| 1 | ARCN1, MGMD
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| ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects.
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| Izumi K, Brett M, Nishi E, Drunat S, Tan ES, Fujiki K, Lebon S, Cham B, Masuda K, Arakawa M, Jacquinet A, Yamazumi Y, Chen ST, Verloes A, Okada Y, Katou Y, Nakamura T, Akiyama T, Gressens P, Foo R, Passemard S, Tan EC, El Ghouzzi V, Shirahige K.
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| Am J Hum Genet 99(2):451-9. doi: 10.1016/j.ajhg.2016.06.011. Epub 2016 Jul 28.
2016
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| 2 | ARCN1
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| Fine mapping of a region of chromosome 11q23.3 reveals independent locus associated with risk of glioma.
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| Chen H, Sun B, Zhao Y, Song X, Fan W, Zhou K, Zhou L, Mao Y, Lu D.
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| PLoS One 7(12):e52864. doi: 10.1371/journal.pone.0052864. Epub 2012 Dec 31.
2012
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| 3 | ARCN1
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| Mutation in archain 1, a subunit of COPI coatomer complex, causes diluted coat color and Purkinje cell degeneration.
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| Xu X, Kedlaya R, Higuchi H, Ikeda S, Justice MJ, Setaluri V, Ikeda A.
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| PLoS Genet 6(5):e1000956.
2010
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| 4 | ARCN1
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| Mutation in archain 1, a subunit of COPI coatomer complex, causes diluted coat color and Purkinje cell degeneration.
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| Xu X, Kedlaya R, Higuchi H, Ikeda S, Justice MJ, Setaluri V, Ikeda A.
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| PLoS Genet 6(5):e1000956. doi: 10.1371/journal.pgen.1000956.
2010
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| 5 | ARCN1
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| The coatomer protein delta-COP, encoded by the archain gene, is conserved across diverse eukaryotes.
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| Tunnacliffe A, van de Vrugt H, Pensotti V, Radice P.
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| Mamm Genome 7(10):784-6. No abstract available. 1996
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| 6 | ARCN1
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| The human archain gene, ARCN1, has highly conserved homologs in rice and drosophila.
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| Radice P, et al.
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| Genomics 26 : 101-106. 1995
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| 7 | ARCN1
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| The ARF1 GTPase-activating protein: zinc finger motif and Golgi complex localization.
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| Cukierman E, Huber I, Rotman M, Cassel D.
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| Science 270(5244):1999-2002.PMID: 8533093 1995
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