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| '''Type''' || '''Notes''' || '''Gene(s)''' || '''[[Collagen disease|Disorders]]'''
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| [[Type-I collagen|I]] || This is the most abundant collagen of the human body. It is present in [[scar]] tissue, the end product when tissue [[healing|heals]] by repair. It is found in [[tendon]]s, skin, artery walls, cornea, the [[endomysium]] surrounding muscle fibers, fibrocartilage, and the organic part of bones and teeth. || [[COL1A1]], [[COL1A2]] || [[Osteogenesis imperfecta]], [[Ehlers–Danlos syndrome]], [[infantile cortical hyperostosis]] a.k.a. Caffey's disease
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| [[Type-II collagen|II]] || [[Hyaline cartilage]], makes up 50% of all cartilage protein. [[Vitreous humour]] of the eye. || [[COL2A1]] || [[Collagenopathy, types II and XI]]
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| [[Type-III collagen|III]] || This is the collagen of [[granulation tissue]] and is produced quickly by young fibroblasts before the tougher type I collagen is synthesized. [[Reticular fiber]]. Also found in artery walls, skin, intestines and the uterus || [[COL3A1]] || [[Ehlers–Danlos syndrome]], [[Dupuytren's contracture]]
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| [[Type-IV collagen|IV]] || [[Basal lamina]]; [[eye lens]]. Also serves as part of the filtration system in [[capillaries]] and the [[Glomerulus (kidney)|glomeruli]] of [[nephron]] in the [[kidney]]. || [[Collagen, type IV, alpha 1|COL4A1]], [[COL4A2]], [[COL4A3]], [[COL4A4]], [[COL4A5]], [[COL4A6]] || [[Alport syndrome]], [[Goodpasture's syndrome]]
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| V || Most interstitial tissue, assoc. with type I, associated with [[placenta]] || [[COL5A1]], [[COL5A2]], [[COL5A3]] || [[Ehlers–Danlos syndrome]] (classical)
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| VI || Most interstitial tissue, assoc. with type I || [[COL6A1]], [[COL6A2]], [[COL6A3]], [[COL6A5]] || [[Ulrich myopathy]], [[Bethlem myopathy]], [[atopic dermatitis]]
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| VII || Forms [[anchoring fibril]]s in [[dermoepidermal junction]]s || [[COL7A1]] || [[Epidermolysis bullosa dystrophica]]
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| VIII || Some [[endothelium|endothelial]] cells || [[COL8A1]], [[COL8A2]] || [[Posterior polymorphous corneal dystrophy 2]]
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| IX || [[FACIT collagen]], cartilage, assoc. with type II and XI fibrils || [[COL9A1]], [[COL9A2]], [[COL9A3]] || [[EDM2]] and [[EDM3]]
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| X || [[Hypertrophic]] and [[Mineralization (biology)|mineralizing]] cartilage || [[COL10A1]] || [[Schmid metaphyseal dysplasia]]
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| XI || Cartilage || [[COL11A1]], [[COL11A2]] || [[Collagenopathy, types II and XI]]
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| XII || [[FACIT collagen]], interacts with type I containing fibrils, [[decorin]] and glycosaminoglycans || [[COL12A1]] || –
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| XIII || Transmembrane collagen, interacts with integrin a1b1, [[fibronectin]] and components of basement membranes like [[nidogen]] and [[perlecan]]. || [[COL13A1]] || –
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| XIV|| [[FACIT collagen]], also known as undulin || [[COL14A1]] || –
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| XV || – || [[COL15A1]] || –
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| XVI || [[FACIT collagen]] || [[COL16A1]] || –
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| [[Collagen XVII|XVII]] || Transmembrane collagen, also known as BP180, a 180 kDa protein || [[COL17A1]] || [[Bullous pemphigoid]] and certain forms of junctional [[epidermolysis bullosa]]
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| [[Type XVIII collagen|XVIII]] || Source of [[endostatin]] || [[COL18A1]] || –
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| XIX || [[FACIT collagen]] || [[COL19A1]] || –
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| XX || – || [[COL20A1]] || –
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| XXI || [[FACIT collagen]] || [[COL21A1]] || –
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| XXII || [[FACIT collagen]] || [[COL22A1]] || –
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| [[Collagen, type XXIII, alpha 1|XXIII]] || MACIT collagen || [[COL23A1]] || –
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| XXIV || – || [[COL24A1]] || –
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| XXV || – || [[COL25A1]] || –
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| XXVI || – || [[EMID2]] || –
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| XXVII || – || [[COL27A1]] || –
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| XXVIII || – || [[COL28A1]] || –
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| XXIX || Epidermal collagen || [[COL29A1]] || Atopic dermatitis
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Translations:Collagen/37/en - Revision history

FuzzyBot: Importing a new version from external source