Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1431 to 1440 of 1806 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1431	22849	CPEB3	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	80315	CPEB4	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	79974	CPED1	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	65250	CPLANE1	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	10815	CPLX1	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	10814	CPLX2	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	339302	CPLX4	Complexin 4	CPX-IV, CPXIV	Coronary artery disease, Hearing loss, Retinopathy
1438	1368	CPM	Carboxypeptidase M	-	Astrocytoma, Endometriosis, Alzheimer disease, Major depressive disorder, Proliferative diabetic retinopathy, Psychiatric disorders, Scoliosis
1439	1369	CPN1	Carboxypeptidase N subunit 1	CPN, SCPN	Anaphylatoxin inactivator deficiency, Carboxypeptidase n deficiency, Dermatomyositis, Nonalcoholic fatty liver disease, Diabetes mellitus type 2
1440	1370	CPN2	Carboxypeptidase N subunit 2	ACBP	Essential tremor

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