Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
1311 to 1320 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1311
Centrosomal protein 135
CEP4, KIAA0635, MCPH8
Auditory neuropathy, Primary microcephaly, Coronary artery disease, Microcephaly

1312
CD68 molecule
GP110, LAMP4, SCARD1
Amyotrophic lateral sclerosis, Psoriatic arthritis, Cholelithiasis, Experimental diabetes, Hyperinsulinism, Diabetes mellitus, type 2, Kidney failure, Liver cirrhosis, Metabolic syndrome, Motor neuron disease, Obesity

1313
CD69 molecule
AIM, BL-AC/P26, CLEC2C, EA1, GP32/28, MLR-3
Arthritis, Experimental arthritis, Autoimmune thyroid disease, Diabetes mellitus type 1, Hashimoto disease, Hypothyroidism, Multiple sclerosis, Non-hodgkins lymphoma, Thyroid disease, Diabetes mellitus, type 1, Diabetes mellitus, type 2

1314
Ciliary rootlet coiled-coil, rootletin
CROCC1, ROLT, TAX1BP2
Alzheimer disease, Gout, Leprosy, Rotator cuff tear, Seasonal allergic rhinitis

1315
CD70 molecule
CD27-L, CD27L, CD27LG, LPFS3, TNFSF7, TNLG8A
Asthma, Astrocytoma, Cardiomyopathy, Central nervous system cancer, Cervical cancer, Lymphocytic leukemia, Combined immunodeficiency disease, Glioblastoma, Glioma, Lymphoproliferative syndrome, Myocarditis, Severe combined immunodeficiency, Viral infection

1316
Centrosomal protein 57
MVA2, PIG8, TSP57
Alzheimer disease, Mosaic variegated aneuploidy, Severe acute respiratory syndrome

1317
CD74 molecule
CLIP, DHLAG, HLADG, II, Ia-GAMMA, p33
Breast neoplasm, Non-small-cell lung carcinoma, Liver cirrhosis, Liver failure

1318
Coiled-coil domain containing 144A
-

1319
CD79a molecule
IGA, IGAlpha, MB-1, MB1
Agammaglobulinemia, Diffuse large b-cell lymphoma

1320
Centrosomal protein 104
CFAP256, GlyBP, JBTS25, KIAA0562, MRT77, ROC22
Autism, Nonsyndromic intellectual disability, Cerebellar ataxia, Ciliopathies, Dental caries, Aplasia of the vermis, Global developmental delay, Intellectual developmental disorder, Joubert syndrome