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
2311 to 2320 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

2311
Centrosomal protein 135
CEP4, KIAA0635, MCPH8
Auditory neuropathy, Primary microcephaly, Coronary artery disease, Microcephaly

2312
Centrosomal protein 152
MCPH4, MCPH9, SCKL5
Primary microcephaly, Color vision deficiency, Congenital microcephaly, Desbuquois syndrome, Insomnia, Microcephaly, Obesity, Seckel syndrome

2313
Centrosomal protein 162
C6orf84, KIAA1009, QN1
Breast cancer, Multiple sclerosis, Obesity, Osteoarthritis

2314
Centrosomal protein 164
NPHP15
Ciliopathy, Metabolic syndrome, Nephronophthisis, Retinitis pigmentosa, Senior-loken syndrome, Diabetes mellitus type 2

2315
Centrosomal protein 170
FAM68A, KAB, KIAA0470
Alzheimer disease, Bronchopulmonary dysplasia, Hypertension, Lung cancer

2316
Centrosomal protein 170B
CEP170R, FAM68C, KIAA0284
Alzheimer disease, Asthma, Central nervous system cancer, Congenital heart defects, Gastroesophageal reflux disease, Glioblastoma, Glioma, Rheumatoid arthritis

2317
Centrosomal protein 19
C3orf34, MOSPGF
Bardet-biedl syndrome, Obesity, Optic atrophy, Retinitis pigmentosa

2318
Centrosomal protein 192
PPP1R62
Breast cancer, Color vision deficiency

2319
Centrosomal protein 20
C16orf63, FOPNL, FOR20, PHSECRG2
Multiple myeloma, Pelvic organ prolapse, Psoriasis

2320
Centrosomal protein 250
C-NAP1, CEP2, CNAP1, CRDHL2
Cone rod dystrophy and hearing loss, Optic atrophy, Retinitis pigmentosa, Usher syndrome