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"
1091 to 1100 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1091
Charcot-Leyden crystal galectin
GAL10, Gal-10, LGALS10, LGALS10A, LPPL_HUMAN
Schizophrenia

1092
Chloride channel accessory 1
CACC, CACC1, CLCRG1, CaCC-1, GOB5, hCLCA1, hCaCC-1
Asthma, Obstructive airway disease

1093
Chloride channel accessory 2
CACC, CACC3, CLCRG2, CaCC-3
Crohn disease, Heart disease, Ileocolitis, Lung neoplasms

1094
Chloride channel accessory 4
CaCC, CaCC2
Autism, Cystic fibrosis

1095
Chloride channel CLIC like 1
ERAC1, MCLC, RP32
Chudley-mccullough syndrome, Deafness, Hearing impairment, Major depressive disorder, Oligodendroglioma, Retinitis pigmentosa

1096
Cardiotrophin like cytokine factor 1
BSF-3, BSF3, CISS2, CLC, NNT-1, NNT1, NR6
Cold-induced sweating syndrome, Crisponi syndrome

1097
Chloride voltage-gated channel 1
CLC1
Becker generalized myotonia, Cerebral palsy, Congenital myotonia, Hyperkalemic periodic paralysis, Metachromatic leukodystrophy, Memory disorders, Migraine, Myocardial infarction, Myopathy, Smith-lemli-opitz syndrome, Myotonia congenita

1098
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

1099
Chloride voltage-gated channel 3
CLC3, ClC-3, NEDHYBA, NEDSBA
Amyotrophic lateral sclerosis, Autism, Neurodevelopmental disorder, Glioma, Nasopharyngeal carcinoma, Non-specific syndromic intellectual disability, Parkinson disease, Schizophrenia, Stomach neoplasms

1100
Chloride voltage-gated channel 4
CLC4, ClC-4, ClC-4A, MRX15, MRX49, MRXSRC
Intellectual disability syndrome, Global developmental delay, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorder, X-linked intellectual disability