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"
1591 to 1600 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1591
Cystatin B
CPI-B, CST6, EPM1, EPM1A, PME, STFB, ULD
Hypohidrotic ectodermal dysplasia, Chorea, Developmental and epileptic encephalopathy, Dyskinesia, Ectodermal dysplasia, Rolandic epilepsy, Esophageal squamous cell carcinoma, Glioblastoma, Meningioma, Progressive myoclonic epilepsy, Intellectual disability, Unverricht-lundborg syndrome

1592
Cleavage stimulation factor subunit 1
CstF-50, CstFp50
Alzheimer disease

1593
Cleavage stimulation factor subunit 2
CSTF64, CstF-64, XLID113
Intellectual developmental disorder, x-linked

1594
Cleavage stimulation factor subunit 3
CSTF-77
Major depressive disorder, Mood disorder

1595
Centriolar satellite-associated tubulin polyglutamylase complex regulator 1
C11orf49
Alzheimer disease, Major depressive disorder, Mood disorder, Peripheral vascular disease, Diabetes mellitus type 2, Vascular disease, Venous thromboembolism

1596
Cancer/testis antigen 55
BJHCC20A, CXorf48, SPGFX7
Male infertility single gene azoospermia, Spermatogenic failure, x-linked

1597
Cutaneous T cell lymphoma-associated antigen 1
CT21.1, CT21.2, CTAGE, CTAGE-1, CTAGE-2
Benign prostatic hyperplasia, Obstructive pulmonary disease, Endometrial cancer, Endometrial neoplasms, Oligodendroglioma

1598
C-terminal binding protein 1
BARS, HADDTS
Attention deficit hyperactivity disorder, Colorectal neoplasms, Intellectual developmental disorder, Substance abuse, Diabetes mellitus type 2, Wolff-parkinson-white syndrome

1599
C-terminal binding protein 2
-
Congenital pulmonary artery atresia, Hearing loss, Hemorrhoid, Metabolic syndrome, Prostate cancer, Prostatic neoplasms, Diabetes mellitus type 2

1600
CST telomere replication complex component 1
AAF-132, AAF132, C17orf68, CRMCC, tmp494178
Bone disease, Brain disease, Calcinosis, Cerebroretinal microangiopathy with calcifications and cysts, Coats plus syndrome, Dyskeratosis congenita, Interstitial lung disease, Metabolic bone disorder, Parkinson disease