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Blm
Bloom syndrome homolog (human)
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On chromosome: 7 40.0 cM
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Mus musculus Bloom syndrome homolog (human) (Blm), transcript variant 2.
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Gene sequence:
Proteins coded by this gene:
References:
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Authors
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Title
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Journal
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Bahr A, De Graeve F, Kedinger C, Chatton B
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Point mutations causing Bloom's syndrome abolish ATPase and DNA helicase activities of the BLM protein.
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Oncogene
Nov. 19, 1998
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Sengupta S, Robles AI, Linke SP, Sinogeeva NI, Zhang R, Pedeux R, Ward IM, Celeste A, Nussenzweig A, Chen J, Halazonetis TD, Harris CC
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Functional interaction between BLM helicase and 53BP1 in a Chk1-mediated pathway during S-phase arrest.
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J Cell Biol
Sept. 13, 2004
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Wang Y, Heddle JA
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Spontaneous and induced chromosomal damage and mutations in Bloom Syndrome mice.
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Mutat Res
Oct. 4, 2004
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Babbe H, Chester N, Leder P, Reizis B
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The Bloom's syndrome helicase is critical for development and function of the alphabeta T-cell lineage.
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Mol Cell Biol
March 1, 2007
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Last modification of this entry: Oct. 6, 2010.
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