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"
1171 to 1180 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1171
Clarin 1
RP61, USH3, USH3A
Branchiootorenal syndrome, Hearing impairment, Optic atrophy, Retinitis pigmentosa, Retinitis pigmentosa-deafness syndrome, Usher syndrome

1172
Clarin 2
DFNB117
Isolated sensorineural deafness, Deafness, Hearing loss, Nonsyndromic hearing loss

1173
Clarin 3
TMEM12, USH3AL1
Parkinson disease

1174
Calsyntenin 1
ALC-ALPHA, CDHR12, CST-1, CSTN1, PIK3CD, XB31alpha, alcalpha1, alcalpha2
Alzheimer disease, Asthma

1175
Calsyntenin 2
ALC-GAMMA, CDHR13, CS2, CSTN2, alcagamma
Asthma, Astrocytoma, Attention deficit hyperactivity disorder, Autism, Central nervous system cancer, Duchenne muscular dystrophy, Glioblastoma, Glioma, Hodgkin lymphoma, Insomnia, Liver neoplasms, Lung cancer, Multiple sclerosis, Oligodendroglioma, Retinal detachment
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1176
Calsyntenin 3
CDHR14, CSTN3, alcbeta
Autism, Schizophrenia

1177
Clathrin light chain A
LCA
Atypical femoral fracture, Bipolar disorder, Color vision deficiency, Fatty liver, Generalized anxiety disorder

1178
Clathrin light chain B
LCB
Lung neoplasms, Obesity

1179
Clathrin heavy chain
CHC, CHC17, CLH-17, CLTCL2, Hc, MRD56
Nonsyndromic intellectual disability, Global developmental delay, Intellectual developmental disorder, Diffuse large b-cell lymphoma, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Noonan syndrome

1180
Clathrin heavy chain like 1
CHC22, CLH22, CLTCL, CLTD
Alzheimer disease, Central nervous system cancer, Congenital insensitivity to pain, Coronary artery disease, Glioblastoma, Glioma