Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
421 to 430 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

421
Casein kappa
CNS10, CSN10, CSNK, KCA
Carcinoma

422
Casein kinase 1 alpha 1
CK1, CK1a, CKIa, HEL-S-77p, HLCDGP1, PRO2975
Biliary atresia, Obstructive pulmonary disease, Craniofacial abnormalities, Esophageal cancer, Insomnia, T-cell leukemia-lymphoma

423
Casein kinase 1 delta
ASPS, CKI-delta, CKId, CKIdelta, FASPS2, HCKID
Advanced sleep phase syndrome, Color vision deficiency, Advanced sleep-phase syndrome

424
Casein kinase 1 epsilon
CKIe, CKIepsilon, HCKIE
Bipolar disorder, Cardiac arrhythmia, Cerebellar ataxia, Developmental and epileptic encephalopathy, Schizophrenia

425
Centrosomal protein 128
C14orf145, C14orf61, LEDP/132
Developmental delay, Epilepsy, Hyperthyroidism, Hypothyroidism, Idiopathic pulmonary fibrosis, Ulcerative colitis

426
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 disorders, Non-specific syndromic intellectual disability, Skin neoplasm

427
C2 calcium dependent domain containing 4A
FAM148A, NLF1
Diabetes mellitus type 2, Esophageal atresia

428
Casein kinase 2 alpha 2
CK2A2, CK2alpha', CSNK2A1
Blood coagulation disorder, Squamous cell carcinoma, Skin neoplasm

429
Casein kinase 2 beta
CK2B, CK2N, CSK2B, Ckb1, Ckb2, G5A, POBINDS
Autism, Nonsyndromic intellectual disability, Squamous cell carcinoma, Malocclusion, Cutaneous lupus erythematosus, Hypothyroidism, Intellectual developmental disorder, T-cell leukemia-lymphoma, Neurodevelopmental disorders, Rheumatoid arthritis, Skin neoplasm, Syndactyly, Systemic lupus erythematosus

430
Codanin 1
CDA1, CDAI, CDAN1A, DLT, PRO1295
Congenital dyserythropoietic anemia, Bipolar disorder