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
3151 to 3160 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

3151
Cubilin
IFCR, IGS, IGS1, MGA1, gp280
Amphetamine or sympathomimetic abuse, Megaloblastic anemia, Autism, Binge eating disorder, Bipolar disorder, Ischemic heart disease, Kidney disease, Colorectal cancer, Coronary artery disease, Deficiency anemia, Focal glomerulosclerosis, Gastroesophageal reflux disease, Gout, Imerslund-grasbeck syndrome, Melanoma
View all (7 more)

3152
CUE domain containing 1
-
Atrial fibrillation, Multiple sclerosis

3153
CUE domain containing 2
C10orf66, bA18I14.5
Autism

3154
Cullin 1
-
Central nervous system cancer, Crohn disease, Glioblastoma, Glioma, Inflammatory bowel disease, Stevens-johnson syndrome, Diabetes mellitus type 2, Ulcerative colitis

3155
Cullin 2
-
Alzheimer disease, Colorectal adenoma, Crohn disease, Inflammatory bowel disease, Moyamoya angiopathy, Ulcerative colitis

3156
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 neoplasms, Pseudohypoparathyroidism, Schizophrenia
View all (1 more)

3157
Cullin 4A
-
Atrial fibrillation, Bipolar disorder, Stevens-johnson syndrome

3158
Cullin 4B
CUL-4B, MRXHF2, MRXS15, MRXSC, SFM2
Global developmental delay, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Teratozoospermia, X-linked intellectual disability

3159
Cullin 5
CUL-5, VACM-1, VACM1
Breast neoplasms, Breast cancer, Rheumatoid arthritis, Triple negative breast cancer, Uterine fibroid

3160
Cullin 7
3M1, CUL-7, KIAA0076, dJ20C7.5
3m syndrome, Autism, Renal cell carcinoma, Desbuquois syndrome