Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
1081 to 1090 of 1338 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

1081
Calreticulin
CALR1, CRT, HEL-S-99n, RO, SSA, cC1qR
Bipolar disorder, Budd-chiari syndrome, Colorectal neoplasm, Diabetes mellitus, Esophageal squamous cell carcinoma, Essential thrombocythemia, Melanoma, Myeloproliferative disorder, Myocardial ischemia, Non-organic psychosis, Schizophrenia, Prostatic neoplasm, Psychotic disorders, Schizoaffective disorder, Sideroblastic anemia
View all (1 more)

1082
Calumenin
-
Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Developmental disability, Peripheral neuropathy

1083
Calcium/calmodulin dependent protein kinase IV
CaMK IV, CaMK-GR, CaMKIV, caMK
Alzheimer disease, Asthma, Autoimmune disease, Autoimmune thyroid disease, Colorectal cancer, Neurodevelopmental disorder, Hypothyroidism, Insomnia, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Periodontitis, Severe combined immunodeficiency, Diabetes mellitus, type 1, Diabetes mellitus, type 2

1084
Complement factor H related 5
CFHL5, CFHR5D, FHR-5, FHR5
Asthma, Atrophic macular degeneration, Hemolytic uremic syndrome, C3 glomerulonephritis, Cholelithiasis, Kidney disease, Mesangiocapillary glomerulonephritis, Age-related macular degeneration

1085
Calcium/calmodulin dependent protein kinase II alpha
CAMKA, CaMKIINalpha, CaMKIIalpha, MRD53, MRT63
Autism, Nonsyndromic intellectual disability, Bipolar disorder, Neurodevelopmental disorder, Crohn disease, Major depressive disorder, Global developmental delay, Hepatolenticular degeneration, Hepatomegaly, Hyperalgesia, Inflammatory bowel disease, Intellectual developmental disorder, Depression, Mitochondrial disease, Neurodevelopmental disorders
View all (3 more)

1086
Chromosome 1 open reading frame 21
PIG13
Systemic lupus erythematosus

1087
ClpB family mitochondrial disaggregase
ANKCLB, ANKCLP, HSP78, MEGCANN, MGCA7, MGCA7A, SCN9, SKD3
3-methylglutaconic aciduria, Severe congenital neutropenia, Leigh syndrome, Microcytic anemia, Neutropenia, Obesity, Scoliosis, Congenital neutropenia

1088
Collagen type XXI alpha 1 chain
COLA1L, FP633
Obstructive pulmonary disease, Color vision deficiency, Psychotic disorders, Schizophrenia, Small cell lung carcinoma

1089
Calcium/calmodulin dependent protein kinase II beta
CAM2, CAMK2, CAMKB, CaMKIIbeta, MRD54
Autism, Nonsyndromic intellectual disability, Brain aneurysm, Cannabis abuse, Congenital neurologic anomalies , Developmental disability, Global developmental delay, Intellectual developmental disorder, Metabolic syndrome, Neurodevelopmental disorder, Neurodevelopmental disorders, Osteoarthritis, Substance-induced psychosis, Schizophrenia, Diabetes mellitus, type 2

1090
Calcium binding protein 39 like
MLAA-34, MO25-BETA, MO2L, bA103J18.3
Insomnia, Parkinson disease