Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Showing genes starting with "C"

1241 to 1250 of 1338 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1241	9134	CCNE2	Cyclin E2	CYCE2	Carcinoma of the head and neck, Endometrioma, Endometriosis, Malignant mesothelioma, Sclerocystic ovaries, Polycystic ovary syndrome
1242	914	CD2	CD2 molecule	LFA-2, SRBC, T11	Breast cancer, Hypothyroidism, Nephrotic syndrome, Rheumatoid arthritis
1243	915	CD3D	CD3 delta subunit of T-cell receptor complex	CD3-DELTA, CD3DELTA, IMD19, T3D	Anorexia, Bare lymphocyte syndrome, Biliary cirrhosis, Dermatitis, Eosinophilia, Exfoliative dermatitis, Immunodeficiency, Immunologic deficiency syndromes, Lymphopenia, Omenn syndrome, Otitis media, Biliary cholangitis, Severe combined immunodeficiency disease
1244	9150	CTDP1	CTD phosphatase subunit 1	CCFDN, FCP1	Acquired kyphoscoliosis, Cataract, Cerebral atrophy, Cerebral cortical atrophy, Charcot-marie-tooth disease, Congenital cataracts, facial dysmorphism, and neuropathy, Congenital clubfoot, Congenital genu recurvatum, Congenital kyphoscoliosis, Developmental delay, Dwarfism, Hypoglycemia, Hypogonadism, Hypogonadotropic hypogonadism, Impaired cognition View all (10 more)
1245	91522	COL23A1	Collagen type XXIII alpha 1 chain	-	Leukemia, Prostate cancer, Prostate cancer, hereditary
1246	916	CD3E	CD3 epsilon subunit of T-cell receptor complex	CD3epsilon, IMD18, T3E, TCRE	Anorexia, Antibody deficiency syndrome, Bare lymphocyte syndrome, Eosinophilia, Exfoliative dermatitis, Gastrointestinal stromal tumor, Immunodeficiency, Immunodeficiency, scid variant, Immunologic deficiency syndromes, Omenn syndrome, Otitis media, Rheumatoid arthritis, Severe combined immunodeficiency disease
1247	9167	COX7A2L	Cytochrome c oxidase subunit 7A2 like	COX7AR, COX7RP, EB1, SCAF1, SCAFI, SIG81	Ischemic stroke, Stroke, Thrombosis
1248	917	CD3G	CD3 gamma subunit of T-cell receptor complex	CD3-GAMMA, CD3GAMMA, IMD17, T3G	Eczema, Immunodeficiency, Immunologic deficiency syndromes, Otitis media, Severe combined immunodeficiency disease
1249	91768	CABLES1	Cdk5 and Abl enzyme substrate 1	CABL1, CABLES, HsT2563, IK3-1	Bipolar disorder, Breast carcinoma, Colorectal cancer, Colorectal neoplasms, Lung adenocarcinoma, Schizoaffective disorder, Schizophrenia
1250	91851	CHRDL1	Chordin like 1	CHL, MGC1, MGCN, NRLN1, VOPT, dA141H5.1	Arcus senilis, Astigmatism, Cataract, Congenital keratoglobus, Coronary heart disease, Glaucoma, Iridodonesis, Lens subluxation, Miosis disorder, Mosaic corneal dystrophy

«««...123 124125126 127...»»»