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"
1601 to 1610 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1601
CCCTC-binding factor
CFAP108, FAP108, MRD21
Alzheimer disease, Neurodevelopmental disorder, Hypothyroidism, Intellectual developmental disorder, Intellectual developmental disorder growth microcephaly, Intellectual developmental disorder dysmorphic microcephaly, Oligodendroglioma, Schizophrenia

1602
CCCTC-binding factor like
BORIS, CT27, CTCF-T, HMGB1L1, dJ579F20.2
Obesity

1603
CTD phosphatase subunit 1
CCFDN, FCP1
Charcot-marie-tooth disease, Congenital cataract facial dysmorphism neuropathy syndrome, Insomnia, Schizophrenia

1604
CTD small phosphatase 1
NIF3, NLI-IF, NLIIF, SCP1
Amyotrophic lateral sclerosis

1605
CTD small phosphatase 2
OS4, PSR2, SCP2
Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Insomnia, Major depressive disorder, Sarcoidosis, Scoliosis

1606
CTD small phosphatase like
C3orf8, HYA22, PSR1, RBSP3, SCP3
Prostate cancer, Schizophrenia

1607
Cardiotrophin 1
CT-1, CT1
Cardiomegaly, Cardiomyopathy, Dilated cardiomyopathy, Hypercholesterolemia, Hypertrophic cardiomyopathy, Hypotension, Diabetes mellitus type 2, Myoclonic epilepsy, Kidney disease, Necrosis, Obesity, Psoriasis

1608
Cystathionine gamma-lyase
CGL, CSE
Amino acid metabolism disorder, Crohn disease, Cystathioninuria, Inflammatory bowel disease, Melanoma, Ulcerative colitis

1609
Collagen triple helix repeat containing 1
-
Barrett esophagus

1610
Cap binding complex dependent translation initiation factor
Gm672, KIAA0427
Androgenetic alopecia, Aortic disease, Eczema, Colorectal cancer, Crohn disease, Gout, Inflammatory bowel disease, Migraine, Rheumatoid arthritis, Scoliosis, Diabetes mellitus type 2, Ulcerative colitis