Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2311 to 2320 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2311
Centrosomal protein 290
3H11Ag, BBS14, CT87, JBTS5, LCA10, MKS4, NPHP6, POC3, SLSN6, rd16
Arima syndrome, Hemolytic uremic syndrome, Bardet-biedl syndrome, Blindness, Cone-rod dystrophy, Congenital kidney anomaly, Congenital disorder of glycosylation, Congenital neurologic anomalies, Cystic kidney disease, Desbuquois syndrome, Encephalocele, Aplasia of the vermis, Global developmental delay, Intellectual developmental disorder, Joubert syndrome
View all (13 more)

2312
Centrosomal protein 295
KIAA1731, SCKL11
Bell's palsy, Central nervous system cancer, Glioblastoma, Glioma, Meckel-gruber syndrome, Neuroblastoma, Scoliosis, Seckel syndrome

2313
CEP295 N-terminal like
DDC8, KIAA1731NL
Eosinophilia, Alzheimer disease, Respiratory system disease

2314
Centrosomal protein 350
CAP350, GM133
Kidney cancer, Kidney neoplasms, Prostate cancer

2315
Centrosomal protein 41
JBTS15, TSGA14
Autism, Obstructive pulmonary disease, Aplasia of the vermis, Joubert syndrome, Retinitis pigmentosa, Venous thromboembolism

2316
Centrosomal protein 43
FGFR1OP, FOP
Ankylosing spondylitis, Basal cell carcinoma, B-cell acute lymphoblastic leukemia, Biliary cirrhosis, Crohn disease, Melanoma, Graves disease, Hypothyroidism, Iga nephropathy, Immune system disease, Inflammatory bowel disease, Keratinocyte carcinoma, Lung cancer, Myasthenia gravis, Biliary cholangitis
View all (9 more)

2317
Centrosomal protein 55
C10orf3, CT111, MARCH, URCC6
Hepatocellular carcinoma, Neurodevelopmental disorder, Hydranencephaly, Non-specific syndromic intellectual disability, Polycystic ovary syndrome

2318
Centrosomal protein 57
MVA2, PIG8, TSP57
Alzheimer disease, Mosaic variegated aneuploidy

2319
Centrosomal protein 57 like 1
C6orf182, bA487F23.2, cep57R
Astrocytoma

2320
Centrosomal protein 63
SCKL6
Primary microcephaly, Desbuquois syndrome, Alzheimer disease, Microcephaly, Seckel syndrome, Hereditary spastic paraplegia