Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2931 to 2940 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2931
Cleavage and polyadenylation specific factor 1
CPSF160, HSU37012, MYP27, P/cl.18
Myopia, Retinitis pigmentosa, Stomach neoplasms

2932
Cleavage and polyadenylation specific factor 2
CPSF100
B-cell acute lymphoblastic leukemia, Kidney disease, Liver disease, Obesity

2933
Cleavage and polyadenylation specific factor 3
CPSF-73, CPSF73, NEDMHS, NEDMHSN
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

2934
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

2935
Carnitine palmitoyltransferase 1A
CPT I, CPT1, CPT1-L, CPTI-L, L-CPT1
Breast neoplasms, Carnitine palmitoyltransferase deficiency, Cataract, Diabetes mellitus, Diabetes mellitus type 2, Fatty acid metabolism disorder, Gout, Kidney failure, Metabolic syndrome, Nonalcoholic fatty liver disease, Obesity, Vitiligo

2936
Carnitine palmitoyltransferase 1B
CPT1-M, CPT1M, CPTI, CPTI-M, M-CPT1, MCCPT1, MCPT1
Cardiomegaly, Colorectal cancer, Fatty acid metabolism disorder, Liver neoplasms, Myocardial ischemia, Narcolepsy, Myopia

2937
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

2938
Carnitine palmitoyltransferase 2
CPT1, CPTASE, IIAE4
Brain disease, Carnitine palmitoyltransferase deficiency, Congenital neurologic anomalies, Myopathy, Systemic lupus erythematosus

2939
Carboxypeptidase vitellogenic like
HVLP
Basal cell carcinoma, Color vision deficiency, Colorectal cancer, Melanoma, Cutaneous squamous cell carcinoma, Endometrial cancer, Keratinocyte carcinoma, Non-melanoma skin carcinoma, Obesity, Prostate cancer, Psoriasis, Psychotic disorders, Seborrheic keratosis, Skin cancer, Skin disease
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2940
CPX chromosome region candidate 1
CT77
Anti-neutrophil antibody associated vasculitis, Major depressive disorder, Prostate cancer