Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
1431 to 1440 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1431
Cytoplasmic polyadenylation element binding protein 3
-
Attention deficit hyperactivity disorder, Breast cancer, Hepatocellular carcinoma, Color vision deficiency, Tourette syndrome, Metabolic syndrome, Schizophrenia, Diabetes mellitus, type 2

1432
Cytoplasmic polyadenylation element binding protein 4
CPE-BP4, hCPEB-4
Ankylosing spondylitis, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Cardiovascular disease, Obstructive pulmonary disease, Crohn disease, Hypertension, Gout, Heart failure, Inflammatory bowel disease, Multiple myeloma, Obesity, Peptic ulcer disease, Prion disease
View all (7 more)

1433
Cadherin like and PC-esterase domain containing 1
C7orf58
Ankle fracture, Bone fracture, Creutzfeldt-jakob disease, Diabetes mellitus, type 2, Upper extremity fracture, Uterine fibroid

1434
Ciliogenesis and planar polarity effector complex subunit 1
C5orf42, Hug, JBTS17, OFD6
Monomelic amyotrophy, Desbuquois syndrome, Encephalocele, Aplasia of the vermis, Global developmental delay, Hodgkin lymphoma, Joubert syndrome, Nephronophthisis, Orofaciodigital syndrome, Polydactyly, Retinitis pigmentosa, Uranostaphyloschisis

1435
Complexin 1
CPX-I, CPX1, DEE63, EIEE63
Behcet disease, Bipolar disorder, Bipolar depression, Major depressive disorder, Developmental and epileptic encephalopathy, Infantile myoclonic epilepsy, Psychotic disorders, Schizophrenia, Vasculitis, Wolff-parkinson-white syndrome

1436
Complexin 2
921-L, CPX-2, CPX2, Hfb1
Attention deficit hyperactivity disorder, Bipolar disorder, Color vision deficiency, Bipolar depression, Major depressive disorder, Insomnia, Obesity, Psychotic disorders, Schizophrenia

1437
Complexin 4
CPX-IV, CPXIV
Coronary artery disease, Hearing loss, Retinopathy

1438
CPM
Carboxypeptidase M
-
Astrocytoma, Endometriosis, Alzheimer disease, Major depressive disorder, Proliferative diabetic retinopathy, Psychiatric disorders, Scoliosis

1439
Carboxypeptidase N subunit 1
CPN, SCPN
Anaphylatoxin inactivator deficiency, Carboxypeptidase n deficiency, Dermatomyositis, Nonalcoholic fatty liver disease, Diabetes mellitus, type 2

1440
Carboxypeptidase N subunit 2
ACBP
Essential tremor