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"
1331 to 1340 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1331
Collagen type VIII alpha 2 chain
FECD, FECD1, PPCD, PPCD2
Alzheimer disease, Corneal dystrophy, Fuchs endothelial dystrophy, Hereditary corneal dystrophy, Keratoconus, Open angle glaucoma, Polymorphous corneal dystrophy, Posterior polymorphous corneal dystrophy

1332
Collagen type IX alpha 1 chain
DJ149L1.1.2, EDM6, MED, STL4
Stickler syndrome, Congenital cartilage disorder, Connective tissue disease, Desbuquois syndrome, Epiphyseal dysplasia, Hearing impairment, Marshall syndrome, Myopia, Optic atrophy, Osteoarthritis, Osteochondrodysplasias, Retinitis pigmentosa, Hearing loss

1333
Collagen type IX alpha 2 chain
DJ39G22.4, EDM2, MED, STL5
Stickler syndrome, Congenital cartilage disorder, Connective tissue disease, Desbuquois syndrome, Epiphyseal dysplasia, Intellectual developmental disorder, Intervertebral disc disease, Marshall syndrome, Meniere disease, Osteochondrodysplasias, Retinitis pigmentosa

1334
Collagen type IX alpha 3 chain
DJ885L7.4.1, EDM3, IDD, MED, STL6
Stickler syndrome, Congenital cartilage disorder, Connective tissue disease, Desbuquois syndrome, Epiphyseal dysplasia, Hearing impairment, Hearing loss, Intervertebral disc disease, Marshall syndrome, Osteochondrodysplasias, Retinal detachment, Nonsyndromic hearing loss

1335
Collectin subfamily member 10
3MC3, CL-10, CL-34, CLL1
3mc syndrome, Asthma, Basal cell carcinoma, Bone disease, Hepatocellular carcinoma, Craniofacial ulnar renal syndrome, Juvenile idiopathic arthritis, Keratinocyte carcinoma, Malpuech facial clefting syndrome, Nasal polyp, Psoriasis, Diabetes mellitus type 1, Diabetes mellitus type 2

1336
Collectin subfamily member 11
3MC2, CL-11, CL-K1-I, CL-K1-II, CL-K1-IIa, CL-K1-IIb, CLK1
3mc syndrome, Carnevale syndrome, Coronary artery disease, Craniofacial abnormalities, Craniofacial ulnar renal syndrome, Desbuquois syndrome, Malpuech facial clefting syndrome, Metabolic syndrome, Oculopalatosekeletal syndrome, Diabetes mellitus type 2

1337
Collectin subfamily member 12
CLP1, NSR2, SCARA4, SRCL
Dementia, Liver cirrhosis, Metabolic syndrome, Obesity, Schizophrenia, Diabetes mellitus type 2

1338
Collagen beta(1-O)galactosyltransferase 1
BSVD3, ColGalT 1, GLT25D1
Brain small vessel disease, Vascular dementia

1339
Collagen beta(1-O)galactosyltransferase 2
C1orf17, ColGalT 2, GLT25D2
Tourette syndrome, Osteoarthritis, Preeclampsia, Diabetes mellitus type 2

1340
Collagen like tail subunit of asymmetric acetylcholinesterase
CMS5, EAD
Alzheimer disease, Congenital myasthenic syndrome, Digestive system disease, Diverticular disease, Diverticulitis, Myasthenic syndrome, Pancreatic cancer