Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
1141 to 1150 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1141
Component of oligomeric golgi complex 8
CDG2H, DOR1
Congenital disorder of glycosylation, Metabolic syndrome, Diabetes mellitus, type 2

1142
Caveolae associated protein 2
PS-p68, SDPR, SDR, cavin-2
Hirschsprung disease, Osteoarthritis, Parkinson disease

1143
Calsequestrin 1
CASQ, CSQ1, PDIB1, VMCQA
Diabetes mellitus type 2, Myopathy, Tubular aggregate myopathy, Vacuolar myopathy, Van buchem disease

1144
Caspase recruitment domain family member 11
BENTA, BIMP3, CARMA1, IMD11, IMD11A, PPBL
Alzheimer disease, Asthma, Astrocytoma, Eczema, Benta disease, Bipolar disorder, Brain aneurysm, Renal cell carcinoma, Central nervous system cancer, Combined immunodeficiency, Combined immunodeficiency disease, Congenital cardiovascular anomaly, Atopic dermatitis, Glioma, Hypothyroidism
View all (17 more)

1145
Calsequestrin 2
PDIB2
Cardiac arrhythmias, Atrial fibrillation, Atrial flutter, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia, Dementia, Hereditary bundle branch system defect, Hypertrophic cardiomyopathy, Long qt syndrome, Polymorphic catecholaminergic ventricular tachycardia, Polymorphic ventricular tachycardia, Vesicoureteral reflux, Wolff-parkinson-white syndrome

1146
Cullin 4B
CUL-4B, MRXHF2, MRXS15, MRXSC, SFM2
Global developmental delay, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, X-linked intellectual disability

1147
Cullin 4A
-
Atrial fibrillation, Bipolar disorder, Stevens-johnson syndrome

1148
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, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Prostatic neoplasm, Pseudohypoparathyroidism
View all (2 more)

1149
CDAN1 interacting nuclease 1
C15orf41, HH114
Alzheimer disease, Congenital dyserythropoietic anemia, Colorectal cancer, Gastroesophageal reflux disease, Willis-ekbom disease

1150
Cullin 2
-
Alzheimer disease, Colorectal adenoma, Crohn disease, Inflammatory bowel disease, Moyamoya angiopathy, Ulcerative colitis