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"
251 to 260 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

251
Calcium modulating ligand
CAML, CDG2Z, GET2
Congenital disorder of glycosylation

252
Cathelicidin antimicrobial peptide
CAP-18, CAP18, CRAMP, FALL-39, FALL39, HSD26, LL37
Rosacea

253
Calmodulin regulated spectrin associated protein 1
CDCBM12
Alzheimer disease, Juvenile arthritis, Colorectal cancer, Cortical dysplasia with other brain malformations, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis, Scoliosis

254
Calmodulin regulated spectrin associated protein family member 2
CAMSAP1L1
Celiac disease, Epilepsy, Generalized epilepsy, Hypothyroidism, Myocardial infarction, Partial epilepsy, Diabetes mellitus type 1, Diabetes mellitus type 2, Venous thromboembolism

255
Calmodulin regulated spectrin associated protein family member 3
KIAA1543, NEZHA, PPP1R80
Female infertility, Pelvic inflammatory disease, Peripheral arterial disease, Uterine inflammatory disease

256
Calmodulin binding transcription activator 1
CANPMR, CECBA
Alzheimer disease, Attention deficit hyperactivity disorder, Cerebellar dysfunction with variable cognitive and behavioral abnormalities, Colorectal cancer, Fatty liver, Gastroesophageal reflux disease, Insomnia, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Migraine, Mood disorder, Nervous system disease, Neurodevelopmental disorder, Neurotic disorder
View all (8 more)

257
Calmodulin binding transcription activator 2
-
Cerebellar dysfunction with variable cognitive and behavioral abnormalities

258
Cullin associated and neddylation dissociated 1
TIP120, TIP120A
Scoliosis

259
Cullin associated and neddylation dissociated 2 (putative)
TIP120B, Tp120b
Atrial fibrillation, Atrial flutter, Cardiac arrhythmia, Cardiomyopathy, Heart failure, Diabetes mellitus type 2

260
Calcium activated nucleotidase 1
DBQD, DBQD1, EDM7, SCAN-1, SCAN1, SHAPY
Desbuquois dysplasia, Desbuquois syndrome, Epiphyseal dysplasia, Larsen syndrome