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"
1041 to 1050 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1041
Calcium and integrin binding family member 2
DFNB48, KIP2, USH1J
Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing impairment, Hearing loss, Retinitis pigmentosa, Usher syndrome

1042
Calcium and integrin binding family member 3
KIP3
Lymphocytic leukemia, Hodgkin lymphoma, Multiple myeloma

1043
CBY1 interacting BAR domain containing 1
BARMR1, FAM92A, FAM92A1, PAPA9
Ciliopathy, Polydactyly, Postaxial polydactyly, Syndactyly

1044
CBY1 interacting BAR domain containing 2
FAM92B
Color vision deficiency, Crohn disease

1045
Capicua transcriptional repressor
MRD45
Androgenetic alopecia, Attention deficit hyperactivity disorder, Autism, Nonsyndromic intellectual disability, Cerebral folate deficiency, Neurodevelopmental disorder, Dias-logan syndrome, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Ocular hypotension, Spinocerebellar ataxia

1046
Cell death inducing DFFA like effector a
CIDE-A
Attention deficit hyperactivity disorder, Congestive heart failure, Heart failure, Liver cirrhosis, Liver neoplasms, Obesity

1047
Cell death inducing DFFA like effector b
-
Anorectal malformation

1048
Cell death inducing DFFA like effector c
CIDE-3, CIDE3, FPLD5, FSP27
Familial partial lipodystrophy, Allergic contact dermatitis, Partial lipodystrophy, Lipodystrophy

1049
Class II major histocompatibility complex transactivator
C2TA, CIITAIV, MHC2D1, MHC2TA, NLRA
Rheumatoid arthritis, Asthma, Eczema, Bare lymphocyte syndrome, Celiac disease, Crohn disease, Gastro-entero-pancreatic neuroendocrine tumor, Inflammatory bowel disease, Juvenile idiopathic arthritis, Systemic lupus erythematosus, Multiple sclerosis, Myocardial infarction, Nasopharyngeal neoplasms, Oligoarticular juvenile idiopathic arthritis, Ulcerative colitis

1050
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