1458
Carnitine palmitoyltransferase 1B
CPT1-M, CPT1M, CPTI, CPTI-M, M-CPT1, MCCPT1, MCPT1
Cardiomegaly, Colorectal cancer, Experimental diabetes, Disorder of fatty acid metabolism, Liver neoplasm, Myocardial ischemia, Narcolepsy, Myopia

1459
Carnitine palmitoyltransferase 1C
CATL1, CPT I-C, CPT1-B, CPT1P, CPTI-B, CPTIC, SPG73
Autoimmune disease, Spastic paraplegia, Color vision deficiency, Gout, Hypothyroidism, Major depressive disorder, Melanoma, Non-neoplastic peripheral nervous system disease, Panic disorder, Peripheral nervous system disease, Peripheral neuropathy, Hereditary spastic paraplegia

1460
Carnitine palmitoyltransferase 2
CPT1, CPTASE, IIAE4
Brain disease, Carnitine palmitoyltransferase deficiency, Congenital neurologic anomalies, Myopathy, Systemic lupus erythematosus