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 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2301
Centrosomal protein 135
CEP4, KIAA0635, MCPH8
Auditory neuropathy, Primary microcephaly, Coronary artery disease, Microcephaly

2302
Centrosomal protein 152
MCPH4, MCPH9, SCKL5
Primary microcephaly, Color vision deficiency, Congenital microcephaly, Desbuquois syndrome, Insomnia, Microcephaly, Obesity, Seckel syndrome

2303
Centrosomal protein 162
C6orf84, KIAA1009, QN1
Breast cancer, Multiple sclerosis, Obesity, Osteoarthritis

2304
Centrosomal protein 164
NPHP15
Ciliopathy, Metabolic syndrome, Nephronophthisis, Retinitis pigmentosa, Senior-loken syndrome, Diabetes mellitus type 2

2305
Centrosomal protein 170
FAM68A, KAB, KIAA0470
Alzheimer disease, Bronchopulmonary dysplasia, Hypertension, Lung cancer

2306
Centrosomal protein 170B
CEP170R, FAM68C, KIAA0284
Alzheimer disease, Asthma, Central nervous system cancer, Congenital heart defects, Gastroesophageal reflux disease, Glioblastoma, Glioma, Rheumatoid arthritis

2307
Centrosomal protein 19
C3orf34, MOSPGF
Bardet-biedl syndrome, Obesity, Optic atrophy, Retinitis pigmentosa

2308
Centrosomal protein 192
PPP1R62
Breast cancer, Color vision deficiency

2309
Centrosomal protein 20
C16orf63, FOPNL, FOR20, PHSECRG2
Multiple myeloma, Pelvic organ prolapse, Psoriasis

2310
Centrosomal protein 250
C-NAP1, CEP2, CNAP1, CRDHL2
Cone rod dystrophy and hearing loss, Optic atrophy, Retinitis pigmentosa, Usher syndrome