Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
231 to 240 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

231
Cation channel sperm associated 1
CATSPER, SPGF7
Alzheimer disease, Male infertility, Spermatogenic failure

232
Cation channel sperm associated 2
-
Deafness, sensorineural, and male infertility, Deafness-infertility syndrome, Lung cancer, Male infertility, Spermatogenic failure, Squamous cell carcinoma, Upper aerodigestive tract neoplasm

233
Calcium and integrin binding family member 3
KIP3
Lymphocytic leukemia, Hodgkin lymphoma, Multiple myeloma

234
Chloride voltage-gated channel 1
CLC1
Cerebral palsy, Hyperkalemic periodic paralysis, Metachromatic leukodystrophy, Memory disorders, Migraine, Myocardial infarction, Myopathy, Smith-lemli-opitz syndrome

235
Chloride voltage-gated channel 2
CIC-2, CLC2, ECA2, ECA3, EGI11, EGI3, EGMA, EJM6, EJM8, FHA2, FHII, HALD2, LKPAT, clC-2
Bipolar disorder, Central nervous system demyelinating disease, Cerebellar ataxia, Cerebral palsy, Cushing syndrome, Epilepsy, Familial focal epilepsy with variable foci, Idiopathic generalized epilepsy, Hyperaldosteronism, Glioma, Intellectual developmental disorder, Myoclonic epilepsy

236
Chloride voltage-gated channel 3
CLC3, ClC-3, NEDHYBA, NEDSBA
Amyotrophic lateral sclerosis, Autism, Neurodevelopmental disorder, Glioma, Nasopharyngeal carcinoma, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Parkinson disease, Schizophrenia, Stomach neoplasms

237
Chloride voltage-gated channel 4
CLC4, ClC-4, ClC-4A, MRX15, MRX49, MRXSRC
Global developmental delay, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorders, X-linked intellectual disability

238
Chloride voltage-gated channel 5
CLC5, CLCK2, ClC-5, DENT1, DENTS, NPHL1, NPHL2, XLRH, XRN, hCIC-K2
Dent disease, Desbuquois syndrome, Hypophosphatemic rickets, Glioma, Nephrolithiasis, Nephrotic syndrome, Proteinuria, Severe acute respiratory syndrome, X-linked nephrolithiasis

239
Chromosome 10 open reading frame 71
CEFIP, CMD1QQ
Alzheimer disease, Cardiomyopathy, Dilated cardiomyopathy, Human immunodeficiency virus infection

240
Cilia and flagella associated protein 70
SPGF41, TTC18
Spermatogenic failure