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
1931 to 1940 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1931
Coiled-coil domain containing 66
-
Gastritis, Nephrotic syndrome, Scoliosis

1932
Coiled-coil domain containing 68
SE57-1
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Coronary artery disease, Fuchs endothelial dystrophy, Hearing loss, Insomnia, Major depressive disorder, Mood disorder, Myocardial ischemia, Neurotic disorder, Obesity, Obsessive-compulsive disorder, Pancreatic cancer
View all (5 more)

1933
Coiled-coil domain containing 69
-
Bulimia, Obstructive pulmonary disease, Obesity, Diabetes mellitus type 2

1934
Coiled-coil domain containing 7
BIOT2, BioT2-A, BioT2-B, BioT2-C, C10orf68
Atrial fibrillation, Color vision deficiency, Focal segmental glomerulosclerosis, Tourette syndrome, Peripheral arterial disease

1935
Coiled-coil domain containing 71
-
Behcet disease, Insomnia

1936
Coiled-coil domain containing 71 like
C7orf74
Atherosclerosis, Cardiovascular disease, Carotid atherosclerosis, Coronary artery disease, Esophageal squamous cell carcinoma, Hypertension, Multiple myeloma

1937
Coiled-coil domain containing 73
NY-SAR-79
Attention deficit hyperactivity disorder, Bipolar disorder, Central nervous system cancer, Glioblastoma, Glioma, Major depressive disorder, Substance abuse

1938
Coiled-coil domain containing 77
-
Obesity, Obstructive sleep apnea syndrome, Diabetes mellitus type 2

1939
Coiled-coil domain containing 78
C16orf25, CNM4, JFP10, hsCCDC78
Centronuclear myopathy, Congenital myopathy, Congenital structural myopathy, Gout

1940
Coiled-coil domain containing 8 subunit of 3M complex
3M3, PPP1R20, p90
3m syndrome, Desbuquois syndrome, Spinocerebellar ataxia