Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "C"
701 to 710 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

701
Cadherin related family member 3
CDH28
Alzheimer disease, Asthma, Atrial fibrillation, Crohn disease, Multiple sclerosis, Obesity

702
Cadherin related family member 4
CDH29, PRO34300
Attention deficit hyperactivity disorder, Autism, Insomnia, Myocardial infarction

703
Cadherin related family member 5
MLPCDH, MU-PCDH, MUCDHL, MUPCDH
Hypothyroidism, Systemic lupus erythematosus, Systemic sclerosis

704
CDAN1 interacting nuclease 1
C15orf41, HH114
Alzheimer disease, Congenital dyserythropoietic anemia, Colorectal cancer, Gastroesophageal reflux disease, Willis-ekbom disease

705
Cyclin dependent kinase 1
CDC2, CDC28A, P34CDC2
Eczema, Hepatocellular carcinoma, Diffuse large b-cell lymphoma

706
Cyclin dependent kinase 10
ALSAS, PISSLRE
Al kaissi syndrome, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Melanoma, Global developmental delay, Major depressive disorder, Schizophrenia

707
Cyclin dependent kinase 11B
CDC2L1, CDK11, CDK11-p110, CDK11-p46, CDK11-p58, CLK-1, PITSLREA, PK58, p58, p58CDC2L1, p58CLK-1
Brachymorphism onychodysplasia dysphalangism syndrome

708
Cyclin dependent kinase 12
CRK7, CRKR, CRKRS
Asthma, Bladder calculus, Coronary artery disease, Diabetes mellitus, Diabetic neuropathy, Alzheimer disease, Tourette syndrome, Hyperopia, Nasopharyngeal neoplasms, Nephrolithiasis, Polycystic ovary syndrome, Prostatic neoplasms, Rheumatoid arthritis, Schizophrenia, Systemic lupus erythematosus
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709
Cyclin dependent kinase 13
CDC2L, CDC2L5, CHDFIDD, CHED, hCDK13
Alzheimer disease, Autism, Congenital heart defects, Congenital heart disease, Congenital heart defect, intellectual disability, facial dysmorphism syndrome, Gastroesophageal reflux disease, Global developmental delay, Intellectual developmental disorder, Neurodevelopmental disorder

710
Cyclin dependent kinase 14
PFTAIRE1, PFTK1
Attention deficit hyperactivity disorder, Hepatocellular carcinoma, Glomerulonephritis, Retinopathy of prematurity, Scoliosis, Substance abuse