Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
571 to 580 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

571
Cordon-bleu WH2 repeat protein like 1
COBLR1
Coronary artery disease, Diabetes mellitus, Diabetic eye disease, Diabetic neuropathy, Diabetic retinopathy, Hyperlipidemia, Gout, Metabolic syndrome, Myocardial ischemia, Nonalcoholic fatty liver disease, Psoriasis, Diabetes mellitus, type 2, Type 2 diabetes nephropathy, Uterine fibroid

572
Cytoplasmic polyadenylation element binding protein 3
-
Attention deficit hyperactivity disorder, Breast cancer, Hepatocellular carcinoma, Color vision deficiency, Tourette syndrome, Metabolic syndrome, Schizophrenia, Diabetes mellitus, type 2

573
Chondroitin sulfate synthase 1
CHSY, CSS1, ChSy-1, TPBS
Ankylosing spondylitis, Bone fracture, Corneal astigmatism, Desbuquois syndrome, Hearing impairment, Immune system disease, Keratoconus, Liver cirrhosis, Non-small cell lung carcinoma, Prostate cancer

574
Ciliogenesis associated kinase 1
ECO, EJM10, ICK, LCK2, MRK, hICK
Attention deficit hyperactivity disorder, Congenital ocular coloboma, Craniodiaphyseal dysplasia, Desbuquois syndrome, Dysgenesis of corpus callosum, Juvenile myoclonic epilepsy, Myoclonic epilepsy, Microphthalmos, Short rib dysplasia-polydactyly syndrome, Substance abuse

575
Connector enhancer of kinase suppressor of Ras 2
CNK2, KSR2, MAGUIN, MRXSHG
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Diabetes mellitus type 2, Insomnia, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Major depressive disorder, Neurodevelopmental disorders, Developmental and epileptic encephalopathy, X-linked intellectual disability, Post-traumatic stress disorder, Psychiatric disorders, Schizophrenia, Diabetes mellitus, type 2
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576
Calsyntenin 1
ALC-ALPHA, CDHR12, CST-1, CSTN1, PIK3CD, XB31alpha, alcalpha1, alcalpha2
Alzheimer disease, Asthma

577
Centrosomal protein 164
NPHP15
Ciliopathies, Metabolic syndrome, Nephronophthisis, Retinitis pigmentosa, Senior-loken syndrome, Diabetes mellitus, type 2

578
Caspase recruitment domain family member 8
CARDINAL, DACAR, DAKAR, NDPP, NDPP1, TUCAN
Gout, Inflammatory bowel disease, Occupational disease, Pleural diseases

579
CD93 molecule
C1QR1, C1qR(P), C1qRP, CDw93, ECSM3, MXRA4, dJ737E23.1
Central nervous system cancer, Glioblastoma, Glioma, Venous thromboembolism

580
Chaperonin containing TCP1 subunit 5
CCT-epsilon, CCTE, HEL-S-69, HSNSP, PNAS-102, TCP-1-epsilon
Breast neoplasm, Neurodevelopmental disorder, Charcot-marie-tooth disease, Human immunodeficiency virus infection, Hereditary sensory neuropathy, Non-specific syndromic intellectual disability, Hereditary spastic paraplegia