Sequence of PLOD2_HUMAN

procollagen-lysine 5-dioxygenase

O00469

737

84686

75935

Valtavaara M.,Papponen H.,Pirttila A.M.,Hiltunen K.,Helander H.,Myllylae R.

Cloning and characterization of a novel human lysyl hydroxylase isoform highly expressed in pancreas and muscle.

J. Biol. Chem.

272

6831-6834

1997

75936

Ota T.,Suzuki Y.,Nishikawa T.,Otsuki T.,Sugiyama T.,Irie R.,Wakamatsu A.,Hayashi K.,Sato H.,Nagai K.,Kimura K.,Makita H.,Sekine M.,Obayashi M.,Nishi T.,Shibahara T.,Tanaka T.,Ishii S.,Yamamoto J.,Saito K.,Kawai Y.,Isono Y.,Nakamura Y.,Nagahari K.,Murakami K.,Yasuda T.,Iwayanagi T.,Wagatsuma M.,Shiratori A.,Sudo H.,Hosoiri T.,Kaku Y.,Kodaira H.,Kondo H.,Sugawara M.,Takahashi M.,Kanda K.,Yokoi T.,Furuya T.,Kikkawa E.,Omura Y.,Abe K.,Kamihara K.,Katsuta N.,Sato K.,Tanikawa M.,Yamazaki M.,Ninomiya K.,Ishibashi T.,Yamashita H.,Murakawa K.,Fujimori K.,Tanai H.,Kimata M.,Watanabe M.,Hiraoka S.,Chiba Y.,Ishida S.,Ono Y.,Takiguchi S.,Watanabe S.,Yosida M.,Hotuta T.,Kusano J.,Kanehori K.,Takahashi-Fujii A.,Hara H.,Tanase T.-O.,Nomura Y.,Togiya S.,Komai F.,Hara R.,Takeuchi K.,Arita M.,Imose N.,Musashino K.,Yuuki H.,Oshima A.,Sasaki N.,Aotsuka S.,Yoshikawa Y.,Matsunawa H.,Ichihara T.,Shiohata N.,Sano S.,Moriya S.,Momiyama H.,Satoh N.,Takami S.,Terashima Y.,Suzuki O.,Nakagawa S.,Senoh A.,Mizoguchi H.,Goto Y.,Shimizu F.,Wakebe H.,Hishigaki H.,Watanabe T.,Sugiyama A.,Takemoto M.,Kawakami B.,Yamazaki M.,Watanabe K.,Kumagai A.,Itakura S.,Fukuzumi Y.,Fujimori Y.,Komiyama M.,Tashiro H.,Tanigami A.,Fujiwara T.,Ono T.,Yamada K.,Fujii Y.,Ozaki K.,Hirao M.,Ohmori Y.,Kawabata A.,Hikiji T.,Kobatake N.,Inagaki H.,Ikema Y.,Okamoto S.,Okitani R.,Kawakami T.,Noguchi S.,Itoh T.,Shigeta K.,Senba T.,Matsumura K.,Nakajima Y.,Mizuno T.,Morinaga M.,Sasaki M.,Togashi T.,Oyama M.,Hata H.,Watanabe M.,Komatsu T.,Mizushima-Sugano J.,Satoh T.,Shirai Y.,Takahashi Y.,Nakagawa K.,Okumura K.,Nagase T.,Nomura N.,Kikuchi H.,Masuho Y.,Yamashita R.,Nakai K.,Yada T.,Nakamura Y.,Ohara O.,Isogai T.,Sugano S.

Complete sequencing and characterization of 21,243 full-length human cDNAs.

Nat. Genet.

36

40-45

2004

75938

Muzny D.M.,Scherer S.E.,Kaul R.,Wang J.,Yu J.,Sudbrak R.,Buhay C.J.,Chen R.,Cree A.,Ding Y.,Dugan-Rocha S.,Gill R.,Gunaratne P.,Harris R.A.,Hawes A.C.,Hernandez J.,Hodgson A.V.,Hume J.,Jackson A.,Khan Z.M.,Kovar-Smith C.,Lewis L.R.,Lozado R.J.,Metzker M.L.,Milosavljevic A.,Miner G.R.,Morgan M.B.,Nazareth L.V.,Scott G.,Sodergren E.,Song X.-Z.,Steffen D.,Wei S.,Wheeler D.A.,Wright M.W.,Worley K.C.,Yuan Y.,Zhang Z.,Adams C.Q.,Ansari-Lari M.A.,Ayele M.,Brown M.J.,Chen G.,Chen Z.,Clendenning J.,Clerc-Blankenburg K.P.,Chen R.,Chen Z.,Davis C.,Delgado O.,Dinh H.H.,Dong W.,Draper H.,Ernst S.,Fu G.,Gonzalez-Garay M.L.,Garcia D.K.,Gillett W.,Gu J.,Hao B.,Haugen E.,Havlak P.,He X.,Hennig S.,Hu S.,Huang W.,Jackson L.R.,Jacob L.S.,Kelly S.H.,Kube M.,Levy R.,Li Z.,Liu B.,Liu J.,Liu W.,Lu J.,Maheshwari M.,Nguyen B.-V.,Okwuonu G.O.,Palmeiri A.,Pasternak S.,Perez L.M.,Phelps K.A.,Plopper F.J.,Qiang B.,Raymond C.,Rodriguez R.,Saenphimmachak C.,Santibanez J.,Shen H.,Shen Y.,Subramanian S.,Tabor P.E.,Verduzco D.,Waldron L.,Wang J.,Wang J.,Wang Q.,Williams G.A.,Wong G.K.-S.,Yao Z.,Zhang J.,Zhang X.,Zhao G.,Zhou J.,Zhou Y.,Nelson D.,Lehrach H.,Reinhardt R.,Naylor S.L.,Yang H.,Olson M.,Weinstock G.,Gibbs R.A.

The DNA sequence, annotation and analysis of human chromosome 3.

Nature

440

1194-1198

2006

75939

Yeowell H.N.,Walker L.C.

Tissue specificity of a new splice form of the human lysyl hydroxylase 2 gene.

Matrix Biol.

18

179-187

1999

75940

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

Genome Res.

14

2121-2127

2004

75941

Zahedi R.P.,Lewandrowski U.,Wiesner J.,Wortelkamp S.,Moebius J.,Schuetz C.,Walter U.,Gambaryan S.,Sickmann A.

Phosphoproteome of resting human platelets.

J. Proteome Res.

7

526-534

2008

75942

Chen R.,Jiang X.,Sun D.,Han G.,Wang F.,Ye M.,Wang L.,Zou H.

Glycoproteomics analysis of human liver tissue by combination of multiple enzyme digestion and hydrazide chemistry.

J. Proteome Res.

8

651-661

2009

75943

Burkard T.R.,Planyavsky M.,Kaupe I.,Breitwieser F.P.,Buerckstuemmer T.,Bennett K.L.,Superti-Furga G.,Colinge J.

Initial characterization of the human central proteome.

BMC Syst. Biol.

5

17-17

2011

75944

van der Slot A.J.,Zuurmond A.-M.,Bardoel A.F.J.,Wijmenga C.,Pruijs H.E.H.,Sillence D.O.,Brinckmann J.,Abraham D.J.,Black C.M.,Verzijl N.,DeGroot J.,Hanemaaijer R.,TeKoppele J.M.,Huizinga T.W.J.,Bank R.A.

Identification of PLOD2 as telopeptide lysyl hydroxylase, an important enzyme in fibrosis.

J. Biol. Chem.

278

40967-40972

2003

75945

Ha-Vinh R.,Alanay Y.,Bank R.A.,Campos-Xavier A.B.,Zankl A.,Superti-Furga A.,Bonafe L.

Phenotypic and molecular characterization of Bruck syndrome (osteogenesis imperfecta with contractures of the large joints) caused by a recessive mutation in PLOD2.

Am. J. Med. Genet. A

131

115-120

2004

75946

Puig-Hervas M.T.,Temtamy S.,Aglan M.,Valencia M.,Martinez-Glez V.,Ballesta-Martinez M.J.,Lopez-Gonzalez V.,Ashour A.M.,Amr K.,Pulido V.,Guillen-Navarro E.,Lapunzina P.,Caparros-Martin J.A.,Ruiz-Perez V.L.

Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome--osteogenesis imperfecta phenotypic spectrum.

Hum. Mutat.

33

1444-1449

2012

75947

Furey C.G.,Choi J.,Jin S.C.,Zeng X.,Timberlake A.T.,Nelson-Williams C.,Mansuri M.S.,Lu Q.,Duran D.,Panchagnula S.,Allocco A.,Karimy J.K.,Khanna A.,Gaillard J.R.,DeSpenza T.,Antwi P.,Loring E.,Butler W.E.,Smith E.R.,Warf B.C.,Strahle J.M.,Limbrick D.D.,Storm P.B.,Heuer G.,Jackson E.M.,Iskandar B.J.,Johnston J.M.,Tikhonova I.,Castaldi C.,Lopez-Giraldez F.,Bjornson R.D.,Knight J.R.,Bilguvar K.,Mane S.,Alper S.L.,Haider S.,Guclu B.,Bayri Y.,Sahin Y.,Apuzzo M.L.J.,Duncan C.C.,DiLuna M.L.,Guenel M.,Lifton R.P.,Kahle K.T.

De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus.

Neuron

99

302-0

2018