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"
1321 to 1330 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1321
Collagen type VII alpha 1 chain
EBD1, EBDCT, EBR1, NDNC8
Dystrophic epidermolysis bullosa, Amelogenesis imperfecta, Anonychia, Breast neoplasms, Non-small-cell lung carcinoma, Colorectal neoplasms, Dominant dystrophic epidermolysis bullosa with absence of skin, Dominant dystrophic epidermolysis bullosa, albopapular type, Duane retraction syndrome, Nail dystrophy, Epidermal nevus, Epidermolysis bullosa, Junctional epidermolysis bullosa, Gout, Hallopeau siemens disease
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1322
Collagen type VIII alpha 1 chain
C3orf7
Atrophic macular degeneration, Breast cancer, Kidney disease, Obstructive pulmonary disease, Congenital abnormalities, Glaucoma, Heart failure, Open angle glaucoma, Age-related macular degeneration

1323
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

1324
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

1325
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

1326
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

1327
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

1328
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

1329
Collectin subfamily member 12
CLP1, NSR2, SCARA4, SRCL
Dementia, Metabolic syndrome, Obesity, Schizophrenia, Diabetes mellitus type 2

1330
Collagen beta(1-O)galactosyltransferase 1
BSVD3, ColGalT 1, GLT25D1
Brain small vessel disease, Vascular dementia