Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2411 to 2420 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2411
CASP8 and FADD like apoptosis regulator
CASH, CASP8AP1, CLARP, Casper, FLAME, FLAME-1, FLAME1, FLIP, I-FLICE, MRIT, c-FLIP, c-FLIPL, c-FLIPR, c-FLIPS, cFLIP
Breast cancer, Lymphocytic leukemia, Hodgkin disease, Leukemia, Lymphoma, Myelodysplastic syndrome, Pancreatic neoplasms

2412
Complement factor properdin
BFD, PFC, PFD, PROPERDIN
Hepatocellular carcinoma, Liver cirrhosis, Stevens-johnson syndrome

2413
CF transmembrane conductance regulator
ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR, dJ760C5.1
Asthma, Autism, Hereditary chronic pancreatitis, Polycystic kidney disease, Azoospermia, Barrett esophagus, Bronchiectasis, Cholecystolithiasis, Obstructive airway disease, Sinusitis, Colorectal neoplasms, Congenital bilateral absence of vas deferens, Connective tissue disease, Coronary artery disease, Cystic fibrosis
View all (15 more)

2414
Glycoprotein hormones, alpha polypeptide
CG-ALPHA, FSHA, GPA1, GPHA1, GPHa, HCG, LHA, TSHA
Atrial fibrillation, Hemiplegia, Ovarian diseases, Follicular thyroid cancer, Uterine polyp

2415
Chorionic gonadotropin subunit beta 1
-
Astrocytoma, Autism, Central nervous system cancer, Glioma

2416
Chorionic gonadotropin subunit beta 3
CGB, CGB5, CGB7, CGB8, LHB, hCGB
Hypogonadism

2417
Chorionic gonadotropin subunit beta 5
CGB, HCG, hCGB
Polycystic ovary syndrome

2418
CGG triplet repeat binding protein 1
CGGBP, p20-CGGBP
Attention deficit hyperactivity disorder, Major depressive disorder, Metabolic syndrome, Orofacial cleft, Substance abuse, Diabetes mellitus type 2

2419
Cingulin
-
Autism, Color vision deficiency, Venous thromboembolism

2420
Cingulin like 1
JACOP, PCING
Atrial fibrillation, Autism, Bipolar disorder, Congenital esophageal anomaly, Diabetic neuropathy, Premature ovarian failure, Schizophrenia, Substance abuse, Hypertension, Diabetes mellitus type 2