[1]
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NUCLEOTIDE SEQUENCE [MRNA], FUNCTION, SUBUNIT, SUBCELLULAR LOCATION, AND VARIANTS ALA-879 AND ARG-2188.
PubMed=11171385 [NCBI, ExPASy, EBI, Israel, Japan]
Li Q.,
Hansen D.,
Killilea A.,
Joshi H.C.,
Palazzo R.E.,
Balczon R.;
"Kendrin/pericentrin-B, a centrosome protein with homology to pericentrin that complexes with PCM-1.";
J. Cell Sci. 114:797-809(2001).
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[2]
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NUCLEOTIDE SEQUENCE [MRNA], AND VARIANT VAL-1038.
Gromley A.S.,
Jurczyk A.,
Sillibourne J.E.,
Halilovic E.,
Doxsey S.J.;
"Vertebrate centrosome proteins that share homology with yeast mitotic exit proteins are required for cytokinesis and cell cycle progression.";
Submitted (MAY-2002) to the EMBL/GenBank/DDBJ databases.
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[3]
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NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 20-3336.
TISSUE=Brain;
DOI=10.1093/dnares/4.5.307; PubMed=9455477 [NCBI, ExPASy, EBI, Israel, Japan]
Ishikawa K.,
Nagase T.,
Nakajima D.,
Seki N.,
Ohira M.,
Miyajima N.,
Tanaka A.,
Kotani H.,
Nomura N.,
Ohara O.;
"Prediction of the coding sequences of unidentified human genes. VIII. 78 new cDNA clones from brain which code for large proteins in vitro.";
DNA Res. 4:307-313(1997).
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[4]
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SEQUENCE REVISION TO 3023.
DOI=10.1093/dnares/9.3.99; PubMed=12168954 [NCBI, ExPASy, EBI, Israel, Japan]
Nakajima D.,
Okazaki N.,
Yamakawa H.,
Kikuno R.,
Ohara O.,
Nagase T.;
"Construction of expression-ready cDNA clones for KIAA genes: manual curation of 330 KIAA cDNA clones.";
DNA Res. 9:99-106(2002).
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[5]
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SEQUENCE REVISION.
Ohara O.;
Submitted (AUG-2003) to the EMBL/GenBank/DDBJ databases.
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[6]
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NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 787-1533.
TISSUE=Trachea;
DOI=10.1038/ng1285; PubMed=14702039 [NCBI, ExPASy, EBI, Israel, Japan]
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).
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[7]
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FUNCTION, SUBCELLULAR LOCATION, TISSUE SPECIFICITY, CALMODULIN-BINDING DOMAIN, AND MUTAGENESIS OF 3196-PHE-ARG-3197; VAL-3203 AND 3208-ARG-LEU-3209.
DOI=10.1073/pnas.97.11.5919; PubMed=10823944 [NCBI, ExPASy, EBI, Israel, Japan]
Flory M.R.,
Moser M.J.,
Monnat R.J. Jr.,
Davis T.N.;
"Identification of a human centrosomal calmodulin-binding protein that shares homology with pericentrin.";
Proc. Natl. Acad. Sci. U.S.A. 97:5919-5923(2000).
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[8]
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PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-1703, AND MASS SPECTROMETRY.
TISSUE=Epithelium;
DOI=10.1073/pnas.0507066103; PubMed=16565220 [NCBI, ExPASy, EBI, Israel, Japan]
Nousiainen M.,
Sillje H.H.W.,
Sauer G.,
Nigg E.A.,
Koerner R.;
"Phosphoproteome analysis of the human mitotic spindle.";
Proc. Natl. Acad. Sci. U.S.A. 103:5391-5396(2006).
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[9]
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INVOLVEMENT IN SCKL4.
DOI=10.1038/ng.2007.80; PubMed=18157127 [NCBI, ExPASy, EBI, Israel, Japan]
Griffith E.,
Walker S.,
Martin C.-A.,
Vagnarelli P.,
Stiff T.,
Vernay B.,
Al Sanna N.,
Saggar A.,
Hamel B.,
Earnshaw W.C.,
Jeggo P.A.,
Jackson A.P.,
O'Driscoll M.;
"Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling.";
Nat. Genet. 40:232-236(2008).
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[10]
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INVOLVEMENT IN MOPD2.
DOI=10.1126/science.1151174; PubMed=18174396 [NCBI, ExPASy, EBI, Israel, Japan]
Rauch A.,
Thiel C.T.,
Schindler D.,
Wick U.,
Crow Y.J.,
Ekici A.B.,
van Essen A.J.,
Goecke T.O.,
Al-Gazali L.,
Chrzanowska K.H.,
Zweier C.,
Brunner H.G.,
Becker K.,
Curry C.J.,
Dallapiccola B.,
Devriendt K.,
Doerfler A.,
Kinning E.,
Megarbane A., ![]()
Meinecke P.,
Semple R.K.,
Spranger S.,
Toutain A.,
Trembath R.C.,
Voss E.,
Wilson L.,
Hennekam R.,
de Zegher F.,
Doerr H.-G.,
Reis A.;
"Mutations in the pericentrin (PCNT) gene cause primordial dwarfism.";
Science 319:816-819(2008).
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