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"
821 to 830 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

821
Centrosomal protein 152
MCPH4, MCPH9, SCKL5
Primary microcephaly, Color vision deficiency, Congenital microcephaly, Desbuquois syndrome, Insomnia, Microcephaly, Obesity, Seckel syndrome

822
Centrosomal protein 162
C6orf84, KIAA1009, QN1
Breast cancer, Multiple sclerosis, Obesity, Osteoarthritis

823
Centrosomal protein 164
NPHP15
Ciliopathy, Metabolic syndrome, Nephronophthisis, Retinitis pigmentosa, Senior-loken syndrome, Diabetes mellitus type 2

824
Centrosomal protein 170
FAM68A, KAB, KIAA0470
Alzheimer disease, Bronchopulmonary dysplasia, Hypertension, Lung cancer

825
Centrosomal protein 170B
CEP170R, FAM68C, KIAA0284
Alzheimer disease, Asthma, Central nervous system cancer, Congenital heart defects, Gastroesophageal reflux disease, Glioblastoma, Glioma, Rheumatoid arthritis

826
Centrosomal protein 19
C3orf34, MOSPGF
Bardet-biedl syndrome, Obesity, Optic atrophy, Retinitis pigmentosa

827
Centrosomal protein 192
PPP1R62
Breast cancer, Color vision deficiency

828
Centrosomal protein 20
C16orf63, FOPNL, FOR20, PHSECRG2
Multiple myeloma, Pelvic organ prolapse, Psoriasis

829
Centrosomal protein 250
C-NAP1, CEP2, CNAP1, CRDHL2
Cone rod dystrophy and hearing loss, Optic atrophy, Retinitis pigmentosa, Usher syndrome

830
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
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