| 1 | ACPS1, MEGF8
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| Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization.
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| Twigg SR, Lloyd D, Jenkins D, Elçioglu NE, Cooper CD, Al-Sannaa N, Annagür A, Gillessen-Kaesbach G, Hüning I, Knight SJ, Goodship JA, Keavney BD, Beales PL, Gileadi O, McGowan SJ, Wilkie AO.
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| Am J Hum Genet 91(5):897-905. doi: 10.1016/j.ajhg.2012.08.027. Epub 2012 Oct 11.
2012
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| 2 | MEGF8
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| Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy.
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| Zhang Z, Alpert D, Francis R, Chatterjee B, Yu Q, Tansey T, Sabol SL, Cui C, Bai Y, Koriabine M, Yoshinaga Y, Cheng JF, Chen F, Martin J, Schackwitz W, Gunn TM, Kramer KL, De Jong PJ, Pennacchio LA, Lo CW.
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| Proc Natl Acad Sci U S A 106(9):3219-24. Epub 2009 Feb 13.
2009
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| 3 | FAT2, CELSR3, CELSR2, MEGF6, MEGF8, MEGF9, LRP4, SLIT1, SLIT3
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| Identification of high-molecular-weight proteins with multiple EGF-like motifs by motif-trap screening.
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| Nakayama M, Nakajima D, Nagase T, Nomura N, Seki N, Ohara O.
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| Genomics 51(1):27-34. 1998
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