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"
811 to 820 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

811
Centromere protein V like 3
CENPVP3
Prostate cancer

812
Centromere protein W
C6orf173, CENP-W, CUG2
Androgenetic alopecia, Attention deficit hyperactivity disorder, Autism, Basal cell carcinoma, Hepatocellular carcinoma, Coronary artery disease, Diabetes mellitus, Diabetic eye disease, Diabetic retinopathy, Myocardial infarction, Neurotic disorder, Psoriasis, Schizophrenia, Scoliosis, Diabetes mellitus type 1
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813
Centromere protein X
CENP-X, D9, FAAP10, MHF2, STRA13
Metabolic syndrome, Diabetes mellitus type 2

814
Centrosomal protein 104
CFAP256, GlyBP, JBTS25, KIAA0562, MRT77, ROC22
Autism, Nonsyndromic intellectual disability, Cerebellar ataxia, Ciliopathy, Dental caries, Aplasia of the vermis, Global developmental delay, Intellectual developmental disorder, Joubert syndrome

815
Centrosomal protein 112
CCDC46, MACOCO, SPGF44
Androgenetic alopecia, Asthma, Atrial fibrillation, Attention deficit hyperactivity disorder, Bone disease, Endometrial cancer, Endometriosis, Spermatogenic failure, Squamous cell carcinoma

816
Centrosomal protein 120
CCDC100, JBTS31, SRTD13
Jeune syndrome, Atrial fibrillation, Breast cancer, Ciliopathy, Coronary artery disease, Desbuquois syndrome, Erythrocytosis, Aplasia of the vermis, Joubert syndrome, Jeune thoracic dystrophy, Metabolic syndrome, Multiple myeloma, Obesity, Prostate cancer, Short rib dysplasia-polydactyly syndrome
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817
Centrosomal protein 126
KIAA1377
Monomelic amyotrophy

818
Centrosomal protein 128
C14orf145, C14orf61, LEDP/132
Developmental delay, Epilepsy, Hyperthyroidism, Hypothyroidism, Idiopathic pulmonary fibrosis, Ulcerative colitis

819
Centrosomal protein 131
AZ1, AZI1, ZA1
Breast cancer, Hepatocellular carcinoma, Crohn disease, Frontotemporal dementia, Inflammatory bowel disease, Male infertility single gene azoospermia, Ulcerative colitis

820
Centrosomal protein 135
CEP4, KIAA0635, MCPH8
Auditory neuropathy, Primary microcephaly, Coronary artery disease, Microcephaly