Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2911 to 2920 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2911
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

2912
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

2913
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

2914
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

2915
Complexin 4
CPX-IV, CPXIV
Coronary artery disease, Hearing loss, Retinopathy

2916
Carboxypeptidase M
-
Astrocytoma, Endometriosis, Alzheimer disease, Major depressive disorder, Proliferative diabetic retinopathy, Psychiatric disorders, Scoliosis

2917
Carboxypeptidase N subunit 1
CPN, SCPN
Anaphylatoxin inactivator deficiency, Carboxypeptidase n deficiency, Dermatomyositis, Nonalcoholic fatty liver disease, Diabetes mellitus type 2

2918
Carboxypeptidase N subunit 2
ACBP
Essential tremor

2919
Copine 1
COPN1, CPN1
Basal cell carcinoma, Schizophrenia

2920
Copine 3
CPN3, PRO1071
Prostatic neoplasms