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"
281 to 290 of 1806 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

281
Calcyphosine like
-
Ankylosing spondylitis, Asthma, Eczema, Autism, B-cell acute lymphoblastic leukemia, Biliary cirrhosis, Dermatitis, Biliary cholangitis, Respiratory system disease, Rhinitis, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2

282
Capping actin protein of muscle Z-line subunit alpha 1
CAPPA1, CAPZ, CAZ1
Esophageal squamous cell carcinoma, Hypertension, Major depressive disorder

283
Capping actin protein of muscle Z-line subunit alpha 2
CAPPA2, CAPZ
Alzheimer disease, Neurodevelopmental disorder, Insomnia, Intellectual developmental disorder, Non-specific syndromic intellectual disability

284
Capping actin protein of muscle Z-line subunit alpha 3
CAPPA3, Gsg3, HEL-S-86
Alzheimer disease, Attention deficit hyperactivity disorder, Chagas cardiomyopathy, Obstructive pulmonary disease, Gastroesophageal reflux disease, Psychiatric disorders, Substance abuse

285
Capping actin protein of muscle Z-line subunit beta
CAPB, CAPPB, CAPZ
Atrial fibrillation, Carcinoma, Obstructive pulmonary disease, Crohn disease, Hypothyroidism, Lung cancer, Psoriasis, Scoliosis

286
Caspase recruitment domain family member 10
BIMP1, CARMA3, IMD89
Autoimmune hepatitis, Immunodeficiency, Open angle glaucoma, Sarcoidosis

287
Caspase recruitment domain family member 11
BENTA, BIMP3, CARMA1, IMD11, IMD11A, PPBL
Alzheimer disease, Asthma, Astrocytoma, Eczema, Benta disease, Bipolar disorder, Brain aneurysm, Renal cell carcinoma, Central nervous system cancer, Combined immunodeficiency, Combined immunodeficiency disease, Congenital cardiovascular anomaly, Atopic dermatitis, Glioma, Hypothyroidism
View all (17 more)

288
Caspase recruitment domain family member 14
BIMP2, CARMA2, PRP, PSORS2, PSS1
Autoinflammatory syndrome, Central nervous system cancer, Erythematosquamous dermatosis, Glioblastoma, Glioma, Hirschsprung disease, Moyamoya disease, Mucopolysaccharidosis, Psoriasis, Psoriasis vulgaris, Seborrheic dermatitis, Skin disease

289
Caspase recruitment domain family member 16
COP, COP1, LLID-114769, PSEUDO-ICE
Jeune syndrome, Bronchopulmonary dysplasia, Major depressive disorder

290
Caspase recruitment domain family member 18
ICEBERG, UNQ5804, pseudo-ICE
Alzheimer disease, Non-small-cell lung carcinoma, Squamous cell carcinoma, Diabetic retinopathy, Willis-ekbom disease