Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2811 to 2820 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2811
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

2812
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

2813
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

2814
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

2815
Collectin subfamily member 12
CLP1, NSR2, SCARA4, SRCL
Dementia, Metabolic syndrome, Obesity, Schizophrenia, Diabetes mellitus type 2

2816
Collagen beta(1-O)galactosyltransferase 1
BSVD3, ColGalT 1, GLT25D1
Brain small vessel disease, Vascular dementia

2817
Collagen beta(1-O)galactosyltransferase 2
C1orf17, ColGalT 2, GLT25D2
Tourette syndrome, Osteoarthritis, Preeclampsia, Diabetes mellitus type 2

2818
Collagen like tail subunit of asymmetric acetylcholinesterase
CMS5, EAD
Alzheimer disease, Congenital myasthenic syndrome, Digestive system disease, Diverticular disease, Diverticulitis, Myasthenic syndrome, Pancreatic cancer

2819
Copper metabolism domain containing 1
C2orf5, MURR1
Alzheimer disease, Color vision deficiency, Copper overload cirrhosis, Coronary artery disease, Hypersensitivity, Liver cirrhosis, Nonalcoholic fatty liver disease, Parkinson disease, Proliferative diabetic retinopathy

2820
COMM domain containing 10
PTD002
Amyotrophic lateral sclerosis, Asthma, Bipolar disorder, Central nervous system cancer, Kidney disease, Obstructive pulmonary disease, Color vision deficiency, Glioblastoma, Glioma, Granulomatosis with polyangiitis, Kidney failure, Major depressive disorder, Neurotic disorder, Schizophrenia