Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "C"
1181 to 1190 of 1806 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

1181
Calsyntenin 1
ALC-ALPHA, CDHR12, CST-1, CSTN1, PIK3CD, XB31alpha, alcalpha1, alcalpha2
Alzheimer disease, Asthma

1182
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
View all (2 more)

1183
Calsyntenin 3
CDHR14, CSTN3, alcbeta
Autism, Schizophrenia

1184
Clathrin light chain A
LCA
Atypical femoral fracture, Bipolar disorder, Color vision deficiency, Fatty liver, Generalized anxiety disorder

1185
Clathrin light chain B
LCB
Lung neoplasms, Obesity

1186
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

1187
Clathrin heavy chain like 1
CHC22, CLH22, CLTCL, CLTD
Alzheimer disease, Central nervous system cancer, Congenital insensitivity to pain, Coronary artery disease, Glioblastoma, Glioma

1188
Collectrin, amino acid transport regulator
NX-17, NX17, TMEM27
Aminoaciduria, Autism, Hepatocellular carcinoma, Urethral obstruction

1189
Clusterin
AAG4, APO-J, APOJ, CLI, CLU1, CLU2, KUB1, NA1/NA2, SGP-2, SGP2, SP-40, TRPM-2, TRPM2
Alzheimer disease, Amyotrophic lateral sclerosis, Juvenile arthritis, Atherosclerosis, Atrophy, Cognition disorder, Dementia, Diabetic retinopathy, Hypertension, Juvenile idiopathic arthritis, Kidney disease, Kidney failure, Lewy body disease, Systemic lupus erythematosus, Melanoma
View all (11 more)

1190
Clusterin associated protein 1
CFAP22, FAP22, IFT38
Aplasia cutis congenita with epibulbar dermoids, Cardiovascular disease, Aplasia of the vermis, Hypertension, Inflammatory bowel disease, Leber congenital amaurosis, Retinitis pigmentosa, Diabetes mellitus type 2