Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2921 to 2930 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2921
Cytoplasmic polyadenylation element binding protein 2
CPE-BP2, CPEB-2, hCPEB-2
Cardiovascular disease

2922
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

2923
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)

2924
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

2925
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

2926
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

2927
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

2928
Complexin 4
CPX-IV, CPXIV
Coronary artery disease, Hearing loss, Retinopathy

2929
Carboxypeptidase M
-
Astrocytoma, Endometriosis, Alzheimer disease, Major depressive disorder, Proliferative diabetic retinopathy, Psychiatric disorders, Scoliosis

2930
Carboxypeptidase N subunit 1
CPN, SCPN
Anaphylatoxin inactivator deficiency, Carboxypeptidase n deficiency, Dermatomyositis, Nonalcoholic fatty liver disease, Diabetes mellitus type 2