Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "C"
1411 to 1420 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1411
Carboxypeptidase A2
-
Hypoxia

1412
Carboxypeptidase A3
MC-CPA
Diverticular disease, Dyslexia, Hypertension

1413
Carboxypeptidase A4
CPA3
Color vision deficiency, Rheumatoid arthritis

1414
Carboxypeptidase A5
-
Color vision deficiency

1415
Carboxypeptidase A6
CPAH, ETL5, FEB11
Alzheimer disease, Benign mesial temporal lobe epilepsy, Cerebral amyloid angiopathy, Cerebral palsy, Epilepsy, Familial temporal lobe epilepsy, Rolandic epilepsy, Temporal lobe epilepsy, Febrile convulsion, Gastroesophageal reflux disease, Generalized epilepsy with febrile seizures plus, Global developmental delay, Intellectual developmental disorder, Oligodendroglioma, Periventricular heterotopia
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1416
C3 and PZP like alpha-2-macroglobulin domain containing 8
ASGD8, K-CAP, VIP
Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Cataract, Colorectal neoplasms, Glaucoma, Hypothyroidism, Multiple sclerosis, Retinal detachment, Selective iga deficiency disease

1417
Centrosome assembly and centriole elongation protein
BM032, CENP-J, CENPJ, LAP, LIP1, MCPH6, SASS4, SCKL4, Sas-4
Primary microcephaly, Congenital microcephaly, Desbuquois syndrome, Lissencephaly, Meniere disease, Microcephaly, Oligodendroglioma, Perisylvian polymicrogyria, Seckel syndrome

1418
Carboxypeptidase B2
CPU, PCPB, TAFI
Amenorrhea, Color vision deficiency, Kidney failure, Obesity

1419
Carboxypeptidase D
GP180
Major depressive disorder, Psychotic disorders

1420
Carboxypeptidase E
BDVS, CPH, IDDHH
Eczema, Ischemic heart disease, Coronary artery disease, Prader-willi-like syndrome, Diabetes mellitus type 2, Endocrine system disease, Lung neoplasms, Myocardial ischemia, Obesity, Pelvic organ prolapse