Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
1661 to 1670 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1661
CUE domain containing 1
-
Atrial fibrillation, Multiple sclerosis

1662
CUE domain containing 2
C10orf66, bA18I14.5
Autism

1663
Cullin 1
-
Central nervous system cancer, Crohn disease, Glioblastoma, Glioma, Inflammatory bowel disease, Stevens-johnson syndrome, Diabetes mellitus, type 2, Ulcerative colitis

1664
Cullin 2
-
Alzheimer disease, Colorectal adenoma, Crohn disease, Inflammatory bowel disease, Moyamoya angiopathy, Ulcerative colitis

1665
Cullin 3
CUL-3, NEDAUS, PHA2E
Alzheimer disease, Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Neurodevelopmental disorder, Dementia, Diverticular disease, Intellectual developmental disorder, Major depressive disorder, Melanoma, Mood disorder, Non-specific syndromic intellectual disability, Prostatic neoplasm, Pseudohypoparathyroidism, Schizophrenia
View all (1 more)

1666
Cullin 4A
-
Atrial fibrillation, Bipolar disorder, Stevens-johnson syndrome

1667
Cullin 4B
CUL-4B, MRXHF2, MRXS15, MRXSC, SFM2
Global developmental delay, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Teratozoospermia, X-linked intellectual disability

1668
Cullin 5
CUL-5, VACM-1, VACM1
Breast neoplasm, Breast cancer, Rheumatoid arthritis, Triple negative breast cancer, Uterine fibroid

1669
Cullin 7
3M1, CUL-7, KIAA0076, dJ20C7.5
3m syndrome, Autism, Renal cell carcinoma, Desbuquois syndrome

1670
Cullin 9
H7AP1, PARC
Syndactyly of the toes, Imperforate anus, Arthritis, Atrial septal defect, Color vision deficiency, Coronary artery disease, Insomnia, Obesity, Peripheral pulmonary artery stenosis, Schizophrenia, Ventricular septal defect