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"
1021 to 1030 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1021
Carbohydrate sulfotransferase 8
GALNAC4ST1, GalNAc4ST, PSS3
Eczema, Autism, Dental caries, Dyslexia, Endometriosis, Inflammatory skin disease, Peeling skin syndrome, Psoriasis

1022
Carbohydrate sulfotransferase 9
GALNAC4ST-2, GalNAc4ST2
Breast cancer, Bronchopulmonary dysplasia, Dental caries, Dyslexia, Generalized anxiety disorder, Major depressive disorder, Scoliosis

1023
Chondroitin sulfate synthase 1
CHSY, CSS1, ChSy-1, TPBS
Ankylosing spondylitis, Bone fracture, Corneal astigmatism, Desbuquois syndrome, Dupuytren contracture, Hearing impairment, Immune system disease, Keratoconus, Non-small cell lung carcinoma, Prostate cancer

1024
Chondroitin sulfate synthase 3
CHSY2, CSS3
Alzheimer disease, Major depressive disorder

1025
Chromosome transmission fidelity factor 18
C16orf41, C321D2.2, C321D2.3, C321D2.4, CHL12, Ctf18, RUVBL
Astrocytoma

1026
Chromosome transmission fidelity factor 8
CTF8, DERPC
Dyslexia

1027
Component of inhibitor of nuclear factor kappa B kinase complex
BPS2, IKBKA, IKK-1, IKK-alpha, IKK1, IKKA, NFKBIKA, TCF16
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bartsocas-papas syndrome, Bone disease, Cleft palate, Cocoon syndrome, Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiency, Congenital skin anomaly, Congenital anomaly of limb, Skin abnormalities, Squamous cell carcinoma, Diabetes mellitus type 2

1028
Churchill domain containing 1
C14orf52, My015, chch
Lung cancer, Squamous cell carcinoma

1029
CHURC1-FNTB readthrough
FNTB, FTase-beta
Lung cancer, Squamous cell carcinoma

1030
Cytosolic iron-sulfur assembly component 1
CIA1, MMDS10, WDR39
Neuromuscular disease