Leprecan

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leucine proline-enriched proteoglycan (leprecan) 1
Identifiers
Symbol	LEPRE1
Entrez	64175
HUGO	19316
OMIM	610339
RefSeq	NM_022356
UniProt	Q32P28
Other data
Locus	Chr. 1 p34.1

Leprecan is a protein associated with osteogenesis imperfecta^[1] type VIII.

References

↑ Cabral WA, Chang W, Barnes AM, et al (March 2007). "Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta". Nat. Genet. 39 (3): 359–65. doi:10.1038/ng1968. PMID 17277775.

Fibril forming	type I COL1A1 COL1A2 type II (COL2A1) type III type V COL5A1 COL5A2 COL5A3 COL24A1 COL26A1

Other	FACIT: type IX COL9A1 COL9A2 COL9A3 type XII (COL12A1) COL14A1 COL16A1 COL19A1 COL20A1 COL21A1 COL22A1 basement membrane: type IV COL4A1 COL4A2 COL4A3 COL4A4 COL4A5 COL4A6 multiplexin: COL15A1 type XVIII COL18A1 Endostatin transmembrane: COL13A1 COL17A1 COL23A1 COL25A1 other: type VI COL6A1 COL6A2 COL6A3 COL6A5 type VII (COL7A1) type VIII COL8A1 COL8A2 type X (COL10A1) type XI COL11A1 COL11A2 COL27A1 COL28A1

Enzymes	Prolyl hydroxylase/Lysyl hydroxylase Cartilage associated protein/Leprecan ADAMTS2 Procollagen peptidase Lysyl oxidase

Other

See also: diseases B proteins: BY STRUCTURE: membrane, globular (en, ca, an), fibrous

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