"The human COL11A2 gene structure indicates that the gene has not evolved with the genes for the major fibrillar collagens."
Vuoristo M.M. , Pihlajamaa T. , Vandenberg P. , Prockop D.J. , Ala-Kokko L.
J. Biol. Chem.270:22873-22881(1995) [PubMed] [Europe PMC] [Abstract]

"The DNA sequence and analysis of human chromosome 6."
Mungall A.J. , Palmer S.A. , Sims S.K. , Edwards C.A. , Ashurst J.L. , Wilming L. , Jones M.C. , Horton R. , Hunt S.E. , Scott C.E. , Gilbert J.G.R. , Clamp M.E. , Bethel G. , Milne S. , Ainscough R. , Almeida J.P. , Ambrose K.D. , Andrews T.D. , Ashwell R.I.S. , Babbage A.K. , Bagguley C.L. , Bailey J. , Banerjee R. , Barker D.J. , Barlow K.F. , Bates K. , Beare D.M. , Beasley H. , Beasley O. , Bird C.P. , Blakey S.E. , Bray-Allen S. , Brook J. , Brown A.J. , Brown J.Y. , Burford D.C. , Burrill W. , Burton J. , Carder C. , Carter N.P. , Chapman J.C. , Clark S.Y. , Clark G. , Clee C.M. , Clegg S. , Cobley V. , Collier R.E. , Collins J.E. , Colman L.K. , Corby N.R. , Coville G.J. , Culley K.M. , Dhami P. , Davies J. , Dunn M. , Earthrowl M.E. , Ellington A.E. , Evans K.A. , Faulkner L. , Francis M.D. , Frankish A. , Frankland J. , French L. , Garner P. , Garnett J. , Ghori M.J. , Gilby L.M. , Gillson C.J. , Glithero R.J. , Grafham D.V. , Grant M. , Gribble S. , Griffiths C. , Griffiths M.N.D. , Hall R. , Halls K.S. , Hammond S. , Harley J.L. , Hart E.A. , Heath P.D. , Heathcott R. , Holmes S.J. , Howden P.J. , Howe K.L. , Howell G.R. , Huckle E. , Humphray S.J. , Humphries M.D. , Hunt A.R. , Johnson C.M. , Joy A.A. , Kay M. , Keenan S.J. , Kimberley A.M. , King A. , Laird G.K. , Langford C. , Lawlor S. , Leongamornlert D.A. , Leversha M. , Lloyd C.R. , Lloyd D.M. , Loveland J.E. , Lovell J. , Martin S. , Mashreghi-Mohammadi M. , Maslen G.L. , Matthews L. , McCann O.T. , McLaren S.J. , McLay K. , McMurray A. , Moore M.J.F. , Mullikin J.C. , Niblett D. , Nickerson T. , Novik K.L. , Oliver K. , Overton-Larty E.K. , Parker A. , Patel R. , Pearce A.V. , Peck A.I. , Phillimore B.J.C.T. , Phillips S. , Plumb R.W. , Porter K.M. , Ramsey Y. , Ranby S.A. , Rice C.M. , Ross M.T. , Searle S.M. , Sehra H.K. , Sheridan E. , Skuce C.D. , Smith S. , Smith M. , Spraggon L. , Squares S.L. , Steward C.A. , Sycamore N. , Tamlyn-Hall G. , Tester J. , Theaker A.J. , Thomas D.W. , Thorpe A. , Tracey A. , Tromans A. , Tubby B. , Wall M. , Wallis J.M. , West A.P. , White S.S. , Whitehead S.L. , Whittaker H. , Wild A. , Willey D.J. , Wilmer T.E. , Wood J.M. , Wray P.W. , Wyatt J.C. , Young L. , Younger R.M. , Bentley D.R. , Coulson A. , Durbin R.M. , Hubbard T. , Sulston J.E. , Dunham I. , Rogers J. , Beck S. more...
Nature425:805-811(2003) [PubMed] [Europe PMC] [Abstract]

Mural R.J. , Istrail S. , Sutton G.G. , Florea L. , Halpern A.L. , Mobarry C.M. , Lippert R. , Walenz B. , Shatkay H. , Dew I. , Miller J.R. , Flanigan M.J. , Edwards N.J. , Bolanos R. , Fasulo D. , Halldorsson B.V. , Hannenhalli S. , Turner R. , Yooseph S. , Lu F. , Nusskern D.R. , Shue B.C. , Zheng X.H. , Zhong F. , Delcher A.L. , Huson D.H. , Kravitz S.A. , Mouchard L. , Reinert K. , Remington K.A. , Clark A.G. , Waterman M.S. , Eichler E.E. , Adams M.D. , Hunkapiller M.W. , Myers E.W. , Venter J.C. more...
Submitted (2005-07) to the EMBL/GenBank/DDBJ databases

"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res.14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]

"The human alpha 2(XI) collagen gene (COL11A2): completion of coding information, identification of the promoter sequence, and precise localization within the major histocompatibility complex reveal overlap with the KE5 gene."
Lui V.C. , Ng L.J. , Sat E.W. , Cheah K.S.
Genomics32:401-412(1996) [PubMed] [Europe PMC] [Abstract]

"Molecular cloning of PARP (proline/arginine-rich protein) from human cartilage and subsequent demonstration that PARP is a fragment of the NH2-terminal domain of the collagen alpha 2(XI) chain."
Zhidkova N.I. , Brewton R.G. , Mayne R.
FEBS Lett.326:25-28(1993) [PubMed] [Europe PMC] [Abstract]

"The human alpha 2(XI) collagen (COL11A2) chain. Molecular cloning of cDNA and genomic DNA reveals characteristics of a fibrillar collagen with differences in genomic organization."
Kimura T. , Cheah K.S.E. , Chan S.D.H. , Lui V.C.H. , Mattei M.-G. , van der Rest M. , Ono K. , Solomon E. , Ninomiya Y. , Olsen B.R.
J. Biol. Chem.264:13910-13916(1989) [PubMed] [Europe PMC] [Abstract]

"Alternative mRNA processing occurs in the variable region of the pro-alpha 1(XI) and pro-alpha 2(XI) collagen chains."
Zhidkova N.I. , Justice S.K. , Mayne R.
J. Biol. Chem.270:9486-9493(1995) [PubMed] [Europe PMC] [Abstract]

"Autosomal recessive disorder otospondylomegaepiphyseal dysplasia is associated with loss-of-function mutations in the COL11A2 gene."
Melkoniemi M. , Brunner H.G. , Manouvrier S. , Hennekam R.C.M. , Superti-Furga A. , Kaeaeriaeinen H. , Pauli R.M. , van Essen T. , Warman M.L. , Bonaventure J. , Miny P. , Ala-Kokko L.
Am. J. Hum. Genet.66:368-377(2000) [PubMed] [Europe PMC] [Abstract]

"Mutations in fibrillar collagens (types I, II, III, and XI), fibril-associated collagen (type IX), and network-forming collagen (type X) cause a spectrum of diseases of bone, cartilage, and blood vessels."
Kuivaniemi H. , Tromp G. , Prockop D.J.
Hum. Mutat.9:300-315(1997) [PubMed] [Europe PMC] [Abstract]

"Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2."
Tompson S.W. , Faqeih E.A. , Ala-Kokko L. , Hecht J.T. , Miki R. , Funari T. , Funari V.A. , Nevarez L. , Krakow D. , Cohn D.H.
Am. J. Med. Genet. A158:309-314(2012) [PubMed] [Europe PMC] [Abstract]

"Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus."
Vikkula M. , Mariman E.C.M. , Lui V.C.H. , Zhidkova N.I. , Tiller G.E. , Goldring M.B. , van Beersum S.E.C. , de Waal Malefijt M.C. , van den Hoogen F.H.J. , Ropers H.-H. , Mayne R. , Cheah K.S.E. , Olsen B.R. , Warman M.L. , Brunner H.G.
Cell80:431-437(1995) [PubMed] [Europe PMC] [Abstract]

"Genetic mapping of ossification of the posterior longitudinal ligament of the spine."
Koga H. , Sakou T. , Taketomi E. , Hayashi K. , Numasawa T. , Harata S. , Yone K. , Matsunaga S. , Otterud B. , Inoue I. , Leppert M.
Am. J. Hum. Genet.62:1460-1467(1998) [PubMed] [Europe PMC] [Abstract]

"Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymueller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome)."
Pihlajamaa T. , Prockop D.J. , Faber J. , Winterpacht A. , Zabel B. , Giedion A. , Wiesbauer P. , Spranger J. , Ala-Kokko L.
Am. J. Med. Genet.80:115-120(1998) [PubMed] [Europe PMC] [Abstract]

"Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha-2(XI) chain of type XI collagen."
Sirko-Osadsa D.A. , Murray M.A. , Scott J.A. , Lavery M.A. , Warman M.L. , Robin N.H.
J. Pediatr.132:368-371(1998) [PubMed] [Europe PMC] [Abstract]

"Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)."
McGuirt W.T. , Prasad S.D. , Griffith A.J. , Kunst H.P.M. , Green G.E. , Shpargel K.B. , Runge C. , Huybrechts C. , Mueller R.F. , Lynch E. , King M.-C. , Brunner H.G. , Cremers C.W.R.J. , Takanosu M. , Li S.-W. , Arita M. , Mayne R. , Prockop D.J. , Van Camp G. , Smith R.J.H. more...
Nat. Genet.23:413-419(1999) [PubMed] [Europe PMC] [Abstract]

"Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus."
Chen W. , Kahrizi K. , Meyer N.C. , Riazalhosseini Y. , Van Camp G. , Najmabadi H. , Smith R.J.H.
J. Med. Genet.42:E61-E61(2005) [PubMed] [Europe PMC] [Abstract]