Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
2301 to 2310 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2301
Centromere protein V like 2
CENPVP2
Prostate cancer

2302
Centromere protein V like 3
CENPVP3
Prostate cancer

2303
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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2304
Centromere protein X
CENP-X, D9, FAAP10, MHF2, STRA13
Metabolic syndrome, Diabetes mellitus type 2

2305
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

2306
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

2307
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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2308
Centrosomal protein 126
KIAA1377
Monomelic amyotrophy

2309
Centrosomal protein 128
C14orf145, C14orf61, LEDP/132
Developmental delay, Epilepsy, Hyperthyroidism, Hypothyroidism, Idiopathic pulmonary fibrosis, Ulcerative colitis

2310
Centrosomal protein 131
AZ1, AZI1, ZA1
Breast cancer, Hepatocellular carcinoma, Crohn disease, Frontotemporal dementia, Inflammatory bowel disease, Male infertility single gene azoospermia, Ulcerative colitis