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
2771 to 2780 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2771
Cordon-bleu WH2 repeat protein
-
Autoimmune disease, Central nervous system cancer, Chromosomal disorder, Glioblastoma, Glioma, Major depressive disorder, Nasal disorder, Oligodendroglioma, Osteoarthritis, Squamous cell carcinoma, Diabetes mellitus type 1, Diabetes mellitus type 2, Vascular disease

2772
Cordon-bleu WH2 repeat protein like 1
COBLR1
Cleft lip and palate, Coronary artery disease, Diabetes mellitus, Diabetic eye disease, Diabetic neuropathy, Diabetic retinopathy, Hyperlipidemia, Gout, Metabolic syndrome, Myocardial ischemia, Nonalcoholic fatty liver disease, Psoriasis, Diabetes mellitus type 2, Type 2 diabetes nephropathy, Uterine fibroid

2773
Cochlin
COCH-5B2, COCH5B2, DFNA9, DFNB110
Isolated sensorineural deafness, Nonsyndromic hearing loss, Congenital hearing disorder, Deafness, Esophageal adenocarcinoma, Hearing impairment, Hearing loss, Hereditary hearing loss, Hypertension, Nephrotic syndrome, Usher syndrome

2774
Component of oligomeric golgi complex 1
CDG2G, LDLB
Congenital disorder of glycosylation, Desbuquois syndrome, Nephrotic syndrome

2775
Component of oligomeric golgi complex 2
CDG2Q, LDLC
Congenital disorder of glycosylation, Ulcerative colitis

2776
Component of oligomeric golgi complex 3
CDG2BB, SEC34
Congenital disorder of glycosylation

2777
Component of oligomeric golgi complex 4
CDG2J, COD1, SWILS
Congenital disorder of glycosylation, Desbuquois syndrome, Gross motor development delay, Metabolic syndrome, Saul-wilson syndrome, Diabetes mellitus type 2

2778
Component of oligomeric golgi complex 5
CDG2I, GOLTC1, GTC90
Atrial fibrillation, Congenital disorder of glycosylation, Coronary artery disease, Dyslexia, Insomnia, Osteoarthritis

2779
Component of oligomeric golgi complex 6
CDG2L, COD2, SHNS
Asthma, Congenital disorder of glycosylation, Intellectual developmental disorder, Multiple sclerosis, Ocular sarcoidosis, Oligoarticular juvenile idiopathic arthritis, Peripheral arterial disease, Polyarticular juvenile idiopathic arthritis, Psoriasis, Respiratory system disease, Rheumatoid arthritis, Squamous cell carcinoma, Juvenile idiopathic arthritis, Systemic lupus erythematosus, Uterine fibroid

2780
Component of oligomeric golgi complex 7
CDG2E
Congenital disorder of glycosylation