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"
1571 to 1580 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1571
Casein kinase 1 gamma 3
CKI-gamma 3, CSNK1G3L
Tourette syndrome, Myocardial infarction

1572
Casein kinase 2 alpha 1
CK2A1, CKII, Cka1, Cka2, OCNDS
Autism, Squamous cell carcinoma, Developmental disability, Intellectual developmental disorder, Alzheimer disease, T-cell leukemia-lymphoma, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Skin neoplasms

1573
Casein kinase 2 alpha 2
CK2A2, CK2alpha', CSNK2A1
Blood coagulation disorder, Squamous cell carcinoma, Skin neoplasms

1574
Casein kinase 2 subunit alpha' interacting protein
CSNKA2IP
Glaucoma, Open angle glaucoma

1575
Casein kinase 2 beta
CK2B, CK2N, CSK2B, Ckb1, Ckb2, G5A, POBINDS
Autism, Nonsyndromic intellectual disability, Squamous cell carcinoma, Malocclusion, Clinodactyly, Cutaneous lupus erythematosus, Hypothyroidism, Intellectual developmental disorder, T-cell leukemia-lymphoma, Neurodevelopmental disorder, Rheumatoid arthritis, Skin neoplasms, Syndactyly, Systemic lupus erythematosus

1576
Chondroitin sulfate proteoglycan 4
CSPG4A, HMW-MAA, MCSP, MCSPG, MEL-CSPG, MSK16, NG2
Basal cell carcinoma, Hepatocellular carcinoma, Gout, Multiple sclerosis, Myopathy, Schizophrenia

1577
Chondroitin sulfate proteoglycan 5
NGC
Schizophrenia

1578
Centrosome and spindle pole associated protein 1
CSPP, CSPP-L, JBTS21
Dandy-walker syndrome, Aplasia of the vermis, Joubert syndrome, Meckel-gruber syndrome, Optic atrophy, Retinitis pigmentosa

1579
Cysteine and serine rich nuclear protein 1
AXUD1, CSRNP-1, FAM130B, TAIP-3, URAX1
Hepatocellular carcinoma, Dilated cardiomyopathy, Lymphocytic leukemia

1580
Cysteine and serine rich nuclear protein 3
FAM130A2, MBU1, PPP1R73, TAIP-2, TAIP2
Attention deficit hyperactivity disorder, Autism, Colorectal cancer, Endometrial neoplasms, Osteoporosis, Diabetes mellitus type 2